MXPA01011219A - Anti-dandruff and conditioning shampoos containing certain cationic polymers - Google Patents
Anti-dandruff and conditioning shampoos containing certain cationic polymersInfo
- Publication number
- MXPA01011219A MXPA01011219A MXPA/A/2001/011219A MXPA01011219A MXPA01011219A MX PA01011219 A MXPA01011219 A MX PA01011219A MX PA01011219 A MXPA01011219 A MX PA01011219A MX PA01011219 A MXPA01011219 A MX PA01011219A
- Authority
- MX
- Mexico
- Prior art keywords
- hair
- composition
- cationic
- conditioning
- weight
- Prior art date
Links
- 239000002453 shampoo Substances 0.000 title claims abstract description 160
- 230000003750 conditioning Effects 0.000 title claims abstract description 156
- 125000002091 cationic group Chemical group 0.000 title claims abstract description 148
- 229920000642 polymer Polymers 0.000 title claims description 100
- 239000000203 mixture Substances 0.000 claims abstract description 282
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 99
- 210000004209 Hair Anatomy 0.000 claims abstract description 74
- 240000005497 Cyamopsis tetragonoloba Species 0.000 claims abstract description 63
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 16
- -1 t riyodot ironin Chemical compound 0.000 claims description 122
- 229920001296 polysiloxane Polymers 0.000 claims description 92
- 125000000217 alkyl group Chemical group 0.000 claims description 36
- 239000000375 suspending agent Substances 0.000 claims description 23
- 230000003698 anagen phase Effects 0.000 claims description 22
- 230000003779 hair growth Effects 0.000 claims description 20
- 239000002245 particle Substances 0.000 claims description 20
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 15
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical group [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 15
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 230000001105 regulatory Effects 0.000 claims description 12
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical group [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 10
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Glycol distearate Chemical group CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 claims description 9
- 150000001735 carboxylic acids Chemical class 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- WCGUUGGRBIKTOS-RRHGHHQTSA-N Ursolic acid Chemical class O=C(O)[C@@]12[C@@H]([C@@H](C)[C@@H](C)CC1)C=1[C@](C)([C@@]3(C)[C@@H]([C@]4(C)[C@H](C(C)(C)[C@@H](O)CC4)CC3)CC=1)CC2 WCGUUGGRBIKTOS-RRHGHHQTSA-N 0.000 claims description 6
- 239000003112 inhibitor Substances 0.000 claims description 6
- 230000002401 inhibitory effect Effects 0.000 claims description 6
- 150000003751 zinc Chemical class 0.000 claims description 6
- XMAYWYJOQHXEEK-OZXSUGGESA-N Ketoconazole Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1OC[C@@H]1O[C@@](CN2C=NC=C2)(C=2C(=CC(Cl)=CC=2)Cl)OC1 XMAYWYJOQHXEEK-OZXSUGGESA-N 0.000 claims description 5
- 229960004125 ketoconazole Drugs 0.000 claims description 5
- PMATZTZNYRCHOR-CGLBZJNRSA-N (3S,6S,9S,12R,15S,18S,21S,24S,30S,33S)-30-ethyl-33-[(E,1R,2R)-1-hydroxy-2-methylhex-4-enyl]-1,4,7,10,12,15,19,25,28-nonamethyl-6,9,18,24-tetrakis(2-methylpropyl)-3,21-di(propan-2-yl)-1,4,7,10,13,16,19,22,25,28,31-undecazacyclotritriacontane-2,5,8,11,14,17 Chemical compound CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O PMATZTZNYRCHOR-CGLBZJNRSA-N 0.000 claims description 4
- BDJRBEYXGGNYIS-UHFFFAOYSA-N Azelaic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 4
- SLJTWDNVZKIDAU-UXEXATSUSA-N Betulonic acid Chemical class C1CC(=O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C(=C)C)[C@H]5[C@H]4CC[C@@H]3[C@]21C SLJTWDNVZKIDAU-UXEXATSUSA-N 0.000 claims description 4
- ZFMITUMMTDLWHR-UHFFFAOYSA-N Loniten Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 claims description 4
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M bromide Chemical group [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 4
- 230000000875 corresponding Effects 0.000 claims description 4
- GDLBFKVLRPITMI-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound ClC1=CC=C2NC(C)=NS(=O)(=O)C2=C1 GDLBFKVLRPITMI-UHFFFAOYSA-N 0.000 claims description 3
- MIJYXULNPSFWEK-GTOFXWBISA-N 3β-hydroxy-Olean-12-en-28-oic acid Chemical class C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CCC(C)(C)C[C@H]5C4=CC[C@@H]3[C@]21C MIJYXULNPSFWEK-GTOFXWBISA-N 0.000 claims description 3
- 108010036949 Cyclosporine Proteins 0.000 claims description 3
- 229960000978 Cyproterone Acetate Drugs 0.000 claims description 3
- UWFYSQMTEOIJJG-FDTZYFLXSA-N Cyproterone acetate Chemical compound C1=C(Cl)C2=CC(=O)[C@@H]3C[C@@H]3[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(C)=O)(OC(=O)C)[C@@]1(C)CC2 UWFYSQMTEOIJJG-FDTZYFLXSA-N 0.000 claims description 3
- CXOFVDLJLONNDW-UHFFFAOYSA-N Epinat Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 claims description 3
- DBEPLOCGEIEOCV-WSBQPABSSA-N Finasteride Chemical compound N([C@@H]1CC2)C(=O)C=C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H](C(=O)NC(C)(C)C)[C@@]2(C)CC1 DBEPLOCGEIEOCV-WSBQPABSSA-N 0.000 claims description 3
- 229960003632 Minoxidil Drugs 0.000 claims description 3
- 229940100243 Oleanolic Acid Drugs 0.000 claims description 3
- MIJYXULNPSFWEK-LXLHWSNGSA-N Oleanolic acid Chemical class C1C[C@H](O)C(C)(C)[C@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CCC(C)(C)C[C@@H]5C4=CC[C@H]3[C@]21C MIJYXULNPSFWEK-LXLHWSNGSA-N 0.000 claims description 3
- 229960002036 Phenytoin Drugs 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 229960001265 ciclosporin Drugs 0.000 claims description 3
- 229960004042 diazoxide Drugs 0.000 claims description 3
- 229960004039 finasteride Drugs 0.000 claims description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M fluoride anion Chemical group [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 3
- 102000004257 potassium channel family Human genes 0.000 claims description 3
- 108020001213 potassium channel family Proteins 0.000 claims description 3
- 150000007949 saponins Chemical class 0.000 claims description 3
- 235000017709 saponins Nutrition 0.000 claims description 3
- 150000003648 triterpenes Chemical class 0.000 claims description 3
- 229940096998 ursolic acid Drugs 0.000 claims description 3
- QGJZLNKBHJESQX-FZFNOLFKSA-N Betulinic acid Chemical class C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C(=C)C)[C@@H]5[C@H]4CC[C@@H]3[C@]21C QGJZLNKBHJESQX-FZFNOLFKSA-N 0.000 claims description 2
- QGJZLNKBHJESQX-CASBDLHJSA-N Betulinic acid Chemical class O=C(O)[C@@]12[C@@H]([C@@H](C(=C)C)CC1)[C@@H]1[C@](C)([C@@]3(C)[C@@H]([C@]4(C)[C@H](C(C)(C)[C@@H](O)CC4)CC3)CC1)CC2 QGJZLNKBHJESQX-CASBDLHJSA-N 0.000 claims description 2
- 210000001772 Blood Platelets Anatomy 0.000 claims description 2
- KQJSQWZMSAGSHN-JJWQIEBTSA-N Celastrol Chemical class C([C@H]1[C@]2(C)CC[C@@]34C)[C@](C)(C(O)=O)CC[C@]1(C)CC[C@]2(C)C4=CC=C1C3=CC(=O)C(O)=C1C KQJSQWZMSAGSHN-JJWQIEBTSA-N 0.000 claims description 2
- JWJOTENAMICLJG-QWBYCMEYSA-N Dutasteride Chemical compound O=C([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)N[C@@H]4CC3)C)CC[C@@]21C)NC1=CC(C(F)(F)F)=CC=C1C(F)(F)F JWJOTENAMICLJG-QWBYCMEYSA-N 0.000 claims description 2
- 229940041033 Macrolides Drugs 0.000 claims description 2
- MDZKJHQSJHYOHJ-LLICELPBSA-N Maslinic acid Chemical class C1[C@@H](O)[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CCC(C)(C)C[C@H]5C4=CC[C@@H]3[C@]21C MDZKJHQSJHYOHJ-LLICELPBSA-N 0.000 claims description 2
- RJKFOVLPORLFTN-STHVQZNPSA-N Progesterone Natural products O=C(C)[C@@H]1[C@@]2(C)[C@H]([C@H]3[C@@H]([C@]4(C)C(=CC(=O)CC4)CC3)CC2)CC1 RJKFOVLPORLFTN-STHVQZNPSA-N 0.000 claims description 2
- RJKFOVLPORLFTN-LEKSSAKUSA-N Syngestrets Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 claims description 2
- 229960000306 Zinc Gluconate Drugs 0.000 claims description 2
- WHMDKBIGKVEYHS-IYEMJOQQSA-L Zinc gluconate Chemical compound [Zn+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O WHMDKBIGKVEYHS-IYEMJOQQSA-L 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000004171 alkoxy aryl group Chemical group 0.000 claims description 2
