US3137622A - Topical therapeutic composition - Google Patents

Topical therapeutic composition Download PDF

Info

Publication number
US3137622A
US3137622A US704277A US70427757A US3137622A US 3137622 A US3137622 A US 3137622A US 704277 A US704277 A US 704277A US 70427757 A US70427757 A US 70427757A US 3137622 A US3137622 A US 3137622A
Authority
US
United States
Prior art keywords
resorcinol
attapulgite
percent
liquid
composition
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
US704277A
Inventor
Albert J Mueller
Paul R Kline
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US704277A priority Critical patent/US3137622A/en
Application granted granted Critical
Publication of US3137622A publication Critical patent/US3137622A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • A61K47/02Inorganic compounds
    • 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

Definitions

  • Certain dermatoses such as for example acne, involve disorders in the oil glands associated with hair follicles, the so called pilosebaceous apparatus. These diseases are characterized by inflammation of the hair follicles and/ or sebaceous glands and in some instances are marked by disfiguring papules, pustules, nodules or crusts. These diseases are frequently chronic and in many individuals are highly resistant to cure,
  • resorcinol and resorcinol monoacetate which function by virtue of their keratolytic and/ or keratoplastic effect, the particular effect depending principally on the concentration of the active ingredient.
  • Dermatological preparations including resorcinol, resorcinol monoacetate or other phenolic compounds are frequently supplied as ointments in oleaginous bases, usually petrolatum with or without fats and waxes and may or may not include anodynes, such as for example bismuth subnitrate, zinc oxide, tale, etc.
  • resorcinol or other hydroxy aromatic compounds in treatment of disorders of the pilosebaceous system is reduced by the presence of oleaginous material therewith since such oleaginous material interferes with the activity of the therapeutic component of the composition. Accordingly, resorcinol is frequently employed in the form of a dilute solution or lotion when used to treat certain dermatoses.
  • resorcinol is frequently employed in the form of a dilute solution or lotion when used to treat certain dermatoses.
  • the use of flowable preparations for the purpose is highly undesirable particularly when the face is the site of the disorder treated because drippings of the medicament from said site can be unpleasant if not noxious, particularly to the hair, eyes, mouth or clothing of the patient.
  • hydroxy aromatic therapeutic agents are advantageously applied in thickened systems.
  • the therapeutic agent is incorporated in a hydrophilic base whereby the composition resists flow unless sufficient mechanical force is applied thereto.
  • An advantage inherent in the use of a gel is that the total quantity of treating material topically applied to any cutaneous site is susceptible to control.
  • Resorcinol preparations including a variety of hydrophilic colloids as the vehicle have been used in medicinals.
  • the efiicacy of resorcinol in such preparations as have been heretofore available is essentially that of the resorcinol in the absence of said colloid.
  • Another object of the instant invention is to provide novel therapeutic compositions and techniques for the treatment of acne with a view to avoiding disadvantages of medicaments or modes of treatment heretofore employed.
  • a more particular object of the invention is the provision of a thickened hydrophilic therapeutic composition in which the thickening agent improves the ability of the principal medicament to combat certain skin disorders.
  • Still another object is the provision of a composition of the character described which is characterized by a remarkable degree of efficacy in the treatment of acne; that is substantially free of adverse side effect when used by the patient in the prescribed manner.
  • compositions of the invention have the property of existing as stable gels or highly thickened systems which turn to a dry composition after a period of controlled residence on the skin.
  • the dry mass, and particularly the 'mineral component of said powder has the property, inter alia, of permitting the primary active agent to function for prolonged periods without introduction to the site of the disorder of deleterious foreign matter, such as for example certain body oils.
  • Said compositions have numerous advantages over ointments, lotions, or solutions heretofore suggested for use in treatment of acne.
  • the subject invention is the result of our surprising discovery that the clay mineral attapulgite, and particularly colloidal attapulgite, has the ability to cooperate with certain hydroxylated aromatic compounds to effectively arrest acne when said attapulgite and said hydroxylated aromatic compound in intimate association with each other, and preferably in the absence of oleaginous material, are applied to the site of such a disorder.
  • liquid dispersions thereof provide suitable hydrophilic thickened or gelled systems which function as ideal carriers for the hydroxylated aromatic compound and such other auxiliary therapeutic agents as may be included in formulations.
  • Clays are naturally-occurring crystalline or semi-crystalline hydrous aluminum silicates frequently associated in nature with minor amounts of impurities such as feldspar, quartz or other impurities.
  • aluminum is replaced in the lattice of the crystal by magnesium, calcium and/ or small amounts of alkali metals.
  • Clay species vary considerably in such physical characteristics as lattice orientation, substitution of aluminum by alkaline earth or alkali metal constituents, quantity and physical state of water associated with the clay and imponderables such as origin of the clay.
  • Kaolinitic clay for example, is a hydrous aluminum silicate which in its raw state comprises as the chief mineral constituent hexagonal platelets of kaolinite, nacrite or dickite.
  • Kaolinitic clays have very low sorptivity for water or other fluids and fail to gel in water or other fluids or otherwise exhibit colloidal properties.
  • clays having as the chief constituent a montmorillonite mineral have layer-like structures and exhibit physical characteristics markedly different from those of kaolinitic clays.
  • the properties of individual species of montmorillonite minerals or clays including a substantial portion of such minerals differ considerably inter se. For example, bentonite,
