Note: Descriptions are shown in the official language in which they were submitted.
CA 02029240 1998-04-20
PHOTOPROTECTION COMPOSITIONS HAVING IMPROVED SUBSTANTIVITY
Frederick Winfield Woodin, Jr.
George Endel Deckner
TECHNICAL FIELD
This invention relates to improved topical compositions having
improved substantivity such as improved water-proofing (e.g., resistance
to perspiration) and rub-off resistance useful for protecting the skin
from the harmful effects of ultraviolet irradiation, such as sunburn and
sun-induced premature aging of the skin.
BACKGROUND OF THE INVENTION
The damaging effects of sunlight on skin are well documented.
Contrary to what most people believe, it is not necessary that one
sunbathe to suffer the ill-effects of excessive UV exposure. In fact,
a lot of damage can be done just by routine day-to-day activities in the
sunlight. Some scientists estimate that over 70 percent of the damage
the sun inflicts on the average person's skin over a lifetime is the
result of simply being outdoors or even sitting by a window.
The major short term hazard of prolonged exposure to sunlight is
erythema (i.e. sunburn). The 290 to 320 nanometer wavelength ultraviolet
radiation range, designated as the "UVB" wavelength range, tends to be
the primary cause of erythema. The 320 to 400 nanometer wavelength
ultraviolet radiation range, designated as the "UVA" wavelength range,
also produces erythema.
In addition to the short term hazard or erythema, there are also
long term hazards associated with UV radiation exposure. One of these
long term hazards is malignant changes in the skin surface. Numerous
epidemiologic studies demonstrate a strong relationship between sunlight
exposure and human skin cancer.
Another long term hazard of ultraviolet radiation is premature
aging of the skin. This condition is characterized by wrinkling and
yellowing of the skin, along with other physical changes such as
cracking, telangiectasis (spider vessels), solar keratoses (growths),
ecchymoses (subcutaneous hemorrhagic lesions), and loss of elasticity
(sagging). The adverse effects associated with exposure to UVA and UVB
wavelength radiation are more fully discussed in DeSimone, "Sunscreen and
Suntan Products", Handbook of Nonprescription Druqs, 7th Ed., Chapter 26,
pp. 499-511 (American Pharmaceutical Association,
~-2- ~n~240
Washington, D.C.; 1982); Grove and Forbes, "A Method for Evaluating
the Photoprotection Action of Sunscreen Agents Against UV-A Radia-
tion", International Journal of Cosmetic Science, 4, pp. 15-24 (1982);
and U.S. Patent 4 387,089, DePolo, issued June 7, 1983. Hence
although the immediate effects of ultraviolet radiation may be cosmet-
ically and socially gratifying, the long-term hazards are cumulative
and potentially serious.
The fact that these effects are taken seriously by the general
public is suggested by considering the sun protection products'
market. This market has grown considerably in recent years and many
new products are introduced each year. What used to be looked upon as
a seasonal business is no longer. Sun protection compounds are now
included in a diversity of personal care products, particularly
cosmetic-type products which are worn on a daily basis.
15Sunblock agents are commercially available to protect the skin
from UV radiation. These agents scatter or reflect ultraviolet
radiation. Examples include titanium dioxide and zinc oxide. Howev-
er, compositions containing these agents are opaque, generally unat-
tractive in color, and are viewed as unacceptable for usage on more
20 than just the nose or tops of the ears. Furthermore, these agents are
- very susceptible to rub-off or wear-off resulting in little or no
protection.
The most common agents for sun protection are sunscreens. These
agents exert their effects through chemical means, i.e., they absorb
25 ultraviolet radiation so that it cannot penetrate the skin. Sun-
screens present the user with several problems. For example, they
must be on the surface of the skin at the time of exposure to be
effective. Sunscreens are preventative so one must anticipate being
in the sun. To be most effective, sunscreens must be on the skin as a
continuous uniform film. Delivering such a film to the surface of the
skin is' very difficult; maintaining the film over time is almost
impossible. Sunscreens must remain on the surface of the skin during
exposure. However, sunscreens are easily rubbed off or washed off by
sweating or swimming and can also be lost be penetration into the
35 Sklll.
To overcome these problems, polymers such as ethyl cellulose,
polyvinyl stearate, polyvinyl pyrollidone and eicosene copolymers
A
- ~Q7~4Q
- 3 -
have been used; however these polymers have not proved entirely
satisfactory. Further, sunscreen compositions containing acrylic acid
copolymers have also been disclosed in U.S. Patent 4,663,157 to Brock,
issued May 5, 1987.