- 229960002255 azelaic acid Drugs 0.000 claims description 2
- 229960004199 dutasteride Drugs 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical group [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 claims description 2
- 239000003120 macrolide antibiotic agent Substances 0.000 claims description 2
- 239000000186 progesterone Substances 0.000 claims description 2
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- 238000009736 wetting Methods 0.000 claims description 2
- 239000011670 zinc gluconate Substances 0.000 claims description 2
- 235000011478 zinc gluconate Nutrition 0.000 claims description 2
- 239000003936 androgen receptor antagonist Substances 0.000 claims 1
- 239000011300 coal pitch Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 description 53
- 239000003599 detergent Substances 0.000 description 29
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- 125000003342 alkenyl group Chemical group 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
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- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 12
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- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 10
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
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- 150000001412 amines Chemical class 0.000 description 6
- OPVLOHUACNWTQT-UHFFFAOYSA-N azane;2-dodecoxyethyl hydrogen sulfate Chemical compound N.CCCCCCCCCCCCOCCOS(O)(=O)=O OPVLOHUACNWTQT-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
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- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
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- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
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- FAGMGMRSURYROS-UHFFFAOYSA-M trihexadecyl(methyl)azanium;chloride Chemical group [Cl-].CCCCCCCCCCCCCCCC[N+](C)(CCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCC FAGMGMRSURYROS-UHFFFAOYSA-M 0.000 description 1
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Abstract
Disclosed are shampoo compositions that provide a superior combination of anti-dandruff efficacy and conditioning, and a method of cleansing and conditioning the hair comprising applying to the hair an effective amount of said compositions. The anti-dandruff and conditioning shampoos comprise:(A) from about 5%to about 50%, by weight of the composition, of an anionic surfactant;(B) from about 0.01%to about 10%, by weight of the composition, of a non-volatile conditioning agent;(C) from about 0.1%to about 4%, by weight of the composition, of an anti-dandruff particulate;(D) from about 0.02%to about 5%, by weight of the composition, of a cationic guar derivative;(i) wherein said cationic guar derivative has a molecular weight from about 50,000 to about 700,000;and (ii) wherein said cationic guar derivative has a charge density from about 0.05%meq/g to about 1.0 meq/g;and (E) water.
Description
ANTISTATIC SHAMPOO AND CONDITIONERS CONTAINING CERTAIN CATIÓNIC POLYMERS
TECHNICAL FIELD OF THE INVENTION The present invention relates to shampoo compositions that provide a superior combination of anti-dandruff efficacy and conditioning. These compositions contain anionic surfactants, conditioning agents, antidandruff particulates, cationic polymers and water. Cationic polymers have certain parameters of molecular weight and charge density that provide improved efficacy of antidandruff shampoo compositions.
BACKGROUND OF THE INVENTION Shampoo compositions comprising various combinations of detergent surfactants and conditioning agents, especially silicone conditioning agents, are known in the art and are commercially available. It has been found that many of these compositions provide excellent cleaning and conditioning performance for the hair. For example, Shampoo Plus Conditioner with Pro-Vitamin-in-One of Pantene® containing anionic surfactants, a cationic polymer and silicone conditioning agents provide excellent benefits of cleaning, conditioning and hair feel at the time of application to the hair Anti-dandruff shampoos are also well known in the art and are also commercially available. Anti-dandruff shampoos usually incorporate an anti-dandruff active agent and detergent surfactants. Among the preferred types of antidandruff agents are crystalline, particulate anti-dandruff agents, such as, for example, sulfur, selenium disulfide and heavy metal salts of pyridinethione. Soluble antidandruff agents, such as, for example, ketoconazole are also known in the art. Anti-dandruff shampoos that also provide conditioning benefits are also known in the art. For example, U.S. Patent No. 5,624,666 exemplifies and claims shampoo compositions containing anionic surfactants, cationic polymers and zinc pyridinethione as an antidandruff agent. U.S. Patent No. 5,624,666 shows that conditioning agents, such as, for example, silicone fluids, can optionally be incorporated into the compositions herein. Anti-Dandruff Shampoo Head & Shoulders® plus conditioner is an example of a commercialized product that provides anti-dandruff and conditioning benefits at the time of shampooing hair. However, some consumers want a shampoo that provides a superior combination of anti-dandruff efficacy and conditioning performance against currently marketed products. This superior combination of efficiency and conditioning can be difficult to achieve. For example, it was previously believed that excellent anti-dandruff efficacy could be achieved by using an optimized coacervate for an efficiency of deposition on the hair and scalp. The coacervates that were deposited more efficiently were considered to be the most preferred for efficacy. Unfortunately, the use of the most efficient coacervates to deposit the antidandruff actives on the hair or scalp can adversely affect the conditioning, specifically the sensation of cleansing the hair.
In order to achieve good conditioning, the level of the anti-dandruff agent could be reduced, resulting in good conditioning, although with an anti-dandruff efficacy less than optimum. However, applicants have now discovered that surprisingly, the bioavailability and scope of the anti-dandruff active agent are much more predictable for efficacy than the deposition efficiency of the active agent on the hair or scalp. In fact, the applicants have found that, in some cases, even when an active antidandruff deposited very well on the hair and scalp, an acceptable anti-dandruff efficacy has not been achieved. On the contrary, a good anti-dandruff efficacy could be achieved in situations where the active anti-dandruff agent has a good reach and was quite bioavailable, although it did not deposit superiorly on the hair or scalp. Thus, for a shampoo composition to provide a superior combination of anti-dandruff efficacy and conditioning compared to known shampoo compositions, it must meet certain criteria with respect to bioavailability and range, although it does not necessarily have to have the ability to deposit the anti-dandruff active agent. so as to superimpose on the hair or scalp. The applicants have further discovered that the excellent bioavailability and scope of the anti-dandruff active agent from the determined shampoo compositions can be achieved if the coacervate formed between the cationic polymer and the anionic surfactant at the time of shampoo dilution has the ability to Smear and is flowable, instead of being elastic in its natural state. The nature of the coacervate is impacted by the level and types of cationic polymer present in the shampoo composition. An object of the present invention is to provide shampoo compositions having a superior combination of anti-dandruff efficacy and conditioning. An object of the present invention is also to provide a method for cleaning and conditioning the hair. These and other objects will be more readily apparent from the following detailed description.
