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Sommaire du brevet 2205548 

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Disponibilité de l'Abrégé et des Revendications

L'apparition de différences dans le texte et l'image des Revendications et de l'Abrégé dépend du moment auquel le document est publié. Les textes des Revendications et de l'Abrégé sont affichés :

  • lorsque la demande peut être examinée par le public;
  • lorsque le brevet est émis (délivrance).
(12) Demande de brevet: (11) CA 2205548
(54) Titre français: COMPOSITION MODIFIANT L'AROME
(54) Titre anglais: FLAVOR MODIFYING COMPOSITION
Statut: Morte
Données bibliographiques
(51) Classification internationale des brevets (CIB):
  • A23L 27/20 (2016.01)
  • A23L 27/30 (2016.01)
(72) Inventeurs :
  • ENGEL, LAWRENCE D. (Etats-Unis d'Amérique)
  • STAGNITTI, GEORGE JR. (Etats-Unis d'Amérique)
(73) Titulaires :
  • CULTOR LTD. (Finlande)
(71) Demandeurs :
  • CULTOR LTD. (Finlande)
(74) Agent: SMART & BIGGAR
(74) Co-agent:
(45) Délivré:
(86) Date de dépôt PCT: 1995-10-16
(87) Mise à la disponibilité du public: 1996-06-13
Licence disponible: S.O.
(25) Langue des documents déposés: Anglais

Traité de coopération en matière de brevets (PCT): Oui
(86) Numéro de la demande PCT: PCT/IB1995/000877
(87) Numéro de publication internationale PCT: WO1996/017527
(85) Entrée nationale: 1997-05-20

(30) Données de priorité de la demande:
Numéro de la demande Pays / territoire Date
08/353,655 Etats-Unis d'Amérique 1994-12-09

Abrégés

Abrégé français

L'invention concerne des compositions modifiant l'arôme comprenant des combinaisons de dihydrochalcone de néohespéridine et de maltol et/ou éthylmaltol. Elle porte également sur les utilisations desdites compositions modifiant l'arôme dans les produits alimentaires.


Abrégé anglais




The present invention is directed to flavor modifying compositions comprising
combinations of neohesperidine dihydrochalcone with maltol and/or ethylmaltol.
Uses of the flavor-modifying compositions is foodstuffs are also disclosed.

Revendications

Note : Les revendications sont présentées dans la langue officielle dans laquelle elles ont été soumises.



-14-

CLAIMS
1. A flavor-modifying composition comprising maltol and neohesperidine
dihydrochalcone.
2. A composition according to claim 1 wherein maltol is present at a level
of from about 5 to about 100 parts per million and neohesperidine dihydrochalcone is
present at a level of from about 0.1 to about 10.0 parts per million.
3. A foodstuff comprising the composition of claim 1.
4. A method of modifying the flavor, body and mouthfeel of a foodstuff
comprising adding to the foodstuff the composition of claim 1.
5. The method of claim 4 wherein said foodstuff is selected from the group
consisting of soft carbonated beverages, soft non-carbonated fruit flavored beverages,
soft non-carbonated beverages, sauces, toppings, meat products, poultry products,
animal feeds, confectionery products, baked goods, alcoholic beverages, savory
snacks, dairy products, condiments, and gravies.
6. A flavor-modifying composition comprising ethylmaltol and
neohesperidine dihydrochalcone.
7. A composition according to claim 6 wherein ethylmaltol is present at a
level of from about 0.1 to about 20 parts per million and neohesperidine
dihydrochalcone is present at a level of from about 0.1 to about 10.0 parts per million.
8. A foodstuff comprising the composition of claim 6.
9. A method of modifying the flavor, body and mouthfeel of a foodstuff
comprising adding to the foodstuff the composition of claim 6.
10. The method of claim 9 wherein said foodstuff is selected from the group
consisting of soft carbonated beverages, soft non-carbonated fruit flavored beverages,
soft non-carbonated beverages, sauces, toppings, meat products, poultry products,
animal feeds, confectionery products, baked goods, alcoholic beverages, savory
snacks, dairy products, condiments, and gravies.
11. A flavor-modifying composition comprising maltol, ethylmaltol and
neohesperidine dihydrochaicone.
12. A composition according to claim 11 wherein maltol is present at a level
of from about 5 to about 100 parts per million, ethylmaltol is present at a level of from
about 0.1 to about 20 parts per million and neohesperidine dihydrochalcone is present
at a level of from about 0.1 to about 10.0 parts per million.





