US2257106A - Dermal lotion - Google Patents

Dermal lotion Download PDF

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Publication number
US2257106A
US2257106A US192796A US19279638A US2257106A US 2257106 A US2257106 A US 2257106A US 192796 A US192796 A US 192796A US 19279638 A US19279638 A US 19279638A US 2257106 A US2257106 A US 2257106A
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United States
Prior art keywords
parts
dermal
alcohol
lotion
film
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US192796A
Inventor
Walter G Christiansen
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ER Squibb and Sons LLC
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ER Squibb and Sons LLC
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Priority to US192796A priority Critical patent/US2257106A/en
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Publication of US2257106A publication Critical patent/US2257106A/en
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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/14Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/368Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0014Skin, i.e. galenical aspects of topical compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/02Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T24/00Buckles, buttons, clasps, etc.
    • Y10T24/14Bale and package ties, hose clamps
    • Y10T24/1402Packet holders

Definitions

  • This invention relates to dermal preparations, such as cosmetic, protective or medicinal lotions,
  • Ethyl oleate is a light-colored, almost odorless, bland, oily substance, which has protective properties similar to those of olive oil and the unique characteristics of solubility in alcohol in all proportions and very low viscosity.
  • a baseof ethyl oleate enables the use of alcohol-soluble perfume materials and/or medicaments for lotions, and, especially in the case of hand lotions, enables desirable modifications by addition of glycerine and/or water without causing separation of the mixture.
  • the higher fatty acid esters of lower aliphatic mono-hydric alcohols can be used as the base or film-forming ingredient of preparations embodying a dermal agent, inter alia, germicidal, fungicidal, emollient, anesthetic, cosmetic, pigmentary or coloring, and ray-absorbing substances, thus, the invention is applicable to dermal preparations such as the following: lotions, e. g. antiseptic, hand, skin-toning, calamine, and sunburn-preventive lotions; creams, e. g.
  • lotions e. g. antiseptic, hand, skin-toning, calamine, and sunburn-preventive lotions
  • creams e. g.
  • lotions for the treatment of ultravioletr afiections of the skin such as acne, blackheads, athlete's feet, and psoriasis
  • insect-bite preparations such as acne, blackheads, athlete's feet, and psoriasis
  • liquid face powders such as dirt, dust, dirt, dirt, and dusting pastes.
  • Example 1 A lotion for the treatment of affections of the skin is prepared by dissolving 10 parts of ethyl oleate in parts of alcohol, and adding Zparts of salicylic acid and 1 part of bergamot oil.
  • Example 2 An antiseptic lotion is prepared by dissolving 50 parts of ethyl oleate in 150 parts of alcohol, and adding 1 part of phenol, 10 parts of camphor,'2 parts of thymol, 3 parts of eugenol, and 1 part of oil of lavender.
  • Example 3 A sun burn-preventive lotion is prepared by dissolving 15 parts of ethyl oleate in 85 parts of alcohol and adding 5 parts of menthyl salicylate and 1 part of oil of lavender.
  • Example 4 A hand lotion is prepared by dissolving 30 parts
  • Example 5 A cold cream is prepared by adding a solution of 1 part of borax in 43 parts of water to a melted mixture of parts of ethyl oleate, 4 parts of spermaceti, and 30 parts of white beeswax, stirring the mixture until cold, and incorporating a perfume material into the emulsion so formed.
  • Example 6 A vanishing cream is prepared by adding 100 7 parts of a 2% aqueous solution of potassium hydroxide to a melted mixture of 20 parts of triplepressed stearic acid and parts of ethyl oleate, stirring the mixture until cold, and incorporating 1' part of a suitable perfume oil into the emulsion so formed; a
  • Example 7 A lotion for the treatment of skin infections I such as athlete's foot is prepared by suitably mixing 3.75 parts of salicylic acid, 7.7 parts 'of benzoic acid; 0.5 part of phenol, parts of ethyl stearate,'1 part oil of Wintergreen, and 73 parts. a of alcohol.
  • Example 8 A brushless shaving cream is prepared by pouring 675 grams of a 1.5% aqueous solution of potasslum hydroxide into a melted mixture of 300 grams stearic acid and 25 grams of butyl palmiv tate.
  • Example 9 An antiseptic lotion is prepared by dissolving 50 parts of isobutyl laurate in 150 parts of alcohol, and adding 1 part of phenol, 10 parts of camphor, 2 parts of thyrnol, 3 parts of eugenol, and 1 part oil of lavender.
  • a dermal lotion essentially comprising a dermal agent and a higher fatty acid ester of a lower aliphatic monohydric alcohol in alcohol solutiqn, and adapted to form a film of the ester in 'combination'wlth the dermal agent.
  • a dermal lotion essentially comprising a dermal agent and ethyl oleate in alcohol solution
  • a dermal lotion essentially comprising a lower aliphatic monohydric alcohol in alcohol so- "lution, and adapted to form a film of the ester in ultraviolet-ray-absorbingsubstance and a higher 5 fatty-acid ester of a lower aliphatic monohydric alcohol in alcohol solution, and adapted to form a film of the'ester in combination with the ultraviolet ray-absorbing substance.
  • a dermal lotion essentially comprising glyc erine and a higher fatty acid ester of a lower aliphatic monohydric alcohol in alcohol solution,