BRIEF DESCRIPTION OF THE INVENTION The present invention relates to shampoo compositions that provide a superior combination of anti-dandruff efficacy and conditioning. These shampoos comprise: (A) between about 5% and 50% by weight, of an anionic surfactant; (B) between about 0.01% and 10% by weight, of a non-volatile conditioning agent; (C) between about 0.1% and 4% by weight, of an antidandruff particulate; (D) between about 0.02% and 5% by weight of a cationic guar derivative; and (E) water. The cationic guar derivative has a molecular weight of between about 50,000 and 700,000, and has a charge density of between about 0.05 meq / g and 1.0 meq / g. The present invention further relates to a method for providing anti-dandruff efficacy and conditioning for hair comprising applying to the hair and scalp an amount of the composition described above that is effective in providing these benefits.
DETAILED DESCRIPTION OF THE INVENTION The shampoo compositions of the present invention provide a superior combination of anti-dandruff efficacy and conditioning. These anti-dandruff and conditioning shampoo compositions may comprise, consist of, or consist essentially of the essential elements and limitations of the invention described herein, as well as any of the additional, optional ingredients, components, or limitations described herein. In particular, these compositions comprise anionic surfactants, conditioning agents, antidandruff particulates, cationic guar and water. At the time of dilution, anionic surfactants and cationic guar form a coacervate. The molecular weight and charge density of the cationic guar will influence the bioavailability and extent of the antidandruff particulate. This is important for antidandruff efficacy and conditioning. The components, including those that can optionally be added, of the shampoo compositions of the present invention, as well as methods for preparation, and methods for use, are described in detail below.
COMPONENTS The anti-dandruff shampoo and conditioner compositions of the present invention comprise an anionic surfactant, a conditioning agent, an antidandruff particulate, a cationic guar derivative and an aqueous carrier, each of these ingredients being described in detail below.
A. Anionic Surfactant The anti-dandruff and conditioning shampoo compositions of the present invention comprise between about 5% and 50% by weight of the composition, preferably between about 8% and 30%, most preferably between about 10% and 25%, most preferably between about 12% and 18% of an anionic detergent surfactant suitable for application to hair or skin. It is believed that the anionic detergent surfactant provides the composition with cleaning performance and foam generation. Additionally, the anionic detergent surfactant forms a coacervate, at the time of aqueous dilution, with the cationic polymer component (described below) of the present invention. It is believed that this coacervate is important to provide the efficacy and conditioning benefits described herein.
The anionic detergent surfactant component may comprise an anionic detergent surfactant, a swi terionic or amphoteric detergent surfactant having a bound entity that is anionic in the pH of the composition or a combination thereof; preferably an anionic detergent surfactant. These surfactants must be physically and chemically compatible with the essential components described herein, and otherwise they should not unduly damage the stability, aesthetics or performance of the product. Examples of anionic detergent surfactants that can be suitably employed in the shampoo compositions herein include, but are not limited to, sulfates, sulfonates, sarcosinates, and sarcosine derivatives.
1. Sulfates Preferred anionic detergent surfactants for use in the anti-dandruff and conditioning shampoo compositions of the present invention are alkyl sulfates and alkyl ether sulfates. These surfactants have the respective formulas ROS03M and R (C2H40) xOS03M, wherein R is an alkyl or alkenyl group of between about C8 and Co., x is an integer having a value of 1 to 10 and M is a cation selected from group consisting of covalently electropositive bonded entities (eg, ammonium), alkanolamines (eg, triethanolamine), monovalent metals (eg, sodium and potassium), polyvalent metal cations (eg, magnesium and calcium) and mixtures thereof . The cation M must be selected so that the anionic detergent surfactant component is soluble in water. The solubility of the surfactant will depend on the particular anionic detergent surfactants and the selected cations. Preferably, R is between about Cs and Cis, more preferably between about Cio, and Cie, most preferably between about C2 and C4, in both alkyl and alkyl ether sulphates. Alkylether sulfates are usually made as condensation products of ethylene oxide and monohydric alcohols of between about C8 and C24. The alcohols can be synthetic or they can be derived from fats, for example coconut oil, palm kernel oil and tallow. Lauryl alcohol and straight chain alcohols derived from coconut oil and palm kernel oil are preferred. These alcohols are reacted with between about 0 and 10, preferably between about 2 and 5, more preferably about 3 moles of ethylene oxide. The resulting mixture of molecular species will have, for example, an average of 3 moles of ethylene oxide per mole of alcohol, and they are sulfated and neutralized. Non-limiting examples of alkyl ether sulfates which can be used in the shampoo compositions of the present invention include sodium and ammonium salts of cocoalkyl triethylene glycol ether sulfate, tallowalkyl triethylene glycol ether sulfate and tallowalkylhexaoxyl ether sulfate. Preferred alkyl ether sulfates are those comprising a mixture of individual compounds, wherein the compounds in the mixture have an average alkyl chain length of between about C 1 and C 1 and an average degree of ethoxylation of between about 1 and 4 moles of ethylene oxide. Specific examples of preferred alkyl sulfates include, but are not limited to: ammonium lauryl sulfate, cocoyl or fat ammonium, potassium lauryl sulfate, potassium cocoyl sulfate, sodium lauryl sulfate, sodium cocoyl sulfate, monoe tanoiamine lauryl sulfate, mono-ethanolamine cocoyl sulfate, lauryl sulfate of diethanolamine, triethanolamine lauryl sulfate, lauri lsul fat or triethylamine, and mixtures thereof. In particular, ammonium lauryl sulfate is preferred. Specific examples of alkyl ether sulphates include, but are not limited to, ammonium laureth sulfate, potassium laureth sulfate, sodium laureth sulfate, monoethanolamine laureth sulfate, diethanolamine laureth sulfate, triethanolamine laureth sulfate, triethylamine laureth sulfate, and mixtures thereof. same. In particular, ammonium laureth sulfate is preferred. Yet another class of sulfate surfactants suitable for use in the antidandruff shampoos and conditioners of the present invention are the sulfated glycerides, an example of which includes, but is not limited to: sodium monoglyceride lauric sulfate.
2. Sulfonates Those anionic detergent surfactants known as olefin sulfonates are also suitable for use in the antidandruff shampoos and conditioners of the present invention. As used herein, the term "olefin sulfonates" refers to compounds that can be produced by the sulfonation of α-olefins by means of sulfur trioxide without complexing, followed by neutralization of the acid reaction mixture under conditions such that any sulfones that have formed in the reaction are hydrolyzed to provide the corresponding hydroxy-alkane sulfonates. Sulfur trioxide can be liquid or gaseous, and usually, but not necessarily, can be diluted by inert diluents, for example by liquid S02, chlorinated hydrocarbons and the like, when used in liquid form, or by air, nitrogen, S02 gaseous and the like, when used in the gaseous form. The α-olefins from which the olefin sulfonates are derived are mono-olefins having from about C C to C24,, preferably from about Ci Ci y to C C-Preferably they are straight-chain olefins. In addition to the true alkane sulphonates and a proportion of hydroxy alcansulphates, the olefin sulfonates may contain small amounts of other materials, for example, alkene disulfonates depending on the reaction conditions, the proportion of reactants, the nature of the olefins. starting and impurities in olefin raw material and secondary reactions during the sulphonation process. A non-limiting example of this mixture of alpha-olefin sulfonate is described in U.S. Patent No. 3,332,880, which is incorporated herein by reference. Another class of sulfonates suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are those anionic detergent surfactants known as β-alkyloxy alkanesulfonates. These surfactants conform to the following formula (I):
wherein R1 is a straight chain alkyl group of between about C6 and C20, R2 is a lower alkyl group of between about Ci and C3, preferably Ci, and M is a water soluble cation, as described above. Still other sulfonates suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are those anionic detergent surfactants known as alkyl aryl sulfonates. Non-limiting examples of alkyl aryl sulfonates include sodium tridecyl benzene sulfonate, sodium dodecyl benzene sulfonate and mixtures thereof. Other sulfonates suitable for use in the anti-dandruff shampoos and conditioners of the present invention are the water-soluble salts of organic reaction products of sulfuric acid according to the formula [R1-S03-M] wherein R1 is an aliphatic hydrocarbon radical, saturated straight or branched chain, between about Cs and C24, preferably between C 0 and C 8; and M is a cation described above. Non-limiting examples of these anionic detergent surfactants are the salts of an organic sulfuric acid reaction product of a hydrocarbon of the methane series, which includes i so, n eo and n-paraffins, and a sulfonating agent, for example S03, H2S0, obtained according to known sulfonating methods. The sulfonation methods may include bleaching and hydrolysis. Preferably, the salts are between about C8 and C2; most preferably between about C1 Z and C18. C 1 to C 8 -sulfonates sulfonated with ammonium and alkali metal are preferred. Still other sulfonates, suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are the reaction products of fatty acids, which are esterified with isethionic acid and neutralized with sodium hydroxide. Preferred fatty acids are those derived from coconut oil or palm kernel oil. Also suitable are the sodium or potassium salts of fatty acid amides of methyl tauride wherein the fatty acids are derived from coconut oil or palm kernel oil. Other similar anionic surfactants are described in U.S. Patent No. 2,486,921; U.S. Patent No. 2,486,922; and U.S. Patent No. 2,396,278, the disclosures of which are incorporated herein by reference. Other sulfonates suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are the succinates, examples of which include but are not limited to: disodium N-octadecylsulfosuccinate, disodium lauryl sulfosuccinate, diammonium lauryl sulfosuccinate, N- (1,2- dicarboxyethyl) -N-octadecylsulfo-succinate tetrasodium, diaminoster of sodium sulfosuccinic acid; diethylester of sodium sulfosuccinic acid and dioctyl esters of sodium sulfosuccinic acid, and mixtures thereof.
