Classifications

• • 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
  • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
  • A61K8/23—Sulfur; Selenium; Tellurium; Compounds 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
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
  • A61K8/11—Encapsulated compositions
• • 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
  • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
  • A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
  • A61K8/4933—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having sulfur as an exocyclic substituent, e.g. pyridinethione
• • 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
  • A61K8/73—Polysaccharides
  • A61K8/737—Galactomannans, e.g. guar; Derivatives thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/006—Antidandruff preparations
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/02—Preparations for cleaning the hair
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
  • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
  • A61K2800/54—Polymers characterized by specific structures/properties
  • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
  • A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic

Definitions

• the present invention relates to shampoo compositions containing antimicrobial agents which provide antidandruff activity
• the present invention relates to shampoo compositions containing antimicrobial agents, preferably particulate antimicrobial agents, in combination with a cationic guar polymer as an antimicrobial agent deposition aid
• compositions are commercially available or otherwise known in the shampoo art These compositions typically comprise particulate, crystalline antimicrobial agents dispersed and suspended throughout the composition Antimicrobial agents used for this purpose include sulfur, selenium sulfide and heavy metal salts of pyridinethione During the shampooing process, these antimicrobial agents deposit on the scalp to provide anti-dandruff activity
• particulate antimicrobial agents are especially difficult in anti- dandruff shampoo compositions containing crystalline suspending agents These suspending agents help disperse and suspend particulate antimicrobial agents in the shampoo composition These suspending agents, however, adversely affect lathering performance It has therefore become conventional practice to enhance the lathering performance of these shampoos by increasing detersive surfactant concentrations or by adding foam boosters, both of which further decrease deposition of particulate antimicrobial agents from the shampoo compositions
• select cationic deposition polymers are especially effective in providing enhanced deposition of antimicrobial agents, especially particulate antimicrobial agents, from a shampoo composition
• the select polymers are cationic derivatives of guar gum which have been found to be most effective when used in combination with crystalline suspending agents and high levels of anionic, amphoteric or zwitterionic surfactant in an anti-dandruff shampoo composition.
• an object of the present invention to provide an anti-dandruff shampoo composition with improved deposition of antimicrobial agents, especially particulate antimicrobial agents, and further to provide for such improved deposition in the presence of crystalline suspending agents and high concentrations of detersive surfactant. It is yet another object of the present invention to provide anti-dandruff shampoo compositions with excellent anti-dandruff activity and reduced concentration of antimicrobial agents.
• the present invention is directed to high lathering, anti-dandruff shampoo compositions with improved deposition of antimicrobial agents, which compositions comprise (a) from about 7% to about 30% by weight of a detersive surfactant selected from the group consisting of anionic surfactant, amphoteric surfactant, zwitterionic surfactant, and combinations thereof; (b) from about 0.1% to about 10% by weight of an antimicrobial agent; (c) from about 0.5% to about 10% by weight of a suspending agent; (d) from about 0.01% to about 1.0% by weight of a cationic guar polymer having a charge density of from about 0.1 to about 3meq/gm, and (e) from about 40% to about 92% by weight of water; wherein at least about 50% by weight ofthe cationic guar polymer is in coacervate form, said coacervate comprising detersive surfactant and cationic guar polymer.
• a detersive surfactant selected from the group consisting
• compositions of the present invention can comprise, consist of, or consist essentially of the essential elements and limitations of the invention described herein, as well any ofthe additional or optional ingredients, components, or limitations described herein.
• the shampoo compositions of the present invention comprise a detersive surfactant selected from the group consisting of anionic surfactants, amphoteric surfactants, zwitterionic surfactants, and combinations thereof.
• the shampoo compositions preferably comprise an anionic surfactant
• the detersive surfactant provides the shampoo compositions with cleaning performance.
• the detersive surfactant component of the shampoo compositions is preferably an anionic surfactant. Concentrations of anionic surfactant can range from about 7% to about 30%, preferably from about 10% to about 25%, more preferably from about 12% to about 22%, by weight ofthe shampoo compositions.
• Anionic surfactants for use in the shampoo compositions include alkyl and alkyl ether sulfates These materials have the respective formulae ROSO3M and RO(C2H4O) x SO3M, wherein R is alkyl or alkenyl of from about 8 to about 30 carbon atoms, x is an integer from 1 to 10, and M is a hydrogen, alkali metal (e.g., lithium, sodium, potassium), alkali earth metal (e.g., beryllium, magnesium, calcium, strontium, barium) ammonium or substituted ammonium.
• alkali metal e.g., lithium, sodium, potassium
• alkali earth metal e.g., beryllium, magnesium, calcium, strontium, barium
• R has from about 10 to about 18 carbon atoms in both the alkyl and alkyl ether sulfates.
