MXPA97006453A - Compositions containing useful benzoyl peroxide in the topical treatment of scaled tissue and reaction to tissue trauma relationship - Google Patents
Compositions containing useful benzoyl peroxide in the topical treatment of scaled tissue and reaction to tissue trauma relationshipInfo
- Publication number
- MXPA97006453A MXPA97006453A MXPA/A/1997/006453A MX9706453A MXPA97006453A MX PA97006453 A MXPA97006453 A MX PA97006453A MX 9706453 A MX9706453 A MX 9706453A MX PA97006453 A MXPA97006453 A MX PA97006453A
- Authority
- MX
- Mexico
- Prior art keywords
- composition
- use according
- region
- benzoyl peroxide
- layer
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 55
- 210000001519 tissues Anatomy 0.000 title claims abstract description 39
- 239000004342 Benzoyl peroxide Substances 0.000 title claims abstract description 28
- OMPJBNCRMGITSC-UHFFFAOYSA-N Incidol Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 235000019400 benzoyl peroxide Nutrition 0.000 title claims abstract description 28
- 230000000699 topical Effects 0.000 title claims abstract description 14
- 206010022114 Injury Diseases 0.000 title description 7
- 238000006243 chemical reaction Methods 0.000 title description 3
- 231100000241 scar Toxicity 0.000 claims abstract description 33
- 239000006210 lotion Substances 0.000 claims description 18
- 239000006071 cream Substances 0.000 claims description 12
- 238000007920 subcutaneous administration Methods 0.000 claims description 9
- JYGXADMDTFJGBT-VWUMJDOOSA-N Cortisol Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 claims description 7
- LXCFILQKKLGQFO-UHFFFAOYSA-N Methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims description 7
- 230000002745 absorbent Effects 0.000 claims description 7
- 239000002250 absorbent Substances 0.000 claims description 7
- 229960000890 hydrocortisone Drugs 0.000 claims description 7
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-Hydroxybenzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 6
- 230000037390 scarring Effects 0.000 claims description 6
- 210000003491 Skin Anatomy 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 claims description 5
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 claims description 5
- 230000003020 moisturizing Effects 0.000 claims description 5
- PZZYQPZGQPZBDN-UHFFFAOYSA-N Aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 claims description 4
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- -1 p-hydroxybenzoic acid ester Chemical class 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 239000003381 stabilizer Substances 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 210000000988 Bone and Bones Anatomy 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 230000000774 hypoallergenic Effects 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 1
- WMGSQTMJHBYJMQ-UHFFFAOYSA-N aluminum;magnesium;silicate Chemical compound [Mg+2].[Al+3].[O-][Si]([O-])([O-])[O-] WMGSQTMJHBYJMQ-UHFFFAOYSA-N 0.000 claims 1
- 210000000746 body regions Anatomy 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- 239000002537 cosmetic Substances 0.000 abstract description 3
- 239000004615 ingredient Substances 0.000 abstract description 2
- 229960003328 benzoyl peroxide Drugs 0.000 description 24
- 230000035876 healing Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 5
- 230000001225 therapeutic Effects 0.000 description 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- 238000001356 surgical procedure Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 206010000496 Acne Diseases 0.000 description 3
- QELSKZZBTMNZEB-UHFFFAOYSA-N Propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 235000012970 cakes Nutrition 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 3
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 3
- 238000002435 rhinoplasty Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000002560 therapeutic procedure Methods 0.000 description 3
- 206010060945 Bacterial infection Diseases 0.000 description 2
- XUGNVMKQXJXZCD-UHFFFAOYSA-N Isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 2
- 210000001331 Nose Anatomy 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 229940009868 aluminum magnesium silicate Drugs 0.000 description 2
- 230000002917 arthritic Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- 201000009910 diseases by infectious agent Diseases 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 229940075495 isopropyl palmitate Drugs 0.000 description 2
- 229960002216 methylparaben Drugs 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- 229960003415 propylparaben Drugs 0.000 description 2
- 230000037307 sensitive skin Effects 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 230000002522 swelling Effects 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 206010073316 Accidental exposures to product Diseases 0.000 description 1
- 206010003246 Arthritis Diseases 0.000 description 1
- 208000006673 Asthma Diseases 0.000 description 1
- 206010015150 Erythema Diseases 0.000 description 1
