Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
CA 02497803 2000-06-29
WO Ol/00117 PCT/US00/17936
DISPOSABLE ARTICLE HAVING SENSOR TO DETECT
IMPENT-ING ELIMINATION OF BODILY WASTE
s
io
FIELD OF THE INVENTION
is The present invention relates to disposable articles and, more
particularly, to
disposable articles having a sensor adapted to detect an input that correlates
to an
impending elimination of 'bodily waste and to provide a signal to the wearer
of the article
of such impending event.
20 BACK,GROUND OF THE INVENTION
Today, disposable articles, such as diapers, pants-type diapers, training
pants,
adult incontinence briefs, sanitary napkins and tampons, are widely used in
infant and
toddler care and in the care of incontinent adults as a means of containing,
isolating and
disposing of bodily wastes. These articles have generally replaced reusable,
washable
zs cloth garments as the preferred means for these applications because of
their convenience
and reliability. The disposable articles respond to a defecation, urination or
discharge
event by absorbing or containing bodily wastes deposited on the article. Some
disposable
articles also signal a defe;cation, urination or discharge event after it has
occurred (e.g.,
wetness indicators, temperature change detection). The articles, however, do
not predict
30 when an event is about to occur and prepare the artiele, wearer or
caregiver for the
occurrence of the predictei event. Current disposable articles have absorbent
material in
a conftguration ready for use at the time of application to the wearer or have
a
configuration that does not become available until the time of a discharge of
bodily waste
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
or shortly thereafter. Bameir cuffs, for example, are in position when the
article is applied
to the wearer. Signaling devices such as thermal or visual indicators or
nocturnal enuresis
alarms signal a urination event only afler the urination has begun. For
example, known
potty training devices, however, detect and signal the wearer once the
defecation or
s urination has begun and do not give the wearer the ability to get to the
bathroom in time
to prevent an accident or beciwetting.
SiJMMARY OF THE INVENTION
The present invention is directed to a disposable article to be fitted to a
wearer.
The disposable article preferably comprises a sensor operatively connected to
the article.
The sensor is adapted to detect electrical activity in the wearer's smooth
colonic muscles,
abdominal muscles, muscles surrounding the wearer's bladder or muscles
surrounding the
wearer's rectum which correlates to an impending elimination of bodily waste
and to
provide a signal to the wearer, a caregiver or an element of the article of
the impending
event.
The present invention also includes an article which includes a sensor adapted
to
detect hen a body cavity of the wearer reaches a predetermined volume and a
signal
mechanism which provides a signal to the wearer, a caregiver or an element of
the article
once the predetermined body cavity volume has been reached.
The invention also iincludes methods for helping an incontinent person achieve
a
temporary contraction of a sphincter muscle by stimulating the muscle in
response to a
detected impending elimination of bodily waste.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a plan view of an article made in accordance with the present
invention
in a flat-out state with portions of the structure being cut-away to more
clearly show the
construction of the article, wherein the article is a diaper.
Figure 2 is a perspective view of a waste bag embodiment of the present
invention.
Figure 3 is a perspective view of one embodiment of a diaper which includes a
waste bag.
2
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WO 01/00117 PCT/US00/17936
Figure 4 shows a diagram of an absorbent article embodiment of the apparatus
of
the present invention.
Figure 5 shows a perspective view of a bodily waste isolation device of the
present
invention in a compressed state before activation.
s Figure 5A shows a sectional view taken along line 5A-5A of Figure 2.
Figures 6A and 6B show an embodiment of a responsive system of the present
invention including an electrically sensitive gel.
Figures 7A, 7B and '7C show a.nother embodiment of a responsive system of the
present invention including a.n electrically sensitive gel.
Figure 8A shows an ideal output function of a discontinuous responsive system
of
the present invention having a single threshold level.
Figure 8B shows an ideal output function of a discontinuous responsive system
of
the present invention having multiple threshold levels.
Figure 9A shows ant exemplary output function of a discontinuous responsive
is system of the present invent:ion along with the first, second and third
derivatives of the
output function.
Figure 9B shows a transfer function of a control system having a series of
first
order lags having an equal time constant.
Figure l 0A shows a block diagrazn of an exemplary open loop responsive
system.
zo Figure lOB shows ,a block diagram of an exemplary closed loop responsive
system.
Figure lOC shows a block diagram of an exemplary open loop responsive system
including a controller.
Figure l OD shows a block diagram of an exemplary closed loop responsive
system
25 including a controller.
Figure 11A is a grap:hical example of an increase in the basal electrical
activity of
an external anal spluncter mi.iscle related to defecation.
Figure 11B is an graphical cxample of a decrease in the basal electrical
activity of
an external anal sphincter muscle related to defecation.
30 Figure 12 shows a diagram of a belt comprising sensors arranged so as to
detect
electrical activity in the wewer's colonic or abdominal wall muscles.
3
CA 02497803 2000-06-29
WO 0 1 /00117 PCT/US00/17936
Figures 13A-13E are graphical examples of how a high amplitude propagating
contraction of the smooth muscle along a human colon plotted over time.
Figure 14 is a graphical representation of the electrical activity measured at
a
wearer's skin surface above a portion of the wearer's colon as well as a
measurement of
s the pressure inside the colon.
DETAILED DESCRIPTION OF THE INVENTION
As used herein, the te:rm "absorbent article" refers to devices which absorb
and
contain body exudates, and niore specifically, refers to devices which are
placed against
or in proximity to the body of the wearer to absorb and contain the various
exudates
discharged from the body. The term "disposable" is used herein to describe
absorbent
articles which generally are n.ot intended to be laundered or otherwise
restored or reused
as an absorbent article (i.e., they are intended to be discarded after a
single use and,
preferably, to be recycled, composted or otherwise disposed of in an
environmentally
compatible manner). A"unitary" absorbent article refers to absorbent articles
which are
formed of separate parts united together to form a coordinated entity so that
they do not
require separate manipulative parts like a separate holder and liner. A
preferred
embodiment of an absorbent article of the present invention is a unitary
disposable
absorbent article, such as the diaper 20 shown in Figure 1. As used herein,
the term
"diaper" refers to an absorbeint article generally worn by infants and
incontinent persons
about the lower torso. The pxesent invention is also applicable to other
absorbent or non-
absorbent articles such as iiacontinence briefs, incontinence undergarments,
absorbent
inserts, diaper holders and lir.iers, colostomy bags for a natural or
artificial anus, feminine
hygiene garments, tampons, wipes, disposable towels, tissues, water absorbing
articles,
oil absorbing articles, spill cleanup bags, desiccant bags, disposable mops,
bandages,
therapeutic wraps, supports, ciisposable heating pads and the like.
Figure 1 is a plan view of the diaper 20 of the present invention in a flat-
out, state
with portions of the structure being cut-away to more clearly show the
construction of the
diaper 20. The portion of tlie diaper 20 which faces the wearer is oriented
towards t.he
viewer. As shown in Figw-e 1, the diaper 20 preferably comprises a liquid
pervious
topsheet 24; a liquid impervious backsheet 26; an absorbent core 28, which is
preferably
4
CA 02497803 2008-06-10
positioned between at least a portion of the topsheet 24 and the bacicsheet
26; side panels
30; elasticized leg cuffs 32; an elastic waist feature 34; and a fastening
system generally
designated 40. Diaper 20 is shown in Figure 1 to have a first waist region 36,
a second
waist region 38 opposed to the first waist region 36 and a crotch region 37
tocated
s between the first waist region and the second waist region. The periphery of
the diaper 20
is defined by the outer edges of the diaper 20 in which the longitudinal edges
50 run
generally parallel to the longitudinal centerline 100 of the diaper 20 and the
end edges 52
run between the longitudinal edges 50 generally parallel to the lateral
centerline 110 of
the diaper 20.
io The chassis 22 of the diaper 20 comprises the main body of the diaper 20.
The
chassis 22 comprises at least a portion of the absorbent core 28 and
preferably an outer
covering layer including the topsheet 24 and the backsheet 26. If the
absorbent article
comprises a separate holder and a liner, the chassis 22 generally comprises
the holder and
the liner. (For example, the holder may comprise one or more layers of
material to fotm
15 the outer cover of the article and the liner may comprise an absorbent
assembly including
a topsheet, a backsheet, and an absorbent core. In such cases, the holder
and/or the liner
may include a fastening element which is used to hold the liner in place
throughout the
time of use.) For unitary absorbent atticles, the chassis 22 comprises the
main structure
of the diaper with other features added to fotm the composite diaper
structure. While the
zo topsheet 24, the backsheet 26, and the absorbent core 26 may be assembled
in a variety of
well known configurations, preferred diaper configurations are described
generally in
U.S. Pat. No. 3,860,003 entitled "Contractible Side Portions for Disposable
Diaper"
which issued to Kenneth B. Buell on January 14, 1975; U.S. Pat. No. 5,151,092
issued to
Buell on September 9, 1992; and U.S. Pat. No. 5,221,274 issued to Buell on
June 22,
25 1993; and U.S. Pat. No. 5,554,145 entitled "Absorbent Article With Multiple
Zone
Structural Elastic-Like Film Web Extensible Waist Feature" which issued to Roe
et al. on
September 10, 1996; U.S. Pat. No. 5,569,234 entitled "Disposable Pull-On Pant"
which
issued to Buell et al. on October 29, 1996; U.S. Pat. No. 5,580,411 entitled
"Zero Scrap
Method For Manufacturing Side Panels For Absorbent Articles" which issued to
Nease et
30 al. on December 3, 1996; and U.S. PatentI3o. 6.004.306 issued December 21.
1999.
CA 02497803 2008-06-10
The backsheet 26 is generally that portion of the diaper 20 positioned
adjacent the
garment facing surface 45 of the absorbent core 28 which prevents the exudates
absorbed
and contained therein from soiling articles which may contact the diaper 20,
such as
bedsheets and undergarments. In preferred embodiments, the backsheet 26 is
impervious
to liquids (e.g., urine) and comprises a thin plastic film such as a
thermoplastic film
having a thickness of about 0.012 mm (0.5 mil) to about 0.051 mm (2.0 mils).
Suitable
backsheet films include those manufactured by Tredegar Industries Ine. of
Terre Haute,
io IN and sold under the trade names X15306, X10962 and X10964. Other suitable
backsheet materials may include breathable materials which permit vapors to
escape from
the diaper 20 while still preventing exudates firom passing through the
backsheet 26.
Exemplary breathable materials may include materials such as woven webs,
nonwoven
webs, composite materials such as film-coated nonwoven webs, and microporous
Slms
such as manufactured by Mitsui Toatsu Co., of Japan under the designation
ESPOIR NO
and by EXXON Chemical Co., of Bay City, TX, under the designation EXXAIRfi.
Suitable breathable composite materials comprising polymer blends are
available from
Clopay Corporation, Cincinnati, OH under the name HYTREL blend P18-3097. Such
breathable composite materials are described in greater detail in PCT
Application No.
zo WO 95/16746, published on June 22, 1995 in the name of E. I. DuPont and
copending
U.S. Pat. No. 5,865,823 issued to Curro on February 2, 1999. Other breathable
backsheets including nonwoven webs and apertured formed films are described in
U.S.
Pat. No. 5,571,096 issued to Dobrin et al. on Novernber 5, 1996.
23 The backsheet 26, or any portion thereof, may be elastically extensible in
one or
more directions. ln one embodiment, the backsheet 26 may comprise a structural
elastic-
Iike film ("SELF") web. A structural elastic-like film web is an extensible
material that
exhibits an elastic-like behavior in the direction of elongation without the
use of added
elastic materials. SELF webs suitable for the present invention are more
completely
30 described in U.S. Pat. No. 5,518,801 entitled Web Materials Exhibiting
Elastic-Like
Behavior, which issued to Chappell, et, al. on May 21, 1996.
6
CA 02497803 2008-06-10
In alternate embodiments, the backsheet 26 niay comprise elastomeric
films, foams, strands, or corrtbinations of these or other suitable materials
with
nonwovens or synthetic films.
The backsheet 26 may be joined to the topsheet 24, the absorbent core 28 or
any
s other element of the diaper 20 by any attachment means known in the art. (As
used
herein, the term "joined" encompasses configurations whereby an element is
directly
secured to another element by affixing the element directly to the other
element, and
configurations whereby an element is indirectly secured to another element by
affixing
the element to intetmediate member(s) which in tum are affixed to the other
element.)
to For example, the attachment means may include a uniform continuous iayer of
adhesive,
a patterned layer of adhesive, or an array of separate lines, spirals, or
spots of adhesive.
One preferred attachment means comprises an open pattetn network of filaments
of
adhesive as disclosed in U.S. Pat. No. 4,573,986 entitled "Disposable Waste-
Containment
Garment", which issued to Minetola et al. on March 4, 1986. Other suitable
attachment
15 tneans include several lines of adhesive filarnents which are swirled into
a spiral pattern,
as is illustrated by the apparatus and methods shown in U.S. Pat. No.
3,911,173 issued to
Sprague, Jr. on October 7, 1975; U.S. Pat. No. 4,785,996 issued to Ziecker, et
al. on
November 22, 1978; and U.S. Pat. No. 4,842,666 issued to Werenicz on June 27,
1989.
Adhesives which have been
zo found to be satisfactory are manufactured by H. B. Fuller Company of St.
Paul,
Minnesota and marketed as HL-1620 and HL-I358-XZP. Alternatively, the
attachment
means may comprise heat bonds, pressure bonds, ultrasonic bonds, dynamic
mechanieal
bonds, or any other suitable attachment means or combinations of these
attachment means
as are known in the ari.