-15-

13. A foodstuff comprising the composition of claim 11.
14. A method of modifying the flavor, body and mouthfeel of a foodstuff
comprising adding to the foodstuff the composition of claim 11.
15. The method of claim 14 wherein said foodstuff is selected from the groupconsisting of soft carbonated beverages, soft non-carbonated fruit flavored beverages,
soft non-carbonated beverages, sauces, toppings, meat products, poultry products,
animal feeds, confectionery products, baked goods, alcoholic beverages, savory
snacks, dairy products, condiments and gravies.
16. A method of reducing the unpleasant aftertaste of a pharmaceutical
composition comprising adding to the pharmaceutical composition a flavor-modifying
composition, said flavor modifying composition selected from the group consisting of:
(a) maltol-neohesperidine dihydrochalcone;
(b) ethylmaltol - neohesperidine dihydrochalcone;
(c) maltol - ethylmaltol - neohesperidine dihydrochalcone.

Description

Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.


CA 02205548 l997-05-20
WO 96117527 ~ ~l1l~9~ Q_



5FLAVOR MODIFYING COMPOSITION
The pr~sent invention relates to flavoring cGr.~l-os~i~r.s. More particularly, it
relates to a flavor modifying cGrl~ro~ oll cGrllp.ia;lly combinations of neohesperidine
dihyJ~ocl ,- -~ne with maltol or ethyl maltol.
r, .~cessecl foodet~ ~s and flavors added to l~r~cessed foodetJ ~ffs typically do not
10have the intense flavor n ':5 C'C ~ ~ -3d wrth consumer ~,rt~ r.ces. For this reason, a flavor
enll~c;..~ agent may be added to ~ot~ le the flavor. In n~ iGI) to ~oter,li~liG~ of
the flavor the flavor enhanc;.,y agent also ~Jululllit~lùs the body and mouthfeel of the
flavor or food~t~ ~.
Two of the most widely used flavor enhancers are maltol and ethyll"~lol. Maltol
15 is a naturally occurring substance found in the bark of young larch trees, pine needles
and chicory. Early comn .ercial pro~uction of maltol was from the destructive distillation
of wood. Natural maltol is usually obtained only in very small qu~ ,lilies by the above
me~hod.
The sy"ll,esis of synthetic maltols as well as other gam~"a-pyrones, such as
20 pyromeconic acid is dQscriLed in United States patent numbers 3,130 204 3,133,089,
3,140,239,3,159,652,3,365,469,3,376,317,3,468,915,3,440,183, and 3,446,629.
The sy"ll,es;s of maltol and ethyl, maltol, along with other yalllrl~a pyrones
using a furfuryl alcohol as a starting l.lalelial is described in United States Patent
numbers 4,082 717 and 4,289,704.
25Neohesperidine dih~,d~ ucl - .... o ne is a ~ Et~-ning agent ~ ared from na, i"gen
a flavanone glycoside occurring naturally in y, ap~f, uit~ by the pr .cess des~;, iL ed in
United States patent numbers 3,087,821 and 3,375,242.
United States Patent number 4,087,588 refers to the use of neohesperidine
dihyJ~ochr'-one as a sw.a~tening agent.
30European Patent Ar F li_Qffon number 600977 refers to the use of neohesperidine
dihyd~ocl,-'oone to pote"lidle the body and mouthfeel of foods and beverages.
United States Patent number 3 653 9~3 refers to a COI"~ ualion of
neohesperidine dihydrochalcone and a sacl ,a" i"ous a~V_- ~tu, ,el as a c Jl~ctcning agent.
European patent ~,-FI~-~;cn number 507598 refers to a combination of
35sucralose and neohesperidi. ,e dihydrocl~alcGne as a sweetening agent.
United States Patent Number 4,581,378 refers to neohesperidine
dihydlochalcone as a sweetening agent in a rodel,licide co~)~positiGI~.