3. Sarcosinates and Sarcosine Derivatives Those anionic detergent surfactants known as sarcosinates and sarcosine derivatives are also suitable for use in the antidandruff shampoos and conditioners of the present invention. Sarcosinates are derivatives of sarcosine and N-methyl glycine, acylated with a fatty acid chloride. They conform to the general formula (II):
OR
II R-C-N-CH2 C-O-O-X I
CH3
wherein RCO- is a fatty acid radical and wherein X is either hydrogen (acid form) or a cationic species, such as, for example, Na + or TEA + (salt form). Non-limiting examples of sarcosinates and sarcosine derivatives include: sodium lauryl sarcoslonate, lauryl sarcosine, cocoyl sarcosine, and mixtures thereof. A preferred sarcosinate is sodium lauryl sarcosinate.
B. Conditioning agent The anti-dandruff and conditioning shampoo compositions of the present invention comprise between about 0.01% and 10% by weight of the composition, preferably between about
0. 1% and more preferably between about 0.1% and 5%, most preferably between about 0.2% and 3.5%, of a conditioning agent suitable for application to hair or skin. It is believed that the conditioning agent provides improved conditioning benefits for the hair, in particular a feeling of hair cleaning and a wet rinsing sensation. The conditioning agent comprises a non-volatile, water-dispersible, water-insoluble liquid, which forms liquid particles emulsified or solubilized by the micelles of the surfactant, in the anionic detergent surfactant component (described above). Suitable conditioning agents for use in the shampoo composition are those conditioning agents generally characterized as silicones (eg, silicone oils, cationic silicones, silicone rubbers, fairly refractive silicones, and silicone resins), organic conditioning oils ( example, hydrocarbon oils, polyolefins, and fatty esters) or combinations thereof, or those conditioning agents that otherwise form dispersed, liquid particles, in the aqueous surfactant matrix of the present. These conditioning agents must be physically and chemically compatible with the essential components of the composition, and should not otherwise unduly impair the stability, aesthetics or performance of the product. The concentration of the conditioning agent in the shampoo composition should be sufficient to provide the desired conditioning benefits, and will be apparent to one of ordinary skill in the art. This concentration can vary with the conditioning agent, the conditioning performance desired, the average size of the conditioning agent particles, the type and concentration of other components and other similar factors.
1. Silicones The conditioning agent of the anti-dandruff and conditioning shampoo compositions of the present invention is preferably an insoluble silicone conditioning agent. The particles of the silicone conditioning agent may comprise volatile silicone, non-volatile silicone, or combinations thereof. Non-volatile silicone conditioning agents are preferred. If volatile silicones are present, this will normally be incidental to their use as a solvent or carrier for the commercially available forms of the ingredients of the non-volatile silicone materials, such as, for example, silicone gums and resins. The particles of the silicone conditioning agent may comprise a conditioning agent with silicone fluid and may also comprise other ingredients, such as, for example, a silicone resin to improve the deposition efficiency of the silicone fluid or improve the luster of the hair (in With a high refractive index (for example, greater than about 1.46), silicone conditioning agents (for example, highly phenylated silicones) are used.
The concentration of the conditioning agent with silicone normally varies between about 0.01% and 10% by weight of the composition, preferably between about 0.1% and 8%, most preferably between about 0.1% and 5%, most preferably between approximately 0.2% and 3%. Non-limiting examples of suitable silicone conditioning agents, and optional suspending agents for the silicone, are described in re-issued United States Patent No. 34,584, U.S. Patent No. 5,104,646, and U.S. Pat. No. 5,106,609, the disclosures of which are incorporated herein by reference. The silicone conditioning agents for use in the anti-dandruff and conditioning shampoo compositions of the present invention preferably have a viscosity, as measured at 25 ° C, of between about 20 and 2,000,000 centistokes ("csk"), most preferably of between about 1,000 and 1,800,000 csk, even more preferably between about 50,000 and 1,500,000 csk, most preferably between about 100,000 and 1,500,000 csk.
The particles of the dispersed silicone conditioning agent typically have an average number of particle diameter ranging from about 0.01 μm to 50 μm. For a small particle application to the hair, the number of average particle diameters normally varies between about 0.01 μm and 4 μm, preferably between about 0.01 μm and 2 μm, more preferably between about 0.01 μm and 0.5 μm. For the application of larger particles to hair, the number of average particle diameters normally varies between about 4 μm and 50 μm, preferably between about 6 μm and 30 μm, more preferably between about 9 μm and 20 μm , most preferably between about 12 μm and 18 μm. Conditioning agents having an average particle size of less than about 5 μm can be deposited more efficiently on the hair. It is believed that small size particles of the conditioning agent are contained within the coacervate that is formed between the anionic surfactant component (described above) and the cationic polymer component (described below), at the time of dilution of the shampoo.
A background material on silicones including the sections that analyze silicone fluids, gums, resins, as well as the manufacture of silicones, are found in Encyclone of Polymer Sci en ce and En gi n eeri n g, vol. 15, 2d ed., Pp 204-308, John Wiley & Sons, Inc. (1989), incorporated herein by reference.
i. Silicone oils Silicone fluids include silicone oils, which are flowable silicone materials having a viscosity, as measured at 25 ° C, less than 1,000,000 csk, preferably between about 5 csk and 1,000,000 csk, more preferably between approximately 10 csk and 100,000 csk. Suitable silicone oils for use in the anti-dandruff and conditioning shampoo compositions of the present invention include polyalkyl siloxanes, polyaryl siloxanes, polyalkylaryl siloxanes, polyether siloxane copolymers and mixtures thereof. Other non-volatile, insoluble silicone fluids having hair conditioning properties can also be used.
