CA2535550A1 - Treatment for acne vulgaris and method of use - Google Patents
Treatment for acne vulgaris and method of use Download PDFInfo
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- CA2535550A1 CA2535550A1 CA002535550A CA2535550A CA2535550A1 CA 2535550 A1 CA2535550 A1 CA 2535550A1 CA 002535550 A CA002535550 A CA 002535550A CA 2535550 A CA2535550 A CA 2535550A CA 2535550 A1 CA2535550 A1 CA 2535550A1
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- Prior art keywords
- treatment
- acne vulgaris
- ethoxylate
- composition
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- 238000011282 treatment Methods 0.000 title claims abstract description 48
- 206010000496 acne Diseases 0.000 title claims abstract description 46
- 208000002874 Acne Vulgaris Diseases 0.000 title claims abstract description 43
- 238000000034 method Methods 0.000 title claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 33
- -1 polyethylene Polymers 0.000 claims abstract description 13
- 239000004698 Polyethylene Substances 0.000 claims abstract description 10
- 229920000573 polyethylene Polymers 0.000 claims abstract description 10
- 108700004121 sarkosyl Proteins 0.000 claims abstract description 10
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 claims abstract description 10
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 claims abstract description 10
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 9
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000011324 bead Substances 0.000 claims abstract description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000004166 Lanolin Substances 0.000 claims abstract description 6
- 229940039717 lanolin Drugs 0.000 claims abstract description 6
- 235000019388 lanolin Nutrition 0.000 claims abstract description 6
- 238000005201 scrubbing Methods 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000006260 foam Substances 0.000 claims abstract description 5
- 239000003381 stabilizer Substances 0.000 claims abstract description 5
- 239000008187 granular material Substances 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 2
- 239000004872 foam stabilizing agent Substances 0.000 claims 1
- 239000012749 thinning agent Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 5
- 230000000699 topical effect Effects 0.000 abstract description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 6
- 125000000524 functional group Chemical group 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 206010033733 Papule Diseases 0.000 description 4
- 230000002757 inflammatory effect Effects 0.000 description 4
- 230000003902 lesion Effects 0.000 description 3
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000003860 topical agent Substances 0.000 description 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 1
- 208000020154 Acnes Diseases 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 208000032544 Cicatrix Diseases 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- 241001635598 Enicostema Species 0.000 description 1
- 206010027626 Milia Diseases 0.000 description 1
- 206010054107 Nodule Diseases 0.000 description 1
- 206010037888 Rash pustular Diseases 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 230000004130 lipolysis Effects 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 208000029561 pustule Diseases 0.000 description 1
- 229960003471 retinol Drugs 0.000 description 1
- 235000020944 retinol Nutrition 0.000 description 1
- 239000011607 retinol Substances 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 230000037387 scars Effects 0.000 description 1
- 210000001732 sebaceous gland Anatomy 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
- A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/075—Ethers or acetals
- A61K31/085—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
Abstract
A treatment for Acne Vulgaris is provided for in a topical treatment. According to the invention, a method is provided for applying composition substances to the infected area, working the composition into the infected area, and removing the composition from the infected area. The composition comprises at least one ethoxylate in combination with Sodium Lauroyl Sarcosinate. Alternatively, the ethoxylate can be exchanged for a methoxylat e or a propoxylate. An inert scrubbing agent, such as polyethylene beads, can also be included. Acetylated lanolin alcohol, sodium Lauroyl Sarcosinate, EDTA, a foam stabilizer, and water can also be added to the composition to assist performance.
Description
1 Invention: Treatment for Acne Vulgaris and Method of Use 2 Inventor: William M. Yarbrough 3 I. FIELD OF THE INVENTION
4 The present invention relates to a composition including surfactants for the treatment of acne vulgaris. Methods of use are also included 6 TI. BACKGROUND OF THE INVENTION AND PRIOR ART
7 Acne vulgaris (or "acne") is a disorder of the sebaceous glands. It is 8 characterized by lesions that are either non-inflammatory or inflammatory papules and 9 nodules. Non-inflammatory papules may be open, commonly referred to as "blackheads", or closed, commonly referred to as "whiteheads". As a group, non-11 inflammatory. papules are called comedones. Closed comedones can lead to 12 inflammatory nodules, papules, and pustules. Severe cases of acne vulgaris can lead to 13 scars characterized by pitting.