• the alkyl ether sulfates are typically made as condensation products of ethylene oxide and monohydric alcohols having from about 8 to about 24 carbon atoms.
• the alcohols can be derived from fats, e.g., coconut oil or tallow, or can be synthetic. Lauryl alcohol and straight chain alcohols derived from coconut oil are preferred. Such alcohols are reacted with between about 0 and about 10, and especially about 3, molar proportions of ethylene oxide and the resulting mixture of molecular species having, for example, an average of 3 moles of ethylene oxide per mole of alcohol, is sulfated and neutralized.
• alkyl ether sulfates which may be used in the shampoo compositions of the present invention are sodium and ammonium salts of coconut alkyl triethylene glycol ether sulfate; tallow alkyl triethylene glycol ether sulfate, and tallow alkyl hexaoxyethylene sulfate.
• Highly preferred alkyl ether sulfates are those comprising a combination of individual compounds, the combination having an average alkyl chain length of from about 10 to about 16 carbon atoms and an average degree of ethoxylation of from about 1 to about 4 moles of ethylene oxide.
• Suitable anionic surfactants are the water-soluble salts of organic, sulfuric acid reaction products of the general formula [ R1 -SO3-M ] where Rj is selected from the group consisting of a straight or branched chain, saturated aliphatic hydrocarbon radicals having from about 8 to about 24, preferably about 10 to about 18, carbon atoms; and M hydrogen, alkali metal (e.g., lithium, sodium, potassium), alkali earth metal (e.g., beryllium, magnesium, calcium, strontium, barium) ammonium or substituted ammonium.
• alkali metal e.g., lithium, sodium, potassium
• alkali earth metal e.g., beryllium, magnesium, calcium, strontium, barium
• surfactants are the salts of an organic sulfuric acid reaction product of a hydrocarbon of the methane series, including iso-, neo-, and n-paraffins, having about 8 to about 24 carbon atoms, preferably about 12 to about 18 carbon atoms and a sulfonating agent, e.g., SO3, H2SO4, obtained according to known sulfonation methods, including bleaching and hydrolysis.
• a sulfonating agent e.g., SO3, H2SO4
• alkali metal and ammonium sulfonated C ] 0-i8 n-paraffins are examples of such surfactants.
• anionic surfactants are the reaction products of fatty acids esterified with isethionic acid and neutralized with sodium hydroxide where, for example, the fatty acids are derived from coconut oil; sodium or potassium salts of fatty acid amides of methyl tauride in which the fatty acids, for example, are derived from coconut oil.
• Other similar anionic surfactants are described in U.S. Patent 2,486,921; U.S. Patent 2,486,922; and U.S. Patent 2,396,278, which descriptions are incorporated herein by reference.
• anionic surfactants suitable for use in the shampoo compositions are the succinnates, examples of which include disodium N-octadecylsulfosuccinnate; disodium lauryl sulfosuccinate; diammonium lauryl sulfosuccinate; tetrasodium N-(l,2-dicarboxyethyl)-N-octadecylsulfosuccinnate; diamyl ester of sodium sulfosuccinic acid; dihexyl ester of sodium sulfosuccinic acid; and dioctyl esters of sodium sulfosuccinic acid.
• succinnates examples of which include disodium N-octadecylsulfosuccinnate; disodium lauryl sulfosuccinate; diammonium lauryl sulfosuccinate; tetrasodium N-(l,2-dicarbox
• Suitable anionic surfactants include olefin sulfonates having about 10 to about 24 carbon atoms.
• olefin sulfonates is used herein to mean compounds which can be produced by the sulfonation of alpha-olefins by means of uncomplexed sulfur trioxide, followed by neutralization of the acid reaction mixture in conditions such that any sulfones which have been formed in the reaction are hydrolyzed to give the corresponding hydroxy-alkanesulfonates.
• the sulfur trioxide can be liquid or gaseous, and is usually, but not necessarily, diluted by inert diluents, for example by liquid SO2, chlorinated hydrocarbons, etc., when used in the liquid form, or by air, nitrogen, gaseous SO2, etc., when used in the gaseous form.
• inert diluents for example by liquid SO2, chlorinated hydrocarbons, etc., when used in the liquid form, or by air, nitrogen, gaseous SO2, etc., when used in the gaseous form.
• alpha-olefins from which the olefin sulfonates are derived from mono-olefins having from about 12 to about 24 carbon atoms, preferably from about 14 to about 16 carbon atoms.
• Straight chain olefins are preferred.
