IP Library Granted Patent US 9,744,119
Granted Patent B2
US 9,744,119 · App. 15/335,917 · Granted Aug 29, 2017

Cosmetic composition and method of preparation

Inventors: Monjit Phukan (Bangalore, IN); Anubhav Saxena (Bangalore, IN); Tushar Navale (Mumbai, IN)
Assignee: Momentive Performance Materials Inc.
A61K8/899A61K8/042A61K8/35A61K8/368A61K8/42A61K8/4926A61K8/602A61K8/891A61K9/06A61K31/455A61K47/34A61Q1/02A61Q17/04A61K2800/95
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Quick Facts
Patent No.
US 9,744,119
App. No.
15/335,917
Granted
Aug 29, 2017
Kind
B2
Abstract

The invention is directed to a cosmetic which comprises an ionic silicone as described herein.

Claims (76)

1. A method of preparing a cosmetic composition comprising an oil phase and optionally an aqueous phase wherein the method comprising

(a) reacting

i) at least one silicone hydride bearing at least two Si—H residues,

ii) at least one cross-linker silicone with two or more Si-unsaturated radicals,

wherein at least one of (i) or (ii) silicone is an ionic silicone having the general formula (I):

M 1 a M 2 b M 3 c D 1 d D 2 e D 3 f T 1 g T 2 h T 3 i Q j   (I)

wherein:

M 1 =R 1 R 2 R 3 SiO 1/2

M 2 =R 4 R 5 R 6 SiO 1/2

M 3 =R 7 R 8 R 9 SiO 1/2

D 1 =R 10 R 11 SiO 2/2

D 2 =R 12 R 13 SiO 2/2

D 3 =R 14 R 15 SiO 2/2

T 1 =R 16 SiO 3/2

T 2 =R 17 SiO 3/2

T 3 =R 18 SiO 3/2

Q=SiO 4/2

where R 1 , R 2 , R 3 , R 5 , R 6 , R 8 , R 9 , R 10 , R 11 , R 13 , R 15 , R 16 are each independently aliphatic, aromatic or fluoro containing monovalent hydrocarbon radicals containing from 1 to about 60 carbon atoms;

where R 4 , R 12 , R 17 are each monovalent radical bearing ion-pairs,

where R 7 , R 14 and R 18 are each independently selected from hydrogen, —OR 20 , unsaturated monovalent radicals or monovalent epoxy group-containing radicals, monovalent sulfur atom-containing radicals and monovalent organosilane groups, wherein R 20 is independently selected from hydrogen, monovalent hydrocarbon radical of from 1 to about 60 carbon atoms,

where the subscript a, b, c, d, e, f, g, h, i, j are zero or positive subject to the following limitations: the sum a+b+c+d+e+f+g+h+i+j is greater than or equal to 2 and less than or equal to 6000, b+e+h is greater than 0; and

iii) an effective amount of precious metal catalyst suitable for facilitating addition cure reaction between i) and ii) to obtain a crosslinked ionic silicone network,

(b) combining the crosslinked ionic silicone network of step (a), at least one cosmeceutical active, and optionally one or more cosmetically acceptable additives;

(c) shearing the combined components of step (b) during and/or after the combining step (b) with a solvent to form a crosslinked ionic silicone network gel, and

(d) adding the crosslinked ionic silicone network gel to an oil phase to obtain the cosmetic composition.

2. The method of claim 1 , wherein the crosslinked ionic silicone network gel comprises 0.1 to 99% of the crosslinked ionic silicone network obtain in step (a) and 0.01% to 25% of the cosmeceutical active.

3. The method of claim 1 , wherein the monovalent radicals R 4 , R 12 , R 17 are each selected from the formula (II):

-A-I x− M n y+ ;  (II)

where A is a spacing group having selected from a divalent hydrocarbon and hydrocarbonoxy group,

where superscripts n and y are independently from 1 to 6 and x is a product of n and y,

where I is an ionic group independently selected from sulfonate —SO 3 − , sulfate —OSO 3 − , carboxylate —COO − , phosphonate —PO 3 2− and phosphate —OPO 3 2− group, where M is hydrogen or a cation independently selected from alkali metals, alkaline earth metals, rare earth metals, transition metals, metals, metal complexes, quaternary ammonium, polymeric cations and phosphonium groups.