CA 02205548 1997-05-20
WO 96117527 PCT/IB95/00877



In one embodiment, the pres~,lt invention is directed to a flavor-modifying
cu"~l~osition CG~ Iiaillg maltol and neohesperidinQ dih~ ùch~ ,e.
r~r,~d is the CG~ -GSit;Gll wherein maltol is present at a level of from about
5 to about 100 parts per million and neohesperidine dihyd~ucl,-',.~ ~e is pr~se"l at a
5 level of from about 0.1 to about 10.0 parts per million.
The pr~ser,l invention is also directed to a foo~st~ff cor"i~,ia;,.g the maltol-neohespiridine dihyd,och-' o ,e co~ o~
The preser,l invention is also u~J to a method of modifying the flavor, body
and mouthfeel of a foo~stl~f by adding to the foorlstuff the maltol-neoi)esperi~ine
10 dihydrochalcone CGI I pO~;YI 1 .
r,~ar,ed is the method wherein said foodstl~ff is sele 1æ~1 from the group
cc: r,si~li, ,9 of soft Cdl Lon~led beverages, soft non-carbonated fruit flavored beverages,
soft non-ca,Lonal~ad beverages, sauces, toppi"gs, meat products, poultry products,
animal feeds, conlec,tionery products, baked goods, alcoholic beverages, savory
15 snacks, dairy products, condiments, and gravies.
In another embodiment, the iolesenl invention is directed to a flavor-modifying
comrosition co"",,i~i"~ ethylmaltol and neohesperidine dihydrochalcone.
fer,ed is the composition wherein ethyl~"allol is preser,l at a level of from
about 0.1 to about 20 parts per million and neohesperidine dihyJ~och~'~one is preser,l
20 at a level of from about 0.1 to about 10.0 parts per million.
The present invention is also directed to a foodstl ~fl coi "pri:,i"g the ethylmaltol-
neohesp6ridine dihyd~ ùcl l - ' ~ ~ ne CGI l ~pO~itiGIl.
The pleser,l invention is also directed to a method of modifying the flavor, body
and mouthfeel of a foo~lstl~ff cGmpri~i"g adding to the foodstuff the ethylmaitol-
25 neohesperi " ,e dihyJ~ ùd~alCGI ,e co" ~pos~iGn.
r~ elled is the method wherein said foo~lst~ff is selectecl from the group
consiali"g of soft carboll~led beverages, soft non-carLol ,aled fruit flavored beverages,
soft non-ca,bol,aled beverages, sauces, toppings, meat products, poultry products,
animal feeds, co"t~ctionery products, baked goods, alcohoiic beverages, savory
30 snacks, dairy products, condiment and gravies.
In still another embodiment, the -present invention is directed to a flavor
modifying comrosiliGn cGm~Jri~il Ig maltol, ethylmaitol and neohesperidine
dihyJ,uch~' ~ne.

CA 02205548 1997-05-20
WO 9611~1S2'1 PCTJ~gS,'. 0 7~



r~ .l is the co"~po~eition wherein maltol is pr~s~nt at a level of from about
5 to about 100 parts per million, ethyb..~llol is ~,r~sellt at a level of from about 0.1 to
" about 20 parts per million and neohesl~t"idine dihydrochalcone is l~r~sent at a level of
from about 0.1 to about 10.0 parts per million.
The ,~r~sel,l invention is also directed to a foo~l~t~ ff c~ JIiailly the maltolethyh.)allol, neohesperidine dih~,d~ucl~ ne cGr.,ros;~iGn.
The ,~,n3se, ll invention is also directed to a method of modifying the flavor, body
and mouthfeel of a foodstl~f compri~ adding to the foo~let~ the maltol-ethyh,~allùl-
neohesperidine dihy-l,ocl~ o ne CG m rositiGn.
Pl~r.æd is the method wherein said foodst~ff is s~l~cted from the group
consi;,li"~ of soft carLonaled beverages, soft non-carLo, laled fruit flavored beverages,
soft non-carbonated beverages, sauces, toFFi.,gs, meat products, poultry products,
animal feeds, cûr,rt,~ionely products, baked goods, alcoholic beverages, savory
snacks, dairy products, condiments and gravies.
The prese"l invention is also directed to a method of reducing the u, ~'----nt
taste of a ~ha,~ ceuticAI com;~o~itiGn cor"~,,iai,.~ adding to the pl)&r,,,Ace-~içAI aflavor
poter,liali"g cGr"pQe~tiGn, said flavor poter,liali"g cGrl ll~osil;Gn 5~ læd from the group
consi~li"~ of
(a) maltol-neohesperidine dihydrocl ,alcone;
(b) ethylmaltol - "eol)esperidine dihydrochalcone; and
(c) maltol - ethylmaltol-neohesperidine dihydrocl,alcone.
One co~, ,pûl)enl of certain flavor-modifying comrositions of the preseol invention
is maltol. Natural or synthetic maltol may be used and in the coulext of the ,,.reser)t
spe~ iç~ n, the term maltol enCoi"r~cses both types. Synthetic maltol is
commercially available from the Food !Solence Group of Pfizer Inc and is sold under the
trade name VeltoP.
Another cGr"ponent of certain flavor-modifying cGr,-poci~iQ"s of the presenl
invention is ethyl maltol. Ethyl maltol is also co"""er~ially available from the Food
Science Group of Pfizer Inc and is sold under the trade name Veltol~ Plus.
Another component of the flavor-pol~r,liali"g comrosition of the presel)t
invention is neol)esperidine dihydlocl1~oone which is commercial available from Linke
and Exquim