  • montmorillonite of which the major component is montmorillonite, exists as a sodium-type montmorillonite which swells in water and as a calcium-type which is non-swelling.
  • Montmorillonite is a layer-like mineral in which th bonding between sheets is weak so that water or other polar molecules can penetrate between sheets and be sorbed.
  • sheets can be swelled apart to the point where the sheets can be colloidally dispersed in the swelling medium.
  • fullers earth usually refers to non-swelling sorptive clays and encompasses both calcium-montmorillonitesand clays comprising the mineral attapulgite.
  • Attapulgus clay sometimes called Attapulgus fullers earth, contains in addition to a majorportion of attapulgite minor amounts 'of montmorillonit minerals, sepiolite, quartz or feldspar.
  • the morphology of attapulgite, an aluminummagnesium silicate mineral differs considerably from that of the layer-like,montmorillonite minerals and from the ened gelatinous systems exhibiting a high degree of thixo-' tropy. High shear is required to bring out the colloidal properties of attapulgite particularly when associated with small quantities of non-colloidal impurities.
  • our invention is practiced by preparing a thickened system including a vaporizable innoxious liquid having attapulgite dispersed therein and incorpo rating into the thickened system 'aihydroxy aromatic comi
  • the carrier for the hydroxy aromatic compound is a thickened system, preferably 'sufiiciently bodied to be a gel, and which is formed by the dispersion of colloidal attapulgite in an innoxious liquid which issubstan'tially vaporizable under ambient conditions of temperature and humidity.
  • Attapulgite refers to the pure mineral .or to a clay'in :which attapulgite is the" chief mineral constituent, such as so called .Attapulgus clay.
  • compositions of our invention comprise a hydroxy aromatic compound, preferably resorcinol or resorcinol monoacetate, in a liquid thickened by dispersion of attapulgite therein,
  • the liquid or liquid mixture is preferably one injwhich 'the hydroxy aromatic compound has good solubility so thatuniform distribution of that compound in the formulation and into the interstices of the attapulgite is facilitated. Furthermore, the liquid'should be sufficiently polarto permit satisfactory dispersion ofthe attapu-lgi'te therein.
  • Particularly useful liquids include water (preferably distilled), ethanol, isopropanol, and mixtures thereof. However, propanol and C-4 alcohols may be-used. T he .ultimate, choicerin liquid composition will be predicated on the determination of desirable rateofevaporation of liquid from the composition: after topical applica -tion.- A particularly useful liquid mixture when resor:
  • cinol is usedis a -50 mixture of water ethanol.
  • a humectant such as for example glycerol, ethylene glycol or sorbitol may be added to'. the liquid.
  • the total liquid is ordinarily about 50 percent byweight of the ultimate v formulation, althoughthe quantity will vary somewhat said attapulgite being present inramount at least equal to a preferred embodiment of the" invention, the thickened system is a gel whereby particulate insoluble material may be included in stable formulations by being suspended'by the gel.
  • Hydroxy aromatic compounds capable of effectively influencing the cure of pilosebaceous disorders include resorcinol, resorcinolmonoacetate, hexylresorcinol, cresol and'metacresyl acetate. 1 Resorcinol and resorcinol'monoacetate are preferred species because of' their'outstanding eflicacy. Phenol has been used as a desquamating agent, however, the toxicity and irritating effects of phenol make it less desirable for the purpose of treating pilosebaceous disorders than resorcinol. An important advantage of resorcinol, particularly when the resorcinolattapulgite ratio is low, is that its high water solubility promotes homogeneous distribution of the compound throughout the composition. Resorcinol monoacetate, on'
  • V is only slightly soluble in water, although readily soluble in alcohol. Accordingly, distribution of resorcinol monoacetate in the composition is facilitated by use of alcohol as the principal fluid in whichsthe attapulgite is dispersed or in admixture with the Water used for the purpose. In general, from about 2to 10 percent byweight of resorcinol or the monoacetate there of is used in formulations of the invention. At lower levels the benefits are minimal. At levels higher than about 10 percent the irritating effect of the ingredient will usually be excessive. However, it will be” understood with variations in. consistency of the composition and use, if' any, of a particulate insolubleanodyne such as for example, zinc oxide, sulfur or talc.
  • a particulate insolubleanodyne such as for example, zinc oxide, sulfur or talc.
  • Colloidal attapulgite is used in the formulation' and servesat least a tri-fold function.
  • the attapulgite forms the gel or thickened systemand provides a suitable flow-resistant vehicle for the hydroxy, aromatic compound; 1 '
  • the attapulgite-bodied vehicle is a suspending agent for any materials present in the formulation in excess of their solubility or which are totally insoluble; 'Thirdly, and of utmost importance, the attapulgite enhances the ability of :the medicinal tocomb'a't the dermatosi's. The reason underlying the'remarkable ability of the attapulgite to cooperate in such a manner with the medicinal ingredient is unknown. Although we do not wish to be bound in any manner to the hypothesis herein set forth, it is felt that theunusual sorptivity and ultimate particl shape of the attapulgite is responsible.
  • the penetration characteristics of the compound into the skin is probably profoundly different from what it would be in the absence of the attapulgite. Furthermore, after all or' a substantial portion (of theliquidis evaporated from the formulation subsequent to topical application, the attapulgite resident at the diseased site is available to sorb bacteria originating therein, deleterious foreign sebaceous matter or sebaceous exudate ofwhich' the inflamed area is the precursor.
  • Attapulgite exerts" a soothing cooling effect when present I "on the 'skin because of its hygroscopic nature.
  • the weight ratio of attapulgite to hydroxyl aromatic material should be at least 1/1 and is more preferably about 2/1 or higher.
  • the attapulgite may be used in its raw state after removal of grit.
  • the mineral is washed to remove impurities and classified as wet or dry methods wellknown to those skilled in the art.