- 229940100242 Glycol Stearate Drugs 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N Glycol stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 210000000088 Lip Anatomy 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- 210000000537 Nasal Bone Anatomy 0.000 description 1
- 229940032067 PEG-20 Stearate Drugs 0.000 description 1
- 231100000614 Poison Toxicity 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229960004063 Propylene glycol Drugs 0.000 description 1
- 208000003251 Pruritus Diseases 0.000 description 1
- 229960004274 Stearic acid Drugs 0.000 description 1
- 206010046736 Urticarias Diseases 0.000 description 1
- 210000003462 Veins Anatomy 0.000 description 1
- 230000000172 allergic Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 201000008937 atopic dermatitis Diseases 0.000 description 1
- 230000003190 augmentative Effects 0.000 description 1
- 230000001580 bacterial Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 239000008294 cold cream Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 238000002316 cosmetic surgery Methods 0.000 description 1
- 230000003247 decreasing Effects 0.000 description 1
- 230000003292 diminished Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000001815 facial Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000005908 glyceryl ester group Chemical group 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000036244 malformation Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 238000010606 normalization Methods 0.000 description 1
- KREXGRSOTUKPLX-UHFFFAOYSA-N octadecanoic acid;zinc Chemical compound [Zn].CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O KREXGRSOTUKPLX-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000059 polyethylene glycol stearate Polymers 0.000 description 1
- 230000002980 postoperative Effects 0.000 description 1
- 230000002335 preservative Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N rac-1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000036620 skin dryness Effects 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-M stearate Chemical compound CCCCCCCCCCCCCCCCCC([O-])=O QIQXTHQIDYTFRH-UHFFFAOYSA-M 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Abstract
The present invention relates to topical application to scar tissue regions of a composition comprising various ingredients commonly used in cosmetic products, such as benzoyl peroxide, leading to a reduction and a softening of the scar tissue
Description
METHOD FOR TOPICAL TREATMENT OF CICATRIZED AND
REACTION TO THE TRAUMA OF THE RELATED TISSUE
BACKGROUND OF THE INVENTION The present invention relates to a method for softening and reducing cutaneous and subcutaneous scar tissue. More specifically, the present invention relates to a method of treating scar tissue by the topical application of a specific composition directly to the areas of the body where healing has occurred, for example, as a result of the trauma accompanying the surgery. Plastic surgery advances have diminished the problem of scarring, both in the layers of the skin (cutaneously) and in the region under the skin (subcutaneously) due to the trauma associated with injury or surgical intervention. However, there is therefore little that can be done to normalize the appearance of specific scar tissue after enough time has elapsed to have stopped the significant natural reduction of scar mass. It has been discovered in Schweiger, U.S. Patent. 4,694,021 ("the '021 patent"), that a composition having a consistency that allows it to form a cake in the region where the healing occurred, advantageously led to a softening and reduction of the scar tissue. In the '021 patent, the preferable composition contained enough water, inter alia, to achieve the desired "cake" consistency, i.e., until the cake has dried and hardened in the composition. In fact, the commercially preferred product of the '021 patent was MUDD®, therefore, the composition preferably had the texture of a compress or face mask. That method for treating scar tissue by the topical application of this specific compound, therefore has been proven to be somewhat impractical and not popular in view of the inconvenience to apply the therapeutic preparation in the form of a voluminous facial mask. Therefore, there is a need to develop a method for treating scar tissue that is (1) easy and convenient to use and (2) produces superiorly effective results. SUMMARY OF THE INVENTION Therefore, it is an object of the present invention to provide a therapeutic method for treating scar tissue which is effective in normalizing the appearance of said tissue, even after the process of natural reduction of healed mass has ceased. It is also an object of the present invention to provide a simple, non-invasive and relatively inexpensive method for smoothing and reducing both cutaneous and subcutaneous scar tissue. It is a further object of the present invention to provide a compound with a practical and comfortable consistency to be used in a method in order to soften and reduce both scar tissue and both subcutaneous and cutaneous tissue.