14 It is believed that acne results from partial rupture of a partially inflamed follicle. The follicle then spills its components, thereby resulting in the development of a 16 perifollicular inflammatory process. Generally, fresh lesions are sterile, but later gram-17 positive diptheroids are present. Many times the skin will have a greasy look to it; this is 18 probably due, at least in part, to the release of fatty acids during lipolysis induced by P.
19 acnes.
Acne can be a serious problem. It generally manifests itself during adolescence 21 and spontaneously resolves in the late teens or early twenties; although for some, it can be 22 a life long problem. Mild to moderate acne is most often treated with topical agents.
INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: . William Yarbrough 1 More severe cases are treated with incision and drainage of lesions, ultraviolet light 2 therapy, and systemic antibiotics.
3 The prior art is replete with compositions for use in the treatment of acne.
4 Topical agents, such as benzoyl peroxide, are thought to decrease bacteria and are often used in the treatment of acne. These treatments are found in many forms, lotions, gels, 6 pads, etc. and are generally available over the counter. Retinol in various forms has been 7 more recently proposed by various Inventors. There are also many soaps used in the 8 treatment of acne. A major shortcoming of most of the prior art is that they often do not 9 penetrate sufficiently and they leave the skin dry.
II. OBJECTS OF THE INVENTION
11 It is an obj ect of the present invention to provide a treatment that helps to alleviate 12 the local signs and symptoms caused by acne vulgaris.
13 It is a further object of the present invention to provide a method of use of the 14 present inventive treatment.
It is yet another object of the present invention to provide a treatment that 16 includes at least a first nonyl phenyl ethoxylate and sodium lauroyl sarcosinate to which a 17 second nonyl phenyl ethoxylate, acetylated lanolin alcohol, EDTA, a foam stabilizer, 18 water, and inert polyethylene granules can be added without altering the effectiveness of 19 the treatment.
It is a yet further object of the present invention to provide a treatment that is safe 21 to use.
INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: William Yarbrough 1 It is yet another object of the present invention to provide such treatment that is 2 topical, can be purchased over the counter, and is economical.
3 IV. SUMMARY OF THE INVENTION
4 The above objects of the invention are provided for in a topical treatment for acne vulgaris. According to the invention, a method is provided for applying a composition of 6 substances to the infected area, working the composition into the infected area, and 7 removing the composition from the infected area. The composition comprises at least 8 one ethoxylate in combination with Sodium Lauroyl Sarcosinate (or "SLS"). An inert 9 scrubbing agent, such as polyethylene beads, can also be included to the formula.
Acetylated lanolin alcohol, a second ethoxylate, EDTA, a foam stabilizer, and water can 11 also be added to the composition without effecting performance.
12 Other formulas that keep the polarity similar to that of the inventive formula will 13 also work. To keep the polarity similar, it is necessary for the compound to have similar 14 characteristics, such as Carbon chains, carbonyl groups, Nitrogen bound to Carbon, Aromatic ring(s), Oxylate groups, and appropriate functional groups at the ends of the 16 individual molecules. The ideal substitute chemicals would have all of the characteristics 17 mentioned above, but it is not necessary to have every one of those as listed. For 18 example, if the functional groups at the ends of the individual molecules are exchanged 19 for other functional groups that retain the ability to undergo an emulsion polymerization, then the effectiveness of the compound is also retained. Another example is to change the 21 ethoxylate to a methoxylate or propoxylate. These formations would still retain a similar INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: William Yarbrough 1 polarity but would be different compounds with different characteristics.
Yet another 2 example would be to exchange triply bound Nitrogen with a doubly bound or perhaps 3 Nitrogen with 4 Carbons bound to it.