• the olefin sulfonates can contain minor amounts of other materials, such as alkene disulfonates depending upon the reaction conditions, proportion of reactants, the nature of the starting olefins and impurities in the olefin stock and side reactions during the sulfonation process
• Another class of anionic surfactants suitable for use in the shampoo compositions are the beta-alkyloxy alkane sulfonates These compounds can be represented by the formula
• R* is a straight chain alkyl group having from about 6 to about 20 carbon atoms
• R2 is a lower alkyl group having from about 1 (preferred) to about 3 carbon atoms
• M hydrogen, alkali metal (e.g , lithium, sodium, potassium), alkali earth metal (e g , beryllium, magnesium, calcium, strontium, barium) ammonium or substituted ammonium
• Preferred anionic surfactants for use in the shampoo compositions include ammonium lauryl sulfate, ammonium laureth sulfate, triethylamine lauryl sulfate, tri ⁇ ethylamine laureth sulfate, triethanolamine lauryl sulfate, triethanolamine laureth sulfate, monoethanolamine lauryl sulfate, monoethanolamine laureth sulfate, diethanolamine lauryl sulfate, diethanolamine laureth sulfate, lauric monoglyceride sodium sulfate, sodium lauryl sulfate, sodium laureth sulfate, potassium lauryl sulfate, potassium laureth sulfate, sodium lauryl sarcosinate, sodium lauroyl sarcosinate, lauryl sarcosine, cocoyl sarcosine, ammonium cocoyl sulfate, am
• the detersive surfactant component of the shampoo compositions may comprise an amphoteric and/or zwitterionic surfactant Concentrations of such surfactants can range from about 0.5% to about 20%, preferably from about 1% to about 10%, by weight of the shampoo compositions
• Amphoteric surfactants for use in the shampoo compositions include the derivatives of aliphatic secondary and tertiary amines in which the aliphatic radical is straight or branched and one of the aliphatic substituents contains from about 8 to about 18 carbon atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate.
• an anionic water solubilizing group e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate.
• Zwitterionic surfactants for use in the shampoo compositions include the derivatives of aliphatic quaternary ammonium, phosphonium, and sulfonium compounds, in which the aliphatic radicals are straight or branched, and wherein one of the aliphatic substituents contains from about 8 to about 18 carbon atoms and one contains an anionic group, e.g., carboxy, sulfonate, sulfate, phosphate, or phos ⁇ phonate.
• anionic group e.g., carboxy, sulfonate, sulfate, phosphate, or phos ⁇ phonate.
• R contains an alkyl, alkenyl, or hydroxy alkyl radical of from about 8 to about 18 carbon atoms, from 0 to about 10 ethylene oxide moieties and from 0 to about 1 glyceryl moiety;
• Y is selected from the group consisting of nitrogen, phosphorus, and sulfur atoms;
• R is an alkyl or monohydroxyalkyl group containing about 1 to about 3 carbon atoms;
• X is 1 when Y is a sulfur atom, and 2 when Y is a nitrogen or phosphorus atom;
• R is an alkylene or hydroxyalkylene of from about 1 to about 4 carbon atoms and Z is a radical selected from the group consisting of carboxylate, sulfonate, sulfate, phosphonate, and phosphate groups
• amphoteric and zwitterionic surfactants also include sultaines and amidosultaines. Sultaines and amidosultaines can be used as foam enhancing surfactants that are mild to the eye in partial replacement of anionic surfactants.
• Sultaines including amidosultaines, include for example, cocodimethylpropylsultaine, stearyldimethylpropylsultaine, lauryl-bis-(2-hydroxyethyl) propylsultaine and the like; and the amidosultaines such as cocoamidodimethylpropylsultaine, stearylamidododimethylpropylsultaine, laurylamidobis-(2-hydroxyethyl) propylsultaine, and the like.
• amidohydroxysultaines such as the Ci2-C ⁇ g hydrocarbyl amidopropyl hydroxy- sultaines, especially C12- 14 hydrocarbyl amido propyl hydroxysultaines, e.g., laurylamidopropyi hydroxysultaine and cocamidopropyl hydroxysultaine.
• Other sultaines are described in U.S. Patent 3,950,417, which descriptions are incor ⁇ porated herein by reference.
