|Publication number||US2853423 A|
|Publication date||Sep 23, 1958|
|Filing date||May 20, 1955|
|Priority date||May 20, 1955|
|Publication number||US 2853423 A, US 2853423A, US-A-2853423, US2853423 A, US2853423A|
|Inventors||La Via Anthony L|
|Original Assignee||Olin Mathieson|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (4), Referenced by (19), Classifications (17)|
|External Links: USPTO, USPTO Assignment, Espacenet|
AEROSOL SUN-SCREENING COMPOSITION Anthony L. La Via, Brooklyn, N. Y., assignor to Olin Mathieson Qhemical Corporation, New York, N. Y., a corporation of Virginia No Drawing. Application May 20, 1955 Serial No. 510,050
Claims. (Cl. 167-90) This invention relates to compositions of matter and more particularly to aerosol compositions useful in protecting against sunburn.
Prior to this invention, various compositions were known which were effective in minimizing or preventing erythema solare, commonly known as sunburn. These compositions can be divided into three classes: greaseless compositions having an alcoholic base; greasy compositions containing vegetable or mineral oil or other tacky components; and water-based emulsions of any suitable oil. More recently, aerosol compositions have been formulated for protection against sunburn. These compositionsinvariably were of the greaseless type employing as a solvent for the sun screening agent, propellent, and other components, an alcohol such as ethanol or isopropanol. The use of an alcoholic solvent, however, is subject to several disadvantages. When such compositions are sprayed, the liquid components, including the alcohol, are dispersed in the form of fine droplets. Under these conditions, and because of the large surface area of the droplets, the alcohol represents a fire hazard, so that all previously known aerosol sunburn preparations were subject to this disadvantage. Furthermore, since the alcohol solvent was highly volatile and evaporated quickly, a second film-forming ingrediout had to be incorporated into the composition in order to assure even distribution of the sun screening agent and protection thereby of the skin.
I have now discovered that these disadvantages can be obviated by the compositions of this invention, which essentially comprise a sun screening agent, a water-repellant, film-forming, liquid carboxylic acid ester vehicle of high flash point (hereinafter referred to simply as the vehicle), a propellent, and optionally but preferably a silicone. I have further discovered that by the use of the vehicles of this invention, not only is the aerosol composition rendered fire proof, but further, since the vehicle serves the dual purpose of a carrier for the various active ingredients of the composition-and a water-repelling film-former on the skin, the quantity of silicone or other film-former previously employed may be reduced or eliminated.
An object of this invention, therefore, is the provision of an aerosol preparation for the prevention of sunburn, which is non-inflammable, easily applied, and which produces on the skin a continuous, substantially invisible, elastic film which provides elfective protection against excessive exposure to erethernogenic actinic light.
Suitable film-forming, liquid carboxylic acid ester vehicles, utilizable in the compositions of this invention, are those which have high flash points (e. g. flash points above about 300 F), are water-repellant, so that they are not readily removed on bathing, form thin films on contact with the skin, so that relatively large areas of skin are covered with the minimum amount of Vehicle and sun screening agent, and Which dissolve at least some and preferably all the other active ingredients of the compositions of this invention.
- esters of higher aliphatic carboxylic acids, such as the esters of higher allcanoic acids (e. g. the mono and polyhydric alcohol esters of capric, lauric, myristic, palmitic, and stearic acid), the esters of higher alkenoic acids (e. g. the mono and polyhydric alcohol esters of citronellic, undecyleni-c, and oleic acid), and the esters of higher alkanedioic acids (e. g. the mono and polyhydric alcohol esters of azelaic and sebacic acid). These esters may be used either singly or in combination as the vehicle of this invention. Specific examples of suitable esters utilizable in the compositions of this invention, include the lower alkyl esters of higher fatty acids (e. g. isopropyl laurate, ethyl myristate, isopropyl myristate, ethyl palmitate, isopropyl palmitate, and butyl stearate), the polyhydric alcohol esters of higher fatty acids (e. g. diglycol laurate, sorbitol monolaurate, mannide monoleate, sorbitan monooleate, sorbitan sesquioleate, and diglycol oleate), and esters of higher alkanedioic acids, such as di-isopr-opyl sebacate. The particularly preferred esters are the mono-lower alkyl esters of higher fatty acids (optimally the lower alkyl esters of higher alkanoic acids).