The silicone oils include polyalkyl or polyarylsiloxanes according to the following formula (III):
wherein R is aliphatic, preferably alkyl or alkenyl, or aryl, R may be substituted or unsubstituted and x is an integer from 1 to about 8,000. Unsubstituted R groups suitable for use in the anti-dandruff shampoo or conditioner compositions of the present invention include, but are not limited to: alkoxy, aryloxy, alkaryl, arylalkyl, arylalkenyl, alkylamine, and aliphatic and aryl substituted groups with ether, substituted with hydroxyl, and substituted with halogen. Suitable R groups also include cationic amines and quaternary ammonium groups. The aliphatic or substituted aryl groups in the siloxane chain may have any structure so long as the resulting silicones remain fluid at room temperature, are hydrophobic, are neither irritating, toxic, or otherwise cause damage when applied to the hair, are compatible with the other components of the shampoo compositions, are chemically stable under normal conditions of use and storage, are insoluble in the shampoo compositions herein and are capable of being deposited on the hair and providing conditioning. The two R groups on the silicon atom of each monomeric silicone unit may represent the same or different groups. Preferably, the two R groups represent the same group. Preferred alkyl and alkenyl substituents are alkyls and alkenyls of Ci to C5, most preferably Ci to C, most preferably Ci to C2. The aliphatic portions of other alkyl-containing groups, alkenyl or alkynyl (such as, for example, alkoxy, alkaryl and alkylamino) can be straight or branched chains and are preferably Ci to C5, more preferably Ci to C4, even more preferably Ci to C3, with the maximum preference from Ci to C2. As discussed above, the R substituents may also contain amino functionalities (eg, alkamino groups), which may be primary, secondary or tertiary amines or quaternary ammonium. These include mono-, di and tri-alkylamino and alkoxyamino groups wherein the chain length of the aliphatic portion is preferably as described above. The R substituents can also be substituted with other groups, such as, for example, halogens (for example, chloride, fluoride and bromide), aliphatic or halogenated aryl groups and hydroxy (for example, hydroxy-substituted aliphatic groups). Suitable halogenated R groups could include, for example, tri-halogenated alkyl groups (preferably tri-fluoro), such as, for example, -RX-CF3, wherein R1 is C1-C3 alkyl. An example of this polysiloxane includes, but is not limited to, polymethyl-3,3,3-trifluoropropylsiloxane. Suitable R groups for use in the antidandruff and conditioning shampoo compositions of the present invention include, but are not limited to: methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl. Specific non-limiting examples of preferred silicones include: polydimethylsiloxane, polydiethylsiloxane and polymethylphenylsiloxane. Polydimethylsiloxane is especially preferred. Other suitable R groups include methyl, methoxy, ethoxy, propoxy and aryloxy. The three R groups in the end caps of the silicone can also represent the same or different groups. The non-volatile polyalkylsiloxane fluids that may be used include, for example, low molecular weight polydimethylsiloxanes. These siloxanes are available, for example, from General Electric Company in their Viscasil R and SF 96 series and from Dow Corning in their Dow Corning 200 series. The polyalkylaryl siloxane fluids that may also be used include, for example, polymethylphenylsiloxanes. These siloxanes are available, for example, from General Electric Company as SF 1075 methylphenyl fluid or from Dow Corning as Cosmetic Grade Fluid 556. Polyethersiloxane copolymers that can be used include, for example, a polypropylene oxide modified polydimethylsiloxane (eg example, Dow Corning DC-1248), although ethylene oxide or mixtures of ethylene oxide and propylene oxide can also be used. The concentrations of ethylene oxide and polypropylene oxide should be sufficiently low to avoid solubility in water and the composition described herein.
Alkylamino-substituted silicones suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention include, but are not limited to, those that conform to the following general Formula (IV):
where x and y are integers. This polymer is also known as "a odimeticone".
ii. Cationic Silicones Cationic silicone fluids suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention include, but are not limited to, those that conform to the general Formula (V)
(?) aG3-a-Si- (-OsiGj • OsiGb (R?) 2-b) m-0-SiG3-a (Ri) wherein G is hydrogen, phenyl, hydroxy, Ci-Cg alkyl and preferably methyl; a is 0 or an integer having a value of 1 to 3, preferably 0; b is 0 or 1, preferably 1; n is a number from 0 to 1,999, preferably from 49 to 149; m is an integer from 1 to 2,000, preferably from 1 to 10; the sum of n and m is a number from 1 to 2,000, preferably from 50 to 150; Ri is a monovalent radical of the formula CqH2qL wherein q is an integer having a value from 2 to 8 and L is selected from the following groups: -N (R2) CH2-CH2-N (R2) 2 -N ( R2) 2 ~ N (R2) 3A ~ -N (R2) CH2-CH2-NR2-H2A "wherein R2 is hydrogen, phenyl, benzyl, a saturated hydrocarbon radical, preferably an alkyl radical of about Ci to C20 and A ~ is a halide ion A particularly preferred cationic silicone corresponding to formula (V) is the polymer known as "trimethylsilylamodimethicone", which is shown in formula (VI) below:
Other cationic silicone polymers that can be used in the anti-dandruff and conditioning shampoo composition of the present invention are represented by the general formula (VII):
wherein R3 is a monovalent hydrocarbon radical of Ci to C? 8, preferably an alkyl or alkenyl radical, such as for example methyl; R is a hydrocarbon radical, preferably an alkylene radical Ci to Cis, or an alkyleneoxy radical of C or a C? 8, and more preferably an alkyleneoxy radical of Ci to C8; Q ~ is a halide ion, preferably chloride; r is a statistical value. average from 2 to 20, preferably from 2 to 8; s is an average statistical value of 20 to 200, and preferably 20 to 50. A preferred polymer of this class is known as UCARE SILICONE ALE 56MR, available from Union Carbide.
iii. Silicone Gums Other optional silicone fluids suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are the insoluble silica sols. These gums are polyorganosiloxane materials that have a viscosity at 25 ° C greater than or equal to 1,000,000 centistokes. Silicone gums are described in U.S. Patent 4,152,416; Noli and Walter, Chemis try and Technology of Sili cones, New York; Academic Press (1968); and in the Data Sheets for the General Electric Silicone Rubber Product SE 30, SE 33, SE 54 and SE 76, all are incorporated herein by reference. The silicone gums will normally have a weight average molecular weight of about 200,000, preferably between about 200,000 and 1,000,000. Specific non-limiting examples of silicone gums suitable for use in the anti-dandruff shampoo and conditioner compositions of the present invention include polydimethylsiloxane, (polydimethylsiloxane) copolymer (methylalvinylsiloxane), poly (dimethylsiloxane) copolymer
(diphenylsiloxane) (methylalvinylsiloxane) and mixtures thereof.
iv. High Refractive Index Silicones Other insoluble, non-volatile silicone fluid conditioning agents which are suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are those known as "high refractive index silicones" having a high refractive index. refractive index of at least about 1.46, preferably at least about 1.48, more preferably at least about 1.52, more preferably at least about 1.55. The refractive index of the polysiloxane fluid in general will be less than 1.70, usually less than about 1.60. In this context, the polysiloxane "fluid" includes oils as well as gums. The polysiloxane fluid with high refractive index includes those represented by the above General Formula (III), as well as cyclic polysiloxanes, such as those represented by the following Formula (VIII):
wherein R is as defined in the above, n is between about 3 and 7, preferably from 3 to about 5. Polysiloxane fluids with high refractive index contain a sufficient amount of substituents R containing aryl to increase the refractive index to the desired level, which was described in the foregoing. In addition, R and n must be selected in such a way that the material is not volatile. Substituents containing aryl include those containing aryl rings of five and six alicyclic and heterocyclic members, and substituents containing rings of five or six fused members. The aryl rings by themselves may be substituted or unsubstituted. Substituents include aliphatic substituents and may include alkoxy substituents, acyl substituents, ketones and halogens (e.g., Cl and Br), amines, etc. Examples of aryl-containing groups include, but are not limited to: substituted and unsubstituted lobes, such as, for example, phenyl and phenyl derivatives, such as, for example, phenyls with C1-C5 alkyl or alkenyl substituents, for example, allylphenyl, methylphenyl and ethylphenyl, vinylphenyls (for example, styrenyl) and phenylalkynes (for example, C2-C4 phenylalkines). The heterocyclic aryl groups include, but are not limited to: substituents derived from furan, imidazole, pyrrole, pyridine, etc. Examples of fused aryl ring substituents include, but are not limited to: naphthalene, coumarin and purine. In general, polysiloxane fluids with high refractive index will have a degree of aryl-containing substituents of at least about 15%, preferably at least about 20%, more preferably at least about 25%, still more preferred at least about 35%, more preferably at least 50%. Normally, the degree of aryl substitution will be less than about 90%, more generally less than about 85%, preferably between about 55% and 80%.