2s The topsheet 24 is preferably positioned adjacent the body surface 47 of
the
absorbent core 28 and may be joined thereto and/or to the backsheet 26 by any
attachment
means known in the art. Suitable attachment means are described above with
respect to
means for joining the backsheet 26 to other elements of the diaper 20. In one
preferred
embodiment of the present invention, the topsheet 24 and the backsheet 26 are
joined
30 directly to each other in some locations and are indirectly joined together
in other
locations by directly joining them to other elements of the diaper 20.
7
CA 02497803 2008-06-10
The topsheet 24 is preferably compliant, soft feeling, and non-irritating to
the
wearer's skin. Further, at least a portion of the topsheet 24 is liquid
pervious, petTnitting
liquids to readily penetrate through its thickness. A suitablc topsheet 24 may
be
manufactured from a wide rangc of materials, such as porous foams; reticulated
foams;
s apertured plastic films; or woven or nonwoven webs of natural fibers (e.g.,
wood or
cotton fibers), synthetic fibers (e.g., polyester or polypropylene fibers), or
a combination
of natural and synthetic fibers. If the topsheets include fibers, the fibers
may be
spunbond, carded, wet-laid, meltblown, hydroentangled, or otherwise processed
as is
known in the art. One suitable topsheet 24 comprising a web of staple length
io polypropylene fibers is manufactured by Veratec, Inc., a Division of
lnternational Paper
Company, of Walpole, Massachusetts under the designation P-8.
Suitable formed film topsheets are described in U.S. Pat. No. 3,929,135,
entitled
"Absorptive Structures Having Tapered Capillaries", which issued to Thompson
on
December 30, 1975; U.S. Pat. No. 4,324,246 entitled "Disposable Absorbent
Article
is Having A Stain Resistant Topsheet", which issued to Mullane, et al. on
April 13, 1982;
U.S. Pat. No. 4,342,314 entitled "Resilient Plastic Web Exhibiting Fiber-Like
Properties",
which issued to Radel, et al. on August 3, 1982; U.S. Pat. No. 4,463,045
entitled
"Macroscopically Expanded Three-Dimensional Plastic Web Exhibiting Non-Glossy
Visible Surface and Cloth-Like Tactile Impression", which issued to Ahr, et
al. on July
20 31, 1984; and U.S. Pat. No. 5,006,394 "Multilayer Polymeric Film" issued to
Baird on
April 9, 1991. Other suitable topsheets 30 are made in accordance with U.S.
Pat. Nos.
4,609,518 and 4,629,643 which issued to Curro et al. on September 2, 1986 and
December 16, 1986, respectively.
Such formed films are available from The Procter & Gamble Company of
Cincinnati,
is Ohio as "DRI-WEAVE" and firom Tredegar Corporation of Terre Haute, Indiana
as
"CLIFF-T."
Preferably, the topsheet 24 is made of a hydrophobic material or is treated to
be
hydrophobic in order to isolate the wearer's skin from liquids contained in
the absorbent
core 28. If the topsheet 24 is made of a hydrophobic material, preferably at
least the
30 upper surface of the topsheet 24 is treated to be hydrophilic so that
liquids will transfer
through the topsheet more rapidly. This diminishes the likelihood that body
exudates will
8
CA 02497803 2008-06-10
flow off the topsheet 24 rather than being drawn through the topsheet 24 and
being
absorbed by the absorbent core 28. The topsheet 24 can be rendered hydrophilic
by
treating it with a surfactant or by incorporating a surfactant into the
topsheet. Suitable
methods for treating the topsheet 24 with a surfactant include spraying the
topsheet 24
s material with the surfactant and immersing the material into the surfactant.
A more
detailed discussion of such a treatment and hydrophilicity is contained in
U.S. Pat. No.
4,988,344 entitled "Absorbent Articles with Multiple Layer Absorbent Layers"
issued to
Reising, et al. on Jan. 29, 1991 and U.S. Pat. No. 4,988,345 entitled
"Absorbent Ariicles
with Rapid Acquiring Absorbent Cores" issued to Reising on Jan. 29, 1991. A
more
io detailed discussion of some suitable methods for incorporating surfactant
in the topsheet
can be found in U.S. Statutory lnvention Registration No. H1670, published on
July 1,
1997 in the names of Aziz et al.
Alternatively, the topsheet 24 may include an apertttred web or film
which is hydrophobic. This may be aecomplished eliminating the hydrophilizing
is treatment step from the production process and/or applying a hydrophobic
treatment to
the topsheet 24, such as a polytetraflouroethylene compound like SCOTCHGUARD
or a
hydrophobic lotion composition, as described below. In such embodimenis, it is
preferred
that the apertures be large enough to allow the penetration of aqueous fluids
iike urine
without significant resistance.
20 Any portion of the topsheet 24 may be coated with a lotion as is known in
the art.
Examples of suitable lotions include those described in U.S. Pat. Nos.
5,607,760 entitled
"Disposable Absorbent Article Having A Lotioned Topsheet Containing an
Emollient and
a Polyol Polyester Immobilizing Agent" which issued to Roe on March 4, 1997;
U.S. Pat.
No. 5,609,587 entitled "Diaper Having A Lotion Topsheet Comprising A Liquid
Polyol
zs Polyester Emollient And An Immobilizing Agent" which issued to Roe on March
11,
1997; U.S. Pat. No. 5,635,191 entitled "Diaper Having A Lotioned Topsheet
Containing
A Polysiloxane Emollient" which issued to Roe et al, on June 3, 1997; and U.S.
Pat. No.
5,643,588 entitled "Diaper Having A Lotioned Topsheet" which issued to Roe et
al, on
July I, 1997. The iotion may function alone or in combination with another
agent as the
30 hydrophobizing treatment described above. The topsheet may also include or
be treated
with antibacterial agents, some examples of which are disclosed in PCT
Publication No.
9
CA 02497803 2000-06-29
WO 01/00117 PCTIUS00/17936
WO 95/24173 entitied "Absorbent Articles Containing Antibacterial Agents in
the
Topsheet For Odor Control" which was published on September 14, 1995 in the
name of
Theresa Johnson. Further, the topsheet 24, the backsheet 26 or any portion of
the topsheet
or backsheet may be embossed and/or matte finished to provide a more cloth
like
s appearance.
The absorbent core 28 may comprise any absorbent material which is generally
compressible, conformable, :non-irritating to the wearer's skin, and capable
of absorbing
and retaining liquids such as urine and other certain body exudates. The
absorbent core
28 may be manufactured i.n a wide variety of sizes and shapes (e.g.,
rectangular,
hourglass, "T"-shaped, asynunetric, etc.) and may comprise a wide variety of
liquid-
absorbent materials conunoiily used in disposable diapers and other absorbent
articles
such as comminuted wood pulp, which is generally referred to as airfelt.
Examples of
other suitable absorbent mate;rials include creped cellulose wadding;
meltblown polymers,
including coform; chemically stiffened, modified or cross-linked cellulosic
fibers; tissue,
is including tissue wraps anci tissue laminates; absorbent foams; absorbent
sponges;
superabsorbent polymers; absorbent gelling materials; or any other known
absorbent
material or combinations of inaterials.
The configuration and construction of the absorbent core 28 may also be varied
(e.g., the absorbent core(s) oir other absorbent structure(s) may have varying
caliper zones,
zo a hydrophilic gradient, a superabsorbent gradient, or lower average density
and lower
average basis weight acquisition zones; or may comprise one or more layers or
structures). However, the total absorbent capacity of t:he absorbent core 28
should be
compatible with the design loading and the intended use of the diaper 20.
Exemplary absorbent: structures for use as the absorbent assemblies are
described
25 in U.S. Pat. No. 4,610,678 entitled "High-Density Absorbent Struct:ures"
issued to
Weisman et al. on September 9, 1986; U.S. Pat. No. 4,673,402 entitled
"Absorbent
Articles With Dual-Layered Cores" issued to Weisman et al. on June 16, 1987;
U.S. Pat.
No. 4,834,735, entitled "High Density Absorbent Members Having Lower Density
and
Lower Basis Weight Acquisition Zones", issued to Alemany et al, on May 30,
1989; U.S.
30 Pat. No. 4,888,231 entitled "Absorbent Core Having A Dusting Layer" issued
to Angstadt
on December 19, 1989; U.S. Pat. No. 5,137,537 entitled "Absorbent Struct:ure
Containing
CA 02497803 2008-06-10
Individualized, Poiyea.tboxylic Acid Crosslinked Wood Pulp Cellulose Fibers"
which
issued to Herron et al. on August 11, 1992; U.S. Pat. No. 5,147,345 entitled
"High
Efficiency Absorbent Articles For Incontinence Management" issued to Young et
al. on
September 15, 1992; U.S. Pat. No. 5,342,338 cntitled "Disposable Absorbent
Article For
Low-Viscosity Fecal Material" issued to Roe on August 30, 1994; U.S. Pat. No.
5,260,345 entitled "Absorbent Foam Materials For Aqueous Body Fluids and
Absorbent
Articles Containing Such Materials" issued to DesMarais et al. on November 9,
1993;
U.S. Pat. No. 5,387,207 entitled "Thin-Until-Wet Absorbent Foam Materials For
Aqueous
Body Fluids And Process For Making Same" issued to Dyer et ai. on February 7,
1995;
io and U.S. Pat. No. 5,625,222 entitled "Absorbent Foam Materials For Aqueous
Fluids
Made From high Intential Phase Emulsions Having Very High Water-To-Oil Ratios"
issued to DesMarais et al. on July 22, 1997.
The diaper 20 may also comprise at least one elastic waist feature 34 that
helps to
provide improved fit and containment. The elastic waist feature 34 is
generally intended
to elastically expand and contract to dynamically fit the wearer's wa-st. The
elastic waist
feature 34 preferably extends at least longitudinally outwardly from at least
one waist
edge 62 of the absorbent core 28 and generally fonns at least a portion of the
end edge 52
of the diaper 20. Disposable diapers are often constructed so as to have two
elastic waist
features, one positioned in the first waist region 36 and one positioned in
the second waist
region 38. Further, while the elastic waist feature 34 or any of its
constituent elements
may comprise one or more separate elements affixed to the diaper 20, the
elastic waist
feature 34 may be constructed as an extension of other elements of the diaper
20, sueh as
the backsheet 26, the topsheet 24, or both the backshect 26 and the topsheet
24.
The elastic waist feature 34 may be constructed in a nurnber of different
configurations including those described in U.S. Pat. No. 4,515,595 issued to
Kievit et al.
on May 7, 1985; U.S. Pat. No. 4,710,189 issued to Lash on December 1, 1987;
U.S. Pat.
No. 5, 151,092 issued to Buell on September 9, 1992; and U.S. Pat. No.
5,221,274 issued
to Buell on June 22, 1993. Other suitable waist configurations may include
waistcap
features such as those described in U.S. Pat. No. 5,026,364 issued to
Robertson on June
il
CA 02497803 2008-06-10
25, 1991 and U.S. Pat. No. 4,816,025 issued to Foreman on March 28, 1989.
The diaper 20 may also include a fastening system 40. The fastening system 40
preferably maintains the first waist region 36 and the second waist region 38
in an
s overlapping configuration so as to provide lateral tensions about the
circumference of the
diaper 20 to hold the diaper 20 on the wearer. The fastening system 40
preferably
comprises tape tabs and/or hook and loop fastening components, although any
other
known fastening means are generally acceptable. Some exemplary fastening
systems are
disclosed in U.S. Pat. No. 3,848,594 entitled "Tape Fastening Systern for
Disposable
io Diaper" issued to Buell on November 19, 1974; U.S. Pat. No. B 1 4,662,875
entitled
"Absorbent Article" issued to Hirotsu et al. on May 5, 1987; U.S. Pat. No.
4,846,815
entitied "Disposable Diaper Having An Improved Fastening Device" issued to
Scripps on
July 11, 1989; U.S. Pat. No. 4,894,060 entitled "Disposable Diaper With
Improved Hook
Fastener Portion" issued to Nestegard on January 16, 1990; U.S. Pat. No.
4,946,527
1s entitled "Pressure-Sensitive Adhesive Fastener And Method of Making Same"
issued to
Battrell on August 7, 1990; and the herein before referenced U.S. Pat. No.
5,151,092
issued to Buell on September 9, 1992; and U.S. Pat. No. 5,221,274 issued to
Buell on
June 22, 1993. The fastening system may also provide a means for holding the
ariicle in a
disposal configuration as disclosed in U.S. Pat. No. 4,963,140 issued to
Robertson et al.
zo on October 16, 1990. In
altemative embodiments, opposing sides of the garment may be seamed or welded
to
form a pant. This allows the article to be used as a pull-on type diaper, such
as a training
pant.
The diaper 20 may also comprise side panels 30. The side panels 30 may be
25 elastic or extensible to provide a more comfortable and contouring fit by
initially
conformably fitting the diaper 20 to the wearer and sustaining this fit
throughout the time
of wear well past when the diaper 20 has been loaded with exudates since the
elasticized
side panels 30 allow the sides of the diaper 20 to expand and contract. The
side panels 30
may also provide more effective application of the diaper 20 because even if
the diaperer
30 pulls one elasticized side panel 30 farther than the other during
application, the diaper 20
will "self-adjust" during wear.