  • the attapulgite may be heat treated to effect sterilization although this step may be omitted when a disinfectant, suitably a halogenated organic compound is included in minor proportion in the formulation. Sterilization should be carried out at temperatures not to exceed about 400 F., and usually I from about 225-400 F., since the gel-forming properties of the material will be reduced.
  • zinc oxide or other anodynes is included in the formulation in relatively large proportions.
  • Colloidal sulfur may be used in lieu of or as a supplement to the zinc oxide.
  • Particulate water-insoluble anodynes are especially desirable because they are retained at the site of application.
  • the waterinsoluble anodyne should be used in finely-divided form so that its retention on the skin is adequate and so that it is non-irritating when applied to the skin.
  • relatively large quantities of insoluble anodynes may be used, they should not be used in amounts exceeding that capable of being stably suspended by the thickened system.
  • Small amounts of other active ingredients such as disinfectants, particularly halogenated disinfectants as exemplified by hexachlorophene and quaternary ammonium salts, may be included in formulations where their use is indicated. These additives may be soluble or insoluble in the liquid component in the system.
  • a preferred method of preparing the compositions of the instant invention includes the preliminary step of forming a thickened or gelled system comprising attapulgite in liquid by use of high shear technique.
  • a thickened or gelled system comprising attapulgite in liquid by use of high shear technique.
  • Suitable high shear equipment includes colloid mills, kinetic energy mills, 3-roll mills and ball mills.
  • the resorcinol or other hydroxy aromatic compound is incorporated into the formulations by high shear technique, suitable by addition in the presence of additional quantities of liquid.
  • the balance of the attapulgite, up to a total of 35 parts by weight, and any other comminuted insoluble material is then blended into the thickened system using a conventional mechanical mixing device.
  • Example I A pharmaceutical preparation demonstrated to be highly effective in the cure of acne was prepared.
  • the composition of the preparation is as follows:
  • Attagel 20 is a purified colloidal form of attapulgite mined in Georgia and sold by Minerals & Chemicals Corporation of America. It can be dispersed to an average particle size of less than 0.1 micron.
  • the Attagel may be dispersed in the water and the alcohol and sheared in a Waring Blendor for about 10 minutes with intermittent stirring to prevent formation of shear planes.
  • the resultant dispersion is a very stiff homogeneous gel. Hexachlorophene and resorcinol are incorporated into' the stiff gel and homogenized therein in the Blendor. The resultant stiff gel is transferred to a low-speed mixer.
  • Example 11 The preparation of the composition of Example I is repeated except that resorcinol isused in the amount of 2.5 percent, based on the total weight of the composition. Such a preparation is preferred to a, 10 percent resorcinol composition when the latter produces in a particular patient severe exfoliation or other adverse effects.
  • Example I or II One hundred patients were treated with compositions of Example I or II over a period of from one to eight months in private practice and in institutions under the supervision of competent dermatologists. Over ninety percent of these patients, many of whom failed to respond to competent treatment with various commonly used modalities, showed satisfactory improvement, with remarkable improvement being noted in many of the cases of acne.
  • Disorders treated comprised severe cystic acne, congestive nodular acne, rosacea, verruca plana juvenilis. Bentonite used in lieu of attapulgite in formulations otherwise identical did not produce the outstanding benefits when used as a control.
  • a thickened hydrophilic therapeutic composition suitable for topical application to the skin in treatment of acne consisting essentially of at least one liquid selected from the group consisting of water, ethanol and isopropanol, from 2 to 10 percent by weight of a hydroxyl aromatic material selected from the group consisting of resorcinol and resorcinol monoacetate, and colloidal attapulgite dispersed in said liquid in an amount at least substantially equal to the weight of said hydroxyl aromatic material, said composition being substantially devoid of oleaginous matter.
  • a thickened hydrophilic therapeutic composition suitable for topical application to the skin in treatment of acne consisting essentially of water, from 2 to 10 percent by weight of resorcinol, and colloidal attapulgite dispersed in said water in an amount within the range of from 2 to 35 percent by weight and at least substantially equal to the weight of said resorcinol, said composition bieng substantially devoid of oleaginous matter.
  • a thickened hydrophilic therapeutic composition suitable for topical application to the skin in treatment of acne consisting essentially of a liquid consisting of water and ethanol, from 2 to 10 percent by weight of resorcinol, and colloidal attapulgite dispersed in said liquid in an amount within the range of from 2 to 35 percent by weight and at least substantially equal to the weight of said resorcinol, said composition being substantially devoid of oleaginous matter.
  • a hydrophilic therapeutic gel suitable for topical application to the skin in treatment of acne consisting essentially of at least one material selected from the group consisting of water, ethanol and isopropanol, from 2 to 10 percent by 'weight of resorcinol, and colloidal attapulgite dispersed in said liquid in an amount within the range of from about 5 to 20 percent by weight and at least substantially equal to the weight of said resorcinol, said composition being substantially devoid of oleaginous matter.
  • a hydrophilic therapeutic gel suitable for topical application to the skin in treatmentof acne consisting" of about 50 percent by weight of a water-ethanol mixture,
  • a hydrophilic therapeutic gel suitable fortopical application to the skin in'treatmen't of acne consisting of about 50 percent by weight of a 50-50 water-ethanol mix- .ture, from 2 to 10 percent by weight of resorcinol, about 20 percent by weight of colloidal attapulgite dispersed in said water-ethanol mixture, and about 1 percent of heXa- 3 chlorophene, the balance being finely divided zinc oxide.