It is therefore an object of the present invention to provide a
topical composition in a stable form, the use of which will prevent both
acute (erythema) and chronic (photoaging) effects of exposure to the sun.
It is also an object of the present invention to provide a topical
composition and a method for preventing these deleterious effects of the
sun without interfering with the tanning response.
It is further an object of the present invention to provide a
photoprotection composition with improved aesthetics which adheres to the
skin and which is less susceptible to rub-off, wear-off or wash-off
without the need for polymeric substantivity aids.
It is a still further object of the present invention to provide a
photoprotection composition which can be applied to the skin in advance
of UV exposure without significant loss of waterproofing efficacy.
These and other objects will become readily apparent from the
detailed description that follows.
SUMMARY OF THE INVENTION
The present invention relates to an oil-in-water sunscreen emulsion
composition having improved substantivity and moisture resistance for
topical use comprising:
(a) from about 1% to about 40% of a sunscreen;
(b) from about 0.01% to about 5~ of an emulsifier selected from the
group consisting of alkyl substituted acrylic acid copolymers, TEA
stearate salts, alkali neutralized monoalkyl phosphates, alkali
neutralized dialkyl phosphates, hydroxy cetyl phosphate, and mixtures
thereof, wherein said alkyl substituted acrylic acid copolymers comprise
from about 9S.9 to 98.8 weight percent of an olefinically unsaturated
carboxylic monomer selected from the group consisting of acrylic,
methacrylic and ethacrylic acids, about 1 to about 3.5 weight percent of
an acrylate ester of the formula
Rl O
1 ll
CH2 = C - C - O - R
~-Q ~4~
- 3a -
wherein R is an alkyl radical containing 10 to 30 carbon atoms and R<sub>1</sub>
is hydrogen, methyl or ethyl, and 0.1 to 0.6 weight percent of a
polymerizable cross-linking polyalkenyl polyether of a polyhydric alcohol
containing more than one alkenyl ether group per molecule wherein the
parent polyhydric alcohol contains at least 3 carbon atoms and at least
3 hydroxyl groups;
(c) from about 1% to about 60% of a wax component having a required
HLB of from about 1-to about 10 comprising:
(i) an ester wax selected from the group consisting of C1040
alcohols esterified with Cl040 fatty acids, diesters of C1040
fatty acids where the alcohol is propylene glycol, ethylene
glycol or glycerin, polyethylene glycol, polypropylene
glycol, polyglycerin, triglycerides or diglycerides of C1040
fatty acids, pentaerythritol tri- or tetra- esters of C1040
fatty acids, C1040 fatty acids of sorbitan triesters, C1040
fatty acids of sucrose polyesters having 3-8 moles of
substitution, myristyl myristate, paraffin, synthetic
Fischer-Tropsche waxes, microcrystalline waxes, castor wax,
partially hydrogenated vegetable oils, behenyl behenrate,
myristyl propionate and mixtures thereof; and
(ii) a wax selected from the group consisting of diester waxes and
triglyceride waxes and mixtures thereof wherein said diester
wax is selected from the group consisting of C18-36 acid
glycol ester and propylene glycol diester waxes and mixtures
thereof, and wherein said triglyceride wax is selected from
the group consisting of shea butter, cocoa butter, C18-36
acid triglyceride, tribehenin, tribehenin (and) calcium
behenate, tristearin, trimyristate, fully hydrogenated
vegetable oils, and mixtures thereof; and
(d) a safe and effective amount of a topical carrier.
~ ~ ,
2029240
The present invention further relates to a method of inhibiting
the deleterious effects of ultraviolet light exposure to skin compris-
ing applying a safe and photoprotectively effective amount of these
compositions.
All percentages and ratios used herein are by weight of the total
composition and all measurements made at 25~C, unless otherwise
designated.
DETAILED DESCRIPTION OF THE INVENTION
In accordance with the present invention, moisture resistant skin
treatment compositions, such as sunscreen and sun block formulations,
and moisturizer formulations are provided, which compositions have
improved moisture resistance and substantivity due to the presence
therein of a specific wax component and are preferably in the form of
a oil-in-water emulsion which contains water, emollients, emulsifiers,
thickeners, preservatives, coloring agents, fragrances, antioxidants
and the like and one or more known ultraviolet absorbing compounds (in
the case of sunscreen or sun block formulations).