12
CA 02497803 2008-06-10
While the diaper 20 of the present invention preferably has the side panels 30
disposed in the second waist region 38, the diaper 20 may be provided with
side panels 30
disposed in the first waist region 36 or in both the first waist region 36 and
the second
waist region 38. (As used herein, the tetm "disposed" is used to mean that an
element(s)
of the diaper is fotmed (joined and positioned) in a particular place or
position as a
unitary structure with other elements of the diaper or as a separate element
joined to
another element of the diaper.) The side panels 30 may be constructed in any
suitable
configurations. Examples of diapers with elasticized side panels are disclosed
in U.S. Pat.
No. 4,857,067, entitled "Disposable Diaper Having Shirred Ears" issued to
Wood, et al.
on August 15, 1989; U.S. Pat. No. 4,381,781 issued to Sciaraffa, et al. on May
3, 1983;
U.S. Pat. No. 4,938,753 issued to Van Gompel, et al. on July 3, 1990; the
herein before
referenced U.S. Pat. No. 5,151,092 issued to Buell on September 9, 1992; and
U.S. Pat.
No. 5, 221,274 issued to Buell on June 22, 1993; U.S. Pat. No. 5,669,897
issued to
LaVon, et al. on September 23, 1997 entitled "Absorbent Articles Providing
Sustained
Dynamic Fit"; U.S. Pat. No. 6,004,306 issued to Robles, et al. on Decetnber
21, 1999
entitled "Absorbent Article With Multi-Directional Extensible Side Panels".
The diaper 20 preferably further includes leg cuffs 32 which provide improved
containment of liquids and other body exudates. Leg cuffs may also be referred
to as leg
bands, side flaps, bamer cuffs, or elastic cuffs. U.S. Pat. No. 3,860,003
describes a
disposable diaper which provides a contractible leg opening having a side flap
and one or
more elastic members to provide an eiasticized leg cuff (a gasketing cuff).
U.S. Pat. Nos.
4,808,178 and 4,909,803 issued to A2iz et al. on February 28, 1989 and March
20, 1990,
respectively, describe disposable diapers having "stand-up" elasticized flaps
(barrier
zs cuffs) which improve the containment of the leg regions. U.S. Pat. Nos.
4,695,278 and
4,795,454 issued to Lawson on September 22, 1987 and to Dragoo on January 3,
1989,
respectively, describe disposabie diapers having dual cuffs, including
gasketing cuffs and
barrier cuffs. ln some embodiments, it may be desirable to treat all or a
portion of the leg
cuffs with a lotion, as described above.
Embodiments of the present invention may also include pockets for receiving
and
containing waste, spacers which provide voids for waste, barriers for limiting
the
13
CA 02497803 2008-06-10
movement of waste in the article, cornpartments or voids which accept and
contain wastc
materials dcposited in the diaper, and the like, or any combinations thereof.
Examples of
pockets and spacers for use in absorbent products are described in U.S. Pat.
No. 5,514,121
issued to Roe et al. on May 7, 1996, entitled "Diaper Having Expulsive
Spacer"; U.S. Pat.
s No. 5,171,236 issued to Dreier et al, on December 15, 1992, entitled
"Disposable
Absorbent Article Having Core Spacers"; U.S. Pat. No. 5,397,318 issued to
Dreier on
March 14, 1995, entitled "Absorbent Article Having A Pocket Cuff"; U.S. Pat.
No.
5,540,671 issued to Dreier on July 30, 1996, entitled "Absorbent Article
Having A Pocket
Cuff With An Apex"; and PCT Application WO 93/25172 published December 3,
1993,
to entitled "Spacers For Use In Hygienic Absorbent Articles And Disposable
Absorbent
Articles Having Such Spacer"; and U.S. Pat. No. 5,306,266, entitled "Flexible
Spacers
For Use In Disposable Absorbent Articles", issued to Freeland on April 26,
1994.
Examples of compartments or voids are disclosed in U.S. Pat. No. 4,968,312,
entitled
"Disposable Fecal Comparttnenting Diaper", issued to Khan on November 6, 1990;
U.S.
is Pat. No. 4,990,147, entitled "Absorbent Article With Elastic Liner For
Waste Material
Isolation", issued to Freeland on February 5, 1991; U.S. Pat. No. 5,062,840,
entitled
"Disposable Diapers", issued to Hoit et al. on November 5, 1991; and U.S. Pat.
No.
5,269,755 entitled "Trisection Topsheets For Disposable Absorbent Articles And
Disposable Absorbent Articies Having Such Trisection Topsheets", issued to
Freeland et
io al. on December 14, 1993. fixamples of suitable transverse barriers are
described in U.S.
Pat. No. 5,554,142 entitled "Absorbent Article Having Multiple Effective
Height
Transverse Partition" issued September 10, 1996 in the name of Dreier et al.;
PCT Patent
WO 94/14395 entitled "Absorbent Article Having An Upstanding Transverse
Partition"
published July 7, 1994 in the name of Freeland, et al.; and U.S. Pat. No.
5,653,703
25 entitled "Absorbent Article Having Angular Upstanding Transverse
Partition", issued
Aug. 5, 1997 to Roe, et al.
Embodiments of the present invention may also include a waste management
device 110 such as is shown in Figure 2. The waste management device 110 may
inctude
30 a waste bag i i 1 to coilect feces, urine or both. The waste bag 111 may
have an aperture
121 and a f]ange 112 surrounding the aperture for preferably adhesive
attachment to the
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WO O1/00117 PCT/US00/17936
perianal area of a wearer. Fizrther, the waste management device 110 has been
found to
be particularly useful and beileficial when used in conjunetion with a
garment, or diaper,
preferably a disposable diaper. One example of a diaper 120 including a waste
bag 111 is
shown in Figure 3. If associated with a diaper 120 or other garment, the waste
bag 111
may be disposed on or joined to any surface of the article. The bag 111 may be
joined to
the article by any known ;means, including any of the joining or attaching
means
described herein and/or anv other joining means such as adhesive, hook and
loop
fasteners, magnetics, belts, ties, straps, snaps, etc. In one embodiment, the
waste bag 11 I
is joined to the topsheet 124 of the diaper 120.
io The waste bag 111 is preferably a flexible receptacle for the containment
of
excreted fecal matter or urine. Thus, the waste bag 111 is preferably liquid
impermeable,
and yet it may be breathable. Further, the waste bag 111 is designed of
sufficient
strength to withstand typical wearing conditions, such as sitting.
The waste bag 111 may comprise one or multiple layers. In one embodiment, the
waste bag I 11 may comprise three layers, preferably one film and two non-
woven layers.
The layers of the bag material may comprise any material, preferably so that
the bag is
liquid impervious. In a preferred embodiment of thc present invention a
laminate may be
formed from a non-woven la;yer and a film.
Suitable film materials for any of the film layers preferably comprise a
thermoplastic material. The thermoplastic material can may be vapor pervious
or
impervious and can be selected from among all types of hot-melt adhesives,
polyolefins
especially polyethylene, polypropylene, amorphous polyolefins, and the like;
material
containing meltable components comprising fibres or polymeric binders
including natural
fibres such as cellulose - wood pulp, cotton, jute, hemp; synthetic fibres
such as
fibreglass, rayon, polyester, polyolefin, acrylic, polyamid, aramid,
polytetrafluroethylene
metal, polyirnide; binders such as bicomponent high melt/low melt polymer,
copolymer
polyester, polyvinyl chloride, polyvinyl acetate/chloride copolymer, copolymer
polyamide, materials comprising blends wherein some of the constituent
materials are
not meltable; air and vapour permeable materials including microporous films
such as
those described above with respect to the backsheet and monolithic breathable
materials
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
such as HYTRELTM available from DuPont and PebaxTM available from ELF Atochem,
France.
The waste bag 111 may have any shape or size. Preferred shapes include flat
circular type bags, cone shaped bags, truncated cone shaped bags and pyramidal
or
s truncated pyramidal shaped bEtgs and flat T shaped bags. Further, the waste
bag 111 rnay
be provided &om a unitary piece of material or a number of separate pieces of
material
whieh may be identical or different and which may be sealed at their
respective
peripheries.
The waste bag 111 may also contain absorbent material. The absorbent material
may comprise any absorbent rnaterial which is capable of absorbing and
retaining liquids.
The absorbent material may comprise a wide variety of liquid-absorbent
materials
commonly used in disposable diapers and other absorbent articles. Some
examples are
described herein with respect to the absorbent core.
The waste bag 111 is provided with an aperture 121 whereby fecal matter or
urine
is received from the body prior to storage within the bag cavity. The aperture
121 is
preferably surrounded by a flange 112 and may be provided in any shape or
size, such as
circular, oblong, heart shaped and may be symmetrical or asymmetrical,
preferably the
aperture has an oblong coni6guration either in the longitudinal or in the
transversal
direction. The flange may comprise projections designed to fit the perineal,
genital
and/or coccygeal area of the wearer.
The flange 112 should be made of soft, flexible and malleable material to
allow
easy placement of the flange 112 to the perianal or uro-genital area. Typical
materials
include nonwoven materials, wovens, open celled thermoplastic foams, closed-
cell
thermoplastic foams, composites of open celled foams and stretch nonwoven, and
films.
The waste bag 111 preferably further comprises a joining or attachment means
to
secure the device to the wearer. Such means may comprise any of the joining or
attachment means described herein or any other suitable joining or fastening
means
known in the art such as straps, belts, hook and loop fasteners, pins, ties,
snaps and/or a
body-compatible adhesive applied to the wearer facing portion of the waste bag
111 or
the flange. Any skin-friendly water resistant pressure sensitive adhesive may
be used to
attach the device to the perianal or uro-genital area of the wearer, such as
hydrocolloid
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WO 01/00117 PCT/US00/17936
adhesives and hydrogel adhesives. Particularly effective adhesives in
providing the
desired adhesive properties to secure the flange to the skin of the wearer at
the sensitive
perianal area, while allowing for relatively painless application and removal,
are formed
from crosslinking polymers vvith a plastisicer to form a 3-dimensional matrix.
s The diaper 20 may also comprise one or more "proactive sensors" 60. As used
in
this application, the term "piroactive sensor" refers to a sensor or sensor
system that is
capable of detecting or monit:oring changes or signals in or on the body of
the wearer, in
the article or in the waste, i.e., inputs, that directly relate or, at a
minimum, correlate to the
occurrence of an impending event related to the bodily waste, the wearer, the
article or a
component or components thereof. Proactive sensors may respond to one or more
specific inputs. Examples of inputs that may be detected by a proactive sensor
of the
present invention in order to predict an impending event include, but are not
limited to,
attitude, pressure, motion, vibration, sound, ultrasonic waves, electrical
activity,
contraction, tension, bloociflow, moisture, temperature, enzymes, bacteria,
pH,
conductivity, resistance, capacitance, inductance or other chemical,
biochemical,
biological, mechanical or ele<;trical properties and/or components of bodily
wastes.
The sensor 60, for ex~unple, may be chemical, mechanical, electrical, thermal,
etc.
A chemical sensor may respond to chemical and/or biochemical inputs such as
enzymes
typically.present in bodily wastes, pH, water, humidity or moisture, and/or
biological
inputs such as bacteria, blood or any other components of bodily wastes such
as feces,
urine, or menses, etc. Examples of chemical or biochemical sensors include
dissolving or
rupturable films, capsules, cells, seals, etc. that dissolve or rupt:ure in
response to a
specific chemical, biochemical or biological input or to a specific class of
chemical,
biochemical or biological inputs. A mechanical sensor may respond to motion,
attitude,
pressure, etc. An example of a mechanical sensor is a bellows-type sensor in
which when
the pelvic floor drops prior to defecation and the pressure pushes down on the
bellows to
inflate a portion of the sensor. A mechanical sensor may also include a sensor
or a
portion of the sensor that is broken or separated under a pre-defined applied
pressure. An
electrical sensor may respond to moisture, urine, feces, menses, pressure,
heat,
temperature, conductance, resistance, capacitance, inductance, etc. An
electrical sensor
may, for example, include a sensor in which a conductive input such as urine
completes
17
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WO 01100117 PCT/US00/17936
an electrical circuit; a sensor in which an input such as pressure, tension or
heat closes an
electrical contact to complete a circuit; a piezoelectric sensor that
generates a signal via
pressure induced by the wearer or a part of the wearer (e.g., frorn motion or
musclc tone);
a piezoelectric transducer that generates an ultrasonic wave when electrically
triggered
s and detects and/or compares "echo" returns, for example to measure the size
of a fluid-
filled cavity such as the bladder or rectum; an ultrasound imaging array; a
sensor in
which the resistance, capacitance or inductance varies in the presence of the
input to
which the sensor responds (c.g., conductance of the wearer's skin); or a
sensor, such as an
EMG sensor, that reccives electrical signals from the body (e.g., frorn the
subcutaneous
rnuscles) of the wearer through a contact such as a skin contact sensor. A
thermal sensor
may be used to detect change.s in temperature.
In yet another embodiment, the sensor may include one or more biosensors as
are
known in the art (e.g., an en::yme sensor, organella sensor, tissue sensor,
microorganism
sensor, or electrochemical sensor). The sensor may be adapted to detect
proteins, sugars,
is bile components, etc. such as described in U.S. Pat. No. 4,636,474 entitled
"Toilet
Apparatus," issued to Kenji Ogura et al. on January 13, 1987. Biosensors may
comprise
bio-recognition systems, typically enzymes or binding proteins such as
antibodies
immobilized onto the surface of physico-chemical transducers. The biosensors
may
detect components of bodily wastes, such as ammonia and phenol (e.g., via
biosensors
comprising enzyme electrodes). A specific strain of bacteria may be detected
via
biosensors employing antibodies raised against that bacterial strain.