CA 02205548 1997-05-20
~1V0 96~175~7 PCTJIB95100877



If the flavor-modifying cGr ~ro~;Gn contains maltol, the maltol is preser,l at alevel of from about 5 to about 100 parts per million.
If the flavor-"~Gdify;..g comr4s~tion contains ethylmaKol, the ethylmaltol is
~,r~se, .1 at a level of from about 0.1 to about 20 parts per million.
The level of neohespe.idine in the flavor modifying co~)~por~tiGn will be from
about 0.1 to about 10.0 parts per million.
Non-limiting examples of food~ ~fs into which the flavor-modifying cor, posiliol)s
may be added include soft c~Lon~led beverages, soft non~arLol.dled fruit flavored
beverages, soft non-c~rl,onaled beverages, sauces, t~rl ..gs, meat products, poultry
products, animal feeds, cor.le.,tiGnery products, baked goods, alcoholic beverages,
savory snacks, dairy products, cGn.li"~enl~ and gravies.
The flavor-modifying CGI~; os~t;Gns of the pr~sent invention may also be added
to pl)ar"~celJticAi coi,-po~ilions, both ethical and overthe counter (OTC).
The flavor-modifying cGrl~rosHiGIls of the ~r~:ser.l invention may also be addedto animal feeds.
Having descril.ed the invention in general terms, ref~rence is now made to
specificexdm~ `es. Itistobeu,-der:,loodthattheseexdr F'esarenotmeanttolimitthe
pr~senl invention, the scope of which is deler",i"ed by the appended claims.
EXAMPLE 1
Diet Cola
Samples of a commercial asp~ larne-sweetened diet cola, alone an
s~ lemer,led with flavor enhancer~, were evaluated by an expert panel of sensoryAcse5sor~ as noted below:
a. The control without added flavor enhancer~ was found to have a good
quality sweetness, a flavor typical of cola, and a somewhat bitter
aJlt ~ le.
b. A sample containing 3 ppm of Veltol Plus was swee~er and more
rounded in flavor than the control.
c. A sample containing 1 ppm of Veltol Plus and 1 ppm of neohesperidine
dihy-l. uchr ~. ~ ne (NHDC) had upfront sweetness which was longer
lasting, a greater flavor impact, and less bittemess than the control.

