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Title: Polar solvent-in-oil emulsions and multiple emulsions
United States Patent: 6,080,394
Inventors: Lin; Zuchen (Midland, MI); Schulz, Jr.; William
James (Midland, MI); Smith; Janet Mary (Bay City, MI)
Assignee: Dow Corning Corporation (Midland, MI)
Appl. No.: 435561
Filed: November 8, 1999
Abstract
One composition is a non-aqueous polar solvent-in-oil emulsion
containing a non-aqueous polar solvent phase dispersed in a silicone oil
continuous phase by an emulsifier. A second composition is a non-aqueous
polar solvent-in-oil-in-water multiple emulsion of the type PS1
/O/w which contains a non-aqueous polar solvent phase PS1
dispersed in a silicone oil as a first continuous phase of a primary
emulsion PS1 /O by an emulsifier. The primary emulsion PS1
/O is dispersed in a second continuous aqueous phase W to form multiple
emulsion PS1 /O/W. A third composition is a non-aqueous polar
solvent-in-oil-in-non-aqueous polar solvent multiple emulsion of the type
PS1 /O/PS2 which contains a non-aqueous polar
solvent phase PS1 dispersed in a silicone oil as a first
continuous phase of a primary emulsion PS1 /O by an emulsifier.
The primary emulsion PS1 /O is dispersed in a second continuous
non-aqueous polar solvent phase PS2 to form multiple emulsion
PS1 /O/PS2.
DETAILED DESCRIPTION OF THE INVENTION
Emulsions are composed of droplets of one liquid dispersed
in a second liquid. Multiple emulsions are composed of droplets of one
liquid dispersed in a second liquid, which is then dispersed in a final
continuous phase. Generally, the internal droplet phase will be miscible
with or identical to the final continuous phase.
For example, in a water-in-oil-in-water multiple emulsion W/O/W, the
internal phase and the external phase are both aqueous. In a non-aqueous
polar solvent-in-oil-in-water multiple emulsion PS1 /O/W, the
internal phase is a non-aqueous polar solvent and external phase is
aqueous. In a non-aqueous polar solvent-in-oil-in-non-aqueous polar
solvent multiple emulsion PS1 /O/PS2, the internal
phase and the external phase are both non-aqueous polar solvents.
For the system PS1 /O/W in which the final continuous phase is
aqueous, the primary emulsion is polar solvent-in-oil emulsion PS1
/O, which is then emulsified into the final aqueous phase W.
For the system PS1 /O/PS2 in which the final
continuous phase is a polar solvent, the primary emulsion is polar
solvent-in-oil emulsion PS1 /O, which is then emulsified into
the final polar solvent phase PS2.
For the purpose of clarity, and in accordance with recognized standards of
nomenclature used for a PS1 /O/W system, the oil phase of the
primary emulsion is designated as O, and the primary emulsion is
designated PS1 /O. Primary emulsion PS1 /O includes
polar solvent phase PS1. After primary emulsion PS1
/O has been further dispersed in the final aqueous phase W, this multiple
emulsion is designated PS1 /O/W. For a PS1 /O/PS2
system, the oil phase of the primary emulsion is again O, and the primary
emulsion is PS1 /O. Primary emulsion PS1 /O includes
polar solvent phase PS1. After primary emulsion PS1
/O has been further dispersed in the final and second polar solvent phase
PS2, this multiple emulsion is designated as PS1
/O/PS2.
Crosslinked elastomeric silicone polyethers which are used in forming
these emulsions, and methods for preparing these crosslinked elastomeric
silicone polyethers are described in detail in the common assignee's U.S.
Pat. No. 5,811,487, incorporated herein by reference.