Exemplary enzyme
electrodes that may be used to detect phenols (e.g. in urine or feces) include
tyrosinase
based electrodes or polyphenol oxidase enzyme electrodes described in U.S.
Pat. No.
5,676,820 entitled "Remote Electrochemical Sensor," issued to Joseph Wang et
al. on
October 14, 1997 and U.S. Pat. No. 5,091,299 entitled "An Enzyme Electrode For
Use In
Organic Solvents," issued to Anthony P. F. Turner et al. on February 25, 1992,
respectively.
The sensor of the present invention may be reversible or irreversible. A
dissolving
film or capsule is an example of an irreversible sensor, while an electrical
sensor that
receives electrical signals from the body of a wearer which may receive
multiple signals
in succession is an example of a reversible sensor.
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A proactive sensor 60 may detect an impending event or detect a parameter that
directly relates, or at a minimum correlates to the occurrence of an impending
event. An
impending event that may be detected or predicted by a proactivc sensor 60 of
the present
invention may include, for example, urination, defecation, heat rash, skin
irritation or
s rash, skin pressure marks, or an illness or medical condition of the wearer
such as an
internal infection (e.g., jaundice), a vitamin deficiency, a bile duct
blockage, candidiasis, a
parasite, a potential chronic skin condition or irritation, etc. A parameter
that correlates to
an event is any measurable input, signal such as one or more of the potential
inputs listed
above, that correlates with the occurrence of the event within the frame of
reference of the
to system (i.e., a signal caused by the waste or the wearer). The proactive
sensor 60 may,
for example, predict the occwTence of a defecation, urination or discharge of
bodily waste
or may detect signals that may precede skin rash or irritation. Proactive
sensors 60 in an
article may measure many dii.ferent inputs in order to predict an event. For
example, the
proactive sensor 60 may moriitor the external anal sphincter muscle for a
contraction or
15 relaxation in the anal sphincter that precedes the release of feces and/or
urine; muscle
activity in one or more of the muscles surrounding a body cavity such as the
bladder, the
colon or the rectum; a separation of the buttocks; a pressure change in the
abdomen; a gas
concentration in the article; a drop in the pelvic floor; or any other
indication that may be
used to predict or anticipate the occurrence of an event such as a defecation,
a urination or
20 a discharge of bodily wastes. Alternatively, a proactive sensor 60 of the
present invention
may detect signals that precede skin irritation. For example, the sensor may
detect
residual fecal contamination of the wearer's skin (e.g., fecal enzyme residue
left on the
wearer's skin after cleaning up a soiled diaper) that may, over time, lead to
irritated skin.
Detection of a high pH, an increased skin hydration resulting in a measurable
increase in
25 conductance or decrease in impedance of skin, a specific microorganism,
fecal enzymes,
etc. may also be used to predict potential skin irritation.
The proactive sensor 60 may be disposed in and/or operatively connected to any
portion of a disposable articlf: that will be exposed to the input that the
sensor is designed
to detect. For the purposes of the present invention, the term "operatively
connected"
30 refers to a means of communication such that the proactive sensor 60 may
signal some
portion of the article 20 when the proactive sensor 60 detects an input. The
proactive
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WO 0I/00117 PCT/US00/17936
sensor 60 may be separate from and operatively connected to another portion
ofthe article
20, another sensor 60, an actuator 70, a controller 80 or some other component
of the
article 20. "Operatively conntseted" may, for example, include a means of
communication
such as an elecfical connection via a conductive wire or member, via a
transmitted signal
s such as radio frequency, infrared or another transmitted frequency
communication.
Alternatively, the sensor 60 rnay be operatively connected via a mechanical
connection
such as a pneumatic or a hydraulic connection.
In article 20, for exarnple, the proactive sensor 60 may be located in the
front
waist region 36, the rear waist region 38 or the crotch region 37 of article
20, and may be
integral with, disposed adjacent to, joined to, or comprise a portion of the
chassis 22, the
topsheet 24, the backsheet 26, the absorbent core 28, side panels 30, leg
cuffs 32, a waist
feature 34, a fastening system 40, the longitudinal 50 or end 52 edges, etc.
The proactive
sensor 60 may be integral with the article 20, or may be installed by the
caretaker or the
wearer. The proactive sensoi- 60 may be completely contained within the
article such as
article 20 or may have a receiving portion located in the article such that it
will come into
contact with the desired input and another portion such as a transmitting
portion located
either in the article or outside. the article. Alternatively, the proactive
sensor 60 may be
external to the article 20 yet operatively connected to some portion of the
article 20 such
that the proactive sensor 60 rnay detect an input external to the article 20
and provide a
signal to a controller 80 and/or an actuator 70. In some embodiments, the
sensor may be
separate from the article, e.g., separately applied to some portion of the
wearer, and/or
may have one or more component separate from the article 20.
In one embodiment, the article 20 may include an extension 220 comprising one
or more sensors 60 as shown in Figure 4. The extension 220 may, for example,
cover at
least a portion of the wearer's abdomen, positioning the proactive sensor(s)
60, such as an
EMG sensor, in proximity to the wearer's colonic or abdominal wall museles.
The
extension 220 may be of an}, suitable shape, size or material, may be elastic
or inelastic,
and may comprise a fastening system, stiffening elements, or a body-adhering
composition, such as a topical adhesive, to maintain alignment of the sensor
with the
target muscles.
CA 02497803 2000-06-29
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The proactive sensor 60 may preferably detect electrical activity in one or
more of
the wearer's muscle groups, including the external anal sphincter, external
urethral
sphincter, colonic muscles (i.e., smooth colonic muscles), muscles of the
abdominal wall,
muscles surrounding the bladcler, muscles surrounding the rectum or muscles
associated
s with any other body cavity or any bodily elimination. Alternatively, the
sensor 60 may
measure the volume of the rectum, bladder or colon and signal the wearer or
caregiver
when the volume reaches a pne-defined threshold for the individual. Although
the actual
volume of the bladder, recturn, colon or other body cavity may be measured, it
may be
more desirable to mcasure certain characteristics of the bladder or other body
cavity
which correspond to a certain volume. For example, it may be sufficient to
measure the
distance between the walls of the cavity, e.g. the bladder walls, and
calculate or otherwise
determine the approximate volume of the cavity. Non-limiting examples of
threshold
values for the bladder or rectum which may be relevant to determining the next
excretion
include about 80 /a of daytime maximum volume or the minimum observed
micturition or
is defecation volume. More specifically, a pre-micturition enuresis alarm for
individual's
having nighttime urinary incontinence may signal the wearer or caregiver, for
example,
when the bladder reaches 80% of the maximum observed daytime bladder volume.
Alternatively, the alarm can iindicate when a predetermined characteristic of
the cavity
(e.g. distance between bladder walls) is met which corresponds to a particular
volume of
the cavity or which corresponcis to imminent urination, defecation or other
bodily activity.
The proactive sensor 60 may further comprise a sensing "system" including two
or
more sensors, each of which may detect the same or different signals from the
same or
different sources. The sensing system may include components that are located
inside,
external to and/or separate from the article. For example, the sensing system
may include
zs a sensor inside the article that detects electrical signals in the external
anal sphincter of the
wearer and a sensor externall:o the article that detects motion, tension or
muscle activity
in the abdomen of the wearer. The sensing system may also or alternatively
include
components other than the sensing elements inside, external to and/or separate
from the
article. The sensing system, for example, may include a transmitter that is
external to the
article and transmits a signal to another part of the sensing system that is
joined to or
disposed in the article 20. In yet other embodiments, the sensor 60 or sensing
system may
21
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WO 01/00117 PCT/US00/17936
be part of a separate device which my be used together with or separately from
the article.
For example, the sensing system may be a completely independent device which
can be
configured to work in conjunction with an article such as a diaper or may be
permanently
or temporarily integrated into such an article.
The article of the present invention may also comprise an actuator 70 (see
Figures
5 and 5A). As used in this application, the term "actuator" refers to a device
that
comprises "potential" and a means of transforming that potential to perform or
activate a
"responsive function." The potential of the actuator 70 may comprise either
stored or
potential energy or stored material. The actuator 70 thus may perform or
activate a
io responsive function by transforming potential energy to kinetic energy or
by releasing or
delivering a stored material. A"responsive function" is dcfined for the
purposes of the
present invention as a function performed upon the bodily waste, the wearer,
the article,
or a component or componer.its thereof, or a signal to the wearer or the
caretaker. A
component of bodily waste niay include, for example, moisture, electrolytes,
enzymes,
is volatile gases, bacteria, blood, etc. A component of the wearer may also
include skin,
genitalia, the anus, the external anal sphincter muscle, etc. A component of
the article
may also include leg cuffs, waist cuffs or other waste barriers and/or
containment
components, side panels, ears, a chassis, an absorbent core, an acquisition
component, a
fastening system, the longituclinal or end edges, etc. Potential energy may be
stored as
Zo mechanical, electrical, chemical or thermal energy. "Kinetic energy" as
used in this
application refers to the cap.acity to do work or to perform a responsive
fnnction as
described above (e.g., expansion of a compressed device, rotation of a twisted
device, a
gel that moves as it changes phases, coating or treatment of skin or feces,
inhibition of an
enzyme, adjustment of pH, etc.).
25 Triggering the creation of a three dimensional structure to capture waste,
for
example, involves responsive functions performed on a component of the article
and,
ultimately, on the waste. Capturing waste, wiping the skin of the wearer,
treating the
feces with a feces modifying agent, or treating the skin with a skin care
composition, for
example, are responsive functions performed on the waste and/or the wearer.
Adjusting
30 the article's geometry (in oiie, two or three dimensions) or physical
properties (e.g.,
bending modulus, geometry, etc.) are examples of responsive functions, which
rnay be
22
CA 02497803 2000-06-29
WO 0 1/00117 PCT/U500/17936
performed on the article. Sigrialing a caretaker and/or the wearer that an
event is about to
occur or stimulating a portion of the wearer's anatomy are examples of
responsive
functions performed on the caretaker and wearer, respectively. An actuator of
a
disposable article may, for exzunple, release or deliver a deodorant, cnzyme
inhibitor, skin
s care composition or pH control agent; capture, wipe, cover, trap,
inunobilize, seal, pump,
or store bodily waste; or trigger the release or creation of a structure or
element designed
to perform one or more of t:hese functions or any other responsive function
upon the
waste, wearer, article, or a component thereof.
An actuator 70 of the present invention may release potential energy to
perform or
activate a responsive functioti upon the waste, the wearer, the article, or a
component
thereof. The release of potential energy may transform mechanical, electrical,
chemical
or thermal potential energy into mechanical, electrical or chemical kinetic
energy to
perform the responsive function. Actuators may be triggered by a threshold
level of an
input to release potential er.tergy to perform a responsive function or may
respond
is continuously to an input as described below. For example, a compressed foam
has stored
compressive mechanical pote,ntial energy and may provide mechanical kinetic
energy
when it is released. A twisted foam has stored torsional mechanical potential
energy that
may provide mechanical kinetic energy, i.e., rotation, when it is released. In
addition,
stored chemical, electrical or thennal energy may be used to release
electrical,
io mechanical, chemical or therrnal kinetic energy. An actuator of a
disposable article, for
example, may include one or more of the following: stored lotion, feces
modification
agents, enzyme inhibitors, pH buffers, dyes, pressurized gas, a compressed
foam, a
twisted foam, a pump, a closed system liquid transport member, an electrically
sensitive
gel, a pH sensitive gel, a salt concentration gel, etc. Potential energy may
be stored in any
25 manner sufficient to maintainJrestrain it until it is required. Examples
include batteries
and/or capacitors, elastically, torsionally, compressively tensioned materials
or structures,
in the form of unreacted reagents, and materials capable of performing
physical or
chemical functions (e.g., absorbents, emollients, pH buffers, enzyme
inhibitors, feces
modification agents; compressed gases, etc.).
30 Alternatively, an actua.tor 70 of the present invention may comprise a
quantity of a
stored material that has the capacity to perform or activate a responsive
funetion upon the
23
CA 02497803 2000-06-29
wo 01/00117 PCT/USOO/17936
waste, the wearer, the article, or any component or components thereof. In one
embodiment, for example, the actuator 70 may release or deliver a stored
material that
performs a responsive functio;n. In this embodiment, the actuator 70 may be
triggered by
a threshold level of an input to discontinuously release or deliver the stored
material at a
s given time or may release or deliver the material continuously. The actuator
70 may, for
example, include stored lotion, skin care compositions, feces modification
agents, enzyme
inhibitors, pH buffers, dyes, e:tc. In certain preferred embodiments, the
material may be
delivered by an actuator 70 such as an expanding resilient rnaterial, a
released high
pressure gas, etc.
In one embodiment of' a bodily waste isolation device 90, as shown in Figures
5
and 5A, the actuator comprises a compressed foam spacer 94 vacuum sealed under
a
water soluble filrn 92 (e.g., << PVA film). Upon receipt of the proper signal
from the
proactive sensor, the actuator closes a switch that releases a small amount of
stored water
to contact and dissolve the water soluble film. This results in the reiease of
the stored
mechanical energy in the compressed foam. The foam expands and forms a spacer
to
provide void volume for the iiicipient feces. Alternatively, the switch
closure may release
two chemicals that combine and create a foaming system, which may protectively
coat the
skin and/or engulf the feces when excretcd. Similar systems to prepare for
imminent
urination events are also included in the scope of this invention.