Description

United States Patent 3,137,622 TGPICAL THERAPEUTIC COMPOSITION Albert J. Mueller, Princeton, N.J., and Paul R. Kline, 30 Lafayette Road W., Princeton, NJ; said Mueller assignor, by mesne assignments, to said Kline No Drawing. Filed Dec. 23, 1957, Ser. No. 704,277 7 Claims. (Cl. 167-58) This invention relates to improved topical therapeutic compositions and particularly to compositions useful in treatment of disorders of the pilosebaceous apparatus. The invention also relates to a method of making such compositions.
Certain dermatoses, such as for example acne, involve disorders in the oil glands associated with hair follicles, the so called pilosebaceous apparatus. These diseases are characterized by inflammation of the hair follicles and/ or sebaceous glands and in some instances are marked by disfiguring papules, pustules, nodules or crusts. These diseases are frequently chronic and in many individuals are highly resistant to cure,
Many medicinals have been used in the treatment of such disorders of the pilosebaceous apparatus. Among the most effective remedial agents are resorcinol and resorcinol monoacetate which function by virtue of their keratolytic and/ or keratoplastic effect, the particular effect depending principally on the concentration of the active ingredient. Dermatological preparations including resorcinol, resorcinol monoacetate or other phenolic compounds are frequently supplied as ointments in oleaginous bases, usually petrolatum with or without fats and waxes and may or may not include anodynes, such as for example bismuth subnitrate, zinc oxide, tale, etc. The effectiveness of resorcinol or other hydroxy aromatic compounds in treatment of disorders of the pilosebaceous system is reduced by the presence of oleaginous material therewith since such oleaginous material interferes with the activity of the therapeutic component of the composition. Accordingly, resorcinol is frequently employed in the form of a dilute solution or lotion when used to treat certain dermatoses. However, the use of flowable preparations for the purpose is highly undesirable particularly when the face is the site of the disorder treated because drippings of the medicament from said site can be unpleasant if not noxious, particularly to the hair, eyes, mouth or clothing of the patient. Hence, hydroxy aromatic therapeutic agents are advantageously applied in thickened systems. Ideally the therapeutic agent is incorporated in a hydrophilic base whereby the composition resists flow unless sufficient mechanical force is applied thereto. An advantage inherent in the use of a gel is that the total quantity of treating material topically applied to any cutaneous site is susceptible to control. Resorcinol preparations including a variety of hydrophilic colloids as the vehicle have been used in medicinals. However, the efiicacy of resorcinol in such preparations as have been heretofore available is essentially that of the resorcinol in the absence of said colloid.
Accordingly, it is a principal object of the subject invention to provide a novel therapeutic composition. of matter suitable for topical application to the skin in treatment of acne which combines in improved and more efiicacious form the remedial and soothing effects of certain known therapeutic materials whereby the individual effects of each of those materials are enhanced and unexpectedly improved by the combination and conjoint application thereof.
Another object of the instant invention is to provide novel therapeutic compositions and techniques for the treatment of acne with a view to avoiding disadvantages of medicaments or modes of treatment heretofore employed.
3,137,622 Patented June 16, 1964 A more particular object of the invention is the provision of a thickened hydrophilic therapeutic composition in which the thickening agent improves the ability of the principal medicament to combat certain skin disorders.
Still another object is the provision of a composition of the character described which is characterized by a remarkable degree of efficacy in the treatment of acne; that is substantially free of adverse side effect when used by the patient in the prescribed manner.
The invention combines in synergistic form and effect certain therapeutic materials which in combination effectively heal, sooth and improve acne, which is a disease involving disorders of the pilosebaceous apparatus. Preferred compositions of the invention have the property of existing as stable gels or highly thickened systems which turn to a dry composition after a period of controlled residence on the skin. The dry mass, and particularly the 'mineral component of said powder, has the property, inter alia, of permitting the primary active agent to function for prolonged periods without introduction to the site of the disorder of deleterious foreign matter, such as for example certain body oils. Said compositions have numerous advantages over ointments, lotions, or solutions heretofore suggested for use in treatment of acne.
Briefly, the subject invention is the result of our surprising discovery that the clay mineral attapulgite, and particularly colloidal attapulgite, has the ability to cooperate with certain hydroxylated aromatic compounds to effectively arrest acne when said attapulgite and said hydroxylated aromatic compound in intimate association with each other, and preferably in the absence of oleaginous material, are applied to the site of such a disorder. When the mineral has colloidal properties liquid dispersions thereof provide suitable hydrophilic thickened or gelled systems which function as ideal carriers for the hydroxylated aromatic compound and such other auxiliary therapeutic agents as may be included in formulations. We are cognizant of the fact that various clays have been topically applied by primitive peoples and that healing qualities have been imputed to the clays. Nevertheless it is recognized by competent dermatologists that the acute inflammatory cutaneous disorders with which We are concerned fail to respond to topical application of attapulgite or other clays, sorptive or non-sorptive. Furthermore, in vivo observations show that bentonitic clays used in lieu of attapulgitein compositions of our invention fail to enhance the therapeutic value of the hydroxy aromatic compound when used therewith in the treatment of acne.
Clays are naturally-occurring crystalline or semi-crystalline hydrous aluminum silicates frequently associated in nature with minor amounts of impurities such as feldspar, quartz or other impurities. In some clays aluminum is replaced in the lattice of the crystal by magnesium, calcium and/ or small amounts of alkali metals. Clay species vary considerably in such physical characteristics as lattice orientation, substitution of aluminum by alkaline earth or alkali metal constituents, quantity and physical state of water associated with the clay and imponderables such as origin of the clay. Kaolinitic clay, for example, is a hydrous aluminum silicate which in its raw state comprises as the chief mineral constituent hexagonal platelets of kaolinite, nacrite or dickite. Kaolinitic clays have very low sorptivity for water or other fluids and fail to gel in water or other fluids or otherwise exhibit colloidal properties. On the other hand, clays having as the chief constituent a montmorillonite mineral have layer-like structures and exhibit physical characteristics markedly different from those of kaolinitic clays. Furthermore, the properties of individual species of montmorillonite minerals or clays including a substantial portion of such minerals differ considerably inter se. For example, bentonite,
of which the major component is montmorillonite, exists as a sodium-type montmorillonite which swells in water and as a calcium-type which is non-swelling.