Polysiloxane fluids with high refractive index are also characterized by relatively high surface tensions as a result of their aryl substitution. In general, the polysiloxane fluids will have a surface tension of at least about 24 dynes / cm2, typically at least about 27 dynes / cm2. The surface tension, for the purposes of the present, is measured by a Nouy ring tensiometer according to Dow Corning Test Method Corporate CTM 0461 (November 23, 1971). The changes in surface tension can be measured according to the above test method or in accordance with ASTM Method D 1331. Preferred high refractive index polysiloxane fluids have a combination of phenyl or phenyl derivative substituents (preferably phenyl), with alkyl substituents, preferably C 1 -C 4 alkyl (most preferably methyl), hydroxy, or C 1 -C 4 alkylamino (especially -R 1 NH 2 NH 2, wherein each R 1 and R 2 independently is an alkyl, alkenyl and / or C? -C3 alkoxy). High refractive index polysiloxanes are available from Dow Corning, Huís America and General Electric.
When silicones with high refractive index are used in the antidandruff shampoo and conditioner compositions of the present invention, they are preferably used with an extension agent, such as a silicone resin or a surfactant, to reduce stress surface in an amount sufficient to improve the extension and, thus, improve the luster (after drying) of the hair treated with the composition. In general, an amount of the extension agent is used which is sufficient to reduce the surface tension of the high refractive index polysiloxane fluid by at least about 5%, preferably at least about 10%, most preferably at least about 15% even more preferably at least about 20%, with the highest preference, of at least about 25%. Reductions in the surface tension of the polysiloxane fluid / spreading agent mixture can provide an improvement in the enhancement of hair shine. Also, the extension agent preferably will reduce the surface tension by at least about 2 dynes / cm2, preferably by at least about 3 dynes / cm2, still more preferably at least about 4 dynes / cm2, and with the greatest preference, in at least about 5 dynes / cm2. The surface tension of the polysiloxane fluid mixture and the extension agent, at the proportions present in the final product, is preferably less than or equal to 30 dynes / cm 2, more preferably less than or equal to about 28 dynes / cm 2, most preferably less than or equal to approximately 25 dynes / cm2. Normally, the surface tension will be in the range of between about 15 dynes / cm2 and 30 dynes / cm2, more typically between about 18 dynes / cm2 and 28 dynes / cm2, and more generally between about 20 dynes / cm2 and 25 dynes / cm2. The weight ratio of the highly spun polysiloxane fluid to the spreading agent in general will be between about 1000: 1 and 1: 1, preferably between about 100: 1 and 2: 1, more preferably between about 50: 1 and 2: 1 and most preferably between about 25: 1 and 2: 1. When fluorinated surfactants are used, the proportions of polysiloxane fluid to particularly high extension agent can be effective due to the efficiency of these surfactants. Thus, it is contemplated that proportions significantly greater than 1000: 1 may be used. Suitable silicone fluids for use in the anti-dandruff and conditioning shampoo compositions of the present invention are set forth in U.S. Patent No. 2,826,551, U.S. Patent No. 3,964,500, U.S. Pat. No. 4,364,837, British Patent 849,433 and Si li with Compo unds, Petrarch Systems, Inc. (1984), all of which are incorporated herein by reference.
v. Silicone resins Silicone resins may be included in the silicone conditioning agent. These resins are highly crosslinked polymeric siloxane systems. Crosslinking is introduced through the incorporation of trifunctional and tetrafunctional silanes with monofunctional or difunctional silanes, or both, during the manufacture of the silicone resin. As is clear to one of ordinary skill in the art, the degree of crosslinking that is required in order to result in a silicone resin will vary according to the specific silane units that are incorporated in the silicone resin. In general, silicone materials having a sufficient level of trifunctional and tetrafunctional siloxane monomer units (and, therefore, a sufficient level of crosslinking) so that they dry to form a rigid or hard film, are considered as resins of sylicon. The ratio of oxygen atoms to silicon atoms is indicative of the level of crosslinking in a particular silicone material. Silicone resins suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention will generally have at least about 1.1 oxygen atoms for each silicon atom. Preferably, the ratio between oxygen atoms: silicon is at least about 1.2: 1.0. Silanes in the manufacture of silicone resins include, but are not limited to: monomethyl-, dimethyl-, trimethyl-, monophenyl-, diphenyl-, methylphenyl-, monovinyl- and methylvinyl-chlorosilanes and tetrachlorosilane, where the methylated silanes are the which are most commonly used. Preferred resins are available from General Electric as GE SS4230 and SS4267. Commercially available silicone resins will generally be supplied in a form dissolved in a volatile or non-volatile, low viscosity silicone fluid. The silicone resins for use herein should be provided and incorporated into the compositions herein in dissolved form, as will be readily apparent to those skilled in the art. Silicone materials and silicone resins, in particular, can be conveniently identified according to an abbreviated nomenclature system well known to those skilled in the art such as the "MDTQ" nomenclature. In this system, the silicone is described according to the presence of several monomeric siloxane units that form the silicone. In summary, the symbol M denotes the monofunctional unit (CH3) 3SiO0.5; D denotes the difunctional unit (CH3) 2SiO; T denotes the trifunctional unit (CH3) SiO? .s; and Q denotes the quadri or tetrafunctional unit Si02. The bonus signs in the unit symbols (for example, M ', D', T 'and Q') denote substituents other than methyl and must be specifically defined each time they are present. Typical alternating substituents include groups such as vinyl, phenyl, amino, hydroxyl, etc. The molar proportions of the different units, either in terms of subscripts in the symbols that indicate the total number of each type of units in the silicone (or an average thereof) or as specifically indicated proportions in combination with the molecular weight, complete the description of the silicone material with the MDTQ system. The high relative molar amounts of T, Q, T 'and / or Q' relative to D, D 'M and / or M' in a silicone resin are indicative of high levels of crosslinking. However, as discussed above, the general level of crosslinking can also be indicated by the oxygen to silicon ratio. Suitable silicone resins for use in the anti-dandruff and conditioning shampoo compositions of the present invention include, but are not limited to: MQ, MT, MTQ, MQ and MDTQ resins. The preferred silicone substituent is methyl. Especially preferred silicone resins are MQ resins, wherein the M: Q ratio is between about 0.5: 1.0 and 1.5: 1.0 and the average molecular weight of the silicone resin is between about 1000 and 10,000. The weight ratio of the non-volatile silicone fluid having a refractive index of less than 1.46, to the silicone resin component, when used, is preferably between about 4: 1 and 400: 1, more preferably between about 9: 1 and 200: 1, most preferably between about 19: 1 and 100: 1, particularly when the silicone fluid component is a polydi-ethylsiloxane fluid or a mixture of polydimethylsiloxane fluid and polydimethylsiloxane gum , as described above. So far, the silicone resin forms part of the same phase in the compositions thereof as the silicone fluid, ie, the active conditioner, the sum of the fluid and the resin must be included in the determination of the level of the conditioning agent of the silicone. silicone of the composition.