To achieve the above objectives, a method for treating scar tissue comprising the step of applying topically to a region of the body where cutaneous or subcutaneous scarring has been presented, has been provided in accordance with one aspect of the present invention. Therapeutically effective amount of a composition comprising benzoyl peroxide, an argillaceous absorbent and at least one ester of hydroxybenzoic acid In a preferred embodiment, the composition mentioned above is applied to the region of the body where the healing occurred, in a sufficient amount such as a light to moderate bed of the composition that covers substantially the entire region of the body affected by the scar. Additionally, in a preferred embodiment, the aforementioned composition is applied to the region of the body where healing has occurred by the repeated application of light to moderate applications of a compos tion having an active ingredient of benzoyl peroxide lotion (hereinafter sometimes referred to as the "preferred composition") The preferred composition is applied in this form, leaving from half a minute to a minute for the medicine to be fixed before gently applying the next portion of the composition on the previous layer Each of said applications of the preferred composition overlaps with the region of the body affected by the underlying scar for maximizing effectiveness With respect to subcutaneous healing at the tip of the nose, the preferred composition is similarly applied in a series of layers on the mucosal membrane on the upper portion of each nostril. Other objects, aspects and advantages of the present invention will be apparent from the following detailed description. However, it should be understood that the detailed description and specific examples, while indicating preferred embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will be apparent to the experts in the art. technique of this detailed description. DETAILED DESCRIPTION OF THE PREFERRED MODALITIES It has been found that a substance having a known use in cosmetic products, but not a well-defined therapeutic effect for treating scar masses, can be used via topical application to effect a reduction and softening of scar tissue , even years after the trauma that caused the healing. Although the physiological basis for this therapeutic effect is not clear, it is thought that the topical application of the substance described above induces (or increases) the natural mechanisms for decalcification and rupture of fibrous material in the masses of scar tissue. Such activity could be in accordance with the observation, described in greater detail below, that topical applications of a composition according to the present invention leads to a reduction of cutaneous and subcutaneous scar tissue and overgrowth of calcified bone after rhinoplasty surgery. A composition useful for treating scar tissue according to the present invention preferably comprises an argillaceous material, such as an aluminum silicate solid, which can act as both an absorbent and a base for the composition. Specifically, an aluminum silicate preferably used as an absorbent and a base for the composition is aluminum magnesium silicate. The composition described above also comprises benzoyl peroxide. Benzoyl peroxide has been used as a bleaching agent for flours, fats, oils and waxes, as well as a drying agent for unsaturated oils. According to Hawley, THE CONDENSED CHEMICAL DICTIONARY 120 (Van Nostrand Co. 1981), benzoyl peroxide has application as "a drying agent for unsaturated oils for pharmaceutical and cosmetic purposes". However, it is not known that any role that affects scar tissue that has been ascribed to topical applications of benzoyl peroxide. A third constituent of a composition employed in the present invention is an ester of p-hydroxybenzoic acid, such as methyl p-hydroxybenzoate ("methyl paraben") propyl p-hydroxybenzoate ("propylparaben"). Such esters are widely used in cold creams, eyeliners and liquid make-up products as preservatives, antimicrobial agents, but there is no known therapeutic activity that has been attributed to them. In the present invention, it is preferable that methyl p-hydroxybenzoate as propyl, they are present in the topically applied composition. A composition used in accordance with the present invention should also contain normal ingredients found in skin cleansers, such as emulsifiers, surfactants, stabilizers, solvents, etc., including, but not limited to. glyceryl ester, isopropyl palmitate, polyethylene glycol stearate (PEG-20), propylene glycol, stearic acid, water, xanthan gum and zinc stearate In any case, it is preferred that the primary benzoyl peroxide-containing composition be substantially applied to the entire region of the scar tissue, preferably in an amount sufficient to form an effective layer "Substantially" in this context denotes that the therapy of the present invention does not require, for effectiveness, a full coverage of the scarred region. However, it is preferred that the area of the body affected by scarring be completely covered with a slight overlap and decreasing the layer in the surrounding regions that are or are thus affected It is also preferable that the composition used to soften and reduce the cutaneous and subcutaneous scar tissue have a light to moderate consistency