Suitable sun screening agents are those which are capable of absorbing and dissipating erythemogenic actinic light and preferably are soluble in the vehicle. Examples of such agents are the esters of p-arninobenzoic acid and p-(lower alkyl substituted)aminobenzoic acid (e. g. the ethyl, propyl, isobutyl, butyl, glyceryl and other higher alcohol esters of p-aminobenzo-ic acid, p-dimethylarninobenzoic acid, and p-diethylaminobenzoic acid) and the esters of salicylic acid and p-arninosalicylic acid (e. g. the ethyl, propyl, isobutyl, benzyl, phenyl, dipropylene glycol and especially the menthyl and homomenthyl esters of salicylic acid and p-aminosalicylic acid). It should be noted, however, that the alcohol moiety of the ester has little effect on the screening activity of the ester, so that virtually any esterifying group may be used. Furthermore, any other of the known sunscreening agents can be used in the compositions of this invention, although those soluble in the vehicle are preferred because they permit the formation of a homogeneous solution.
In contrast to previously known aerosol preparations,
the use of a silicone or other additional film-forming substance is not absolutely essential in the compositions of this invention, since the novel vehicles of this invention serve the dual purpose of solvent and Water-repellent filmformer on the skin. However, to prevent any frothing upon contact of the aerosol spray with the skin, it is desirable that a silicone, particularly a silicone fluid, also be incorporated in the compositions of this invention. Any relatively water-insoluble silicone is utilizable, as long as it is dermatologically acceptable and preferably soluble in the vehicle. Utilizable silicones include the silicone fluids such as aryl polysiloxanes (e. g. phenyl polysiloxanes), cyclic alkyl polysiloxanes (e. g. cyclic ethyl silicone tetramer), alkyl polysiloxanes (e. g. ethyl polysiloxanes and methyl polysiloxanes) and mixed polysiloxanes (e. g. methyl phenyl polysiloxanes). The viscosity of these preferred silicone fluids can range anywhere from about 25 to 15,000 centistrokes.
To prepare the sun-screening film-forming active ingredients of the aerosols of this invention, the vehicle, sun screening agent, and silicone (if any) are intermixed in any order or together. Other ingredients such as a perfume or an insect repellent may also be added if desired. The proportion of sun screening agent to vehicle is not critical, but rather depends on the efiicacy of the sun screening agent and hence the maximum dilution of the agent which is possible Without making the composition ineffective. The preferred ratio of sun screening agent to vehicle, however, is in the order of one part by Weight of the former to about one to about fifty parts by weight of the latter (optimally one part of sun screening agent to about seven to about ten parts of vehicle). If a silicone is used, it is preferably present in relatively small amounts, not exceeding about 40% (preferably less than about 25%) of the total weight of active ingredients.
The active ingredients are then mixed with a suitable propellent in a valved pressure container, such as one customarily employed in the aerosol industry. Suitable propellents are those which individually or in mixture have a gauge pressure less than about 50 pounds per square inch at 70 F. For use with the active ingredients of this invention, the propellent preferably is one which has a gauge pressure in the range of about: 20 to 35 lbs/in. at 70 F. (optimally about 25 to 30 lbs/in? at 70 F.). Suitable propellents which can be used either alone or in mixture to give a gauge pressure in the hereinbefore recited ranges include the halogenated lower alkanes, such as trichlorornonofluoromethane, dichlorodifluoromethane, monochloridifluoromethane, trichlorotrifiuoroethane, and dichlorctetrafluoroethane. A particularly preferred propellent for the active ingredients in the compositions of this invention is one consisting of about equal proportions of trichloromonofluoromethane and dichlorodifluoromethane.
The proportion of active ingredients to propellent is not critical, but preferably should be such that there is sulficient propellent present to expel substantially the entire amount of active ingredients from the container as a spray. For this purpose, the propellent is added in the proportion of about one to about 20 parts of propellent by weight per one part of active ingredients (an optimal composition being one wherein the propellent is present in a ratio of 1 to 5 parts of propellent per part of active ingredients).
The following examples illustrate the invention:
Example 1 To 100.0 g. of homomenthyl salicylate is added with stirring 7.5 g. of a perfuming agent, such as Perfume G. D. 6763, Givaudan-Delawanna, 50.0 g. of a silicone fluid (e. g. a methyl phenyl polysiloxane of 75 ctsks. viscosity), and finally enough isopropyl palmitate to bring the mixture to a weight of 1,000.0 g., the mixture having a fiash point above 310 F. The finished mixture is then strained through a fine muslin and filled into 6 ounce valved pressure cans using a ratio of 20% by Weight of the solution to 80% by weight of a propellent, the propellent being an equal mixture of trichloromonofluoromethane and dichlorodifluoromethane. The cans are then sealed to give a final composition having a gauge pressure of about 28 lbs/in. at 70 F.