The formulation of the invention is preferably an oil-in-water
type emulsion since this type of emulsion affords better cosmetic feel
to the product. However, the product could also be formulated as a
water-in-oil emulsion, cream base, or oil base. Depending upon the
choice of ingredients, the formulation has a semi-solid cream-like
consistency which can be packaged in a plastic squeeze tube or it has
a lotion type consistency which can be packaged in a plastic squeeze
container. The container can include a flow-type cap or pump-type
dispenser.
Sunscreens. A wide variety of conventional sunscreening agents
are suitable for use in the present invention. Segarin, et al., at
Chapter VIII, pages 189 et seq., of Cosmetics Science and TechnologY,
disclose numerous suitable agents. Specific suitable sunscreening
agents include, for example: p-Aminobenzoic acid, its salts and its
derivatives (ethyl, isobutyl, glyceryl esters; p-dimethylaminobenzoic
acid); Anthranilates ti.e., o-aminobenzoates; methyl, menthyl, phenyl,
benzyl, phenylethyl, linalyl, terpinyl, and cyclohexenyl esters);
Salicylates (octyl, amyl, phenyl, benzyl, menthyl, glyceryl, and
dipropyleneglycol esters); Cinnamic acid derivatives (menthyl and
benzyl esters, -phenyl cinnamonitrile; butyl cinnamoyl pyruvate);
Dihydroxycinnamic acid derivatives (umbelliferone, methylumbelli-
2029240
ferone, methylaceto-umbelliferone); Trihydroxycinnamic acid deriva-
tives (esculetin, methylesculetin, daphnetin, and the glucosides,
esculin and daphnin); Hydrocarbons (diphenylbutadiene, stilbene);
Dibenzalacetone and benzalacetophenone; Naphtholsulfonates (sodium
salts of 2-naphthol3,6-disulfonic and of 2-naphthol-6,8-disulfonic
acids); Dihydroxy-naphthoic acid and its salts; o- and p-Hydroxybi-
phenyldisulfonates; Coumarin derivatives (7-hydroxy, 7-methyl, 3-
phenyl); Diazoles (2-acetyl-3-bromoindazole, phenyl benzoxazole,
methyl naphthoxazole, various aryl benzothiazoles); Quinine salts
(bisulfate, sulfate, chloride, oleate, and tannate); Quinoline deriva-
tives (8-hydroxyquinoline salts, 2-phenylquinoline); Hydroxy- or
methoxy-substituted benzophenones; Uric and vilouric acids; Tannic
acid and its derivatives (e.g., hexaethylether); (Butyl carbityl)
(6-propyl piperonyl) ether; Hydroquinone; Benzophenones (Oxybenzene,
Sulisbenzone, Dioxybenzone, Benzoresorcinol, 2,2',4,4'-Tetrahydroxy-
benzophenone, 2,2'-Dihydroxy-4,4'-dimethoxybenzophenone, Octabenzone;
4-Isopropyldibenzoylmethane; Butylmethoxydibenzoylmethane; Etocrylene;
and 4-isopropyl-di-benzoylmethane.
Of these, 2-ethylhexyl p-methoxycinnamate, 4,4'-t-butyl methoxy-
dibenzoylmethane, 2-hydroxy-4-methoxybenzophenone, octyldimethyl
p-aminobenzoic acid, digalloyltrioleate, 2,2-dihydroxy-4-methoxybenzo-
phenone, ethyl 4-[bis(hydroxypropyl)]aminobenzoate, 2-ethylhexyl2-
cyano-3,3-diphenylacrylate, 2-ethylhexysalicylate, glyceryl p-amino-
benzoate, 3,3,5-trimethylcyclohexysalicylate, methylanthranilate,
p-dimethyl- aminobenzoic acid or aminobenzoate, 2-ethylhexyl p-di-
methylamino- benzoate, 2-phenylbenzimidazole-5-sulfonic acid 2-(p-
dimethylaminophenyl)-S-sulfonicbenzoxazoic acid and mixtures of these
compounds, are particularly useful.
Preferred sunscreens useful in the compositions of the present
invention are 2-ethylhexyl p-methoxycinnamate, butylmethoxydibenzoyl-
methane, 2-hydroxy-4-methoxybenzophenone, octyldimethyl p-aminobenzoic
acid, 2,2' dihydroxy-4-methoxybenzophenone and ethyl hexyl salicylate
and mixtures thereof.