In other embodiments, the responsive system may include an actuator that
alerts
the caretaker or the wearer of' an impending event such as a defecation or a
urination. If
the responsive system alerts the caretaker, for example, the caretaker may
prepare to
change the artiele to minimize the amount of time that the bodily waste is in
contact with
the skin of the wearer, may ensure that a bedpan or an absorbent article is in
place to
contain the bodily waste when it is eliminated, or may aid the wearer in
getting to the
bathroom before the elimination of the bodily waste. If the responsive system
alerts the
wearer, the responsive systenn may act as a signaling device that alerts the
wearer of an
impending defecation or urination before the actual event. In another
embodiment, the
responsive system may actually stimulate a portion of the wearer's anatomy in
response
to the system's sensing of the impending event. Thus, the responsive system
can, for
example, stimulate the wearer to contract the urethral or anal sphincter
muscle prior to an
24
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
impending defecation or urination. This may provide the wearer with enough
time to
make it to a toilet or to fit liim or herself with an appropriate absorbent or
other waste
receiving article prior to the waste actually leaving the body.
Alternatively, the sensor and/or actuator may comprise a closed system liquid
s transport member. A"closed system liquid transport member" or "transport
member"
comprises a liquid filled mernber having an iniet port and outlet port, which
upon receipt
of even a little amount of liquid at the inlet port practically immediately
releases liquid at
the outlet port. The liquid released from the outlet port may serve as an
input signal to a
sensor. For example, the liquid may be water, which is released when the
transport
member imbibes urine at ari inlet port, which acts to dissolve a seal to
release stored
mechanical energy to create .a feces void space. Alternatively, the transport
member may
itself trigger an actuator (e.g., mix with agents to perform a chemical
reaction), or may
perform at least a portion of the actuator function (e.g., the released water
is imbibed by a
super absorbent polymer an=anged in a particular geometry, which swells and
forms a
is feces void volume). Liquici transport through such transport members is
based upon
direct suction rather than on capillarity. The liquid is transported through a
region into
which no significant quantity of air (or other gas) may enter. The driving
force for liquid
flowing through such a member can be created by a liquid sink (e.g., a
capillary or
osmotic absorbent structure) or source in liquid connection with the member.
Thus, a
liquid transport member must have a relatively high liquid permeability.
There are preferably at least two regions within the transport member with
different pore sizes, namely the one or more port region(s) having smaller
pores and the
inner region having a much larger pore size. The inner region of transport
member has a
permeability that is relatively high compared to the permeability of a port
region (a higher
liquid pen:neability provides less flow resistance), which can be a part of an
outer/wall
region circumscribing the inner/bulk region. Nonlimiting examples of high
porosity
materials suitable for use as the inner region material include fibrous
structures
comprising polyolefin, PET, cellulose, and cellulose-based frbers, and porous,
open celled
foam such as reticulated foains, cellulose sponges, polyurethane foams, and
HIPE foams.
In one embodiment, the voids of the inner region are essentially completely
filled with an
essentially incompressible flizid. The term "essentially completely" refers to
the situation,
CA 02497803 2000-06-29
WO 01100117 PCTlUS00l17936
where sufficient void volurne of the. inner region is filled with the liquid
such that a
continuous flow path between inlet and outlet ports can be established.
The port regions of the transport member comprise materials which are
permeable
for the transport liquid, but not for the ambient gas (like air) once they are
wetted with the
transport liquid. Often, such materials are described as membranes, which are
defined as
regions that are permeable for liquid, gas or a suspension of particles in a
liquid or gas.
The membrane may for example comprise a microporous region to provide liquid
permeability through the capillaries. In an alternative embodiment, the
membrane may
comprise a monolithic regiori comprising a block-copolymer through which the
liquid is
transported via diffusion. Exemplary membranes for the port regions include
celluloseacetate membranes, such as also disclosed in United States Patent No.
5,108,383
entitled "Membranes For Atisorbent Ariicles" issued to White on April 28,
1992, PET
films as disclosed in EP-A-0451797, nitrocellulose membranes, cellulosenitrate
membranes, PTFE membranes, polyamide membranes, and polyester. Other suitable
materials are woven polymeric meshes, such as polyamide or polyethylene meshes
as
available from Verseidag in Geldern-Waldbeck, Germany, or SEFAR in
Riischlikon,
Switzerland.
The actuator 70 may alternatively comprise an electrically sensitive gel.
Electrically sensitive gels are polymeric gcl networks that, when at least
partially swollen
with water, change volume and/or geometry under the application of an electric
current or
field. For example, certain p,aztially ionized polyacrylamide gels will
undergo anisotropic
contraction of about 50 % under weak electric fields (e.g., 0.5 volts/cm) when
immersed
in acetone and water. Altemative electrically sensitive gels may undergo
electrically
indueed bending in the presenee of water and a surfactant or may undergo an
oscillating
wave motion when subjected to an oscillating electric field. It is believed
that local
shrinkage may be induced in a portion of the gel, e.g., one side of a gel
element, by
concentrating positively charged surfactant molecules on the negatively
charged gel
polymer in an electric field. Changing the intensity and/or the polarity of
the field
induces a movement in the gE:l as one side decreases in length (e.g,, a gel
formed in a strip
may curl). Electrically sensitive gels may comprise variable geometries such
as
rectangular, circular, reticulared grid, etc. patterns in order to provide a
valve to release a
26
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
material, allow a bodily waste to flow through, prevent a bodily waste from
flowing
through, eneapsulate a bodily waste, etc. as they change volume and/or
geometry. An
electrically sensitive gel formed in a strip, for example, may be bent to
provide an
available void space for when electrical activity in the external anal
sphincter muscle
s predictive of defecation or urination is detected. In Figures 6A and 613,
for example, a
strip of electrically sensitive gel 494 is shown in a circuit in which fecal
moisture may
bridgc the contacts 485 and allow current to flow from battery 487 to the
electrically
sensitive gel 494 either bending or straightening the strip. Alternatively, an
electrically
sensitive gel 594 formed in a reticulated grid pattern, such as shown in
Figures 7A, 7B
and 7C, may be electrically induced to swell or shrink when an inuninent
urination is
detected to form a valve that allows and/or prevents urine flow to another
portion of the
article 20. Figure 7A, for ex,ample, shows a circuit including a reticulated
grid pattern of
an electrically sensitive gel. Figures 7B and 7C further show a microscopic
view of the
grid in a shrunk 593 and in a swelled 595 configuration, respectively. An
exemplary
material is a weakly cross-linked PAMPs gel (poly(acrylamido-2-methyl propane)
sulphonic acid). This type of gel may perform various functions such as
applying or
delivering a chemical feces treatment agent. Other exemplary electrically
sensitive gels
are described in United States Patent No. 5,100,933 issued to Tanaka on March
31, 1990
and WO 9202005. Altematively, pH sensitive gels or salt concentration
sensitive gels
that change volume and/or geometry at specific pH or salt concentrations,
respectively,
may be used as an actuator of the present invention.
The actuator 70 may be disposed in and/or operatively connected to any portion
of
disposable article that will a11ow the actuator to perform a responsive
function upon the
bodily waste, the wearer, the article, or a component thereof. In article 20,
for example,
the actuator 70 may be located in the front waist region 36, the rear waist
region 38 or the
crotch region 37 of article 20, and may be integral with, disposed adjacent to
or joined to
a component of the chassis 22, the topsheet 24, the backsheet 26, the
absorbent core 28,
side panels 30, leg cuffs 32, a waist feature 34, a fastening system 40, the
longitudina150
or end 52 edges, etc. The actuator 70 may also be completely contained within
the article
such as article 20, may have a portion located in the article and a portion
located outside
the article 20, or may be completely external to the article 20. An actuator
70 or a portion
27
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
of an actuator 70 may be operatively connected to one or more sensors 60, onc
or more
controllers 80, another portion of the actuator 70 or anothcr portion of the
article 20.
Further, the actuator 70 may be integral with the article 20, or may be
installcd by the
caretaker or the wearer.
s The article 20 may also include a controller 80. A"controllcr" is defined
for the
purposes of this applicatiori as a device that receives an input from a sensor
and
determines if one or more ac:tions are to be taken. The controller may receive
a signal
from the sensor 60 and direct the actuator 70 to perform a responsive function
upon the
bodily waste, the wearer, the article or a component thereof. Alternatively,
the actuator
70 may receive the signal dii=ectly from the sensor 60 and perform a
responsive function
upon the wearer, the waste, the article or a component thereof A controller
may include
materials that undergo chem:ical or physical change, may be a chemical,
mechanical or
electrical device that processes information from a sensor, etc. For example,
in an article
having a compressed plastic foam material encapsulated and restrained under
vacuum by
is a moisture soluble bag, the sensor 60 may comprise the moisture soluble
bag. The
physical and chemical characteristics of the film, i.e., the type of polymer,
the thiclrness,
etc., that determine how much of the input must be present before the film
will dissolve
act as the controller 80 and determine the threshold level of input that must
be met before
the controller 80 allows the actuator 70 to release stored energy to perform a
responsive
function. The actuator 70 is the combination of the compressed foam and the
loss of
vacuum, which allows release of the stored mechanical energy of the compressed
foam.
In this example, the controller 80 acts as a one-time switch. An electrical
controller 80
that receives signals from the sensor 60 such as electrical activity of
muscles of the
wearer, however, may receive and monitor multiple electrical signals and may
repeatedly
trigger the actuator. The cotitroller may be integral with the sensor
component, integral
with the actuator component, or a separate component of the system.
The controller 80 may be disposed in and/or operatively connected to any
portion
of a disposable article that w:ill allow the controller 80 to receive a signal
from the sensor
60 and to provide a signal to the actuator 70. In article 20, for example, the
controller 80
may be located in the front vraist region 36, the rear waist region 38 or the
erotch region
37 of article 20, and may be integral with, disposed adjacent to or joined to
the chassis 22,
28
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/I7936
or a component of the topshe:et 24, the backsheet 26, the absorbent core 28,
side panels
30, leg cuffs 32, a waist featiLre 34, a fastening system 40, the longitudinal
50 or end 52
edges, etc. The controller 80 may bc intcgral with the article 20, or may be
installed by
the caretaker or the wearer. The controller 80 may be completely contained
within the
s article such as article 20, may have a portion located in the article and a
portion located
outside the article, or may be located completely outside the article 20. A
controller 80 or
a portion of a controller 80 may be operatively connected to one or more
sensors 60, one
or more actuators 70, another portion of the controller 80 or another portion
of the article
20. The controller 80, for example, may receive a signal from the sensor 60
and provide a
signal to the actuator 70, e.g., by a radio frequency (rf) transmission.
Although distinct structural elements may perform the sensor 60, actuator 70
and
controller 80 functions, the sensor 60, actuator 70 and/or controller 80
functions of the
present invention need not bes perforcned by distinct structural elements. The
sensor 60
and controller 80 functions, for example, may be performed by the same
structural
element such as a film that d:issolves in contact with a component of a bodily
waste. In
this example, the film acts as a sensor and responds to the input component of
bodily
waste. The physical and cheniical characteristics of the film, i.e., the type
of polymer, the
thickness, ete., that detenmine how much of the input must be present before
the film will
dissolve act as the controller and determine the threshold level of input that
must be met
before the controller allows the actuator to release stored energy to perform
a responsive
function.
A"responsive systerri" is defined for the purposes of this application as a
system
that includes a sensor 60 and an actuator 70 that acts upon the bodily waste,
the wearer,
the article, or a component or components thereof when the sensor 60 detects
the
appropriate triggering input. Upon sensing a given input parameter, the
actuator 70
effects the release of stored eriergy or the release or delivery of stored
material to perform
a responsive function. When the proactive sensor 60 detects an impending
event, the
actuator effects the release of stored energy. By detecting an input signal
prior to the
impending event, a responsive system in the article may be triggered to
prepare for the
event or to signal the caregiver or the wearer of the impending event. This
allows
construction of articles in which the waste-management technology is initially
"hidden"
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CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
or unobtrusive, but which is available at, or just before, the moment of need
and/or in
which the article may provide the caregiver or the wearer the opportunity to
prepare for an
event in advance. Regardless of the specific input, the proactive sensor 60 in
these
embodiments may trigger an actuator to perform an action on the article, the
wearer or the
s environment to prepare for the occurrence of the event or provide a signal
to the caregiver
that the impending event is about to occur. For example, if an impending
defecation or
urination is to be detected via the electrical activity of the external anal
sphincter muscles,
the system is preferably triggered (i.e., the responsive system is activated)
by a signal
related to the reflexive contraction of or the relaxation of the anal
sphincter. The actuator
io may then perfomz a function such as treating the wearer's skin to prevent
or minimize
skin irritation; preparing a bcidily waste management device by activating a
fecal void
spacer; opening a valve to allow urine to flow into a storage device;
releasing an enzyme
inhibitor, skin care composition, pH control agent, or other skin treatment
aids as known
in the art; or providing an audible, tactile, or visual warning signal to the
caregiver or the
15 wearer. If the sensor 60 comprises a sensing system, one actuator may be
triggered by
different sensors and/or signals, or different actuators may be triggered by
different
sensors and/or signals. Altematively, one sensor and/or signal may trigger
multiple
actuators.
A responsive system inay respond in either a"continuous" or a"discontinuous"
20 manner. As used in this application, a"continuous responsive system" refers
to a
responsive system in which the output is quantitatively dependent upon the
quantity of the
input, i.e., continuously increasing quantities of the input are required to
effect
continuously increasing quantities of the output, or where the output of the
responsive
system comprises a passive release of a stored material. A super absorbent
polymer
25 placed in an absorbent core of an article, for example, provides a
continuous response in
which the output is quantitatively dependent upon the quantity of the input,
i.e., as
increasing quantities of liquici waste contact the super absorbent polymer, an
increasing
amount of the polymer contains that liquid until the capacity of the polymer
is exhausted.