In the formulation of Example 1, the perfurning agent is, of course, an optional ingredient and may be eliminated if desired. Furthermore, the specific ingredients and pro portions may be changed Within the limits hereinbefore noted Without qualitatively affecting the nature of the final composition.
The following examples illustrate other utilizable compositions, which are mixed and formulated as in Example 1:
Example 2 One part of active ingredients consisting of:
Percent Homomenthyl salicylate 10.0 Isopropyl palmitate 90.0
is mixed with three parts of a propellent consisting of 40% dichlorodifluoromethane and 60% dichlorotetrafluoroethane.
4 Example 3 One part of active ingredients consisting of:
Percent Dipropyleneglycol salicylate 50.0 A methyl phenyl polysiloxane of 50 ctsks, viscosity [Silicone 81431 (G. E.)] 5.0 isopropyl palmitate 15.0 Isopro-pyl myristrate 15.0 isopropyl laurate -1 15.0
is mixed with nine parts of a propellent consisting of an equal mixture of dichlorodifluoromethane and trichlorotrifluoroethane.
Example 4 One part of active ingredients consisting of:
Percent Ethyl p-diethylaminobenzoate 10.0 A methyl. phenyl polysiloxane of 75 ctsks. viscosity [Silicone DC 555] 25.0 Diisopropyl sebacate 65.0
is mixed with one part of a propellent consisting of 10% monochlorodifiuoromethane and dichlorotetrafiuoroethane.
Example 5 One part of active ingredients consisting of:
Percent lsobutyl p-aminosalicylate 10.0
A methyl phenyl polysiloxane of 35 ctsks. viscosity [Silicone DC 701] 5.0 Diglycol laurate 40.0 Isopropyl palmitate 45.0
is mixed with three parts of a propellent consisting of 40% dichlorodifluoromethane and 60% trichlorotrifluoroethane.
Example6 One part of active ingredients consisting of:
Percent Solprotex (digalloyloleate) 25.0 A methyl polysiloxane of 12,000 ctsks. viscosity [Silicone D0200] 25.0
Sorbitol monolaurate 50.0
is mixed with eight parts of a propellent consisting of an equal mixture of trichloromonofluoromethane and dichlorodifluoromethane.
Example7 One part of active ingredients consisting of:
Percent Ethyl p-dimethylaminobenzoate 20.0 A methyl polysiloxane of 500 ctsks. viscosity [Silicone 8-96 (G. E.)] 10.0 Sorbitan monooleate 35.0 Sorbitan sesquioleate 35.0
is mixed with three part of a propellent consisting of 10% monochlorodifluoromethane and 90% trichloromonofluoromethane.
The compositions of Examples 2 through 7 may be perfumed if desired.
The invention may be variously otherwise embodied within the scope of the appended claims.
1. An aerosol composition consisting essentially of: a sun-screening agent; a propellant; and a water-repellent, film-forming liquid ester vehicle of high flash point, said ester having an acid moiety selected from the group consisting of higher alkanoic acids, higher alkenoic acids and higher alkanedioic acids, said acids having not more than 18 carbon atoms, and an alcohol moiety selected from the group consisting of saturated, unsubstituted lower aliphatic monohydric alcohols, lower alkylene glycols of low molecular weight, sorbitol and mannitol.
2. The composition of claim 1 which also contains a polysiloxane fluid.
3. The composition of claim 1 wherein the vehicle is a lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms.
4. The composition of claim 1 in which the film-forming vehicle is present in the proportion of about one to about fifty parts by weight per part by weight of sun-screening agent, and in which the propellant is present in the proportion of about one to about twenty parts by weight per part by weight of combined sun-screening agent and filmforming vehicle.
5. The composition of claim 4 wherein the vehicle is a lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms. 7
6. The composition of claim 5 wherein the sun-screening agent is selected from the group consisting of the esters of p-aminobenzoic acid, p-(lower-alkyl-substituted) aminobenz-oic acid, salicylic acid and p-aminosalicylic acid.