A safe and photoprotectively effective amount of sunscreen may be
used in the sunscreen compositions of the present invention. By "safe
and photoprotectively" is meant an amount sufficient to provide
photoprotection when the composition is applied not so much as to
-6-
cause any side effects or skin reactions. Generally from about 1% to
about 30%, preferably from about 2% to about 20%, of the composition
may comprise a sunscreening agent. Exact amounts will vary depending
upon the sunscreen chosen and the desired Sun Protection Factor (SPF).
SPF is a commonly used measure of photoprotection of a sunscreen
against erythema. This number is derived from another parameter, the
minimal erythemal dose (MED). MED is defined as the "lease exposure
dose at a specified wavelength that will elicit a delayed erythema
response". The MED indicates the amount of energy reaching the skin
and the responsiveness of the skin to the radiation. The SPF of a
particular photoprotector is obtained by dividing the MED of protected
skin by the MED of unprotected skin. The higher the SPF, the more
effective the agent in preventing sunburn. The SPF value tells how
many times longer a person can stay in the sun with use of the sun-
screen (compared to a person with unprotected skin) before that person
will experience 1 MED. For example, utilizing a sunscreen with an SPF
of 6 will allow an individual to stay in the sun six times longer
before receiving l MED. As the SPF value of a sunscreen increases,
the less chance exists for development of tanning of the skin.
Commercially available sunscreening products have SPF values ranging
from 2 to 50.
Also particularly useful in the present invention are sunscreens
such as those disclosed in Sabatelli, U.S. Patent No. 4,937,370
(granted June 26, 1990) and Sab~telli et al., European
Application Serial No. 87201184.6 (filed June 22, 1987
published February 3, 1988). The sunscreening
agents disclosed therein have, in a single molecule, two distinct
chromophore moieties which exhibit different ultra-violet radiation
absorption spectra. One of the chromophore moieties absorbs pre-
dominantly in the UVB radiation range and the other absorbs strongly
in the UVA radiation range.
These sunscreening agents provide higher efficacy, broader UV
absorption, lower skin penetration and longer lasting efficacy rela-
tive to conventional sunscreens.
Preferred members of this class of sunscreening agents are 4-
N,N-(2-ethylhexyl)methylaminobenzoic acid ester of 2,4-dihydroxybenzo-
phenone; N,N-di-(2-ethylhexyl)-4-aminobenzoic acid ester with 4-hy-
droxydibenzoylmethane; 4-N,N(2-ethylhexyl) methylaminobenzoic acid
B
-7--
.~
ester with 4-hydroxydibenzoylmethane; 4-N,N-(2-ethylhexyl)methylamino-
benzoic acid ester of 2-hydroxy-4-(2-hydroxyethoxy)benzophenone;
4-N,N-(2-ethylhexyl) methylaminobenzoic acid ester of 4-(2-hydroxyeth-
oxy)dibenzoylmethane; N-N-di-(2-ethylhexyl)-4-aminobenzoic acid ester
of 2-hydroxy-4-(2-hydroxyethoxy)benzophenone, and N,N-di-(2-ethyl-
hexyl)4-aminobenzoic acid ester of 4-(2-hydroxyethoxy)dibenzoylmethane
and mixtures thereof.
Emulsifier. The compositions of the present invention also
essentially comprise at least one emulsifier. Preferred is the use of
alkyl substituted acrylic acid copolymers comprising polymers of a
monomeric mixture containing 95.9 to 98.8 weight percent of an ole-
finically unsaturated carboxylic monomer selected from the
group consisting of acrylic, methacrylic and ethacrylic acids, about 1
to about 3.5 weight percent of an acrylate ester of the formula
Rl O
CH2=~ - ~ - 0 - R
wherein R is an alkyl radical containing 10 to 30 carbon atoms and R~
is hydrogen, methyl or ethyl, and 0.1 to 0.6 weight percent of a
polymer-izable cross-linking polyalkenyl polyether of a polyhydric
alcohol containing more than one alkenyl ether group per molecule
wherein the parent polyhydric alcohol contains at least 3 carbon atoms
and at least 3 hydroxyl groups.
Preferably, these polymers contain from about 96 to about 97.9
weight percent of acrylic acid and from about 2.5 to about 3.5 weight
percent of acrylic esters wherein the alkyl group contains 12 to 22
carbon atoms, and Rl is methyl, most preferably the acrylate ester is
stearyl methacrylate. Preferably, the amount of crosslinking monomer
is from about 0.2 to 0.4 weight percent. The preferred crosslinking
monomers are allyl pentaerythritol, trimethylolpropane diallylether or
allyl sucrose. These polymers are fully described in U.S. Patent
4,509,949, Huang et al., issued April 5, 1985.