A stoichiometric chemical reaction is another example of a system having a
continuous
30 response to increasing outptut. In the reaction A+ excess B-~ C, for
example, the
amount of excess B convertc:d to C is stoichiometrically and, therefore
"continuously,"
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
related to the amount of A available in the system. One example of a
continuous
responsive system in which an inflatable spacer inflates to provide a void
volume to store
feces via a stoichiometric chemical reaction when a liquid such as urine
contacts a gas
evolving material, i.e., a coritinuous responsive system, is described in
United States
s Patent No. 5,330,459 entitled "Disposable Absorbent Article Having An
Inflatable
Spacer," issued to Gary D. Lavon et al. on July 19, 1994. Another example of a
continuous responsive system in which a disposable article that improves the
fit on the
wearer by a liquid such as urine dissolving a film to release a leg cuff that
has been held
in an expanded state is described in United States Patent No. 4,246,900
entitled "Diaper
Including Moisture-responsive Seal Means," issued to Schroder et al. on
January 27,
1981. A responsive system that passively releases a stored material, however,
generally
provides a continuous response regardless of how the material itself is
released because
the actual responsive function. performed upon the bodily waste, the wearer,
the article, or
a component thereof is perfonned by the material, not by the release of the
material.
is Thus, whether the material is released continuously in response to a given
input, or
released discontinuously at a single time when a threshold of a given input is
detected, the
responsive function performed by the released material is performed such that
continuously increasing quantities of the input are required to effect
continuously
increasing quantities of the ouitput until the material released is exhausted.
A"discontinuous responsive system" of the present invention, however, refers
to a
responsive system that has an output function that is essentially independent
of the
quantity of the input beyond a threshold level. For example, when one or more
threshold
levels of a given input are met, the responsive system may release all or a
pre-designated
portion of its stored energy or deliver, i.e., actively transport, all or a
pre-designated
portion of its stored materia.l to perform a specific responsive function. In
an ideal
embodiment of the present invention, the output function, f(x), includes
a"step" function
as shown in Figure 8A. In. this embodiment, the rate of change in the output
with
increasing levels of input (d(output)/d(input)), i.e., the slope or first
derivative f(x) of the
output function f(x), is preferably essentially zero when the amount of input
is above or
below the threshold level. Ai: the threshold level, however, the d(output)/
d(input) rate of
change preferably approaches infinity. Thus, in the ideal discontinuous
response, the
31
CA 02497803 2000-06-29
WO Oll00117 PCTNS00/17936
limit of the fianction f(x-e) as e->0 is not equal to the limit of the
function f(x+e) as e-+0,
i.e., lim f(x-s) # lim f(x+8).
E-+0 E-+0
The present invention, however, recognizes that in the physical world an ideal
s instantaneous step change at the threshold level is not necessary and may
not even be
possible in many instances. In a preferred embodiment, it is only necessary
that the
output function have a virtual step change with very little change in the
input at or around
the threshold level of the input. Thus, the present invention contemplates a
discontinuous
responsive system of the present invention having an output function that
responds in a
io sufficiently discontinuous manner in the transition region such that the
output function
has at least a minimum relative degree of steepness in the transition region.
While not
wishing to be limited to a particular method of describing or modeling a
discontinuous
system, in a preferred methocl of determining whether a given output function
performs in
a sufficiently discontinuous tnanner as defined for the purposes of the
present invention,
ts the slope of the output curve at the inflection point is compared with the
relative slope of
a line between the first and last points of the transition region. For
example, Figure 9A
shows a graph of an exempla:ry output function, f(x) along with aligned graphs
of the first,
f(x), and second, f'(x), and third, f"(x), derivatives of the exemplary output
function.
The output function f(x) describes the effect of the in put (x or I) on the
output or
20 response (R(I)). For purpose:s of the present invention, the transition
region is defined as
the region between the relative maxima, R(Ii), and the minima, R(IZ), of the
second
derivative, f'(x), of the outpiit function, f(x). The relative maxima, R(I,),
and the relative
minima, R(I2), are points at which the third derivative, f"(x), equals zero.
The inflection
point, Io, is defined as the point in the transition region at which the
second derivative,
is f'(x), equals zero, i.e.,
dZR ~
-- I = 0.
dIZ I I=Io
32
CA 02497803 2000-06-29
WO 01100117 PCT/US00/17936
The comparison of the slope of the output function at the inflection point to
the slope of a
line between the first and the last points of the transition region can be
described by the
equation:
dR aRT)
s - ~ = k .
di f I=Io ( AIT )
In this equation dR/dI at the inflection point is the first derivative of the
output function at
that point. The term DIT is the change in the input to the responsive system
between the
first, I,, and last, IZ, points of the transition region, i.e., I. - I,_ and
the term A RT is the
io change in the response of ttie output function between the first and last
points of the
transition region, i.e., R(I2) - R(I,). The coefficient k is a proportional
constant that
describes the relative steepness of the slope of the output function at the
inflection point,
Io, compared to the slope of a line between the first and last points of the
transition region.
In order that the responsive system have a discontinuous output function, the
proportional
is constant k must be at least about 2.0, preferably at least about 3.0, more
preferably at least
about 5.0, even more preferably at least about 10.0, with at least about 100.0
being the
most preferred.
In certain embodimen.ts, the relative degree of steepness in the transition
region of
a discontinuous responsive system may also be modeled by a transfer function
of a
20 control system having a series of an integer number, n, first order lags
with an equal time
constant. The transfer function of the responsive system is defined for the
purposes of the
present invention as the ratio of the Laplace transforms of the output
(responding
variable) to the input (disturbing variable). See, e.g., Robert H. Perry & Don
Green,
Perrv's Chemical Engineers' Hand ook, Sixth Ed., Chap. 22 (McGraw Hill, Inc.
1984).
25 As shown in Figure 913, the relative degree of steepness of an output
function may be
approximated by the formula: KG(s) = K/(Ts + 1) in which KG(s) is the
transfer
function, K is a proportional element, T is the time constant of the system,
and n is the
integer number of first order time lags. In this model, as the number n
increases, the
steepness of the output function in the transition region increases, and the
model begins to
30 approximate a discontinuous responsive system. Certain discontinuous
responsivc
33
CA 02497803 2000-06-29
WO Ol/00117 PCT/US00/17936
systems of the present invention preferably may be modeled by the above
formula when n
is greater than or equal to about 25, with n being greater than or equal to
about 50 being
more preferred, and n being greater than or equal to about 100 being the most
preferred.
As shown in Figure 8A, a responsive system of the present invention may
include
s a single threshold level at which the responsive system may release all of
its stored energy
to perform a specific responsive function or may include multiple threshold
levels at
which the system may release a pre-designated portion of its stored energy to
perform one
or more specific responsive functions at each of the threshold levels. In an
embodiment
having a single threshold level, for example, the responsive system may
release all of its
storcd cnergy to perform the entire responsive function when that threshold
level is met.
In such a single threshold embodiment, In this example, the discontinuous
responsive
system includes a system that has two states such as on or off. When a
threshold quantity
of an input such as bodily waste is present in the absorbent article, the
responsive system
may perform a single resporisive function upon the waste, the wearer, the
article or a
component thereof, such as enveloping the waste away from the skin of the
user. Thus,
the discontinuous responsive system may perform a one-time "switch-like"
function that
changes from one state to another in the presence of a threshold level of an
input.
Alternatively, as shown in Figure 813, the responsive system may have multiple
threshold levels such as 1,1 and I,2 at which when each threshold level is met
the system
zo may release a given "quanta" of energy or deliver a given quantity of
material to perform
a specific responsive functioii. In this embodiment, when each threshold level
is met, a
portion of the entire responsive function may be performed and/or different
independent
responsive functions may be performed in response to different threshold
levels being
met. For example, a resporisive system may monitor a fecal enzyme and when
each
threshold enzyme level is nlet may deliver an equal or unequal quantity of
enzyme
inhibitor(s) or lotion, or deliver a pH buffer at the first threshold level
and perform
another responsive function such as delivering a quantity of enzyme
inhibitor(s) at the
second threshold level. In each transition region, the responsive system
responds
essentially the same as the trELnsition region in the single threshold
embodiment described
above.
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CA 02497803 2000-06-29
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In addition, a responsive system may monitor multiple inputs such as moisture
and/or one or more fecal enzymes and perform one or more responsive functions
when
the threshold levels of the iiifferent inputs are met or may perform one
responsive
function only when two or rnore of the threshold levels of the different
inputs are met.
Thus, a controller may monitor multiple different inputs and perform a
different
responsive function when the threshold level of the different inputs are met.
Alternatively, the controller may perform a logic OR-gate type function such
that a
responsive function may be performed when one or more threshold levels of the
multiple
inputs are met. The controller may also perfonm a logic AND-gate type function
such that
io a responsive function may tie performed when each threshold level of two or
more
different inputs is met.
The responsive systern may also comprise a"closed loop" or an "open loop"
system. A"closed loop" system, which is also referred to as a"feedback control
loop"
system, includes distinct sensor 60 and actuator 70 components and performs a
responsive
function upon the input. In some preferred embodiments, the system may also
use a
detection or a measurement of an element or a paramcter of the output
condition as at
least one trigger of the responsive function that is perfomlcd upon the input.
The output
condition may be the state of the input condition after the actuator 70 has
had the
opportunity to perform a responsive function on the input condition. For
example, if the
sensor 60 is monitoring the hydration level of the skin and the hydration
level reaches a
threshold level, i.e., the output condition of the responsive system, the
responsive system
may release a predetermined quantity of a desiccant to bring the hydration of
the skin
back to the desired target hydration or hydration range or may release a
desiccant until the
hydration retums to the target hydration or the hydration range. An absorbent
material
such as a super absorbent polymer that continually absorbs a liquid input
until the liquid
has ali been absorbed or the capacity of the polymer has been reached,
however, is not
considered to comprise a closed loop system because the absorbent material
does not have
distinct sensor 60 and actuator 70 components. The responsive function may be
perfonned when the output condition reaches a threshold level, or may be
performed only
when the output condition and one or more other conditions are met. Acting
upon the
input may include acting upon the element sensed, e.g., sensing pH and acting
upon the
CA 02497803 2000-06-29
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pH, or may include acting upon a composition of which the eiemcnt sensed is an
integral
component, e.g., sensing a fecal enzyme or fecal moisture and acting upon
feces. As
described above, a feedback control loop systcm includes at least two distinct
components: the sensor 60 and the actuator 70. The sensor 60 detects an event,
or a
s parameter associated with that event. The actuator 70 receives a signal and
performs a
responsive function on the :input condition detected by the sensor 60. The
feedback
control loop may further include a controller 80. In this case, the sensor 60
may provide a
signal to the controller 80, aiid the controller 80 may direct the actuator 70
to perform a
responsive function upon th.e input condition. The controller 80 may be a
separate
component of the responsive system or the controller function may be performed
by the
sensor 60 and/or the actuator 70.
A preferred embodiment of a closed loop control system of the present
invention
comprises an electrical sensor capable of detecting changes in the magnitude
of electrical
activity of sphincter muscles, particularly the external anal sphincter,
related to imminent
release or the potential for release of bodily waste and a means to deliver an
electrical
impulse (or electrical stimula,tion) as required to the perianal skin of the
wearer to induce
a temporary contraction of tlhe sphincter muscle to function as a continence
aid. (This
process may be alternatively referred to as dynamic graciloplasty nerve
stimulation in the
medical literature.) For the purpose of this invention, the electrical
activity herein
referred to as the electrical activity of the external anal sphincter may
additionally include
electrical activity from other muscles, including, but not limited to, pelvic
floor muscles
associated with the external anal sphincter, or other muscles such as the
extemal urethral
sphincter, the muscles of the colon, the muscles surrounding the bladder or
the rectum or
other muscles associated witll elimination of waste from the body. Optionally,
a visible,
zs audible, and/or tactile (i.e., vibrating) signal is delivered to the wearer
and/or caregiver,
alerting them of the potential for waste elimination.
The electrical impulsE; may consist of one or more pulses of electricity or
may be a
continuous impulse. While the maximum strength of the electrical impulse may
be as
high as about 35 volts, the electrical impulse preferably has a voltage in the
range of
about 0.05 to about 5 Volts and more preferably in the range of about 0.3 to
about 1 Volt.
Preferably, the electrical impulse current is in the range of about 0.1 to
about 100 mA.