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dermatology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Cosmetics (AREA)

Description

Patented Sept. 30, 1941 2,257,106 v DERMAL LOTION Walter G. Christians'en, Glen Ridge,
N. J., as-
signor to E. R. Squibb & Sons, New York, N.'Y., a corporation of New York I No Drawing.
6 Claims.
Application February 26, 1938, Serial No. 192,796
This invention relates to dermal preparations, such as cosmetic, protective or medicinal lotions,
creams, and the like.-
' Numerous dermal preparations embody fixed oils, such as olive oil, as the base or film -forming ingredient. Such preparations, however, are not readily distributed over theskin, and cause an objectionable sense of oiliness. Moreover, these oils, being at best only slightly soluble in alcohol, can not be used as the base or film-forming ingredient of alcoholic dermal lotions.
It is the object of this invention to provide dermal preparations-especially alcoholic lotions embodying alcohol-soluble perfume materials and/or medicamentswhich spread readily over the skin and form a very thin, soft, pliable film causing no objectionable sense of oiliness.
It has been found that higher fatty acid esters of lower aliphatic monohydric alcohols, and notably ethyl oleate, are excellently suited for use as the base or film-forming ingredient of dermal preparations. Ethyl oleate, for example, is a light-colored, almost odorless, bland, oily substance, which has protective properties similar to those of olive oil and the unique characteristics of solubility in alcohol in all proportions and very low viscosity. Because of its very low viscosity, it spreads readily over the skin, leaving a very thin, almost indiscernible, soft, pliable, oily film causlng no objectionable sense of oiliness: being soluble in alcohol, it enables the provision of alcoholic dermal lotions which are especially easily distributed over the skin, much like a toilet water, and leave, on evaporation of the alcohol, a thin, uniform, and protective film of ethyl oleate either alone or in combination with desired medicament and/or cosmetic materials. Moreover, a baseof ethyl oleate enables the use of alcohol-soluble perfume materials and/or medicaments for lotions, and, especially in the case of hand lotions, enables desirable modifications by addition of glycerine and/or water without causing separation of the mixture.
The higher fatty acid esters of lower aliphatic mono-hydric alcohols, notably ethyl oleate, can be used as the base or film-forming ingredient of preparations embodying a dermal agent, inter alia, germicidal, fungicidal, emollient, anesthetic, cosmetic, pigmentary or coloring, and ray-absorbing substances, thus, the invention is applicable to dermal preparations such as the following: lotions, e. g. antiseptic, hand, skin-toning, calamine, and sunburn-preventive lotions; creams, e. g. cold, vanishing, massage, shaving, and lanolin creams; lotions for the treatment of ultravioletr afiections of the skin, such as acne, blackheads, athlete's feet, and psoriasis; insect-bite preparations; liquid face powders; and hand-cleansing pastes.
Among the other higher fatty acid esters of lower aliphatic monohydric alcohols used in the practice of this invention are The following examples are illustrative of the invention, the parts being by weight:
Example 1 A lotion for the treatment of affections of the skin is prepared by dissolving 10 parts of ethyl oleate in parts of alcohol, and adding Zparts of salicylic acid and 1 part of bergamot oil.
Example 2 An antiseptic lotion is prepared by dissolving 50 parts of ethyl oleate in 150 parts of alcohol, and adding 1 part of phenol, 10 parts of camphor,'2 parts of thymol, 3 parts of eugenol, and 1 part of oil of lavender. I
Example 3 A sun burn-preventive lotion is prepared by dissolving 15 parts of ethyl oleate in 85 parts of alcohol and adding 5 parts of menthyl salicylate and 1 part of oil of lavender.
Example 4 A hand lotion is prepared by dissolving 30 parts Example 5 A cold cream is prepared by adding a solution of 1 part of borax in 43 parts of water to a melted mixture of parts of ethyl oleate, 4 parts of spermaceti, and 30 parts of white beeswax, stirring the mixture until cold, and incorporating a perfume material into the emulsion so formed.
Example 6 A vanishing cream is prepared by adding 100 7 parts of a 2% aqueous solution of potassium hydroxide to a melted mixture of 20 parts of triplepressed stearic acid and parts of ethyl oleate, stirring the mixture until cold, and incorporating 1' part of a suitable perfume oil into the emulsion so formed; a
Example 7 A lotion for the treatment of skin infections I such as athlete's foot is prepared by suitably mixing 3.75 parts of salicylic acid, 7.7 parts 'of benzoic acid; 0.5 part of phenol, parts of ethyl stearate,'1 part oil of Wintergreen, and 73 parts. a of alcohol.
Example 8 A brushless shaving cream is prepared by pouring 675 grams of a 1.5% aqueous solution of potasslum hydroxide into a melted mixture of 300 grams stearic acid and 25 grams of butyl palmiv tate.
Example 9 An antiseptic lotion is prepared by dissolving 50 parts of isobutyl laurate in 150 parts of alcohol, and adding 1 part of phenol, 10 parts of camphor, 2 parts of thyrnol, 3 parts of eugenol, and 1 part oil of lavender.
The invention may be variously otherwise embodied, within the scope of the appended claims.
I claim:
medicament and a higher fatty acid ester of a 2,257,106 1. A dermal lotion essentially comprising a dermal agent and a higher fatty acid ester of a lower aliphatic monohydric alcohol in alcohol solutiqn, and adapted to form a film of the ester in 'combination'wlth the dermal agent.
2. A dermal lotion essentially comprising a dermal agent and ethyl oleate in alcohol solution,
and adapted to form a film of ethyl oleate in combination with the dermal agent,
3. A dermal lotion essentially comprising a lower aliphatic monohydric alcohol in alcohol so- "lution, and adapted to form a film of the ester in ultraviolet-ray-absorbingsubstance and a higher 5 fatty-acid ester of a lower aliphatic monohydric alcohol in alcohol solution, and adapted to form a film of the'ester in combination with the ultraviolet ray-absorbing substance.
6. A dermal lotion essentially comprising glyc erine and a higher fatty acid ester of a lower aliphatic monohydric alcohol in alcohol solution,
and adapted to form a film of theester in combination with the glycerine.
' WALTER G. CHRISTIANSEN.
US192796A 1938-02-26 1938-02-26 Dermal lotion Expired - Lifetime US2257106A (en)