The carboxylic monomers useful in the production of polymers used
in this invention are the olefinically-unsaturated carboxylic acids
containing at least one activated carbon-to-carbon olefinic double
bond, and at least one carboxyl group.
The preferred carboxylic monomers are the acrylic acids having
the general structure:
~_ -8~ 4 ~
R2
CH 2 =C - COOH,
wherein R2 is a substituent selected from the class consisting of
hydrogen, halogen, and the cyanogen (--C=N) groups, monovalent alkyl
radicals, monovalent alkaryl radicals and monovalent cycloaliphatic
radicals. Of this class, acrylic, methacrylic, and ethacrylic acid
are most preferred. Another useful carboxylic monomer is maleic
anhydride or the acid. The amount of acid used will be from about
95.5 to about 98.9 weight percent of the total monomers used. More
preferably the range will be from about 96 to about 97.9 weight
percent.
The polymers are crosslinked with a polyfunctional vinylidene
monomer containing at least 2 terminal CH2<groups, including for
example, butadiene, isoprene, divinyl benzene, divinyl naphthlene,
allyl acrylates, and the like. Particularly useful crosslinking
monomers for use in preparing the copolymers are polyalkenyl poly-
ethers having more than one alkenyl ether grouping per molecule. The
most useful possess alkenyl groups in which an olefinic double bond is
present attached to a terminal methylene grouping, CH2=C<. Most
preferred from this class is Carbomer 1342 (available as Carbopol 1342
from B.F. Goodrich).
Also useful are TEA stearate salts, alkali neutralized mono- and
di- alkyl phosphates including diethanolamine mono- and di- cetyl
phosphate (available from Givaudan as Amphisol) and hydroxy cetyl
phosphate (available from Henkel as Forlanit E).
The emulsifiers used in the present invention should be dispers-
able (but not soluble) in water.
The emulsifier typically comprises in total from about 0.01% to
about 5%, preferably from about 0.05% to about 3%, and most preferably
from about 0.05% to about 1%, of the compositions of the present
inventlon.
Wax Component. An essential component of the compositions herein
is a wax component having a required HLB of from about 1 to about 10,
preferably from about 1 to about 8, more preferably from about 1 to
about 6 and most preferably from about 1 to about 5 comprising:
(i) an ester wax; and
(ii) a wax selected from the group consisting of diester waxes
and triglyceride waxes and mixtures thereof.
* Trade mark
-9-
Preferably, the ratio of (i) to (ii) ranges from about 10:1 to
about 1:1, more preferably from about 5:1 to about 1:1 and most
preferably from about 3:1 to about 1:1.
The HLB (short for "Hydrophile-Lipophile Balance") value system
is fully described, and values for various materials are provided, in
the publication The HLB Svstem. A Time-Savinq Guide to Emulsifier
Selection (published by ICI Americas Inc., Wilmington, Delaware;
1984).
Useful ester waxes include C10-C40 alcohols esterfied with
o C10-C40 fatty acid, diesters of C10-C40 fatty acid where the alcohol
is propylene glycol, ethylene glycol, polyethylene glycol, polypropy-
lene glycol, polyglycerin, or glycerin, triglycerides or diglycerides
of C10-C40 fatty acid, pentaerythitol tri- or tetra- esters of C10-C40
fatty acids, C10-C40 fatty acids of sorbitan triesters, C10-C40 fatty
acids of sucrose polyesters having 3-8 moles of substitution, myristyl
myristate, paraffin, synthetic waxes such as Fischer-Tropsche waxes,
microcrystalline waxes, castor wax, partially hydrogenated vegetable
oils, behenyl behenrate and myristyl propionate and mixtures thereof.
Useful diester waxes include Synchrowax ERL-C (available from
20 Croda) and propylene glycol diester waxes including ethylene glycol
distearate and glycol distearate. Useful triglyceride waxes include
Shea Butter, Cocoa Butter, Synchrowax HGL-C, Synchrowax~HRC, Synchro-
wax HRS-C (all available from Croda Inc.), tristearin, trimyristate
and fully hydrogenated vegetable oils and mixtures thereof. Preferred
25 is a mixture of diester and triglyceride waxes in a ratio of from
about 5:1 to about 1:1 and more preferably from about 4:1 to about
1:1.