2. Organic Conditioning Oils The conditioning component of the anti-dandruff and conditioning shampoo compositions of the present invention can also comprise between about 0.05% and 3% by weight of the composition, preferably between about 0.08% and 1.5%, most preferably between about 0.1% and 1%, of at least one organic conditioning oil as the conditioning agent, either alone or in combination with other conditioning agents, such as, for example, silicones (described above). It is believed that these organic conditioning oils provide the shampoo composition with improved conditioning performance when used in combination with the essential components of the composition, and in particular when used in combination with cationic polymers (described below). Conditioner oils can be added to give luster and shine to hair. Additionally, they can improve dry brushing and dry hair feeling. It is believed that most of all these organic conditioning oils are solubilized in the shampoos of the surfactant of the shampoo composition. It is also believed that this solubilization in the micelles of the surfactant contributes to the improved hair conditioning performance of the shampoo compositions herein. Organic conditioning oils suitable for use as the conditioning agent herein are preferably water-insoluble, low-viscosity liquids selected from hydrocarbon oils, polyolefins, fatty esters and mixtures thereof. The viscosity, as measured at 40 ° C, of these organic conditioning oils is preferably between about 1 centipoise and 200 centipoise, more preferably between about 1 centipoise and 100 centipoise, most preferably between about 2 centipoise and 50 centipoise. centipoises
i. Hydrocarbon Oils Organic conditioning oils suitable for use as conditioning agents in the anti-dandruff and conditioning shampoo compositions of the present invention include, but are not limited to, hydrocarbon oils having at least about 10 carbon atoms, such as, for example, cyclic hydrocarbons. , straight chain aliphatic hydrocarbons (saturated or unsaturated), and branched chain aliphatic hydrocarbons
(saturated or unsaturated), which include polymers and mixtures thereof. The straight chain hydrocarbon oils, preference is between about Ci2 and C? 9. Branched chain hydrocarbon oils, which include hydrocarbon polymers, will normally contain more than 19 carbon atoms. Specific non-limiting examples of these hydrocarbon oils include paraffin oil, mineral oil, saturated and unsaturated dodecane, saturated and unsaturated tridecane, saturated and unsaturated tetradecane, saturated and unsaturated pentadeca, saturated and unsaturated hexadecane, polybutene, polydecene, and mixtures thereof. same. Branched-chain isomers of these compounds can also be used, as well as of larger chain length hydrocarbons, examples of which include saturated or unsaturated, highly branched alkanes, such as, for example, the isomers substituted with permethyl, for example , the isomers of hexadecane and eicosane substituted with permethyl, such as for example, 2,2,4,4,6,6,8,8-dimethyl-10-methylundecane and
2, 2, 4, 4, 6, 6-dimethyl-8-methannonnon, available from Permethyl Corporation. The hydrocarbon polymers such as, for example, polybutene and polydecene. A preferred hydrocarbon polymer is polybutene, such as, for example, the copolymer of isobutylene and butene. A commercially available material of this type is polybutene L-14 from Amoco Chemical Corporation.
ii. Polyolefins Organic conditioning oils for use in the anti-dandruff and conditioning shampoo compositions of the present invention may also include liquid polyolefins, more preferably liquid poly-α-olefins, most preferably hydrogenated liquid poly-α-olefins. The polyolefins to be used herein are prepared by the polymerization olefinic monomers of between C4 and C4, preferably of between about e and C2. Non-limiting examples of olefinic monomers for use in the preparation of the polyolefin liquids herein include ethylene, propylene, 1-butene, 1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1- tetradecene, branched chain isomers such as, for example, 4-methyl-1-pentene, and mixtures thereof. Olefin-containing refinery feedstocks or effluents are also suitable for preparing polyolefin liquids. Preferred hydrogenated α-olefin monomers include, but are not limited to: 1-hexene for 1-hexadecenes, 1-octene for 1-tetradecene, and mixtures thereof.
iii. Fatty esters Other organic conditioning oils suitable for use as the conditioning agent in the anti-dandruff and conditioning shampoo compositions of the present invention include, but are not limited to, fatty esters having at least 10 carbon atoms. These fatty esters include esters with hydrocarbyl chains derived from fatty acids or alcohols (eg, mono-esters, polyhydric alcohol esters, and di- and tri-carboxylic acid esters). The hydrocarbyl radicals of the fatty esters thereof may include or have covalently bonded thereto other compatible functional groups, such as, for example, amides and alkoxy entities (eg, ethoxy or ether bonds, etc.). Suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are alkyl and alkenyl esters of fatty acids having from about C 6 and C 2 aliphatic chains, and alkyl and alkenyl esters of fatty alcohol carboxylic acid having an aliphatic chain derived from C and C22 alkyl and / or alkenyl alcohol, and mixtures thereof. Specific examples of preferred fatty esters include, but are not limited to, isopropyl isostearate, hexyl laurate, isohexyl laurate, isohexyl palmitate, isopropyl palmitate, decyl oleate, isodecyl oleate, hexadecyl stearate, decyl stearate, isopropyl isostearate. , dihexyldecyl adipate, lauryl lactate, myristyl lactate, cetyl lactate, oleyl stearate, oleyl oleate, oleyl myristate, lauryl acetate, cetyl propionate and oleyl adipate. Other fatty esters suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are esters of the monocarboxylic acid of the general formula R'COOR, wherein R 'and R are alkyl or alkenyl radicals, and the sum of the atoms of carbon in R 'and R is at least 10, preferably at least 20. The monocarboxylic acid ester need not necessarily contain at least one chain with at least 10 carbon atoms; instead, the total number of carbon atoms of the aliphatic chain must be at least 10. Specific non-limiting examples of monocarboxylic acid esters include: isopropyl myristate, glycol stearate and isopropyl laurate. Still other fatty esters suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are di- and tri-alkyl and alkenyl esters of carboxylic acids, such as, for example, esters of carboxylic acids of C4 to C8 (e.g. Ci a Cío esters, preferably Ci ae, succinic acid, glutaric acid, adipic acid, hexanoic acid, heptanoic acid and octanoic acid). Specific non-limiting examples of di- and tri-alkyl and alkenyl esters of carboxylic acids include isocetyl stearoyl stearate, diisopropyl adipate and triestearyl citrate. Other fatty esters suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are those known as polyhydric alcohol esters. These polyhydric alcohol esters include alkylene glycol esters, such as, for example, esters of mono- and di-fatty acid of ethylene glycol, esters of mono- and di-fatty acid of diethylene glycol, esters of mono- and di-fatty acid of polyethylene glycol, esters of propylene glycol mono- and di-fatty acid, polypropylene glycol monooleate, polypropylene glycol monostearate 2000, ethoxylated propylene glycol monostearate, glyceryl mono and digraso acid esters, polyglycerol poly fatty acid esters, ethoxylated glyceryl monostearate, mono-stearate 1, 3-butylene glycol, 1,3-butylene glycol distearate, fatty acid ester and polyoxyethylenepolyol, fatty acid and sorbitan esters, and polyoxyethylene sorbitan fatty acid esters. Still other fatty esters suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are glycerides, among which are included, namely, mono-, di- and t-glycerides, preferably di- and t-glycerides, most preferably triglycerides. For use in the shampoo compositions described herein, the glycerides are preferably the mono-, di-, and tri-esters of glycerol and long chain carboxylic acids, such as, for example, carboxylic acids from Cío to C2.2- A variety of these types of materials can be obtained from vegetable and animal fats and oils, such as, for example, castor oil, safflower oil, cottonseed oil, corn oil, olive oil, cod liver oil. , almond oil, avocado oil, palm oil, sesame oil, lanolin oil and soy. Synthetic oils include, but are not limited to: triolein dilaurate and tristearin. Other fatty esters suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are synthetic water-insoluble fatty esters. Some preferred synthetic esters are in accordance with the general Formula (IX):
wherein R1 is an alkyl, alkenyl, hydroxyalkyl or hydroxyalkenyl group of C to Cg, preferably a saturated alkyl group, more preferably a saturated linear alkyl group; n is a positive integer that has a value of 2 to 4, preferably 3; and Y is an alkyl, alkenyl, alkyl or alkenyl substituted with hydroxy or carboxy, having between about 2 and 20 carbon atoms, preferably between about 3 and 14 carbon atoms. Other preferred synthetic esters are in accordance with the general Formula (X):
wherein R2 is an alkyl, alkenyl, hydroxyalkyl or hydroxyalkenyl group of C8 to Cio; preferably a saturated alkyl group, more preferably a linear, saturated alkyl group; n and Y are as previously defined in the Formula
(X) It is believed that the preferred synthetic esters provide an improved wet hair feel when used in combination with the essential components of the shampoo compositions of the present invention, particularly when used in combination with the cationic polymer component (described below). ). These synthetic esters improve the feeling of wet hair by reducing the viscosity or feeling of excessively conditioned hair that has been conditioned by a cationic polymer. Specific non-limiting examples of synthetic fatty esters for use in the anti-dandruff and conditioning shampoo compositions of the present invention include: P-43 (C 8 -C 10 trimethylolpropane triester), MCP-684 (3,3-dietanol-tetra-ester) 1,5 pentadiol), MCP 121 (C 8 -C 6 adipic acid diester), all are available from Mobil Chemical Company.