4 V. DETAILED DESCRIPTION OF THE INVENTION
Chemical analysis and research has revealed that two of the component parts of 6 the inventive composition are principally involved in its effectiveness as an acne 7 treatment: an ethoxylate and Sodium Lauroyl Sarcosinate ("SLS"). The ethoxylate is 8 preferably a nonyl phenol ethoxylate.
9 The Inventor has also found, however, that other formulas that keep the polarity similar to that of the inventive formula will also work. To keep the polarity similar, it is 11 necessary for the compound to have similar characteristics, such as Carbon chains, 12 carbonyl groups, Nitrogen bound to Carbon, Aromatic ring(s), Oxylate groups, and 13 appropriate functional groups at the ends of the individual molecules. The ideal 14 substitute chemicals would have all of the characteristics mentioned above, but it is not necessary to have every one of those as listed. For example, if the functional groups at the 16 ends of the individual molecules are exchanged for other functional groups that retain the 17 ability to undergo an emulsion polymerization, then the effectiveness of the compound is 18 also retained. Another example is to change the ethoxylate to a methoxylate or 19 propoxylate. These formations would still retain a similar polarity but would be different compounds with different characteristics. Yet another example would be to exchange INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: William Yarbrough 1 triply bound Nitrogen with a doubly bound or perhaps Nitrogen with 4 Carbons bound to 2 it.
3 The inventor has also discovered that the addition of an inert scrubbing agent 4 improves the action of the inventive composition. The beads should be large enough to be effective but not so large as to cause abrasions. The inventor suggests beads in the 6 range of 5 to SO microns with an average size being approximately 25 microns or 50 7 mesh.
8 To make the inventive composition, an exact ratio of ethoxylate to SLS is not 9 critical. The only requirement is that the ethoxylate is completely reacted with the SLS, creating a polymer. This will vary with the ethoxylate used, but the Inventor has 11 determined that a ratio of ethoxylate-to- SLS of 1. S :2 is preferred. The amount by weight 12 of polyethylene beads can vary according to the grittiness desired. The Inventor has 13 found that a formula of ethoxylate:SLS:polyethylene of 40:20:40 is preferred but that 14 formulas of other concentrations are useful. Thus, for production purposes, formulas having SLS ranging from 10 to 20 % by weight, ethoxylate ranging from 20 to 40 % by 16 weight, and polyethylene beads from 20 to 50% by weight are reasonable. But again, the 17 formula is not restricted to these ranges, which ranges are presented for example purposes 18 only.
19 Also, a cutting agent that does not chemically react with the composition may be added. The cutting agent makes the overall composition flow more easily, thereby INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: William Yarbrough 1 enabling more packaging options, such as tubes. The cutting agent must be added only in 2 sufficient amount that it promotes flow but does not effect the action of the composition.
3 In use, an sufficient amount of the composition is used to cover the infected area, 4 the composition is applied to an infected area and worked over the area by a scrubbing motion. After sufficient time has elapsed to ensure that the infected area has been 6 adequately exposed to the composition such that they area feels clean, approximately ten 7 to thirty seconds for the typical person, the area is rinsed cleaned.
7 Acne vulgaris (or "acne") is a disorder of the sebaceous glands. It is 8 characterized by lesions that are either non-inflammatory or inflammatory papules and 9 nodules. Non-inflammatory papules may be open, commonly referred to as "blackheads", or closed, commonly referred to as "whiteheads". As a group, non-11 inflammatory. papules are called comedones. Closed comedones can lead to 12 inflammatory nodules, papules, and pustules. Severe cases of acne vulgaris can lead to 13 scars characterized by pitting.
14 It is believed that acne results from partial rupture of a partially inflamed follicle. The follicle then spills its components, thereby resulting in the development of a 16 perifollicular inflammatory process. Generally, fresh lesions are sterile, but later gram-17 positive diptheroids are present. Many times the skin will have a greasy look to it; this is 18 probably due, at least in part, to the release of fatty acids during lipolysis induced by P.
19 acnes.
Acne can be a serious problem. It generally manifests itself during adolescence 21 and spontaneously resolves in the late teens or early twenties; although for some, it can be 22 a life long problem. Mild to moderate acne is most often treated with topical agents.
INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: . William Yarbrough 1 More severe cases are treated with incision and drainage of lesions, ultraviolet light 2 therapy, and systemic antibiotics.
3 The prior art is replete with compositions for use in the treatment of acne.
4 Topical agents, such as benzoyl peroxide, are thought to decrease bacteria and are often used in the treatment of acne. These treatments are found in many forms, lotions, gels, 6 pads, etc. and are generally available over the counter. Retinol in various forms has been 7 more recently proposed by various Inventors. There are also many soaps used in the 8 treatment of acne. A major shortcoming of most of the prior art is that they often do not 9 penetrate sufficiently and they leave the skin dry.
II. OBJECTS OF THE INVENTION
11 It is an obj ect of the present invention to provide a treatment that helps to alleviate 12 the local signs and symptoms caused by acne vulgaris.
13 It is a further object of the present invention to provide a method of use of the 14 present inventive treatment.
It is yet another object of the present invention to provide a treatment that 16 includes at least a first nonyl phenyl ethoxylate and sodium lauroyl sarcosinate to which a 17 second nonyl phenyl ethoxylate, acetylated lanolin alcohol, EDTA, a foam stabilizer, 18 water, and inert polyethylene granules can be added without altering the effectiveness of 19 the treatment.
It is a yet further object of the present invention to provide a treatment that is safe 21 to use.
INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: William Yarbrough 1 It is yet another object of the present invention to provide such treatment that is 2 topical, can be purchased over the counter, and is economical.
3 IV. SUMMARY OF THE INVENTION
4 The above objects of the invention are provided for in a topical treatment for acne vulgaris. According to the invention, a method is provided for applying a composition of 6 substances to the infected area, working the composition into the infected area, and 7 removing the composition from the infected area. The composition comprises at least 8 one ethoxylate in combination with Sodium Lauroyl Sarcosinate (or "SLS"). An inert 9 scrubbing agent, such as polyethylene beads, can also be included to the formula.
Acetylated lanolin alcohol, a second ethoxylate, EDTA, a foam stabilizer, and water can 11 also be added to the composition without effecting performance.
12 Other formulas that keep the polarity similar to that of the inventive formula will 13 also work. To keep the polarity similar, it is necessary for the compound to have similar 14 characteristics, such as Carbon chains, carbonyl groups, Nitrogen bound to Carbon, Aromatic ring(s), Oxylate groups, and appropriate functional groups at the ends of the 16 individual molecules. The ideal substitute chemicals would have all of the characteristics 17 mentioned above, but it is not necessary to have every one of those as listed. For 18 example, if the functional groups at the ends of the individual molecules are exchanged 19 for other functional groups that retain the ability to undergo an emulsion polymerization, then the effectiveness of the compound is also retained. Another example is to change the 21 ethoxylate to a methoxylate or propoxylate. These formations would still retain a similar INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: William Yarbrough 1 polarity but would be different compounds with different characteristics.
Yet another 2 example would be to exchange triply bound Nitrogen with a doubly bound or perhaps 3 Nitrogen with 4 Carbons bound to it.
4 V. DETAILED DESCRIPTION OF THE INVENTION
Chemical analysis and research has revealed that two of the component parts of 6 the inventive composition are principally involved in its effectiveness as an acne 7 treatment: an ethoxylate and Sodium Lauroyl Sarcosinate ("SLS"). The ethoxylate is 8 preferably a nonyl phenol ethoxylate.
9 The Inventor has also found, however, that other formulas that keep the polarity similar to that of the inventive formula will also work. To keep the polarity similar, it is 11 necessary for the compound to have similar characteristics, such as Carbon chains, 12 carbonyl groups, Nitrogen bound to Carbon, Aromatic ring(s), Oxylate groups, and 13 appropriate functional groups at the ends of the individual molecules. The ideal 14 substitute chemicals would have all of the characteristics mentioned above, but it is not necessary to have every one of those as listed. For example, if the functional groups at the 16 ends of the individual molecules are exchanged for other functional groups that retain the 17 ability to undergo an emulsion polymerization, then the effectiveness of the compound is 18 also retained. Another example is to change the ethoxylate to a methoxylate or 19 propoxylate. These formations would still retain a similar polarity but would be different compounds with different characteristics. Yet another example would be to exchange INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: William Yarbrough 1 triply bound Nitrogen with a doubly bound or perhaps Nitrogen with 4 Carbons bound to 2 it.