Waxes useful in the compositions of this invention are disclosed
in the following U.S. Patent 4, 049, 792, to Elsnau, issued September
20, 1977; U.S. Patent 4,151,272, to Geary et al., issued April 24,
1975; U.S. Patent 4,229,432, to Geria, issued October 21, 1980; U.S.
Patent 4,280,994~ to Turney, issued July 28, 1981; U.S. Patent
4,126,679, to Davy et al., issued November 21, 1978; and European
Patent Application Publication Number 117,070, to May, published
August 29, 1984, "The Chemistry and Technology of Waxes", A.H. Warth,
2nd Edition, reprinted in 1960, Reinhold Publishing Corporation, pp.
* Trade mark
~ -10-
391-393 and 421; "The Petroleum Chemicals Industry", R.F. Goldstein
and A.L. Waddeam, 3rd Edition (1967), E & F.N. Span Ltd., pp 33-40;
"The Chemistry and Manufacture of Cosmetics", M.G. DeNavarre, 2nd
edition (1970), Van Nostrand ~ Company, pp 354-376; and in "Ency-
clopedia of Chemical Technology:, Vol. 24, Kirk-Othmer, 3rd Edition
(1979) pp 466-481.
OPTIONAL COMPONENTS
Emollients. The compositions of the present invention preferably
comprise at least one emollient. Preferred emollients are volatile
silicone oils, non-volatile emollients, and the highly branched
hydrocarbons known as the Permethyl*99 through 108A series (available
from Permethyl Corporation) and mixtures thereof. The compositions of
the present invention more preferably comprise at least one volatile
silicone oil which functions as a liquid emollient, or especially in a
mixture of volatile silicone oils and non-volatile emollients. The
term "volatile", as used herein, refers to those materials which have
a measurable vapor pressure at ambient temperature.
Volatile silicone oils useful in the compositions of the present
invention are preferably cyclic. The following formula illustrates
cyclic volatile polydimethylsiloxanes useful in the compositions
disclosed herein:
C CH3
[Si ~]n
CH3
wherein n equals about 3 to about 7. Linear polydimethylsiloxanes
contain from about 3 to about 9 silicon atoms per molecule and have
the following general formula:
(CH3)3si-o-[si(cH3) 2 -O]n-Si(CH3)3
wherein n equals about 1 to about 7. Linear volatile silicone materi-
als generally have viscosities of less than about 5 centistokes at25~C while cyclic materials typically have viscosities of less than
about 10 centistokes. A description of various volatile silicone oils
is found in Todd, et al., "Volatile Silicone Fluids for Cosmetics",
Cosmetics & Toiletries, 91, pages 27-32 (1976).
Examples of preferred volatile silicone oils useful herein
include: Dow Corning* 344, Dow Corning 345, and Dow Corning 200
(manufactured by Dow Corning Corp.); Silicone 7207 and Silicone 7158
* Trade mark
' ~2 ",'
~,
4 ~ ~
'~ -11 -
(manufactured by the Union Carbide Corp.); SF 1202 (manufactured by
General Electric); and SWS-03314 (manufactured by SWS Silicones,
Inc.).
The present compositions also preferably contain one or more
non-volatile emollients. Such materials include fatty acid and fatty
alcohol esters, hydrocarbons, non-volatile silicone oils, and mixtures
thereof. Emollients among those useful herein are described in
Cosmetics. Science and Technoloq~ 27-104 (M. Balsam and E. Sagarin,
Ed.; 1972), and U.S. Patent 4,202,879, to Shelton, issued May 13, 1980.
Non-volatile silicone oils useful as an emollient material
include polyalkylsiloxanes, polyalkylarylsiloxanes, and polyether-
siloxane copolymers. The essentially non-voiati~e polyalkyl siloxanes
useful herein include, for example, polydimethyl siloxanes with
viscosities of from about 5 to about 100,000 centistokes at 25~C.
5 Among the preferred non-volatile emollients useful in the present
compositions are the polydimethyl siloxanes having viscosities from
about 10 to about 400 centistokes at 25~C. Such polyalkyl siloxanes
include the Vicasil~series (sold by General Electric Company) and the
Dow Corning 200 series (sold by Dow Corning Corporation). Polyalkyl-
20 aryl siloxanes include polymethylphenyl siloxanes having viscositiesof from about 15 to about 65 centistokes at 25~C. These are avail-
able, for example, as SF 1075 methylphenyl fluid (so]d by General
Electric Company) and 556 Cosmetic Grade Fluid (sold by Dow Corning
Corporation). Useful polyether siloxane copolymers include, for
25 example, a polyoxyalkylene ether copolymer having a viscosity of about
1200 to 1500 centistokes at 25~C. Such a fluid is available as
SF-1066 organosilicone surfactant (sold by General Electric Company).