Generally, such crosslinked elastomeric silicone polyethers are prepared
by reacting an .tbd.Si--H containing polysiloxane (A) and a mono-alkenyl
polyether (B) in the presence of a platinum catalyst, until an .tbd.Si--H
containing siloxane with polyether groups (C) is formed. The --Si-H
containing siloxane with polyether groups (C) is then reacted with an
unsaturated hydrocarbon (D) such as an alpha, omega-diene, in the presence
of a solvent (E) and a platinum catalyst, until a silicone elastomer is
formed by crosslinking and addition of .tbd.SiH across double bonds in the
alpha, omega-diene (D).
These crosslinked elastomeric silicone polyethers can be generally
described as constituting polymeric molecules which are crosslinked
together to form gels consisting of three-dimensional molecular polymeric
networks containing tens, hundreds, and thousands of crosslinked units
between and among the polymeric molecules. Typically, these crosslinked
elastomeric silicone polyethers contain and are swollen by 65 to 98
percent by weight of an oil.
Both U.S. Pat. No. 5,811,487 and U.S. Pat. No. 5,889,108 contain extensive
lists of appropriate oils which can be used, among which are, for example,
(i) volatile polydimethylsiloxanes such as hexamethyldisiloxane,
octamethyltrisiloxane, and decamethylcyclopentasiloxane, (ii) nonvolatile
polydimethylsiloxanes having a viscosity generally in the range of about 5
to about 1,000 centistoke (mm.sup.2 /s), and (i) fragrances such as musk
and myrrh.
Organic oils such as natural oils derived from animal, vegetable, or
mineral sources, are also suitable. Modern cosmetic oils, for example, are
most representative, and among common organic oils known to be safe for
cosmetic purposes are almond oil, apricot kernel oil, avocado oil, cacao
butter (theobroma oil), carrot seed oil, castor oil, citrus seed oil,
coconut oil, corn oil, cottonseed oil, cucumber oil, egg oil, jojoba oil,
lanolin oil, linseed oil, mineral oil, mink oil, olive oil, palm kernel
oil, peach kernel oil, peanut oil, rapeseed oil, safflower oil, sesame
oil, shark liver oil, soybean oil, sunflower seed oil, sweet almond oil,
tallow (beef) oil, tallow (mutton) oil, turtle oil, vegetable oil, whale
oil, and wheat germ oil.
While the term non-aqueous polar solvent is intended to include solvents
generally, when the emulsions and multiple emulsions are intended for
personal care application, then the non-aqueous polar solvent should be
one recognized as being cosmetically acceptable. Representative of some
cosmetically acceptable non-aqueous polar solvents which can be used are,
for example, monohydroxy alcohols such as ethyl alcohol and isopropyl
alcohol; diols and triols such as propylene glycol and glycerol,
respectively; glycerol esters such as glyceryl triacetate (triacetin),
glyceryl tripropionate (tripropionin), and glyceryl tributyrate (tributyrin);
and polyglycols such as polyethylene glycol. In applications other than
personal care, these and other more suitable types of non-aqueous polar
solvents can be employed.
In using crosslinked elastomeric silicone polyethers for preparing
non-aqueous polar solvent-in-oil emulsions consisting of a non-aqueous
polar solvent disperse phase and an oil continuous phase, the non-aqueous
polar solvent phase may contain a non-aqueous polar solvent soluble active
ingredient, and the oil phase may contain an oil soluble active
ingredient.
Some representative non-aqueous polar solvent soluble active ingredients
for the non-aqueous polar solvent phase of the non-aqueous polar
solvent-in-oil emulsion and multiple emulsion are (i) non-aqueous polar
solvent soluble Vitamins, (ii) non-aqueous polar solvent soluble drugs
including activated antiperspirant salts such as aluminum chlorohydrate
and aluminum-zirconium trichlorohydrate, or (iii) .alpha.-hydroxy acids
such as glycolic acid, lactic acid, tartaric acid, and citric acid, i.e.,
fruit acids. In this latter instance, i.e., (iii), significant benefits
can be realized as fruit acids have been alleged to be capable of
diminishing fine skin lines and pigmentation spots, as well as stimulating
collagen which allows the skin to repair itself.
