Hydrophilically-modified silicone compositions

Patent metadata

Field	Value
Publication number	US-9624334-B2
Application number	US-201013503639-A
Country	US
Kind code	B2
Filing date	Oct 19, 2010
Priority date	Oct 23, 2009
Publication date	Apr 18, 2017
Grant date	Apr 18, 2017

Abstract

In various embodiments, provided are hydrophilically-modified silicone compositions comprising substantially spherical elastomeric microparticles, methods of making such compositions, and silicone pastes, personal care, and healthcare products comprising such silicone compositions.

First claim

The invention claimed is:

1. A method for the preparation of a silicone composition, the method comprising:
(I) co-polymerizing
Component (A), at least one organopolysiloxane having an average of at least two free radical polymerizable groups per molecule that is selected from the group consisting of a methacryloxypropyl-terminated polydimethylsiloxane, an acryloxypropyl-terminated polydimethylsiloxane, an (acryloxypropyl)methylsiloxane-dimethylsiloxane copolymer; and a combination thereof; and
Component (B), at least one organic co-monomer having an average of at least one free radical polymerizable group per molecule that is selected from the group consisting of benzyl methacrylate, tetrahydrofuryl methacrylate, 2-hydroxyethyl methacrylate, dimethylaminoethyl methacrylate, N-vinyl formamide, 4-vinyl pyridine, N,N-dimethylacrylamide, N-isopropylacrylamide, and a combination thereof, with a weight ratio of Component (A) to Component (B) of about 1:4 to about 19.2:1;

wherein co-polymerization occurs in the presence of
Component (C), at least one organoborane free radical initiator selected from the group consisting of triethylborane-propanediamine, triethylborane-butyl imidazole, triethylborane-methoxypropylamine, and a combination thereof;
Component (D), water;
Component (E), at least one organonitrogen-reactive compound; and
oxygen;

while maintaining a temperature of from about 5° C. to about 95° C. to form hydrophilically-modified silicone elastomeric microparticles; and
(II) recovering the silicone elastomeric microparticles and dispersing them in at least one absorbable fluid that is immiscible with Component (D) to form a paste comprising the silicone elastomeric microparticles with at least some of the absorbable fluid absorbed therein.

2. The method according to claim 1 , wherein the silicone elastomeric microparticles are formed by adding Component (C) to a dispersion or emulsion comprising Component (A), Component (B), Component (D), and Component (E) or by adding Component (E) to a dispersion or emulsion comprising Component (A), Component (B), Component (C) and Component (D).

3. The method according to claim 1 , wherein the absorbable fluid is selected from silicones, including linear and cyclosiloxanes comprising decamethylcyclopentasiloxane and organic solvents, including C8-C20 isoparaffins, isododecane, isohexadecane, esters selected from isotridecyl isononanoate, PEG-4 diheptanoate, isostearyl neopentanoate, tridecyl neopentanoate, cetyl octanoate, cetyl palmitate, cetyl ricinoleate, cetyl stearate, cetyl myristate, coco-dicaprylate/caprate, decyl isostearate, isodecyl oleate, isodecyl neopentanoate, isohexyl neopentanoate, octyl palmitate, dioctyl malate, tridecyl octanoate, myristyl myristate, octododecanol, or mixtures of octyldodecanol, acetylated lanolin alcohol, cetyl acetate, isododecanol, polyglyceryl-3-d isostearate, and any combination thereof.

4. The method according to claim 1 , wherein the temperature is maintained at from about 10° C. to about 35° C.

5. The method according to claim 1 , wherein optional Component (E) is selected from acetic acid, citric acid, acrylic acid, polyacrylic acid, isophorone diisocyanate, and any combination thereof.

6. The method according to claim 1 , wherein co-polymerization occurs in the presence of, or the silicone elastomeric microparticles formed are treated with, Component (F), at least one active ingredient suitable for use in personal care and healthcare products.

7. The method according to claim 1 , wherein co-polymerization occurs in the presence of Component (G), at least one emulsifier.

8. The method according to claim 6 , wherein Component (F) is selected from vitamins, sunscreens, plant extracts, fragrances or perfumes, topical drug actives, proteins, enzymes, antiperspirants, deodorants, moisturizers, antifungal agents, antimicrobial agents, and any combination thereof.

9. The method according to claim 7 , wherein Component (G) is selected from secondary alcohol ethoxylates, polyglycol-modified trimethsilylated silicate, polyglycol-modified siloxanes, polyglycol-modified silicas, ethoxylated quaternary ammonium salt solutions, cetyltrimethylammonium chloride solutions, and any combination thereof.

Assignees

• Ahn Dongchan
• Huang Qi
• Puscau Maria M
• Schulz William
• Thompson James
• Wier Kevin
• Dow Corning

Inventors

• Ahn Dongchan
• Huang Qi
• Puscau Maria M
• Schulz William
• Thompson James
• Wier Kevin

Classifications

• A61K2800/654

  The particulate/core comprising macromolecular material · CPC title

• A61K8/89

  Polysiloxanes · CPC title

• A61Q15/00

  Anti-perspirants or body deodorants (deodorisation of air A61L9/00) · CPC title

• C08F4/52

  selected from boron, aluminium, gallium, indium, thallium or rare earths (C08F4/14 takes precedence) · CPC title

• A61K2800/412

  Microsized, i.e. having sizes between 0.1 and 100 microns · CPC title