Polysiloxane ethylene glycol ether copolymers are preferred copolymers
for use in the present compositions.
Non-polar fatty acid and fatty alcohol esters useful herein as an
emollient material include, for example, di-isopropyl adipate, isopro-
pyl myristate, isopropyl palmitate, ethyl hexyl palmitate, isodecyl
neopentanoate C12-C15 alcohol benzoate, diethyl hexyl maleate, PPG 14
butyl ether and PPG-2 myristyl ether propionate. Hydrocarbons such as
isohexadecane (e.g., Permethyl lOlA supplied by Presperse), petrolatum
and USP light (e.g. Klearol~) or heavy (e.g. Kaydol~) mineral oils
are also useful as emollients.
* Trade mark
~:B
20292~0
-12-
The emollients typically comprise in total from about 1% to about
50%, preferably from about 1% to about 25%, and more preferably from
about 1% to about 10X by weight of the compositions of the present
invention.
The following non-limiting examples illustrate embodiments of the
subject invention wherein both essential and optional ingredients are
combined. It i s to be understood that these examples are for illus-
trative purposes only and are not to be construed as limiting the
scope of the invention thereto.
EXAMPLE I
An oil-in-water emulsion prepared by combining the following
components utilizing conventional mixing techniques.
A B C
Comconents % Weiqht % Wei~ht % Wei~ht
Water, purified q.s. q.s. q.s.
Carbopol 1342 0.15 0.15 0.15
Carbopol g34 0.30 0.20 0.20
Escalol 507 (octyl dimethyl PABA)2.00 2.00 2.00
Octyl Methoxycinnamate 2.00 2.00 2.00
Stearic Acid 2.50 2.50 2.50
C12 15 alcohols benzoate 10.00 10.00 10.00
Myristyl myristate 1.00 1.00 1.00
Shea Butter 1.00 1.00 1.00
Triethanolamine 99% 0.45 1.00 0.30
Cyclomethicone 2.00 2.00 2.00
Propyl paraben 0.20 0.20 0.20
Methyl paraben 0.30 0.30 0.30
OMDM Hydantoin 0.20 0.20 0.20
Fragrance 0.50 0.50 0.50
Amphisol (DEA-cetyl phosphate) -- -- 1.0
This emulsion is useful for topical application to inhibit damage
caused by acute or chronic UV exposure. Use of an amount of this
composition sufficient to deposit about 2.0 mg/cm2 of the sunscreening
agent to the skin prior to UV exposure is appropriate.
2029240
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EXAMPLE II
An oil-in-water emulsion prepared by combining the following
components utilizing conventional mixing techniques.
B
Com w nents % w/w %w/w
Water, purified q.s. q.s.
Carbopol 1342 0.15 0.15
Carbopol 934 0.20 0.20
Octyl Dimethyl PABA 8.00 8.00
Octyl Methoxycinnamate 4.00 4.00
Benzophenone-3 4.00 4.00
C 12 -15 alcohols benzoate 5.00 5.00
Octyldodecyl Stearoyl Stearate 5.00 5.00
Castor Wax MP 70 2.00 2.00
Cyclomethicone 3.00 3.00
Triethanolamine 99% 0.35 0.60
Synchrowax HRC 2.00 2.00
Propyl paraben 0.15 0.15
Methyl paraben 0.20 0.20
Benzyl alcohol 0.30 0.30
Fragrance 0.50 0.50
Hydrocetyl phosphate -- 1.00
This emulsion is useful for topical application to inhibit damage
caused by acute or chronic UV exposure. Use of an amount of this
composition sufficient to deposit about 2.0 mg/cm2 of the sunscreening
agent to the skin prior to UV exposure is appropriate.
2029240
-14-
EXAMPLE III
An oil-in-water emulsion prepared by combining the following
components utilizing conventional mixing techniques.
Comwnents % w/w
Water, purified q.s.