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2498727A (en) * 1946-11-23 1950-02-28 Lanolin Plus Cosmetics Inc Isopropyl palmitate solution of lanolin cosmetic
US2809166A (en) * 1957-10-08 Skin cleanser composition
US2853423A (en) * 1955-05-20 1958-09-23 Olin Mathieson Aerosol sun-screening composition
US2865859A (en) * 1956-11-09 1958-12-23 Irwin I Lubowe Solubilizing of mineral, vegetable, animal oils for cosmetic, pharmaceutical and industrial purposes
US3122475A (en) * 1960-02-25 1964-02-25 Schaeppi Ag Dr Circulatory adjuvant shell elements for cardiac glycoside suppository cores
US3873537A (en) * 1971-05-28 1975-03-25 Squibb & Sons Inc 1-Imidocarbonyl-2-(1H)-pyridones and method of preparing same
US4016264A (en) * 1975-07-14 1977-04-05 The University Of Utah Wart treatment with phosphonoacetic acid or derivatives thereof
FR2416011A1 (en) * 1978-02-06 1979-08-31 Logan Srl EMOLLIENT PRODUCT FOR HAIR SHAVING, APPLICABLE DIRECTLY ON THE WIRE OF A RAZOR AND METHODS OF APPLICATION
WO1982000249A1 (en) * 1980-07-17 1982-02-04 S Reinke Emulsion for facial massage and shaving
EP0186258A2 (en) * 1984-05-17 1986-07-02 Haviva Rivkin Lotion for blemished scin (comprising thymol)
US4883654A (en) * 1987-01-09 1989-11-28 Young Deborah A Cosmetic preparation
DE4237367A1 (en) * 1992-11-05 1994-05-11 Beiersdorf Ag Antimycotic cosmetic and dermatological preparations containing fatty acid esters
US5519059A (en) * 1994-08-17 1996-05-21 Sawaya; Assad S. Antifungal formulation

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2809166A (en) * 1957-10-08 Skin cleanser composition
US2498727A (en) * 1946-11-23 1950-02-28 Lanolin Plus Cosmetics Inc Isopropyl palmitate solution of lanolin cosmetic
US2853423A (en) * 1955-05-20 1958-09-23 Olin Mathieson Aerosol sun-screening composition
US2865859A (en) * 1956-11-09 1958-12-23 Irwin I Lubowe Solubilizing of mineral, vegetable, animal oils for cosmetic, pharmaceutical and industrial purposes
US3122475A (en) * 1960-02-25 1964-02-25 Schaeppi Ag Dr Circulatory adjuvant shell elements for cardiac glycoside suppository cores
US3873537A (en) * 1971-05-28 1975-03-25 Squibb & Sons Inc 1-Imidocarbonyl-2-(1H)-pyridones and method of preparing same
US4016264A (en) * 1975-07-14 1977-04-05 The University Of Utah Wart treatment with phosphonoacetic acid or derivatives thereof
FR2416011A1 (en) * 1978-02-06 1979-08-31 Logan Srl EMOLLIENT PRODUCT FOR HAIR SHAVING, APPLICABLE DIRECTLY ON THE WIRE OF A RAZOR AND METHODS OF APPLICATION
WO1982000249A1 (en) * 1980-07-17 1982-02-04 S Reinke Emulsion for facial massage and shaving
EP0186258A2 (en) * 1984-05-17 1986-07-02 Haviva Rivkin Lotion for blemished scin (comprising thymol)
EP0186258A3 (en) * 1984-05-17 1987-06-03 Haviva Rivkin Lotion for blemished scin (comprising thymol)
US4883654A (en) * 1987-01-09 1989-11-28 Young Deborah A Cosmetic preparation
DE4237367A1 (en) * 1992-11-05 1994-05-11 Beiersdorf Ag Antimycotic cosmetic and dermatological preparations containing fatty acid esters
US5519059A (en) * 1994-08-17 1996-05-21 Sawaya; Assad S. Antifungal formulation

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