• amphoteric surfactants are the aminoalkanoates of the formula R-NH(CH2) n COOM, the iminodialkanoates of the formula R-N[(CH2) m COOM]2 and mixtures thereof, wherein n and m are integers from 1 to 4, R is Cg - C22 alkyl or alkenyl, and M is hydrogen, alkali metal, alkaline earth metal, ammoruum or alkanolammonium
• suitable aminoalkanoates include n-alkylamino-propionates and n-alkyliminodipropionates, specific examples of which include N-lauryl- -beta-amino propionic acid or salts thereof, and N-lauryl-beta-imino-dipropionic acid or salts thereof, and mixtures thereof
• amphoteric surfactants include those represented by the formula
• R ⁇ is alkyl or alkenyl having from about 8 to about 22 carbon atoms, preferably from about 12 to about 16 carbon atoms
• R ⁇ is hydrogen or CH 2 CO 2 M
• R 3 is CH 2 CH 2 OH or CH 2 CH 2 OCH 2 CH2COOM
• R 4 is hydrogen, CH 2 CH 2 OH, or CH 2 CH 2 OCH2CH 2 COOM
• Z is CO 2 M or CH 2 CO 2 M
• n is the integer 2 or 3, preferably 2
• M is a hydrogen, alkali metal (e g , lithium, sodium, potassium), alkali earth metal (e.g., beryllium, magnesium, calcium, strontium, barium) ammonium or substituted ammonium
• This type of surfactant is sometimes classified as an imidazoline-type amphoteric surfactant, although it does not necessarily have to be derived, directly or indirectly, through an imidazoline intermediate.
• MIRANOL Suitable materials of this type are marketed under the trade name MIRANOL and are understood to comprise a complex mixture of species, and can exist in protonated and non-protonated species depending upon pH with respect to species that can have a hydrogen at R ⁇ All such variations and species are meant to be encompassed by the above formula
• surfactants of the above formula are monocarboxylates and dicarboxylates
• examples of these materials include cocoamphocarboxypropionate, cocoamphocarboxypropionic acid, cocoamphocarboxyglycinate (alternately referred to as cocoamphodiacetate), and cocoamphoacetate
• amphoteric surfactants include those sold under the trade names MIRANOL C2M CONC N.P , MIRANOL C2M CONC O P , MIRANOL C2M SF, MIRANOL CM SPECIAL (Miranol, Ine ), ALKATERIC 2CIB (Alkaril Chemicals), AMPHOTERGE W-2 (Lonza, Ine ), MONATERIC CDX-38, MONATERIC CSH-32 (Mona Industries), REWOTERIC AM-2C (Rewo Chemical Group), and SCHERCOTERIC MS-2 (Scher Chemicals)
• Betaine surfactants (zwitterionic) suitable for use in the shampoo compositions are those represented by the formula
• R 1 is COOM or CH(OH)CH 2 SO 3 M
• R2 is lower alkyl or hydroxyalkyl
• R 3 is lower alkyl or hydroxyalkyl
• R is a member selected from the group consisting of hydrogen and lower alkyl
• R5 is higher alkyl or alkenyl
• Y is lower alkyl, preferably methyl
• m is an integer from 2 to 7, preferably from 2 to 3
• n is the integer 1 or 0, and
• M is a hydrogen, alkali metal, alkali earth metal, ammonium or substituted ammonium.
• lower alkyl or “hydroxyalkyl” means straight or branch chained, saturated, aliphatic hydrocarbon radicals and substituted hydrocarbon radicals having from one to about three carbon atoms such as, for example, methyl, ethyl, propyl, isopropyl, hydroxypropyl, hydroxyethyl, and the like
• higher alkyl or alkenyl means straight or branch chained satu ⁇ rated (i e , "higher alkyl”) and unsaturated (i.e , "higher alkenyl”) aliphatic hydrocarbon radicals having from about eight to about 20 carbon atoms such as, for example, lauryl, cetyl, stearyl, oleyl, and the like.
• higher alkyl or alkenyl includes mixtures of radicals which may contain one or more intermediate linkages such as ether or polyether linkages or non-functional substitutents such as hydroxyl or halogen radicals wherein the radical remains of hydrophobic character.
• Suitable surfactant betaines ofthe above formula wherein n is zero include the alkylbetaines such as cocodimethylcarboxymethylbetaine, lauryldimethylcarboxymethylbetaine, lauryl dimethyl-alpha-carboxyethylbetaine, cetyldimethylcarboxymethylbetaine, lauryl-bis-(2-hydroxyethyl)carboxymethyI- betaine, stearyl-bis-(2-hydroxypropyl)carboxymethylbetaine, oleyl- dimethyl-gamma-carboxypropylbetaine, lauryl-bis-(2-hydroxypropyl)- alpha-carboxyethylbetaine, etc.
• alkylbetaines such as cocodimethylcarboxymethylbetaine, lauryldimethylcarboxymethylbetaine, lauryl dimethyl-alpha-carboxyethylbetaine, cetyldimethylcarboxymethylbetaine, lauryl-bis-(2-
• Suitable sulfobetaines include cocodimethylsulfopropyl- betaine, stearyldimethylsulfopropylbetaine, and lauryl-bis-(2-hydroxyethyl)sulfopropylbetaine.