Carbopol 1342 0.15
Carbopol 940 0.20
Octyl Dimethyl PABA 8.00
Octyl Methoxycinnamate 3.00
Benzophenone-3 3.00
Isostearyl Benzoate 5.00
Cocoa Butter 2.00
Behenyl Behenate 3.00
Triethanolamine 94% 0.35
Dimethicone (350 cts) 2.00
Propyl paraben 0.20
Methyl paraben 0.35
DMDM Hydantoin 0.30
Fragrance 0.50
This emulsion is useful for topical application to inhibit damage
caused by acute or chronic UV exposure. Use of an amount of this
composition sufficient to deposit about 2.0 mg/cm2 of the sunscreening
agent to the skin prior to UV exposure is appropriate.
-15- ~ 4 ~
-
EXhMPLE IV
An oil-in-water emulsion prepared by combining the following
components utilizing conventional mixing techniques.
Components % w/w
Water, purified q.s.
Carbopol 1342 0.35
Octyl Methoxycinnamate 8.00
Benzophenone-3 3.00
Octyl Salicylate 3.00
Ethylene Glycol stearate 0.50
Synchrowax ERC (synthetic diester) 3.00
Tristearin 2.00
Triethanolamine 99% 0.35
Isostearyl benzoate 10.00
Octyldodecyl stearoyl stearate 5.00
Propyl paraben 0.25
Methyl paraben 0.30
Germall 115 0.30
Fragrance 0.80
This emulsion is useful for topical application to inhibit damage
caused by acute or chronic UV exposure. Use of an amount of this
composition sufficient to deposit about 2.0 mg/cm2 of the sunscreening
agent to the skin prior to UV exposure is appropriate.
* Trade mark
-B
2029240
-16-
EXAMPEE V
An oil-in-water emulsion prepared by combining the following
components utilizing conventional mixing techniques.
ComDonents % w/w
Water, purified q.s.
Carbopol 1342 0.20
Carbopol 940 0.10
Octyl dimethyl PABA 8.00
Menthyl anthranilate 5.00
Cetyl palmitate 3.00
Ethylene Glycol Distearate 3.00
Isodecyl Neopentanoate (Dermol 105) 2.00
Triethanolamine 99~ O.BO
Cyclomethicone (Dow Corning 344) 1.50
Propyl paraben 0.15
Methyl paraben 0.20
DMDM Hydantoin 0.35
Fragrance 1.00
This emulsion is useful for topical application to inhibit damage
caused by acute or chronic UV exposure. Use of an amount of this
composition sufficient to deposit about 2.0 mg/cm2 of the sunscreening
agent to the skin prior to UV exposure is appropriate.
2029240
-17-
EXAMPLE VI
An oil-in-water emulsion prepared by combining the following
components utilizing conventional mixing techniques.
ComDonents ~Ow/w
Water, purified q.s.
Carbopol 934 0.20
Carbopol 1342 0.15
Disodium EDTA 0.10
Octyl dimethyl PABA 2.00
Octyl Methoxycinnamate 2.00
Isostearyl benzoate 10.00
Octyldodecyl stearoyl stearate5.00
Myristyl myristate 2.00
Shea Butter 2.00
Ethylene Glycol stearate 0.20
Triethanolamine g9% 0.35
Cyclomethicone 2.00
Propyl paraben 0.15
Methyl paraben 0.25
Butylene Glycol 2.00
Benzyl alcohol 0.30
DMDM Hydantoin 0.40
Fragrance 1.00
This emulsion is useful for topical application to inhibit damage
caused by acute or chronic UV exposure. Use of an amount of this
composition sufficient to deposit about 2.0 mg/cm2 of the sunscreening
agent to the skin prior to UV exposure is appropriate.
''~ -18- ~ 2 4 ~
EXAMPLE VII
An oil-in-water emulsion prepared by combining the following
components utilizing conventional mixing techniques.
Components % w/w
Water, purified q.s.
Carbopol 1342 0.15
Carbopol 940 0.15
Octyl methoxycinnamate8.00
Octyl salicylate 3-00
Benzophenone-3 3.00
C12-15 alcohols benzoate8.00
Isodecyl Neopentanoate3.00
Wecobee-m (Hydrogenated vegetable oil) 3.00
Satulan (Hydrogenated lanolin) 2.00
Synchrowax HGL 3.00
Dimethicone (350 cts) 2.50
Triethanolamine 99% 0.30
Glycerin 2.00
Propyl paraben 0.20
Methyl paraben 0.30
Germall 115 ~ ~ 40
This emulsion is useful for topical application to inhibit damage
caused by acute or chronic UV exposure. Use of an a~ount of this
composition sufficient to deposit about 2.0 mg/cm2 of the sunscreening
agent to the skin prior to UV exposure is appropriate.
A