== ==
CA 02205548 1997-05-20
~IYO 96117527 1 . ~ 877



EXAMPLE 2
Tar,yeri"e Flavor
eo~s solutions containing 0.1% l~ e,i..e flavor, 5% sucrose, and 0.15%
citric acid, alone and supplel"er,led with flavor enl-ancerY, were evaluated by expert
5 sensory panelists as noted below:
a. The control without flavor ~nl .ancera was aldehydic, tart, and typical of tange.;. ,e.
b. A sample containing 5 ppm of Veltol was slightly less acidic.
c. A sample containing 2 ppm of Veltol Plus was sweet, less acidic, and
juicier than the control.
d. A sample containing 2 ppm NHDC, 3 ppm of Veltol, and 1 ppm of Veltol
Plus had a flavor profile which was fuller, juicier, and more intense than
that of the control.
EXAMPLE 3
Original Fat Free Style Barbecue Sauce
A standard original fat free style barbecue sauce was ev~ t~d
The barbecue sauce was then dosed with various levels of Veltol, Veltol-Plus,
and NHDC com~ nalions with both Veltol and Veltol-Plus. These were then coln,oar~d
to the standard barbecue sauce:
a. Standard barbecue sauce was acidic, spicy, and thin.
b. Veitol at a level of 50ppm i"creased the spice notes.
c. Veltol-Plus at a level of 1 Opm increased s~ etl ess, and reduced the acid
bite.
d. NHDC at 2ppm along with 30ppm Veltol and 5ppm Veltol-Plus made the
25 body cr~ar ,ier, rounded the flavor, increased spice notes, and red~ced acid bite.
EXAMPLE 4
Dark (Bittersweet) Chocolate
A standard dark (bittersweet) chocolate product was evaluated with Veltol, and
NHDC and Veltol combinations. The products made contained 1 00ppm of Veltol, 1 ppm
30 NHDC along with 100ppm of Veltol.
a. Standard dark (bille,_.vcct) chocolate was typical.
b. Veltol at 1 00ppm i- .creased creaminess, sweetness, and chocol~~^
char~..ter.

CA 02205548 1997-05-20
WO96/17527 P~ CE7~



c. NHDC at 1ppm along with 100ppm of Veltol also i,.cleased body,
mouthfeel, and incr~ased the ChOCGI-l e Cllar~ 1el. There was no siy~ r~nce
b~.w6~n the enh~ncer,~e"l that Veltol at 100ppm had on the aLL~d~

CA 02205548 1997-05-20
~10 ~6r~7527 PCTJlB95JOn877


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CA 02205548 1997-05-20
WO 96r~7s27 PCT/IB95/00877




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Dessin représentatif

Désolé, le dessin représentatatif concernant le document de brevet no 2205548 est introuvable.

États administratifs

Pour une meilleure compréhension de l'état de la demande ou brevet qui figure sur cette page, la rubrique Mise en garde , et les descriptions de Brevet , États administratifs , Taxes périodiques et Historique des paiements devraient être consultées.

États administratifs

Titre Date
Date de délivrance prévu Non disponible
(86) Date de dépôt PCT 1995-10-16
(87) Date de publication PCT 1996-06-13
(85) Entrée nationale 1997-05-20
Demande morte 2002-10-16

Historique d'abandonnement

Date d'abandonnement Raison Reinstatement Date
2001-10-16 Taxe périodique sur la demande impayée

Historique des paiements

Type de taxes Anniversaire Échéance Montant payé Date payée
Le dépôt d'une demande de brevet 300,00 $ 1997-05-20
Taxe de maintien en état - Demande - nouvelle loi 2 1997-10-16 100,00 $ 1997-10-16
Enregistrement de documents 100,00 $ 1998-06-30
Enregistrement de documents 100,00 $ 1998-06-30
Taxe de maintien en état - Demande - nouvelle loi 3 1998-10-16 100,00 $ 1998-09-24
Taxe de maintien en état - Demande - nouvelle loi 4 1999-10-18 100,00 $ 1999-09-21
Taxe de maintien en état - Demande - nouvelle loi 5 2000-10-16 150,00 $ 2000-09-22
Titulaires au dossier

Les titulaires actuels et antérieures au dossier sont affichés en ordre alphabétique.

Titulaires actuels au dossier
CULTOR LTD.
Titulaires antérieures au dossier
ENGEL, LAWRENCE D.
PFIZER INC.
STAGNITTI, GEORGE JR.
Les propriétaires antérieurs qui ne figurent pas dans la liste des « Propriétaires au dossier » apparaîtront dans d'autres documents au dossier.
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Description du
Document 
Date
(yyyy-mm-dd) 
Nombre de pages   Taille de l'image (Ko) 
Revendications 1997-05-20 2 73
Page couverture 1997-08-08 1 23
Abrégé 1997-05-20 1 34
Description 1997-05-20 13 477
Cession 1997-05-20 4 165
PCT 1997-05-20 12 406
Correspondance 1997-07-17 1 29
Cession 1998-06-30 13 492