. Montmorillonite is a layer-like mineral in which th bonding between sheets is weak so that water or other polar molecules can penetrate between sheets and be sorbed.
In the case of sodium montmorillonites, .the'
that in the treatment of disordersin someindividuals less than 2 percent and more than aboutv percent of resorcinol or resorcinol monoacetate is indicated.
sheets can be swelled apart to the point where the sheets can be colloidally dispersed in the swelling medium. The
I term fullers earth usually refers to non-swelling sorptive clays and encompasses both calcium-montmorillonitesand clays comprising the mineral attapulgite. Attapulgus clay, sometimes called Attapulgus fullers earth, contains in addition to a majorportion of attapulgite minor amounts 'of montmorillonit minerals, sepiolite, quartz or feldspar. The morphology of attapulgite, an aluminummagnesium silicate mineral, differs considerably from that of the layer-like,montmorillonite minerals and from the ened gelatinous systems exhibiting a high degree of thixo-' tropy. High shear is required to bring out the colloidal properties of attapulgite particularly when associated with small quantities of non-colloidal impurities.
More specifically, our invention is practiced by preparing a thickened system including a vaporizable innoxious liquid having attapulgite dispersed therein and incorpo rating into the thickened system 'aihydroxy aromatic comi The carrier for the hydroxy aromatic compound is a thickened system, preferably 'sufiiciently bodied to be a gel, and which is formed by the dispersion of colloidal attapulgite in an innoxious liquid which issubstan'tially vaporizable under ambient conditions of temperature and humidity.
It will be understood that the term attapulgite as used herein refers to the pure mineral .or to a clay'in :which attapulgite is the" chief mineral constituent, such as so called .Attapulgus clay. A typical chemical analysis ofan' Attapulgus clay expressed inrterms of theoxides "present is tabulated belowon a'volatile-free basis sit) 67.0 A1203 -.V- MgO v a 11.0 7 F6 0;; ..l v i ,CaO a 2.5 Others l 3.0
pound which when applied to the site of certain dermai toses has a kerotolytic or keretoplastic effect. Compositions of our invention comprise a hydroxy aromatic compound, preferably resorcinol or resorcinol monoacetate, in a liquid thickened by dispersion of attapulgite therein,
to and preferably at least double that of the hydroxy aromatic compound. Auxiliary therapeutic agents such as for example certain anodynes, humectants, antiseptic and antibiotics may be included in the. composition. Pursuant Percent The liquid or liquid mixture ispreferably one injwhich 'the hydroxy aromatic compound has good solubility so thatuniform distribution of that compound in the formulation and into the interstices of the attapulgite is facilitated. Furthermore, the liquid'should be sufficiently polarto permit satisfactory dispersion ofthe attapu-lgi'te therein. Particularly useful liquids include water (preferably distilled), ethanol, isopropanol, and mixtures thereof. However, propanol and C-4 alcohols may be-used. T he .ultimate, choicerin liquid composition will be predicated on the determination of desirable rateofevaporation of liquid from the composition: after topical applica -tion.- A particularly useful liquid mixture when resor:
cinol is usedis a -50 mixture of water ethanol. When the evaporation of theliquid is tobe restricted,a humectant, such as for example glycerol, ethylene glycol or sorbitol may be added to'. the liquid. f The total liquid is ordinarily about 50 percent byweight of the ultimate v formulation, althoughthe quantity will vary somewhat said attapulgite being present inramount at least equal to a preferred embodiment of the" invention, the thickened system is a gel whereby particulate insoluble material may be included in stable formulations by being suspended'by the gel.
Hydroxy aromatic compounds capable of effectively influencing the cure of pilosebaceous disorders include resorcinol, resorcinolmonoacetate, hexylresorcinol, cresol and'metacresyl acetate. 1 Resorcinol and resorcinol'monoacetate are preferred species because of' their'outstanding eflicacy. Phenol has been used as a desquamating agent, however, the toxicity and irritating effects of phenol make it less desirable for the purpose of treating pilosebaceous disorders than resorcinol. An important advantage of resorcinol, particularly when the resorcinolattapulgite ratio is low, is that its high water solubility promotes homogeneous distribution of the compound throughout the composition. Resorcinol monoacetate, on'
V the other hand, is only slightly soluble in water, although readily soluble in alcohol. Accordingly, distribution of resorcinol monoacetate in the composition is facilitated by use of alcohol as the principal fluid in whichsthe attapulgite is dispersed or in admixture with the Water used for the purpose. In general, from about 2to 10 percent byweight of resorcinol or the monoacetate there of is used in formulations of the invention. At lower levels the benefits are minimal. At levels higher than about 10 percent the irritating effect of the ingredient will usually be excessive. However, it will be" understood with variations in. consistency of the composition and use, if' any, of a particulate insolubleanodyne such as for example, zinc oxide, sulfur or talc.
Colloidal attapulgite is used in the formulation' and servesat least a tri-fold function. First, by virtue of its colloidal properties, the attapulgite forms the gel or thickened systemand provides a suitable flow-resistant vehicle for the hydroxy, aromatic compound; 1 'Secondly,
the attapulgite-bodied vehicle is a suspending agent for any materials present in the formulation in excess of their solubility or which are totally insoluble; 'Thirdly, and of utmost importance, the attapulgite enhances the ability of :the medicinal tocomb'a't the dermatosi's. The reason underlying the'remarkable ability of the attapulgite to cooperate in such a manner with the medicinal ingredient is unknown. Although we do not wish to be bound in any manner to the hypothesis herein set forth, it is felt that theunusual sorptivity and ultimate particl shape of the attapulgite is responsible. Sincethe hydroxy aromatic: compound is associated with the minute particlesofatta pulgit e the penetration characteristics of the compound into the skin is probably profoundly different from what it would be in the absence of the attapulgite. Furthermore, after all or' a substantial portion (of theliquidis evaporated from the formulation subsequent to topical application, the attapulgite resident at the diseased site is available to sorb bacteria originating therein, deleterious foreign sebaceous matter or sebaceous exudate ofwhich' the inflamed area is the precursor.
attapulgite exerts" a soothing cooling effect when present I "on the 'skin because of its hygroscopic nature.
From about 0.5 to about-5.0 percent by weight of the liquid phase of attapulgi'te is required for thickenin'g'the' Furthermore, 'the 1 v liquid whereas from about 5.0 to 20.0 percent by weight will produce gellation. For satisfactory formulations the weight ratio of attapulgite to hydroxyl aromatic material should be at least 1/1 and is more preferably about 2/1 or higher. When the quantity of attapulgite is more than can be satisfactorily dispersed in the liquid by high shear it may be agitated into the previously thickened system. The attapulgite may be used in its raw state after removal of grit. Preferably the mineral is washed to remove impurities and classified as wet or dry methods wellknown to those skilled in the art. The attapulgite may be heat treated to effect sterilization although this step may be omitted when a disinfectant, suitably a halogenated organic compound is included in minor proportion in the formulation. Sterilization should be carried out at temperatures not to exceed about 400 F., and usually I from about 225-400 F., since the gel-forming properties of the material will be reduced.