3 The inventor has also discovered that the addition of an inert scrubbing agent 4 improves the action of the inventive composition. The beads should be large enough to be effective but not so large as to cause abrasions. The inventor suggests beads in the 6 range of 5 to SO microns with an average size being approximately 25 microns or 50 7 mesh.
8 To make the inventive composition, an exact ratio of ethoxylate to SLS is not 9 critical. The only requirement is that the ethoxylate is completely reacted with the SLS, creating a polymer. This will vary with the ethoxylate used, but the Inventor has 11 determined that a ratio of ethoxylate-to- SLS of 1. S :2 is preferred. The amount by weight 12 of polyethylene beads can vary according to the grittiness desired. The Inventor has 13 found that a formula of ethoxylate:SLS:polyethylene of 40:20:40 is preferred but that 14 formulas of other concentrations are useful. Thus, for production purposes, formulas having SLS ranging from 10 to 20 % by weight, ethoxylate ranging from 20 to 40 % by 16 weight, and polyethylene beads from 20 to 50% by weight are reasonable. But again, the 17 formula is not restricted to these ranges, which ranges are presented for example purposes 18 only.
19 Also, a cutting agent that does not chemically react with the composition may be added. The cutting agent makes the overall composition flow more easily, thereby INVENTION: Treatment for Acne Vulgaris Treatment and Method of Use INVENTOR: William Yarbrough 1 enabling more packaging options, such as tubes. The cutting agent must be added only in 2 sufficient amount that it promotes flow but does not effect the action of the composition.
3 In use, an sufficient amount of the composition is used to cover the infected area, 4 the composition is applied to an infected area and worked over the area by a scrubbing motion. After sufficient time has elapsed to ensure that the infected area has been 6 adequately exposed to the composition such that they area feels clean, approximately ten 7 to thirty seconds for the typical person, the area is rinsed cleaned.
Claims (32)
1. A Treatment for Acne Vulgaris comprising sodium lauroyl sarcosinate and a nonyl phenyl ethoxylate in combination.
2. The treatment for Acne Vulgaris of Claim 1 further including a second nonyl phenyl ethoxylate.
3. The treatment for Acne Vulgaris of Claim 1 further including acetylated lanolin alcohol.
4. The treatment for Acne Vulgaris of Claim 1 further including polyethylene granules.
5. The treatment for Acne Vulgaris of Claim 1 further including water.
6. The treatment for Acne Vulgaris of Claim 1 further including ethylenediaminetetraacetic acid.
7. The treatment for Acne Vulgaris of Claim 1 further including a foam stabilizing agent.
8. The treatment for Acne Vulgaris of Claim 1 further including a cutting agent.
9. The cutting agent of Claim 8 being selected from the group of aqueous based solutions and oil based solutions.
10. The treatment for Acne Vulgaris of Claim 1 wherein the ethoxylate is exchanged for a methoxylate.
11. The treatment for Acne Vulgaris of Claim 1 wherein the ethoxylate is exchanged for a propoxylate.
12. A treatment for Acne Vulgaris comprising an ethoxylate, sodium lauroyl sarcosinate, and scrubbing means.
13. The treatment for Acne Vulgaris of Claim 12 wherein the scrubbing mean is polyethylene beads.
14. The treatment for Acne Vulgaris of Claim 12 further including a cutting agent.
15. The treatment for Acne Vulgaris of Claim 12 wherein the ethoxylate is exchanged for a methoxylate.
16. The treatment for Acne Vulgaris of Claim 12 wherein the ethoxylate is exchanged for a propoxylate.
17. A treatment for Acne Vulgaris comprising: a first ethoxylate, a second ethoxylate, acetylated lanolin alcohol, sodium lauroyl sarcosinate, EDTA, a foam stabilizer, water, and inert polyethylene granules.