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Preferably, the stimulation frequency is in the range of about 10 to about 100
Hz, more
preferably in the range of about 20 to about 80 Hz, and even more preferably
in the range
of about 60 to about 80 Hz. If the impulse is a pulse (one or a multiplicity
of pulses), the
duration of each pulse is preferably in the range of about 0.1 to about 5 ms
and more
s preferably in the range of about 0.5 to about 1 ms. In certain embodiments
where the
impulse comprises a multiplicity of pulses, the entire set of pulses, or
"pulse train", may
have a duration of about 0.1 second to about 15 seconds with an interval
between pulse
trains of between about 1 second and about 60 seconds. Preferably, the
electrical
stimulation voltage, frequency, the number and frequency of pulses in a pulse
train, and
io the number and duration of and spacing between pulse trains may be modified
and/or
controlled by the wearer or the caregiver. Any electrical circuit as known in
the art
capable of ineeting these parameters may be used to deliver or control the
electrical
stimulation to the external anal sphincter or other body location. For
example, a 3 volt
watch battery with a pulse generating system may operatively connected with a
proactive
is sensor, such as an EMG surfa.ce electrode as described herein, and be used
to deliver one
or more electrical impulses to the wearer's skin in the perianal region. One
exemplary
electrical stimuiation device is the Prosper e.i.s. 5000 system available from
the
Dr. Rowedder Biomedizinische Geraete in Muehbrook, Germany. This device may be
alternatively used with an adhesive EMG surface electrode as described herein.
zo In alternative embodiments of stimulation (i.e., contraction) of the
external
sphincter muscles as a continence aid, the signal from the sensor may be
directed to
another site on the wearer's body to elicit the anorectal reflex. For example,
the sensor
may trigger an electrical or rnechanical stimulation of the perineal skin, the
skin at the
back of the wearer's knee, the sole of the foot, or any other site that
results in the
25 expression of the anorectal reilex.
The feedback control l.oop may be "non-modulating" or "modulating." In a"non-
modulating" feedback control loop responsive system the responsive system acts
as a one-
time switch in which the actuator perfonns a responsive function on the input
when the
threshold level of the output condition is met. For example, the sensor 60 may
detect a
30 specific microorganism, and the actuator 70 may signal the caretaker of a
potential
incipient infection. In this example, the actuator 70 acts upon the input
detected by the
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WO 01/00117 PCT/US00/17936
sensor 60. If the sensor 60 detects electrical signals in the external anal
sphincter of the
wearer to predict an imminent defecation and the actuator 70 releases a
compressed foam
material to create a shaped void of sufficicnt volume to contain feces,
however, the
actuator 70 acts upon someth.ing other than the input detected by the sensor
60, i.e., acts
upon the feces instead of the electrical activity in the sphincter muscles and
is thercfore
not a feedback control loop. A"modulating" feedback control loop, however,
includes a
sensor 60, an actuator 70 and a controller 80. In a modulating feedback
control loop, the
output condition is monitored constantly or repeatedly, and the controller 80
directs the
actuator to perform a resporsive function on the input in order to maintain
the output
io condition at a desired set p0int or within a desired range. A modulating
responsive
system may constantly or repeatedly measure sphincter muscle electrical
activity and send
a signal to the sphincter muscles to keep the anal sphincter closed for a
desired period of
time to provide a feedback control loop responsive system.
An "open loop" systein, however, is a system that responds to the input to
perform
a responsive function without using feedback, i.e., the output has no effect
upon the
sensed input entering the system. An open loop system may include a responsive
system
that has a single device that performs the functions of both the sensor 60 and
the actuator
70 or may have distinct sensor 60 and actuator 70 components in which the
actuator acts
upon something other than the input. A super absorbent polymer placed in an
absorbent
core of a disposable absorbent article, for example, provides an open loop
response
because the polymer only includes a single device that performs the functions
of the
sensor 60 and actuator 70. Alternatively, an open loop responsive system may
include a
sensor 60 that detects bodily waste or a component of that bodily waste, and
an actuator
70 that performs a responsive function in a continuous or a discontinuous
manner on
something other than the input detected by the sensor 60. As above, for
example, the
sensor 60 may detect sphincter muscle electrical activity, and the actuator 70
may capture
or store feces.
A block diagram of an exemplary open loop responsive system having a sensor 60
and an actuator 70 is shown in Figure 10A. A block diagram of an altemative
open loop
responsive system including a sensor 60, an actuator 70 and a controller 80 is
shown in
Figure IOC. A block diagraLrn of an exemplary closed loop responsive system
having a
38
CA 02497803 2000-06-29
WO 0 1/00117 PCT/US00/17936
sensor 60 and an actuator 70 is shown in Figure lOB. A block diagram of an
alternative
closed loop responsive systerri including a sensor 60, an actuator 70 and a
controller 80 is
shown in Figure IOD.
Other responsive systems are described in United States Patent Application
s Numbers 09/106,424 entitled "Disposable Article Having A Discontinuous
Responsive
System" filed on June 29, 1998, which has been allowed; 09/107,563 entitled
"Disposable
Article Having A Responsive System Including A Feedback Control Loop" filed on
June
29, 1998, which has been allowed; and 09/106,225 entitled "Disposable Article
Having A
Responsive System Including A Mechanical Actuator" filed on June 29, 1998 (P&G
Case
Number 7199), each of which is incorporated herein by reference.
An example of a diape:r 20 of the present invention including a proactive
sensor is
shown in Figure 1. In this embodiment, a skin contact sensor system comprises
an
electrical sensor 60 that includes three electrodes 64, 65 and 66. An
electrical sensor 60
of the present invention may include two or more electrodes. In one
embodiment,
electrodes 64 and 65 may be active and electrode 66 may be a Teference
electrode. This
allows for a bimodal electrical pickup. The skin contact sensor system may be
releasably
secured to the skin of the wearer in order to receive electrical signals from
a muscle or
muscle group of the wearer. For example, the skin contact sensor may be placed
as close
as possible to the anus of the iuearer so that the probe may detect signals
from the external
anal sphincter muscle, which is anatomically near the skin at the point of the
anal orifice.
If the sensor is not self-adhesive, an electroconductive, adhesive gel may be
placed on the
electrode of the skin contact probe before it is placed on the skin. In this
embodiment, the
skin contact sensors may be placed on the wearer by the caretaker, or may be
integral with
the article such that they are automatically aligned and attached to the
wearer's skin near
the anal perimeter when the a.rticle is placed on the wearer. A 7mm adhesive
disposable
surface electrode manufactured by Dantec Medical A/S of Skovlunde, Denmark,
which
may be connected to a Dantec EMG (Type 14 D 11) receiver unit, for example, is
believed
to be useful for the present invention. In this example, the Dantec EMG unit
may be set,
for example, at a time base of 20 msec/division resulting in a screen sweep
time of 0.2
seconds. The gain amplifier may be set at 20 V/division. A proactive sensor
in this
embodiment may vary in size and manufacture and may optionally be integral
with the
39
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WO 01/00117 PCT/US00/17936
body of the article. The unit that receives the signal from the sensor(s) may
be separate
from the article or may be ir.itegral with the article. If the receiver unit
is separate from
the article (i.e., a telemetry, based system), the article may additionally
comprise a
transmitter to transmit the signal to the receiver. This may be accomplished,
for example,
s via an infrared (IR) or radiofi=equency (RF) telemetry device. The settings
for the sensor,
transmitter (if required), and receiver may vary according to the specific
type of signal,
sensor embodiment, and function to be performed.
The surface electrodes 64, 65 and 66 of the skin contact sensor system in the
above embodiment measure electrical signals in a muscle fiber or a group of
muscle
fibers. If the electrodes measure the electrical activity of a group of muscle
fibers, the
total potential change involves a greater mixture of frequencies. Preferably,
the skin
contact sensor or sensor system is capable of detecting electrical activity
throughout a
frequency range including frorn about 5 Hz to about 500 Hz, and more
preferably
including from about 10 to about 350 Hz. Preferably, the electrodes utilize
two active
Is electrodes 64 and 65 and one; reference electrode 66 for a bimodal
electrical pickup. The
electrical activity measured by the surface electrodes includes a combination
of EMG
signals, other physiologic signals present on the skin surface such as EKG and
electrodermal activity, and environmental artifacts such as 60 Hz from
electronic
equipment or radio frequency interference. When bimodal electrodes are used in
combination with a differential amplifier, only those signals which are not
detected in
common by the two active electrodes are allowed to pass. Because a substantial
portion
of the common mode signals picked up by the electrodes are not EMG signals, it
may be
advantageous to reject signals common to both active electrodes. This common
mode
rejection provides a cleaner, more discrete signal from the sensor.
In altemative embodiments, the electrical skin contact sensor of the present
invention may be any other- commercially available EKG (electrocardiogram) or
EMG
(electromyogram) electrode and/or measuring system. For example, the MyoTrace
200,
available from Noraxon U.S.A., Inc. of Scottsdale, AZ, comprises a wideband
electrode
capable of sensing muscle electrical activity in the 16 Hz to 500 Hz range
(this is
appropriate for the slow-twitch muscles of the pelvic floor). Another
commercially
available EMG sensing system is the MyoSense system available from MIE Medical
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
research Ltd., of Leeds, U.K. Other suitable adhesive surface electrodes
include
electrodes available from Medicotest A/S of Olstykke, Denmark as M-00-S, N-00-
S, M-
00-A/F, BS 3400, BS3500, FtR, and BRS, as well as electrodes available from
Multi Bio
Sensor, Inc. of El Paso, TX, as 3ST3, 3SG3-N, and 2DT2. Other suitable
electrical
sensors are disclosed in iJS Patents 5,785,040; 5,727,549; 5,337,748;
5,203,330;
5,255,677, all of which are incorporated herein by reference. The electrodes
of the
present invention preferably comprise an electrically conductive adhesive to
maintain
uninterrupted contact with the wearer's skin.
In additional altemative embodiments of the present invention, the telemetry
io system may be any commerci.ally available EMG or EKG telemetry system. One
suitable
telemetry system is available from Noraxon U.S.A., Inc, as the Telemyo system,
comprising a battery-operatecl wearable transmitter. Another suitable
telemetry system is
available from MIE Medical Research Ltd. as the MT8 Telemetry System. Another
suitable telemetry system is disclosed in US Patent 5,704,351.
is For embodiments in which an imminent defecation or urination is detected,
the
proactive sensor 60 may respond to a signal related to either the reflexive
contraction of
or the relaxation of the extenlal anal sphincter, or to electrical activity in
one or more of
the muscles sunounding the: rectum or bladder. In one embodiment of t.he
present
invention detect the contraction of the extemal anal sphincter as a signal of
imminent or
zo potential defecation. For example, in continent adults and older children
and babies, the
rapid filling of the rectum with feces from the sigmoid junction (i.e., the
lower region of
the colon) causes the externa.l anal sphincter to reflexively (i.e.,
involuntarily) contract.
This reflex is referred to as the anorectal reflex. A sharp increase in the
extemal anal
sphineter muscle activity acecampanies the contraction of the external anal
sphineter and is
zs detectable as an EMG signal via the sensors of the present invention. This
reflex is absent
in the newborn human infant and generally begins to develop affter about one
year of age.
Therefore, embodiments of the present invention intended to detect increased
external
anal sphincter activity as a precursor of defecation may be generally more
applicable to
older babies (older than about 1 year of age). The increase in external anal
sphincter
30 eleetrical activity that signals rectal filling is preferably at least
about 2 times the basal
41
CA 02497803 2000-06-29
WO O1/00117 PCT/US00/17936
external anal sphincter musc:le activity, but may be at least about 3 times
the basal
activity, at least about 5 times the basal activity or more.
In other prefen:ed erribodiments, the sensor detects sharp decreases in, or
the
absence of, the electrical activity of the external anal sphincter. These
decreases occur
when the external anal sphincter relaxes to open the rectal neck just prior
to, or during,
defecation. Generally, the electrical activity of the external anal sphincter
muscle will
drop sharply for at least severral seconds as the muscles relax. The activity
is at or close to
zero immediately preceding and during the elimination process. In these
embodiments, a
sensor 60 may be triggered by precipitous drops in muscle electrical activity,
preferably
drops of greater than or equal to about 50 %. More preferably, the sensor 60
may be
triggered by drops of greater than or equal to about 75 %, or equal to about
95 %.
Since muscular electrical activity is typically "noisy", an averaged value of
the
amplitude (i.e., absolute value of the signal) should be used for comparison
of the external
anal sphincter activity under various conditions (e.g., basal state and
stimulated
is conditions). Figure lla is a graphical representation (Electrical Activity
of Anal
Sphincter v. Time) of a sharp increase in the external anal sphincter
electrical activity
related to the extension of the rectum (i.e., for a normal adult) that is
useful as a signal of
imminent or potential defecation. The figure shows a basal sphincter muscle
electrical
activity level (a) followed by rectal filling which results in an increase in
the magnitude of
electrical activity of the sphincter muscle related to the anorectal reflex
(b). Figure l lb is
a graphical representation of a sharp decrease in the external anal sphincter
electrical
activity related to imminent or current defecation. The sphincter muscle
activity during
defecation (c) is shown between the anorectal reflex electrical activity (b)
and the basal
electrical activity (a), which is typical.
Preferably, the target or "trigger" level of muscle electrical activity
increase or
decrease that results in the s:ignaling of the wearer or caregiver or the
application of an
electrical stimulus may be varied or controlled by the wearer or caregiver
based on
differences between individu.al wearers. In certain embodiments, one or more
sequences
of electrical stimuli to be delivered to a portion of the wearer's anatomy
(e.g., the perianal
skin) based on the particular detected muscle electrical signal may be pre-
programmed
into a controller operatively associated with the sensor/actuator (i.e.,
stimulation device).
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WO 01/00117 PCT/US00/17936
In one exemplary embodiment of the present invention, as shown in Figure 12,
the
article may comprise a belt :230 including at least one sensor 60 to be fitted
or secured
around at least a portion of t:hc wcarcr's lower abdomen generally
corresponding to the
location of the transverse, descending, and/or sigmoid colon. At least a
portion of the belt
s 230 may be elastically extensible so as to accommodate local changes in the
wearer's
dimensions and to provide a sufficiently snug fit to hold the sensor 60 in the
target
location while the belt 230 is worn. The belt 230 may be secured around the
wearer's
abdomen by any fastening system as known in the art, including adhesive tapes,
topical
adhesives, mechanical fasteners such as hook and loop fasteners, buttons, and
the like.