Pursuant to an embodiment of the invention, zinc oxide or other anodynes is included in the formulation in relatively large proportions. Colloidal sulfur may be used in lieu of or as a supplement to the zinc oxide. Particulate water-insoluble anodynes are especially desirable because they are retained at the site of application. The waterinsoluble anodyne should be used in finely-divided form so that its retention on the skin is adequate and so that it is non-irritating when applied to the skin. Although relatively large quantities of insoluble anodynes may be used, they should not be used in amounts exceeding that capable of being stably suspended by the thickened system.
Small amounts of other active ingredients such as disinfectants, particularly halogenated disinfectants as exemplified by hexachlorophene and quaternary ammonium salts, may be included in formulations where their use is indicated. These additives may be soluble or insoluble in the liquid component in the system.
A preferred method of preparing the compositions of the instant invention includes the preliminary step of forming a thickened or gelled system comprising attapulgite in liquid by use of high shear technique. When the total quantity of mineral called for in a particular formulation exceeds that which is capable of being colloidally dispersed in the liquid only a fraction of the total may be preliminarily dispersed. Suitable high shear equipment includes colloid mills, kinetic energy mills, 3-roll mills and ball mills. The resorcinol or other hydroxy aromatic compound is incorporated into the formulations by high shear technique, suitable by addition in the presence of additional quantities of liquid. The balance of the attapulgite, up to a total of 35 parts by weight, and any other comminuted insoluble material is then blended into the thickened system using a conventional mechanical mixing device.
The following examples are given only for the sake of further illustrating the invention and are not to be construed as limiting the scope thereof.
Example I A pharmaceutical preparation demonstrated to be highly effective in the cure of acne was prepared. The composition of the preparation is as follows:
Attagel 20 is a purified colloidal form of attapulgite mined in Georgia and sold by Minerals & Chemicals Corporation of America. It can be dispersed to an average particle size of less than 0.1 micron. In the preparation of the composition, the Attagel may be dispersed in the water and the alcohol and sheared in a Waring Blendor for about 10 minutes with intermittent stirring to prevent formation of shear planes. The resultant dispersion is a very stiff homogeneous gel. Hexachlorophene and resorcinol are incorporated into' the stiff gel and homogenized therein in the Blendor. The resultant stiff gel is transferred to a low-speed mixer. The zinc oxide is then added to the mass and stirred into the composition at increasing rates of speed for about 30 minutes. The resultant product is a smooth creamy unctuous-feeling suspension. Example 11 The preparation of the composition of Example I is repeated except that resorcinol isused in the amount of 2.5 percent, based on the total weight of the composition. Such a preparation is preferred to a, 10 percent resorcinol composition when the latter produces in a particular patient severe exfoliation or other adverse effects.
One hundred patients were treated with compositions of Example I or II over a period of from one to eight months in private practice and in institutions under the supervision of competent dermatologists. Over ninety percent of these patients, many of whom failed to respond to competent treatment with various commonly used modalities, showed satisfactory improvement, with remarkable improvement being noted in many of the cases of acne. Disorders treated comprised severe cystic acne, congestive nodular acne, rosacea, verruca plana juvenilis. Bentonite used in lieu of attapulgite in formulations otherwise identical did not produce the outstanding benefits when used as a control.
It will be understood that the invention is susceptible to variation without departing from the spirit and scope thereof.
We claim:
1. A thickened hydrophilic therapeutic composition suitable for topical application to the skin in treatment of acne consisting essentially of at least one liquid selected from the group consisting of water, ethanol and isopropanol, from 2 to 10 percent by weight of a hydroxyl aromatic material selected from the group consisting of resorcinol and resorcinol monoacetate, and colloidal attapulgite dispersed in said liquid in an amount at least substantially equal to the weight of said hydroxyl aromatic material, said composition being substantially devoid of oleaginous matter.
2. A thickened hydrophilic therapeutic composition suitable for topical application to the skin in treatment of acne consisting essentially of water, from 2 to 10 percent by weight of resorcinol, and colloidal attapulgite dispersed in said water in an amount within the range of from 2 to 35 percent by weight and at least substantially equal to the weight of said resorcinol, said composition bieng substantially devoid of oleaginous matter.
3. A thickened hydrophilic therapeutic composition suitable for topical application to the skin in treatment of acne consisting essentially of a liquid consisting of water and ethanol, from 2 to 10 percent by weight of resorcinol, and colloidal attapulgite dispersed in said liquid in an amount within the range of from 2 to 35 percent by weight and at least substantially equal to the weight of said resorcinol, said composition being substantially devoid of oleaginous matter.
4. A hydrophilic therapeutic gel suitable for topical application to the skin in treatment of acne consisting essentially of at least one material selected from the group consisting of water, ethanol and isopropanol, from 2 to 10 percent by 'weight of resorcinol, and colloidal attapulgite dispersed in said liquid in an amount within the range of from about 5 to 20 percent by weight and at least substantially equal to the weight of said resorcinol, said composition being substantially devoid of oleaginous matter.
5. A hydrophilic therapeutic gel suitable for topical application to the skin in treatmentof acne consisting" of about 50 percent by weight of a water-ethanol mixture,
I from 2- to 10 percent by weight of resorcinol, and about 20 percent .by weight of colloidal attapulgite dispersed in said water-ethanol'mixture, the balance being finely divided zincoxide. f
6. A hydrophilic therapeutic gel. suitable fortopical application to the skin in'treatmen't of acne consisting of about 50 percent by weight of a 50-50 water-ethanol mix- .ture, from 2 to 10 percent by weight of resorcinol, about 20 percent by weight of colloidal attapulgite dispersed in said water-ethanol mixture, and about 1 percent of heXa- 3 chlorophene, the balance being finely divided zinc oxide.
7. A hydrophilic therapeutic gel suitable for topical ber1956 ,pp.1111- 1 112.
I References Cited in the file of this patent Kulchar: Arch. Dermatologyand Syphilology, vol. 44
Perrnagel, Bulletin Chemicals Corp, Philadelphia, Pa., 7 pp No. P53, Attapulgus Mineral and brochure. v Franburg: Drug and Cosmetic Industry, vol. 66,"No. 5, May 1950, pp. 580-581. 5 I 7 .Harry: Cosmetic Materials,Leonard Hill Ltd., London Registered Us. Trademark 561,218 (for 1 0w volatile fullers earth), July.8, 1952.
US. Dispensatory, 25th ed, Lippincott Co Philadelv phia,Pa. (1955),pp. 734-736.
- Harry; 'Modern Cosmeticology,
Ltd., London (1955); pp. 273-274.
Malkinson: Clinical VMedicine, vol. 3,
o. 1 1', Nove 4m ed;, I ;eonard Hill I