• amido betaines and amidosulfo betaines for use in the shampoo compositions include the amidocarboxybetaines, such as cocoamidodimethylcarboxymethylbetaine, laurylamidodi- methylcarboxymethylbetaine, cetylamidodimethylcarboxymethylbetaine, laurylamido-bis-(2-hydroxyethyl)-carboxymethylbetaine, cocoamido-bis-(2-hydroxyethyl)-carboxymethylbetaine, etc
• Amido sulfobetaines include cocoamidodimethylsulfopropylbetaine, stearylamidodimethylsulfopropylbetaine, and lauryl- amido-bis-(2-hydroxyethyl)-sulfopropylbetaine.
• the shampoo compositions of the present invention are preferably free of highly solubilizing surfactants such as N-acyl amino acid surfactants.
• substantially free means that the shampoo compositions preferably contain no more than about 1%, more preferably no more than about 0.5%, even more preferably no more than about 0.25%, most preferably essentially zero percent, of highly solubilizing surfactants by weight ofthe shampoo compositions
• the shampoo compositions may comprise N-acyl amino acid surfactants as a secondary optional surfactant or as the detersive surfactant component ofthe shampoo compositions.
• N-acyl amino acid surfactants are well known surfactants for use in a variety of products. A description of these surfactants and their synthesis can be found, for example, in Anionic Suractants. Part II. Surfactant Science Series. Vol. Ill, edited by Warner M. Linfield, Marcel Dekker, Inc. (New York and Basel), pp 581-617 (1976), which description is incorporated herein by reference.
• N-acyl amino acid surfactants for use in the shampoo compositions herein include N-acyl hydrocarbyl acids and salts thereof, which can be represented by the formula wherein Rl is a alkyl or alkenyl radical having from about 8 to about 24 carbon atoms, preferably from about 12 to about 18 carbons atoms, R ⁇ is hydrogen, alkyl having from about 1 to about 4 carbon atoms, phenyl, or CH2COOM, preferably alkyl having from about 1 to about 4 carbon atoms, more preferably alkyl having from about 1 to about 2 carbon atoms; R3 is (CR 4 )2 or alkoxy having from about 1 or about 2 carbon atoms, wherein each R 4 is independently hydrogen or alkyl having from about 1 to about 6 carbon atoms or alkylester thereof, n is an integer from 1 to 4, preferably 1 or 2, and M a hydrogen, alkali metal (e g , lithium, sodium, potassium), alkali earth metal (e g , beryll
• the highly solubilizing surfactants described hereinabove when used in combination with the guar cationic polymers described hereinafter, are less effective in providing improved deposition of the antimicrobial agent ofthe shampoo compositions herein. It has also been found that, by increasing the cationic charge density of the guar cationic polymer in the presence of these highly solubilizing surfactant, the less effective antimicrobial agent deposition can be improved substantially In the presence of the highly solubilizing surfactants in the shampoo compositions herein, therefore, the cationic guar polymer should have a cationic charge density of from about 0 9meq/g to about 4meq/g, preferably between about 1.0 and 3meq/g.
• the shampoo compositions of the present invention comprise a safe and effective amount of an antimicrobial agent
• the antimicrobial agent provides the shampoo compositions with antimicrobial activity
• the antimicrobial agent is preferably a crystalline particulate that is insoluble in, and dispersed throughout, the shampoo compositions Effective concentrations of such antimicrobial agents generally range from about 0.1% to about 5%, more preferably from about 0 3% to about 5%, by weight of the shampoo compositions
• Suitable antimicrobial agents include sulfur, octopirox, selenium sulfide, and pyridinethione salts
• Selenium sulfide is a preferred particulate antimicrobial agent for use in the shampoo compositions, effective concentrations of which range from about 0 1% to about 5 0%, preferably from about 0 3% to about 2 5%, more preferably from about 0 5% to about 1 5%, by weight of the shampoo compositions
• Pyridinethione antimicrobial agents are highly preferred particulate antimicrobial agents for use in the shampoo compositions, concentrations of which range from about 0 1% to about 3%, preferably about 0 3% to about 2%, by weight of the shampoo compositions
• Preferred pyridinethione salts are those formed from heavy metals such as zinc, tin, cadmium, magnesium, aluminum and zirconium Zinc salts are most preferred, especially the zinc salt of l-hydroxy-2-pyridinethione (zinc pyridinethione, ZPT)
• Other cations such as sodium may also be suitable
• Particularly preferred are 1- hydroxy-2-pyridinethione salts in platelet particle form, wherein the particles have an average size of up to about 20 microns, preferably up to about 8 microns, most preferably up to about 5 microns
• Pyridinethione antimicrobial agents are well known in the shampoo art, and are described, for example, in U S Patent 2,809,971, U.S Patent 3,236,733, U S Patent 3,753, 196, U.S. Patent 3,761,418, U.S Patent 4,345,080, U S Patent 4,323,683, U S Patent 4,379,753, and U.S. Patent 4,470,982, which descriptions are inco ⁇ orated herein by reference
• Sulfur may also be used as the particulate antimicrobial agent in the shampoo compositions herein Effective concentrations of the particulate sulfur are generally from about 1% to about 5%, more preferably from about 2% to about 5%, by weight of the compositions
• Octopirox and related salts and derivatives may also be used as the antimicrobial agent in the shampoo compositions
• Such antimicrobial agents are soluble in the shampoo composition and, therefore, do not disperse throughout the composition as crystalline particulates as do the other antimicrobial agents described hereinbefore Suspending or Thickening Agent
• the shampoo compositions ofthe present invention comprise a suspending or thickening agent to help maintain dispersion of particulate antimicrobial agents throughout the composition.