Any portion of the belt 230 or any of the sensors 60 may alternatively be
affixed to the
wearer directly via the use of topical adhesives or other body adhering
compositions,
which are described in more detail below. In any case, at least one sensor 60,
such as an
EMG sensor, is preferably h[eld in contact with the wearer's skin by the belt
230. In
embodiments having multiple sensors, it is generally preferred to have a
multiplicity of
is sensors 60 contact the skin at intervals along a path corresponding to at
least a portion of
the transverse, descending and/or sigmoid colon.
Body adhering compositions suitable for use in the present invention may be in
any form, including, but not limited to gels, lotions, films, webs or the
like. Some
exemplary body adhesives include adhesives, gelatin, petrolatum, waxes such as
silicone
or petroleum waxes, oils sucli as silicone or petroleum based oils, skin care
compositions
or ingredients thereof. Other topical adhesives include, but are not limited
to, hydrogel
or hydrocolloid adhesives such as acrylic based polymeric adhesives, and the
like. (Some
exemplary hydrogel and/or hydrocolloid a.dhesives are disclosed in U.S. Pat.
Nos.
4,231,369; 4,593,053; 4,699,146; 4,738,257; and 5,726,250; each of which is
incorporated by reference hei-ein.) The topical adhesives may also include any
"medical
adhesive" which is compatible for use with biological tissue, such as skin.
Acrylic
medical adhesives suitable for use as body adhering compositions 80, include
adhesives
available from Adhesive Research, Inc., of Glen Rock, PA, under the
designations MA-
46, MA-312, "MTTM" High MVTR adhesive, and AS-17. Rubber-based medical
adhesives, such as SB-2 from Adhesive Research Inc. may also be suitable.
Other
exemplary adhesives include Dow Corning Medical Adhesive (Type B) available
from
43
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
Dow Corning, Midland, lV1I; "MEDICAL A.DHESIVE" from Hollister Inc., of
Libertyville, IL; 3M Spray A.dhesives #79, 76, 77 and 90 available frorn the
3M Corp. of
St. Paul, MN; and "MATISOL" liquid adhesive available from Ferndale
Laboratories of
Femdale, MI. Other medical adhesives are described in U.S. Pat. Nos.
4,078,568;
s 4,140,115; 4,192,785; 4,393,080; 4,505,976; 4,551,490; 4,768,503 and
polyacrylate and
polymethacrylate hydrogel adhesives are disclosed in U.S. Pat. Nos. 5,614,586
and
5,674,275; the disclosure of' each of which is incorporated by reference
herein. Yet
another exemplary adhesive comprising polyvinyl pyrollidone and a multi-
functional
amine-containing polymer is disclosed in WO 94/13235A1. (The disclosure of
each of
these references is incorporated herein by reference.) Alternative body
adhering means
which may be used in plac<: of or in addition to those described above include
static
electricity, suction and the like. In any case, it is preferred that the body
adhering
composition permit vapors t:o pass (i.e., breathable), be compatible with the
skin and
otherwise skin friendly.
is To obtain the desired characteristics, the body adhering composition may
comprise: from 0.5 to 20 /~, preferably 5% to 15%, by weight of a
macromolecular
polymeric substance or a mixture of such substances soluble or swellable in
the below
mentioned plasticizer(s). As not limiting examples such macromolecular or
polymeric
substances can be natural and/or synthetic such as natural gums or derivatives
such as
natural gums and gelatins, their derivatives and alginates; polyacrylics;
polyvinyl alcohol;
polyethylene oxide; polyvinylpyrrolidon (PVP) or polyvinylethers, their
copolymers and
derivatives; cellulose derivatives; Block Copolymer Thermoplastic Elastomers
and
preferably Styrenic block C'opolymers and more preferably the hydrogenated
grades
StyroUEthylene-Butylene/Styrol (SEBS), Styrene/Isoprene/Styrene (SIS), and
StyroVEthylene-Propylene/Styrol (SEPS). Further, preferred body adhesive
compositions
may comprise from 45 to 99.5% by weight, preferably from 51 to 99.5% by
weight, of a
plasticizing substance or a niixture of plasticizing substances, which are
liquid at room
temperature. As non-limiting examples the plasticizer can be water, various
alcohols (like
in particular glycerol), gylcols and their ethers, polyglycols, liquid
polybutenes, esters
such phtalates, adipates, stearates, palmitates, sebacates, or myristates,
natural or synthetic
oils such as vegetable oils, mineral oils, or combinations thereof. Further,
the body
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CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
adhesive may include from 0% to 50% by weight of the composition, preferably
0% to
600% by weight of the macrornolecular polymeric substance, of a tackifying
resin whose
main scope is to tailor the Tg especially in systems based on synthctic
polymers. Also,
preferred body adhesives may include from 0 to 10% and more preferably from 0
to 5%
by weight of substances for facilitating and stabilizing the gel and the gel
forming process
both of hydrophilic or hydrophobic liquid plasticizers. These may be for oily
systems,
e.g., the fatty acids of Ce to CZZ, their metallic salts and their polyoxo-
derivatives; lanolin
derivatives; silica; bentonite, montmorillonite and their derivatives;
polyamides, waxes or
mixtures thereof.
Common additives known in the art as preservative, antioxidants, anti UV,
pigments, mineral fillers, rheology modifiers and the like can also be
comprised in
quantities up to 10% each. Also, when chemical crosslinks are formed in the
system, a
cross-linking agent can be present preferably in quantities up to 5% by
weight. Chemical
crosslinking can be formed also by mutual neutralization of polymers having
different
functionalities as in the reaction between acid polyacrylics and
polysaccharides.
Suitable skin care coinpositions which may be used as, with, or in place of
the
body adhesives include Category I actives as defined by the U.S. Federal Food
and Drug
Administration's (FDA) Tentative Final Monograph on Skin Protectant Drug
Products for
Over-the-Counter Human Use, which presently include: alantoin, aluminum
hydroxide
io gel, calamine, cocoa butter, diimethicone, cod liver oil (in combination),
glycerine, kaolin,
petrolatum, lanolin, mineral oil, shark liver oil, white petrolatum, talc,
topical starch, zinc
acetate, zinc carbonate, zinc oxide, and the like. Other potentially useful
materials are
Category III actives as defiiied by the U.S. Federal Food and Drug
Administration's
Tentative Final Monograph on Skin Protectant Drug Products for Over-the-
Counter
Human Use tentative final r.nonograph on skin protectant drug products for
over-the-
counter human use, which presently include: live yeast cell derivatives,
aldioxa,
aluminum acetate, microporous cellulose, cholecalciferol, colloidal oatmeal,
cysteine
hydrochloride, dexpanthanol, Peruvian balsam oil, protein hydrolysates,
racemethionine,
sodium bicarbonate, Vitamin A, and the like. Many of the FDA monographed skin
care
ingredients are eurrently utilized in commercially available skin care
products, such as "A
AND D" Ointment, "VASELINE" Petroleum Jelly, "DESITIN' Diaper Rash Ointment
CA 02497803 2000-06-29
w0 01/00117 PCT/US00/17936
and Daily Care Ointment, "GOLD BOND" Medicated Baby Powder, "AQUAPHOR"
Healing Ointment, "BABY h1AGIC" Baby Lotion, "JOHNSON'S ULTRA SENSITIVE"
Baby Cream, Joliunson's baby lotion, lip balms, etc. Other suitable skin care
compositions
(e.g., lotions) are described in detail in U.S. Pat. No. 5,643,588; U.S. Pat.
No. 5,607,760;
s U.S. Pat. No. 5,609587; anci U.S. Pat. No. 5,635,191; each of these
references being
incorporated herein by reference.
In alternative embodiments of the present invention, one or more sensors may
be
arranged so as to detect patteins of high colonic muscle electrical activity,
"bursts", which
appear to travel from the proximal end of the transverse colon (i.e., near the
hepatic
flexure) along the colon to, the distal end of the descending colon (i.e.,
near the
rectosigmoid junction). These high amplitude electrical "spikes" or "bursts",
commonly
termed "migrating long spike: bursts" ("MLSBs"), or "Migrating Electrical
Activity" are
associated with progressive contraction of the colonic muscles that creates a
pressure
wave along the colon, transporting the luminal contents of the colon, i.e.,
feces, to the
rectum, where they become available for defecation. MLSBs typically have a
duration of
about 30 seconds, an amplibade of about 100 to 500 V, and a conduction
velocity or
approximately 15 mm/second and may be detected at the skin surface using the
EMG
sensors positioned above the colon. (A more detailed discussion of migrating
long spike
bursts can be found in the article entitled "Electromyography and Manometry of
the
Pelvic Colon - a Contribution to the Understanding of its Function", Medeiros,
J. A., et
al., Europ J Gastro Hepat vol. 8, pp. 453-459 (1996), which is incorporated by
reference
herein.) The pressure waves that move feces through the colon are commonly
referred to
a high amplitude propagating contractions or "HAPC"s. A graphical
representation of the
output from a sensor monitoring the electrical activity associated with HPAC's
over time
is shown in Figures 13A-:13F. The MSLB's are designated 250 and are shown
sequentially at predetermined intervals as the contents of the wearer's colon
are
transported through the colon. In Figures 13A-13F, the horizontal axis
represents the
length of the colon from the cecum to the rectum as one moves from left to
right on the
axis. As the contents move through the colon, the signal migrates toward the
rectum.
The output shown on the graphs 13A-13F is sequenced such that the measurement
depicted in Figure 13B was taken subsequent to the measurement taken show in
Figure
46
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
13A, and so forth, through Figure 13F. Thus, the Figures show a graphical
representation
of the movement of the colon's contents, as represented by a pressure wave,
over time as
one moves from Figure 13A to Figure 13F.
In one particular embodiment of the present invention, it has been found that
a
s single sensor, such as an EMGJ sensor, located against the skin of the user
in the general
region of the sigmoid colon vvas capable of detecting electrical spikes as the
contents of
the colon were moved tow&rd the user's rectum. The Amplitude of the spikes was
generally found to be in the range of about 40 - 100 V, the frequency was
found to be in
the range of about 0.1 Hz to about 10 Hz, and the duration was in the range of
about 5 to
about 50 seconds. (It should be noted that the ranges described above are only
exemplary,
and that the different parameters could be monitored in different ranges, as
desired. In
just one example, the frequency of the spikes could be monitored in much
broader range,
such as frorn about 0.05 Hz to about 500 Hz and the Amplitude may be monitored
at 10
V or greater.) A graphical example of the output of the sensor 60 is shown in
Figure 14
and is designated 260, while representation of the pressure inside the colon
associated
with the electrical activity is designated 270. As would be noted by one of
skill in the art,
the units of the pressure 260 and electrical activity 270 output would be
different, but
could be any suitable units, such as mmHg and V, respectively.
In an alternative embodiment of the present invention in the form of a pre-
zo micturition enuresis alarm, the article may comprise a monitoring system
including a
piezoelectric transducer that nieasures the volume of a fluid-filled cavity in
the body, such
as a bladder or rectum. Wheri stimulated, the piezoelectric transducer sends
an ultrasonic
pulse into the abdomen. The pulse may be sent out at any pre-defined or random
interval.
The time delay or phase shift in the reflection of the ultrasonic pulse by the
various layers
zs or components of the abdomen is then detected by the transducer. The signal
may be
processed so as to calculate the distance between the front and back walls of
the bladder
or other cavity and to estimatte the relative volume of the bladder or other
cavity versus a
reference state, such as a maximum observed volume. When a predetermined
threshold
parameter is met, the system signals the wearer or caregiver or sends the
information to
30 another system or device which stores the information or otherwise responds
to the input.
47
CA 02497803 2000-06-29
WO 01/00117 PCT/US00/17936
The piezoelectric transducer is preferably oriented appropriately so as to
direct the
ultrasonic pulse to the targel: cavity. In one suitable embodiment, the
transducer has a
frcquency in thc range of 3 to 5 MHz and is driven by an RF (radiofrequency)
transmitter.
A high-voltage half-wavelength pulse (e.g., a pulse of 45 to 80 Hz with a 30
nano-sec rise
s time and a 150 non-second duty time) generates the ultrasound burst. An
exemplary
piezoelectric transducer and associated electrical/processing system suitable
for use with
the present invention is desc:ribed in more detail in the article "Design of a
Miniaturized
Ultrasonic Bladder Monitor and Subsequent Preliminary Evaluation on 41
Patients",
Petrican, P., et al., EE Trartsactions on Rehabilitation En ineering, Vol. 6,
No.l, March
io 1998, which is incorporated by reference herein.
While particular embodiments and/or individual features of the present
invention
have been illustrated and described, it would be obvious to those skilled in
the art that
various other changes and rriodifications can be made without departing from
the spirit
and scope of the invention. Further, it should be apparent that all
combinations of such
is embodiments and features Eire possible and can result in preferred
executions of the
invention. Therefore, the appended claims are intended to cover all such
changes and
modifications that are within the scope of this invention. Also, although the
present
invention is illustxated and ciescribed primarily with respect to a disposable
diaper, the
present invention is not limit:ed to this embodiment. The present invention
may also be
20 used, for example, in articles that are applied directly to a wearer (e.g.,
to the perianal or
perineal regions of the wearer) prior to the application of a disposable
diaper or in place
of a disposable diaper, in a pull-on diaper, a diaper insert, a sanitary
napkin, a tampon,
etc. It is therefore intended to cover in the appended claims all such changes
and
modifications that are within the scope of this invention.
48