The common assignee's U.S. Pat. No. 5,948,855 contains an extensive list
of some appropriate non-aqueous polar solvent soluble Vitamins and
non-aqueous polar solvent soluble drugs which can be used, among which are
Vitamin C, Vitamin B1, Vitamin B2, Vitamin B6,
Vitamin B12, niacin, folic acid, biotin, and pantothenic acid.
The non-aqueous polar solvent soluble vitamin can be used in the
non-aqueous polar solvent-in-oil emulsions and multiple emulsions in
amounts of from 0.01 to about 50 percent by weight.
The common assignee's U.S. Pat. No. 5,948,855 also contains an extensive
list of some appropriate oil soluble active ingredients such as vitamins
and drugs which can be used in the oil phase of the non-aqueous polar
solvent-in-oil emulsions and multiple emulsions, among which are vitamins,
including but not limited to, Vitamin A1, RETINOL, C2
-C18 esters of RETINOL, Vitamin E, TOCOPHEROL, esters of
Vitamin E, and mixtures thereof. RETINOL includes trans-RETINOL,
13-cis-RETINOL, 11-cis-RETINOL, 9-cis-RETINOL, and 3,4-didehydro-RETINOL.
Other vitamins which are appropriate include RETINYL ACETATE, RETINYL
PALMITATE, RETINYL PROPIONATE, .alpha.-TOCOPHEROL, TOCOPHERSOLAN,
TOCOPHERYL ACETATE, TOCOPHERYL LINOLEATE, TOCOPHERYL NICOTINATE, and
TOCOPHERYL SUCCINATE. The oil-soluble vitamin or drug can be used in the
non-aqueous polar solvent-in-oil emulsions and multiple emulsions in
amounts of from 0.01 to about 50 percent by weight.
In forming the primary emulsion PS1 /O, it is preferred to use
0.1 to 99 percent by weight of the non-aqueous polar solvent phase PS1,
which amount includes the weight of the non-aqueous polar solvent and any
non-aqueous polar solvent soluble active ingredient such as a vitamin(s)
which may be carried therein. The oil phase O of the primary emulsion PS1
/O is used in an amount of about 1 to 99.9 percent by weight, which amount
includes the weight of the elastomeric silicone polyether, the oil, and
the oil soluble vitamin(s) or oil soluble active ingredient included
therein.
Preferably, the non-aqueous polar solvent phase including the weight of
the non-aqueous polar solvent and any non-aqueous polar solvent soluble
active ingredient comprises 20 to 95 percent by weight of primary emulsion
PS1 /O, while the oil phase including the weight of the
elastomeric silicone polyether, the oil, and the oil soluble vitamin(s) or
oil soluble active ingredient comprises 15 to 80 percent by weight of
primary emulsion PS1 /O.
Multiple emulsions PS1 /O/W can then be prepared by simply
mixing together about 0.1 to 70 percent by weight of the primary emulsion
PS1 /O, with about 30 to 99.9 percent by weight of the final
continuous phase W, which latter amount includes the weight of any water
soluble active ingredient(s) contained in final continuous phase W.
Generally, any active ingredient referred to above as being an appropriate
active ingredient for addition to the non-aqueous polar solvent phase is
also an appropriate active ingredient for addition to the final continuous
phase W. Multiple emulsions of the type PS1 /O/PS2
are prepared in a similar manner.
Claim 1 of 8 Claims
1. A composition comprising a non-aqueous polar
solvent-in-oil emulsion containing a non-aqueous polar solvent phase
dispersed in a silicone oil continuous phase by an emulsifier, the
emulsifier being a crosslinked elastomeric silicone polyether which
constitutes polymeric molecules crosslinked together to form a gel
consisting of three-dimensional molecular polymeric networks containing
crosslinking units between and among the polymeric molecules, the
crosslinked elastomeric silicone polyether containing and being swollen
with about 65 to about 98 percent by weight of the silicone oil.
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