4. The method of claim 1 wherein the monovalent radicals R 4 , R 12 , R 17 are each independently selected from zwitterions having the formula (III):

—R′—NR″ 2 + —R′″—I  (III)

where R′ is a divalent hydrocarbon radical containing from 1 to about 60 carbon atoms, where R″ is monovalent hydrocarbon radical containing from 1 to about 60 carbon atoms, and

where R′″ is divalent hydrocarbon radical containing from 2 to about 20 carbon atoms; and, I is an ionic group independently selected from sulfonate —SO 3 − , sulfate —OSO 3 − , carboxylate —COO − , phosphonate —PO 3 2− group and phosphate —OPO 3 2− group.

5. The method of claim 1 , wherein the crosslinking reaction mixture is reacted by condensation, hydrosilylation, free-radical polymerization, ring opening polymerization and combinations thereof.

6. The method of claim 5 , wherein the reaction is carried out neat or in presence of the cosmetically acceptable additive.

7. The method of claim 1 , wherein said crosslinked ionic silicone network comprises a physical blend of the ionic silicone of the formula (I) with structuring polymer and/or networks other than the said ionic silicone (I).

8. The method of claim 1 wherein the combined components of step (b) further comprises film-forming additives selected from the group comprising of polysilicone dimethicone, polysilicone acrylate copolymer, dimethylsiloxane/3-thiopropyl methyl siloxane copolymer, vinylpyyrolidone/vinylacetate copolymer, polyvinylacetate, starch, polyquaternium-4, polyquaternium-11, acrylates/steareth-2 methacrylate crosspolymer, vinylacetate/vinyl neodecanoate copolymer, polyester-5, cetyl ethylhexanoate, vinyl acetate, crotonate/vinyl neodecanoate copolymer, 2-acryamido-2-methyl propane sulfonic acid/acrylic acid copolymer, acryamido-2-methyl propane sulfonic acid/acrylic acid/acryl methacrylate copolymer, polyacrylamide, C13-C14 isoparaffin, laureth-7, octylacrylamide, acrylate/butylaminoethylmethacrylate copolymer, and combinations thereof.

9. The method of claim 1 wherein the combined components of step (b) further comprises cross-linked matrixes selected from the group comprising of non-ionic silicone cross-polymers, urethane cross-polymer, acrylated cross-polymers, cross-linked polysaccharides and combinations thereof.

10. The method of claim 1 , wherein the cosmeceutical active is selected from the group consisting of photoprotective agents, self-tanning agents, desquamating agents, depigmenting agents, moisturizing agents, skin lightening agents, anti-aging ingredients, anti-wrinkle agents and combinations thereof.

11. The method of claim 1 , wherein the crosslinked ionic silicone network obtain in step (a) is combined with the cosmetically acceptable additive prior to forming the combination with the cosmeceutical active.

12. The method of claim 1 , wherein the cosmeceutical active is present in the crosslinking reaction mixture with the ionic silicone of formula (I).

13. The method of claim 1 , wherein the cosmeceutical active is kept separate from the crosslinking reaction mixture with the ionic silicone of formula (I), and then both are combined following the formation of the ionic silicone network to form the crosslinked ionic silicone network gel in-situ during a topical application of the cosmetic composition.

14. A method of preparing a cosmetic composition comprising an oil phase and optionally an aqueous phase, wherein the method comprising

1) reacting a silicone hydride with an oxirane-functionalized ionic silicone, an oxirane ring-opening polymerization catalyst, a carrier solvent; and optionally, one or more silicon hydride activators to obtain a crosslinked ionic silicone network by the ring-opening polymerization of oxirane moiety with hydride;

2) shearing the crosslinked ionic silicone network of step 1) in the presence of at least one cosmeceutical active and optionally one or more cosmetically acceptable additives during and/or after polymerization of step 1) with at least a carrier solvent to form a crosslinked ionic silicone network gel; and

3) adding the crosslinked ionic silicone network gel of step 2) to an oil phase of the cosmetic composition;

wherein the oxirane-functionalized ionic silicone has the general formula (I):

M 1 a M 2 b M 3 c D 1 d D 2 e D 3 f T 1 g T 2 h T 3 i Q j   (I)

wherein:

M 1 =R 1 R 2 R 3 SiO 1/2

M 2 =R 4 R 5 R 6 SiO 1/2

M 3 =R 7 R 8 R 9 SiO 1/2

D 1 =R 10 R 11 SiO 2/2

D 2 =R 12 R 13 SiO 2/2

D 3 =R 14 R 15 SiO 2/2

T 1 =R 16 SiO 3/2

T 2 =R 17 SiO 3/2

T 3 =R 18 SiO 3/2

Q=SiO 4/2

where R 1 , R 2 , R 3 , R 5 , R 6 , R 8 , R 9 , R 10 , R 11 , R 13 , R 15 , R 16 are each independently aliphatic, aromatic or fluoro containing monovalent hydrocarbon radicals containing from 1 to about 60 carbon atoms;

where R 4 , R 12 , R 17 are each monovalent radical bearing ion-pairs,

where R 7 , R 14 and R 18 are each independently selected from hydrogen, —OR 20 , unsaturated monovalent radicals or monovalent epoxy group-containing radicals, monovalent sulfur atom-containing radicals and monovalent organosilane groups, wherein R 20 is independently selected from hydrogen, monovalent hydrocarbon radical of from 1 to about 60 carbon atoms,

where the subscript a, b, c, d, e, f, g, h, i, j are zero or positive subject to the following limitations: the sum a+b+c+d+e+f+g+h+i+j is greater than or equal to 2 and less than or equal to 6000, b+e+h is greater than 0.

15. The method of claim 14 wherein the monovalent radicals R 4 , R 12 , R 17 are selected from the formula (II):

-A-I x− M n y+ ;  (II)

where A is a spacing group having selected from a divalent hydrocarbon and hydrocarbonoxy group,

where superscripts n and y are independently from 1 to 6 and x is a product of n and y,

where I is an ionic group independently selected from sulfonate —SO 3 − , sulfate —OSO 3 − , carboxylate —COO − , phosphonate —PO 3 2− and phosphate —OPO 3 2− group, more specifically sulfonate —SO 3 − , where M is hydrogen or a cation independently selected from alkali metals, alkaline earth metals, rare earth metals, transition metals, metals, metal complexes, quaternary ammonium, polymeric cations and phosphonium groups.

16. The method of claim 14 wherein the monovalent radicals R 4 , R 12 , R 17 are independently selected from zwitterions having the formula (III):

—R′—NR″ 2 + —R′″—I  (III)

where R′ is a divalent hydrocarbon radical containing from 1 to about 60 carbon atoms, where R″ is monovalent hydrocarbon radical containing from 1 to about 60 carbon atoms, and

where R′″ is divalent hydrocarbon radical containing from 2 to about 20 carbon atoms; and, I is an ionic group independently selected from sulfonate —SO 3 − , sulfate —OSO 3 − , carboxylate —COO − , phosphonate —PO 3 2− group and phosphate —OPO 3 2− group.

17. The method claim 14 wherein the crosslinking reaction mixture is reacted by condensation, hydrosilylation, free-radical polymerization, ring opening polymerization and combinations thereof.

18. The method of claim 14 wherein the cosmeceutical active is selected from the group consisting of photoprotective agents, self-tanning agents, desquamating agents, depigmenting agents, moisturizing agents, skin lightening agents, anti-aging ingredients, anti-wrinkle agents and combinations thereof.

Assignments (9)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (063213/0472) Recorded Oct 22, 2025
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 073168/0715 →
RELEASE OF SECURITY INTEREST Recorded Jul 18, 2025
From: KOOKMIN BANK NEW YORK BRANCH
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 072039/0906 →
FIRST LIEN TERM LOAN PATENT SECURITY AGREEMENT Recorded Mar 31, 2023
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 063213/0472 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Mar 31, 2023
From: BNP PARIBAS
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 063259/0133 →
RELEASE OF SECURITY INTEREST Recorded Mar 30, 2023
From: KOOKMIN BANK NEW YORK
To: MOMENTIVE PERFORMANCE MATERIALS INC.
Reel/Frame 063197/0373 →
SECURITY INTEREST Recorded Mar 30, 2023
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: KOOKMIN BANK NEW YORK BRANCH
Reel/Frame 063197/0475 →
ABL PATENT AGREEMENT Recorded Jun 5, 2019
From: MOMENTIVE PERFORMANCE MATERIALS INC.; MOMENTIVE PERFORMANCE MATERIALS GMBH
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 049388/0252 →
SECOND LIEN TERM LOAN PATENT AGREEMENT Recorded Jun 5, 2019
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: KOOKMIN BANK, NEW YORK BRANCH, AS ADMINISTRATIVE AGENT
Reel/Frame 049388/0220 →
FIRST LIEN TERM LOAN PATENT AGREEMENT Recorded Jun 5, 2019
From: MOMENTIVE PERFORMANCE MATERIALS INC.
To: BNP PARIBAS, AS ADMINISTRATIVE AGENT
Reel/Frame 049387/0782 →
Continuity (2)
Continuation In Part 14572108 · Dec 16, 2014
Related Publication 20170042787A1 · Feb 16, 2017