Claims (1)

1. A THICKENED HYDROPHILIC THERAPEUTIC COMPOSITOR SUITABLE FOR TOPICAL APPLICATION TO THE SKIN IN TREATMENT OF ACNE CONSISTING ESSENTIALLY OF AT LEAST ONE LIQUID SELECTED FROM THE GROUP CONSISTING OF WATER, ETHANOL AND ISOPROPANOL, FROM 2 TO 10 PERCENT BY WEIGHT OF A HYDROXYL AROMATIC MATERIAL SELECTED FROM THE GROUP CONSISTING OF RESORCINOL AND RESORCINOL MONOACETATE, AND COLLOIDAL ATTAPULGITE DISPERSED IN SAID LIQUID IN AN AMOUNT AT LEAST SUBSTANTIALLY EQUAL TO THE WEIGHT OF SAID HYDROXYL AROMATIC MATERIAL, SAID COMPOSITION BEING SUBSTANTIALLY DEVOID OF OLEAGINOUS MATTER.
US704277A 1957-12-23 1957-12-23 Topical therapeutic composition Expired - Lifetime US3137622A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US704277A US3137622A (en) 1957-12-23 1957-12-23 Topical therapeutic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US704277A US3137622A (en) 1957-12-23 1957-12-23 Topical therapeutic composition

Publications (1)

Publication Number Publication Date
US3137622A true US3137622A (en) 1964-06-16

Family

ID=24828806

Family Applications (1)

Application Number Title Priority Date Filing Date
US704277A Expired - Lifetime US3137622A (en) 1957-12-23 1957-12-23 Topical therapeutic composition

Country Status (1)

Country Link
US (1) US3137622A (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3258398A (en) * 1965-02-24 1966-06-28 Vienna Beauty Products Co Acidic aqueous alkali metal alginate and lanolin acne vulgaris preparation
US3322621A (en) * 1962-01-16 1967-05-30 Hollichem Corp Thixotropic quaternary ammonium aromatic cyclic imides
US3337434A (en) * 1964-01-15 1967-08-22 Mc Donnell Douglas Corp Method of electrolytic etching metals using a gel electrolyte
US4005191A (en) * 1974-06-04 1977-01-25 Clark Mary G Topical ointment composition
US4704280A (en) * 1986-12-19 1987-11-03 Bates Harry L Cosmetic lotion
US4810496A (en) * 1985-02-19 1989-03-07 Jensen Charles A Treatment of skin and inflammatory disorders
US4968510A (en) * 1985-02-19 1990-11-06 Jensen Charles A Method of treating arthritis
US5069912A (en) * 1985-02-19 1991-12-03 Jensen Charles A Method of treating spastic colitis
US20050187129A1 (en) * 2004-02-06 2005-08-25 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Detergent composition
US20060269504A1 (en) * 2003-04-15 2006-11-30 James Alexander G Use of alkyl resorcinols in the treatment of acne
US7687650B2 (en) 2006-02-03 2010-03-30 Jr Chem, Llc Chemical compositions and methods of making them
US7867522B2 (en) 2006-09-28 2011-01-11 Jr Chem, Llc Method of wound/burn healing using copper-zinc compositions
US7897800B2 (en) 2006-02-03 2011-03-01 Jr Chem, Llc Chemical compositions and methods of making them
US7927614B2 (en) 2006-02-03 2011-04-19 Jr Chem, Llc Anti-aging treatment using copper and zinc compositions
US8273791B2 (en) 2008-01-04 2012-09-25 Jr Chem, Llc Compositions, kits and regimens for the treatment of skin, especially décolletage
US8952057B2 (en) 2011-01-11 2015-02-10 Jr Chem, Llc Compositions for anorectal use and methods for treating anorectal disorders
US9427397B2 (en) 2009-01-23 2016-08-30 Obagi Medical Products, Inc. Rosacea treatments and kits for performing them