in weight and texture, thus providing an effective yet comfortable vehicle for topically delivering a pharmaceutically effective amount of the preferred composition. For this purpose, a composition that is particularly preferred to be used for the purpose of treating scar tissue in accordance with the present invention includes 10% BENZOYL PEROXIDE LOTION (manufactured by KMart Corporation, Troy Michigan), an acne medication that it has a formulation comprising 10% benzoyl peroxide, glyceryl monostearate, isopropyl palmitate, aluminum magnesium silicate, methylparaben, propylparaben, PEG-20 stearate, propylene glycol, stearic acid, water, xanthan gum and stearate of zinc, which falls within the preceding description. The periodic topical applications of the 10% BENZOYL PEROXIDE LOTION, to a region of the nose that has been healed, both cutaneously and subcutaneously, by major rhinoplasty surgery or in some way associated with a reduction in the mass of scar tissue, a concomitant softening of remaining scar tissue and a recession in tracing overgrowth which has caused an apparent thickness of the nasal bone. The present invention was made when a LOTION OF
% BENZOYL PEROXIDE, marketed to help cure acne, was applied in order to alleviate bacterial infection in the right nasal window. The scar tissue from a surgical rhinoplasty procedure many years before was located at the nasal tip at the time of this treatment for bacterial infection. After four days of treatment of infection with 10% BENZOYL PEROXIDE LOTION, not only did it alleviate the discomfort of the infection, as expected, but it also reduced the scar tissue and also presented a more normal appearance of the nasal tip. , the result of which was very unexpected. The continuous application of 10% BENZOYL PEROXIDE LOTION resulted in the continuous reduction of scar tissue in the following months. Additionally, the scar tissue softened as it was reduced in size. These effects of the therapy, after the present invention, were particularly unexpected since the surgery that caused the healing that was treated, was performed approximately from seventeen to eighteen years before, that is, the treatment was effective after it ceased well from the treatment. significant postoperative normalization of damaged tissue. The maximum benefit of the present invention was realized about one to one hour and one quarter of the time that the 10% BENZOYL PEROXIDE LOTION was applied. It is thought that the maximum benefit occurs while the lotion is wet, thus corresponding to the time frame mentioned above for the application of the preferred composition. The formation of layers of the composition helps to ensure that the lotion will not dry very quickly and therefore shortens the benefit period. After the treatment, the dry residue was washed with water. A light application of hydrocortisone cream and / or nonprescription moisturizer can be used to help avoid or mitigate red coloring and scale formation. A multiplier effect can be shown when two to three topical treatments of the BENZOYL PEROXIDE LOTION The 10% are carried out in close proximity to one another, generally one to fifteen minutes apart. The results of said effect may offer increased scarring and / or accelerated scarring on the results caused by the same number of treatments spaced by a day. Another improvement technique, which may lengthen and / or reinforce the therapeutic effect of the preferred composition of In accordance with the present invention, a moderate to severe application of the 10% BENZOYL PEROXIDE LOTION is added from twenty-five to thirty-five minutes after the application of the original layers and while the first application is still wet. In any case, if two or more treatments are performed with several minutes of separation in order to help achieve accelerated, augmented, elongated or reinforced results, it is preferable that the applications of the preferred composition, particularly the latter, be preceded with a light application of hydrocortisone cream without prescription and / or a light application of moisturizing lotion. Additionally, the last layer treatment should preferably be followed by the application of the hydrocortisone cream and possibly a moisturizing lotion (as opposed to a moisturizing cream, since in one example the cream tended to promote bacterial inflammation), in order to avoid irritation to the area being treated In view of the present invention, it is thought that benzoyl peroxide is an agent that generally helps the body repair itself of excess tissue formations and fluids caused by the tissue damaged Such damage could be presented from the outside of the trauma, that is, the burned tissue, or also from events that occur naturally such as arthritis. Consequently, it is ensured that large quantities of BENZOYL PEROXIDE LOTION AT 10% could reduce the time of cure and the degree of "permanence" of the damage and can help disqualification and reduce arthritic malformations in the hand Additional, it is understood that an appropriately acceptable solution of benzoyl peroxide could be injected into a smovin 'tissue of the joint in order to help alleviate arthritic problems In this vein, a permissible solution of benzoyl peroxide could be effective for related surgical uses. However, according to the dermatological consultation, approximately 