18. The treatment for Acne Vulgaris of Claim 17 wherein the first ethoxylate is exchanged for a methoxylate.
19. The treatment for Acne Vulgaris of Claim 17 wherein the first ethoxylate is exchanged for a propoxylate.
20. A treatment for Acne Vulgaris comprising an ethoxylate, sodium lauroyl sarcosinate, and EDTA.
21. The treatment for Acne Vulgaris of Claim 20 wherein the ethoxylate is exchanged for a methoxylate.
22. The treatment for Acne Vulgaris of Claim 20 wherein the ethoxylate is exchanged for a propoxylate.
23. A method for treating Acne Vulgaris comprising the steps of:
preparing a composition comprising an ethoxylate and sodium lauroyl sarcosinate;
applying the composition to an infected area;
permitting the composition to remain on the infected area a sufficient amount of time to enable the composition of matter to cause an effect; and, removing the composition from the infected area.
preparing a composition comprising an ethoxylate and sodium lauroyl sarcosinate;
applying the composition to an infected area;
permitting the composition to remain on the infected area a sufficient amount of time to enable the composition of matter to cause an effect; and, removing the composition from the infected area.
24. The method of Claim 23 wherein preparing the composition further includes adding second ethoxylate.
25. The method of Claim 23 wherein preparing the composition further includes adding acetylated lanolin alcohol.
26. The method of Claim 23 wherein preparing the composition further includes adding acetylated polyethylene granules.
27. The method of Claim 23 wherein preparing the composition further includes adding water.
28. The method of Claim 23 wherein preparing the composition further includes EDTA.
29. The method of Claim 23 wherein preparing the composition further includes a foam stabilizer.
30. The method of Claim 23 further including the step of adding a thinning agent to the composition.
31. The method of Claim 23 wherein the ethoxylate is exchanged for a methoxylate.
32. The method of Claim 23 wherein the ethoxylate is exchanged for a propoxylate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2003/025207 WO2005018629A1 (en) | 2003-08-12 | 2003-08-12 | Treatment for acne vulgaris and method of use |
Publications (1)
Publication Number | Publication Date |
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CA2535550A1 true CA2535550A1 (en) | 2005-03-03 |
Family
ID=34215304
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA002535550A Abandoned CA2535550A1 (en) | 2003-08-12 | 2003-08-12 | Treatment for acne vulgaris and method of use |
Country Status (5)
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EP (1) | EP1656128A4 (en) |
JP (1) | JP2007521234A (en) |
AU (1) | AU2003264053A1 (en) |
CA (1) | CA2535550A1 (en) |
WO (1) | WO2005018629A1 (en) |
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GB1539031A (en) * | 1975-02-22 | 1979-01-24 | Beecham Group Ltd | Pharmaceutical compositions |
US4147782A (en) * | 1976-06-24 | 1979-04-03 | William H. Rorer, Inc. | Pharmaceutical detergent composition |
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US6423746B1 (en) * | 1999-07-03 | 2002-07-23 | The William M. Yarbrough Foundation | Urushiol induced contact dermatitis and method of use |
US7008963B2 (en) * | 1999-07-03 | 2006-03-07 | The William M. Yarbrough Foundation | Urushiol induced contact dermatitis solution |
-
2003
- 2003-08-12 EP EP03818329A patent/EP1656128A4/en not_active Withdrawn
- 2003-08-12 CA CA002535550A patent/CA2535550A1/en not_active Abandoned
- 2003-08-12 AU AU2003264053A patent/AU2003264053A1/en not_active Abandoned
- 2003-08-12 WO PCT/US2003/025207 patent/WO2005018629A1/en active Application Filing
- 2003-08-12 JP JP2005508238A patent/JP2007521234A/en not_active Abandoned
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EP1656128A4 (en) | 2007-02-28 |
EP1656128A1 (en) | 2006-05-17 |
AU2003264053A1 (en) | 2005-03-10 |
WO2005018629A1 (en) | 2005-03-03 |
JP2007521234A (en) | 2007-08-02 |
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