• a suspending or thickening agent Any known suspending or thickening agent may be used in the shampoo compositions, provided that it is physically and chemically compatible with the essential components of the shampoo composition described herein, or does not otherwise unduly impair product stability, aesthetics or performance.
• Crystalline suspending agents are preferred for suspending the particulate antimicrobial agent in the shampoo compositions.
• the selected suspending agent at the selected concentration, should help maintain the suspension for at a period of at least one month, preferably at least three months, more preferably at least about twenty-four months, at ambient temperatures.
• effective concentrations of the crystalline suspending agent range from about 0.5% to about 10%, preferably from about 0.5% to about 5%, more preferably about 1% to about 4%, most preferably about 1% to about 3%, by weight ofthe shampoo composition.
• concentrations of the crystalline suspending agent should be minimized to achieve only the desired property.
• Preferred crystalline suspending agents are acyl derivatives and amine oxides, especially acyl derivatives, especially those which can be solubilized in a premix solution and then be recrystallized upon cooling.
• These materials comprise long chain (e.g., C8-C22 preferably C i -C22» rnore preferably C16-C22) aliphatic groups, i.e., long chain acyl derivative materials and long chain amine oxides, as well as mixtures of such materials.
• ethylene glycol long chain esters alkanol amides of long chain fatty acids, long chain esters of long chain fatty acids, glyceryl long chain esters, long chain esters of long chain alkanolamides, and long chain alkyl dimethyl amine oxides, and combinations thereof.
• Crystalline suspending agents are described, for example, in U.S. Patent 4,741,855, which description is incorporated herein by reference.
• Suitable suspending agents for use in the shampoo compositions herein include ethylene glycol esters of fatty acids preferably having from about 14 to about 22 carbon atoms, more preferably 16-22 carbon atoms. More preferred are the ethylene glycol stearates, both mono and distearate, but particularly the distearate containing less than about 7% ofthe mono stearate.
• Other suspending agents include alkanol amides of fatty acids, preferably having from about 16 to about 22 carbon atoms, more preferably about 16 to 18 carbon atoms.
• Preferred alkanol amides are stearic monoethanolamide, stearic diethanolamide, stearic monoisopropanolamide and stearic monoethanolamide stearate
• Other long chain acyl derivatives include long chain esters of long chain fatty acids (e.g., stearyl stearate, cetyl palmitate), glyceryl esters (e.g , glyceryl distearate) and long chain esters of long chain alkanol amides (e g , stearamide diethanolamide distearate, stearamide monoethanolamide stearate)
• Ethylene glycol esters of long chain carboxylic acids, long chain amine oxides, and alkanol amides of long chain carboxylic acids in addition to the preferred materials listed above, may be used as suspending agents.