2% of the population is allergic to 10% benzoyl peroxide Therefore, it is conceivable that a person with the need to use said composition to soften and reduce scar tissue cutaneous or subcutaneous , could develop an immediate allergic reaction or after the continuous application of said composition The consequences could result in a simple urticaria or swelling (normal) and / or moderate asthma (the dermatological consultation indicates that this type of reaction is unusual) Additionally, in this regard, the literature of the PEROXIDE LOTION OF B 10% ENZOYL, marketed by KMart Corporation, set under "WARNINGS", For external use only. The use of other topical acne medications at the same time or immediately after using this product may increase skin dryness or irritation. If you have very sensitive skin or if you are sensitive to benzoyl peroxide, this product may cause irritation, characterized by redness, burning, itching, detachment, a medication should be used unless directed by a doctor. Skin, or possibly swelling Moderate irritation may be reduced by using the product less frequently or in a lower concentration If irritation becomes very severe, discontinue use, if irritation persists, consult a doctor. Keep away from eyes, lips and mouth In case of accidental ingestion, get professional help or contact immediately to a Poison Control Center Avoid contact with hair, fabrics or carpets since benzoyl peroxide will cause bleaching It is possible, with those with traditionally sensitive skin, that the application of the BENZOYL PEROXIDE LOTION AT 10% is routinely preceded with a 1% hydrocortisone cream application without prescription and after treating with the same cream to mitigate reddish coloration and dryness. With or without 1% hydrocortisone cream, softening and reduction of scar tissue would occur. The above invention has been described with reference to the particularly preferred embodiments. Those skilled in the art recognize that various modifications can be made to the invention without departing from the spirit and scope thereof.
Claims (1)
- CLAIMS 1 The use of a therapeutically effective amount of a composition comprising, in combination (a) benzoyl peroxide as an active ingredient, and (b) an argillaceous absorbent and at least one p-hydroxybenzoic acid ester, in the preparation of an agent for use in a method for treating scar tissue, wherein said composition is applied topically to a body region where subcutaneous scarring or overgrowth of calcified bone occurred. The use according to claim 1, wherein said absorbent consists essentially of an aluminum silicate 3 The use according to claim 2, wherein said aluminum silicate absorbent consists essentially of magnesium aluminum silicate 4 The use according to claim 2 wherein said ester of p-acid hydroxybenzoic acid is, at least, the ester selected from the group consisting of methyl p-hydroxybenzoate and p-hydroxybenzoate Propyl 5 The use according to claim 1 wherein said composition further comprises one or more cleaning helpers selected from a group consisting of emulsifiers, surfactants, stabilizers and solvents. The use according to claim 1 wherein said amount of said The composition applied to such region of the body is sufficient to form a layer of said composition that substantially covers the aforementioned region. The use according to claim 6, wherein a layer of such a therapeutically effective amount of a composition is applied in a light to moderate thickness. The use according to claim 7, further comprising, prior to said topical application of such a layer of the aforementioned composition, the step of applying to said region of the body an amount of a second composition that is sufficient to form a layer of said second composition covering substantially all of said region, said second composition consisting essentially of a hypoallergenic cream. The use according to claim 7, further comprising, following said topical application of such a layer of the aforementioned composition, the step of applying to said region of the body an amount of a second composition that is sufficient to form a layer of such a composition. second composition substantially covering all said region, said second composition consisting essentially of said hypoallergenic cream. The use according to claim 8, wherein said second composition consists essentially of 1% hydrocortisone cream and / or a moisturizing lotion. 11. The use according to claim 9, wherein said second composition consists essentially of 1% hydrocortisone cream and / or a moisturizing lotion. 12. The use according to claim 1, wherein the natural reduction of healed mass in such region of the body has been stopped prior to the application of said composition. The use according to claim 1, wherein said composition comprises benzoyl peroxide, an argillaceous absorbent, at least one p-hydroxybenzoic acid ester and one or more skin cleansing aids selected from a group consisting of emulsifiers, surfactants, stabilizers and solvents.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US39400095A | 1995-02-24 | 1995-02-24 | |
US394000 | 1995-02-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
MX9706453A MX9706453A (en) | 1998-07-31 |
MXPA97006453A true MXPA97006453A (en) | 1998-11-09 |
Family
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