7. The composition of claim 6 wherein the propellant comprises a halogenated lower alkane.
8. The composition of claim 5 wherein the sun-screening agent is homomenthyl salicylate.
9. An aerosol composition consisting essentially of a halogenated lower alkane propellant and sun-screeningfilm-forming active ingredients consisting essentially of homomenthyl salicylate, a mono-lower alkyl ester of a higher alkanoic acid having not more than 18 carbon atoms, and a polysiloxane fluid, wherein said homo- References Cited in the file of this patent UNITED STATES PATENTS 2,257,106 Christiansen Sept. 30, 1941 2,446,272 Farris Aug. 3, 1948 2,639,213 Barth May 19, 1953 FOREIGN PATENTS 84,595 Argentina May 22, 1947 OTHER REFERENCES Soap and Sanitary Chem., Sept. 1953, pp. 142, 143, 145, 147, 153 and 155.
E. G. Tajkowski et al.: Proc. of the Sci. Sec. of Toilet Goods Asso., No. 20, Dec. 1953, pp. 1-7.
E. N. Cooper: Chem. Ind., Dec. 1948, pp. 970, 972 and 1058.
G. S. Pears: Perf. and Ess. Oil Rec., Mar. 1953, pp. 84-90, 101.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US2257106 *||Feb 26, 1938||Sep 30, 1941||Squibb & Sons Inc||Dermal lotion|
|US2446272 *||Jul 1, 1947||Aug 3, 1948||Lockheed Aircraft Corp||Fire extinguisher fluid|
|US2639213 *||Mar 21, 1950||May 19, 1953||Price Driscoll Corp||Mold parting surface and method of application|
|AR84595A *||Title not available|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3081232 *||Dec 27, 1960||Mar 12, 1963||Warner Lambert Pharmaceutical||Iodine preparation and method of disinfecting the skin|
|US3175950 *||Jul 22, 1960||Mar 30, 1965||Armour Pharmaceutrical Company||Sunscreening preparations|
|US3275520 *||May 29, 1962||Sep 27, 1966||Gen Aniline & Film Corp||Methods for protecting the skin against actinic radiations|
|US3403207 *||Nov 14, 1966||Sep 24, 1968||Ernest Ohlsson||Method of and composition for screening erythema inducing ultraviolet bands|
|US3479428 *||Jul 8, 1964||Nov 18, 1969||Boots Pure Drug Co Ltd||Sunscreen composition and method of using the same|
|US4001391 *||Sep 16, 1971||Jan 4, 1977||Plough, Inc.||Means for depositing aerosol sprays in buttery form|
|US4036951 *||Jan 16, 1976||Jul 19, 1977||Synergistics, Inc.||Ultra-violet filtration with certain aminosalicylic acid esters|
|US4069309 *||Sep 19, 1972||Jan 17, 1978||Avon Products, Inc.||Cationic skin substantive sunscreen composition and method|
|US4107290 *||Aug 18, 1976||Aug 15, 1978||L'oreal||Anti-solar polymers, method of making the same and cosmetic compositions containing the same|
|US4217344 *||Dec 29, 1977||Aug 12, 1980||L'oreal||Compositions containing aqueous dispersions of lipid spheres|
|US4793990 *||Jan 17, 1983||Dec 27, 1988||L'oreal||Use of coffee bean oil as a sun filter|
|US4940574 *||Dec 22, 1988||Jul 10, 1990||Plough, Inc.||Non-aqueous high SPF sunscreen oils|
|US5268166 *||Jul 9, 1992||Dec 7, 1993||Elizabeth Arden Company, Division Of Conopco, Inc.||Cosmetic application system|
|US5447715 *||May 17, 1989||Sep 5, 1995||Scholl Inc.||Non-aqueous suncare compositions having high SPF values|
|US5518712 *||Nov 18, 1993||May 21, 1996||Stewart; Ernest||Water resistant sunscreen protection and insect repellent compound|
|US5756075 *||Mar 25, 1993||May 26, 1998||Schering-Plough Healthcare Products, Inc.||Apparatus and method for sunless tanning|
|US5916541 *||May 1, 1996||Jun 29, 1999||Stewart; Ernest G.||Water resistant sunscreen and insect repellent composition|
|WO1994000104A1 *||Jun 23, 1993||Jan 6, 1994||Stewart Ernest G||Water resistant sunscreen protection and insect repellent compound|
|WO1995019161A1 *||Nov 16, 1994||Jul 20, 1995||Stewart Ernest G||Improved water resistant sunscreen protection and insect repellent compound|
|U.S. Classification||424/47, 424/60|
|International Classification||A61Q17/04, A61K8/368, C08F218/00, A61K8/37, A61K8/44, A61K8/30, C08F218/04|
|Cooperative Classification||A61K8/445, A61Q17/04, A61K8/368, A61K8/37|
|European Classification||A61K8/37, A61K8/44G, A61K8/368, A61Q17/04|