• Suspending agents also include long chain amine oxides such as alkyl (C16-C22) dimethyl amine oxides, e.g., stearyl dimethyl amine oxide
• acyl derivatives that can be used include N,N-dihydrocarbyl ( i2"C22 ' preferably C j ⁇ -C i ) amido benzoic acid and soluble salts thereof (e.g , Na and K salts), particularly N,N-di(Ci6-C ] g, and hydrogenated tallow) amido benzoic acid species of this family, which are commercially available from Stepan Company (Northfield, Illinois, USA)
• the crystalline suspending agent can be inco ⁇ orated into the shampoo compositions herein by solubilizing it into a solution containing water and the anionic sulfate surfactant at a temperature above the melting point of the suspending agent The suspending agent is then recrystallized, typically by cooling the solution to a temperature sufficient to induce crystallization
• suitable suspending agents for use in the shampoo compositions include that can be used include polymeric thickeners, such as carboxyvinyl polymers, examples of which are described in U.S. Patent 2,798,053, and U.S Patent 4,686,254, which descriptions are inco ⁇ orated herein by reference
• suitable carboxyvinyl polymers include Carbopol® 934, -940, -941, -956, -980, -981, -1342, and -1382, all commercially available from B F. Goodrich Company
• suspending agents include those which impart a gel-like viscosity to the composition, such as water soluble or colloidally water soluble polymers like cellulose ethers (e.g., hydroxyethyl cellulose), guar gum, polyvinyl alcohol, polyvinyl pyrrolidone, hydroxypropyl guar gum, starch and starch derivatives, and other thickeners, viscosity modifiers, gelling agents, xanthan gum and combinations thereof
• water soluble or colloidally water soluble polymers like cellulose ethers (e.g., hydroxyethyl cellulose), guar gum, polyvinyl alcohol, polyvinyl pyrrolidone, hydroxypropyl guar gum, starch and starch derivatives, and other thickeners, viscosity modifiers, gelling agents, xanthan gum and combinations thereof
• the shampoo compositions of the present invention comprise a cationic guar polymer having a select charge density
• the cationic guar polymer in combination with the essential components of the compositions, provides improved deposition of the antimicrobial agent onto the scalp and other areas of the skin
• Concentrations of the cationic deposition polymer range from about 0 01% to about 1 0%, preferably from about 0 01% to about 0 5%, more preferably from about 0 02% to about 0 25%, by weight ofthe shampoo compositions.
• the cationic guar polymer for use in the shampoo composition is further defined as having a cationic charge density of from about O Olmeq/g to about 3meq/g, preferably from about 0 lmeq/g to about 2meq/g, more preferably from about 0 8 to about 1 8meq/g, wherein at least about 50%, preferably about 100%, by weight ofthe cationic guar polymer forms coacervates with detersive surfactant in the shampoo compositions
• the formed coacervates are in the form of hydrated, dispersed colloids that are insoluble in the shampoo compositions
• the cationic guar polymers for use in the shampoo compositions are cationically substituted galactomannan (guar) gum derivatives
• the molecular weight of such derivatives ranges generally from about 2,000 to about 3,000,000 Guar gum for use in preparing these guar gum derivatives is typically obtained as a naturally occurring material from the seeds of the guar plant
• the guar molecule itself is a straight chain mannan branched at regular intervals with single membered galactose units on alternative mannose units The mannose units are linked to each other by means of beta (1-4) glycosidic linkages
• the galactose branching arises by way of an alpha (1-6) linkage
• Cationic derivatives of the guar gums are obtained by reaction between the hydroxyl groups of the polygalactomannan and reactive quaternary ammonium compounds
• the degree of substitution of the cationic groups onto the guar structure must be sufficient to provide the requisite cationic charge density described hereinbefore.
• Suitable quaternary ammonium compounds for use in forming the guar cationic polymers include
• R4 is a halohydrin group of the formula
• R5 is C 1-C3 alkylene and X is chlorine or bromine, and Z is an anion such as Cl", Br, or HSO4-
• Cationic guar polymers (cationic derivatives of guar gum) formed from the reagents described hereinbefore are represented by the formula
• the cationic guar polymer is guar hydroxypropyltrimethylammonium chloride, which can be more specifically represented by the formula
• Suitable cationic guar polymers include hydroxypropylated cationic guar derivatives
• the shampoo compositions of the present invention are aqueous systems which comprise from about 40% to about 92%, preferably from about 50% to about 85%, more preferably from about 60% to about 80%, water by weight of the compositions
• the pH of the shampoo compositions ranges, in general, from about 2 to about 10, preferably from about 3 to about 9, more preferably from about 4 to about 8, most preferably from about 5 5 to about 7 5
• the pH should be adjusted according to the isoelectric point ofthe selected surfactant to maintain an anionic species on the selected surfactant prior to forming a coacervate with the cationic guar polymer described herein