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3322621A (en) * 1962-01-16 1967-05-30 Hollichem Corp Thixotropic quaternary ammonium aromatic cyclic imides
US3337434A (en) * 1964-01-15 1967-08-22 Mc Donnell Douglas Corp Method of electrolytic etching metals using a gel electrolyte
US3258398A (en) * 1965-02-24 1966-06-28 Vienna Beauty Products Co Acidic aqueous alkali metal alginate and lanolin acne vulgaris preparation
US4005191A (en) * 1974-06-04 1977-01-25 Clark Mary G Topical ointment composition
US4810496A (en) * 1985-02-19 1989-03-07 Jensen Charles A Treatment of skin and inflammatory disorders
US4968510A (en) * 1985-02-19 1990-11-06 Jensen Charles A Method of treating arthritis
US5069912A (en) * 1985-02-19 1991-12-03 Jensen Charles A Method of treating spastic colitis
US4704280A (en) * 1986-12-19 1987-11-03 Bates Harry L Cosmetic lotion
US20060269504A1 (en) * 2003-04-15 2006-11-30 James Alexander G Use of alkyl resorcinols in the treatment of acne
US7285521B2 (en) 2004-02-06 2007-10-23 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Detergent composition comprising predominantly soap and palygorskite clay
US20050187129A1 (en) * 2004-02-06 2005-08-25 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Detergent composition
US7687650B2 (en) 2006-02-03 2010-03-30 Jr Chem, Llc Chemical compositions and methods of making them
US7897800B2 (en) 2006-02-03 2011-03-01 Jr Chem, Llc Chemical compositions and methods of making them
US7927614B2 (en) 2006-02-03 2011-04-19 Jr Chem, Llc Anti-aging treatment using copper and zinc compositions
US8148563B2 (en) 2006-02-03 2012-04-03 Jr Chem, Llc Chemical compositions and methods of making them
US7867522B2 (en) 2006-09-28 2011-01-11 Jr Chem, Llc Method of wound/burn healing using copper-zinc compositions
US8273791B2 (en) 2008-01-04 2012-09-25 Jr Chem, Llc Compositions, kits and regimens for the treatment of skin, especially décolletage
US8505730B2 (en) 2008-01-04 2013-08-13 Jr Chem, Llc Compositions, kits and regimens for the treatment of skin, especially décolletage
US9427397B2 (en) 2009-01-23 2016-08-30 Obagi Medical Products, Inc. Rosacea treatments and kits for performing them
US8952057B2 (en) 2011-01-11 2015-02-10 Jr Chem, Llc Compositions for anorectal use and methods for treating anorectal disorders

Similar Documents

Publication Publication Date Title
US3137622A (en) Topical therapeutic composition
US3535422A (en) Stable benzoyl peroxide composition
Davis et al. Wound healing. Oral and topical activity of Aloe vera
US4387107A (en) Stable benzoyl peroxide composition
DE60212847T2 (en) TOPICALLY APPLICABLE MEDICINAL FORMULATION
WO2010018418A1 (en) Formulation based on micronized clinoptilolite as therapeutic agent providing highly bioavailable silicon
US4252796A (en) Stable water-in-oil emulsions
PT2504012E (en) Use of an oleo gel containing triterpene for healing wounds
US4124720A (en) Therapeutic hydrodispersible emulsion
PT93638A (en) A process for the preparation of a composition for the topical application of vitamin A
DE102005045145A1 (en) Use of octenidine dihydrochloride in semisolid preparations
CA2425780C (en) Composition with a base of a therapeutically active compound, in particular honey, for the treatment of wounds
US5879717A (en) Wound healing compositions containing iodine and sucrose
AU2014257984A1 (en) Composition for use in reducing scab formation and promoting healing
DE60018409T2 (en) USE OF ANTISEPTICA FOR THE PREPARATION OF MEDICAMENTS FOR THE PROPHYLAXIS AND THE TREATMENT OF INFECTIONS AND / OR FUNCTIONAL TISSUE FORMATIONS IN THE BODY'S INSECTS
JPH0825908B2 (en) Use of sucralfate wet gel as a carrier for topically active pharmaceuticals or cosmetics
US5270042A (en) Medicinal salve composition
US4117120A (en) Medication for herpes simplex and canker sores
EP1293194A1 (en) Physically stable sprayable gel composition
EP0683670B1 (en) Wound-healing compositions containing iodine and a sugar
EP1196159B1 (en) Use of tosylchloramide(s) for treating diseases of the skin, mucous membranes, organs and tissues
CA2285012C (en) Remedy for external application, and use of an oil-in-water emulsion for said remedy
Ricciatti-Sibbald et al. Dermatologic vehicles
DE102007002073A1 (en) Medium for use during care and antimicrobial treatment of skin, for topical dermatological application, and for therapeutic skin and sore treatment, comprises benzalkonium chloride, which is basically exclusive pharmaceutically active
Semkina Ointments, gels, liniments, and creams containing phytopreparations (a review)