• the shampoo compositions ofthe present invention may further comprise one or more optional components known for use in shampoo compositions, provided that the optional components are physically and chemically compatible with the essential components described herein, or do not otherwise unduly impair product stability, aesthetics or performance Concentrations of such optional components typically range from about 0.001% to about 10% by weight ofthe shampoo compositions
• Optional components include preservatives, conditioning agents, styling polymers, organic solvents, pearlescent aids, foam boosters, nonionic surfactants, pH adjusting agents, perfumes, proteins, dyes, skin active agents, sunscreens, vitamins, and viscosity adjusting agents
• preservatives conditioning agents, styling polymers, organic solvents, pearlescent aids, foam boosters, nonionic surfactants, pH adjusting agents, perfumes, proteins, dyes, skin active agents, sunscreens, vitamins, and viscosity adjusting agents
• the shampoo compositions of the present invention are used in a conventional manner for cleaning hair and controlling dandruff on the scalp
• the shampoo compositions herein are also useful for cleansing the skin and other areas of the body such as underarm and groin areas
• An effective amount of the composition typically from about 1 g to about 20 g of the composition, for cleaning hair, skin or other area of the body, is applied to the hair, skin or other area that has preferably been wetted, generally with water, and then rinsed off
• Application to the hair typically includes working the shampoo composition through the hair such that most or all ofthe hair is contacted with the shampoo composition
• compositions illustrated in Examples I-XX illustrate specific embodiments of the shampoo compositions of the present invention, but are not intended to be limiting thereof Other modifications can be undertaken by the skilled artisan without departing from the spirit and scope of this invention These exemplified embodiments of the shampoo compositions of the present invention provide excellent cleansing of hair and dandruff control
• compositions can be prepared by conventional formulation and mixing techniques Component amounts are listed as weight percents and exclude minor materials such as diluents, filler, and so forth The listed formulations, therefore, comprise the listed components and any minor materials associated with such components Examples I - XVI
• Ethylene Glycol Distearate 1.50 1 50 1.50 1 50 1 50 1 50
• composition provides excellent hair cleansing, lathe ⁇ ng, antimicrobial agent deposition on the scalp and dandruff control Component
• each of the compositions described in Examples XVII to XIX from 50% to 100% by weight of the detersive surfactants are added to a jacketed mix tank and heated to about 74°C with slow agitation to form a surfactant solution.
• pH modifiers disodium phosphate, disodium phosphate
• Ethylene glycol distearate (EGDS) and fatty alcohols are then added to the mixing vessel and allowed to melt. After the EGDS is melted and dispersed (usually about 5-10 minutes), preservative (if used) is added and mixed into the surfactant solution.
• Example XX Each exemplified composition provides excellent hair cleansing, lathering, antimicrobial agent deposition on the scalp, and dandruff control.
• Example XX Each exemplified composition provides excellent hair cleansing, lathering, antimicrobial agent deposition on the scalp, and dandruff control.
• the resulting mixture is passed through a heat exchanger where it is cooled to about 35°C and collected in a finishing tank As a result of this cooling step, the EGDS crystallizes to form a crystalline network in the product
• the remainder of the detersive surfactant and other components are added to the finishing tank with agitation to ensure a homogeneous mixture Cationic guar polymer is dispersed in water as a 0.5-2.5% aqueous solution before addition to the final mix.
• viscosity and pH modifiers are added to the mixture to adjust product viscosity and pH to the extent desired.
• the resulting composition provides excellent hair cleansing, lathering, antimicrobial agent deposition on the scalp and dandruff control

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• 1997
  • 1997-01-06 BR BR9707216A patent/BR9707216A/pt not_active Application Discontinuation
  • 1997-01-06 TR TR1998/01453T patent/TR199801453T2/tr unknown
  • 1997-01-06 HU HU9900641A patent/HUP9900641A3/hu unknown
  • 1997-01-06 CN CN97193079A patent/CN1213294A/zh active Pending
  • 1997-01-06 KR KR1019980705796A patent/KR19990082074A/ko not_active Application Discontinuation
  • 1997-01-06 CA CA002242932A patent/CA2242932A1/en not_active Abandoned
  • 1997-01-06 CZ CZ982296A patent/CZ229698A3/cs unknown
  • 1997-01-06 JP JP9526858A patent/JPH11503175A/ja active Pending
  • 1997-01-06 AU AU16910/97A patent/AU1691097A/en not_active Abandoned
  • 1997-01-06 WO PCT/US1997/000081 patent/WO1997026854A1/en not_active Application Discontinuation
  • 1997-01-06 EP EP97902829A patent/EP0920298A1/en not_active Withdrawn
  • 1997-01-24 CO CO97003302A patent/CO4770889A1/es unknown
  • 1997-01-27 AR ARP970100320A patent/AR013558A1/es not_active Application Discontinuation
  • 1997-01-28 ZA ZA9700696A patent/ZA97696B/xx unknown
  • 1997-01-28 PE PE1997000047A patent/PE56898A1/es not_active Application Discontinuation
• 1998
  • 1998-07-28 MX MX9806050A patent/MX9806050A/es unknown

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