3. Other conditioning agents also suitable for use in the compositions herein are the conditioning agents described by The Procter & Gamble Company in U.S. Patent Nos. 5,674,478 and 5,750,122, both of which are hereby incorporated by reference in their entirety. Also suitable for use herein are those conditioning agents described in U.S. Patent Nos. 4,529,586 (Clairol), 4,507,280 (Clairol), 4,663,158 (Clairol), 4,197,865 (L'Oreal), 4,217,914 (L'Oreal), 4,381,919 (L'Oreal) and 4,422,853 (L'Oreal), all descriptions are incorporated herein by reference.
Some other preferred silicone conditioning agents for use in the compositions of the present invention include: Abil® 201 (dimethicone / PG-propi copolymer Idimeton sodium thiosulfate), available from Goldschmidt; DC Q2-8220 (trimethylsilyl amodimetone) available from Dow Corning; DC 949 (amodimethicone, cetrimonium chloride and Tridoceth-12), available from Dow Corning; DC 749 (cyclomethicone and rimet ilsiloxysilicate), available from Dow Corning; DC2502 (cetyl dimethicone), available from Dow Corning; BC97 / 004 and BC 99/088 (silicone microemulsions with amino functional group), available from Basildon Chemicals; GE 'SME253 and SM2115-D2 and SM2658 and SF1708 (silicone microemulsions with amino functional group), available from General Electric; siliconized salvia seed oil, available from Croda; and those silicone conditioning agents described by GAF Corp. in U.S. Patent No. 4,834,767 (quaternized amino lactam), by Biosil Technologies in U.S. Patent No. 5,854,319 (reactive silicone emulsions containing amino acids) and by Dow Corning in U.S. Patent No. 4,898,585 (polysiloxanes), all descriptions are incorporated herein by reference.
C. Anti-Dandruff Particulate The anti-dandruff and conditioning shampoo compositions of the present invention comprise between about 0.1% and 4% by weight of the composition, preferably between about 0.1% and 3%, most preferably between about 0.3% and 2%. %, of an antidandruff particulate suitable for application to hair or skin. The anti-dandruff particulate must be physically and chemically compatible with the essential components of the composition and should not otherwise unduly damage the stability, aesthetics or performance of the product.
1. Pyridintion salts Pyridinthione anti-dandruff particulates, especially l-hydroxy-2-pyridinthione salts, are fairly preferred particulate antidandruff agents for use in the anti-dandruff and conditioning shampoo compositions of the present invention. The concentration of the pyridinethione anti-dandruff particulate normally varies between about 0.1% and 4% by weight of the composition, preferably between about 0.1% and 3%, most preferably between about 0.3% and 2%. The pyridinethion salts include those formed of heavy metals such as for example zinc, tin, cadmium, magnesium, aluminum and zirconium, preferably zinc, more preferably the zinc salt of l-hydroxy-2-pyridinethione (known as " zinc pyridinethione "or" ZPT "), most preferably salts of l-hydroxy-2-pyridin-ione in particle form in platelet, wherein the particles have an average size of up to about 20μ, preferably up to about 5μ , most preferably up to about 2.5μ. The salts formed from other cations, such as, for example, sodium, may also be suitable. Anti-dandruff pyridinone agents are described, for example, in U.S. Patent No. 2,809,971; U.S. Patent No. 3,236,733; U.S. Patent No. 3,753,196; U.S. Patent No. 3,761,418; U.S. Patent No. 4,345,080; U.S. Patent No. 4,323,683; U.S. Patent No. 4,379,753; and U.S. Patent No. 4,470,982, all are incorporated herein by reference. It is contemplated that when ZPT is used as the anti-dandruff particulate in the shampoo compositions herein, that hair growth or regeneration can be stimulated or regulated, or both, or that hair loss can be reduced or inhibited, or that The hair may appear thicker or with more volume.
2. Selenium sulfide Selenium sulfide is a particulate antidandruff agent suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention, effective concentrations thereof ranging from about 0.1% to 4% by weight of the composition, preferably between about 0.3% and 2.5%, more preferably between about 0.5% and 1.5%. Selenium sulfide is generally taken into consideration as a compound having one mole of selenium and two moles of sulfur, although it can also be a cyclic structure which is in accordance with the general formula SexSy, where x + y = 8. Average particle diameters for selenium sulfide are usually less than 15 μm, as measured by direct laser light scattering device (eg, Malvern 3600 instrument), preferably less than 10 μm. Selenium sulfide compounds are described, for example, in U.S. Patent No. 2,694,668; U.S. Patent No. 3,152,046; U.S. Patent No. 4,089,945; and U.S. Patent No. 4,885,107, all descriptions are incorporated herein by reference.
3. Sulfur Sulfur can also be used as the particulate antidandruff agent in the anti-dandruff and conditioning shampoo compositions of the present invention. Effective concentrations of the particulate sulfur are usually between about 1% and 4% by weight of the composition, preferably between about 2% and 4%.
D. Cationic Guar Derivatives The antidandruff shampoo and conditioner compositions of the present invention comprise between about 0.02% and 5% by weight of the composition, preferably between about 0.05% and 3%, most preferably between about 0.1% and 1.5%, most preferably between about 0.5% and 1%, of a cationic guar suitable for application to hair or skin. It is believed that guars provide an anti-dandruff efficacy and enhanced conditioning for the shampoo compositions described herein. These cationic guars must be physically and chemically compatible with the essential components described herein and should not otherwise unduly damage the stability, aesthetics or performance of the product.
1. Characteristics of the cationic guars The cationic guars useful in the present invention should be selected and should be present at a level such that the cationic polymers are soluble in the shampoo composition and that they are preferably soluble in a complex coacervate phase in the composition. of shampoo, at the time of dilution. This coacervate is described in detail later. The physical properties of cationic guars and suitable counterions are also detailed.
i. Coacervate ormado from the cationic polymer At the time of dilution of the shampoo composition, a coacervate is formed between the cationic polymer and the anionic detergent surfactant component (described above) of the present invention. It is believed that the cationic entity of the polymers binds with the cationic entity of the surfactant to form an insoluble complex that precipitates at the time of dilution (the coacervate). Complex coacervates of the cationic polymer can also be formed with other optional anionic components of the shampoo composition (described below). The formation of the coacervate depends on a variety of criteria, such as, for example, molecular weight, concentration of the component and proportion of the ionic interacting components, ionic strength (which includes the modification of the ionic strength, for example, by the addition of salts ), charge density of cationic and anionic components, pH and temperature. Coacervate systems and the effect of these parameters have been described, for example, in J. Caelles, et al., "Anionic and Cationic Compounds in Mixed Systems", Cosm e ti cs & Toi l e tri es, vol. 106, (April 1991), pp. 49-54; C. J. van Oss, "Coacervation, Complex-Coacervation and
Flocculation ", J. Di spersi on Sci en ce an d Tech., Vol.9 (5.6), (1988-89), pp 561-73, and in DJ Burgess," Practical Analysis of Complex Coacervate Systems ", J. of Coll oid and Infa ce Science, Vol 140, No. 1, (November 1990), pp 227-38, all descriptions are incorporated herein by reference The shampoo compositions described herein , usually have a proportion of an anionic detergent surfactant component for the cationic polymer component of between about 25: 0.02 and 1: 1, preferably between about 20: 0.1 and 12: 1. It is believed that coacervates provide conditioning benefits , especially conditioning benefits during the use of the product when the hair is wet, by helping to deposit the conditioning agents on the hair and scalp It is also known in the art that coacervates aid in the deposition of other types of particulates It is known that or it occurs when concentrating the particulates within the limits of the coacervate at the time of dilution. It has also been found that the characteristics of the polymer in these compositions can affect the bioavailability / range of the anti-capping particulates, these characteristics include molecular weight and charge density of the cationic guar polymer. Guar with low molecular weight are preferred, guar with low charge density are preferred. Guar with low molecular weight and low charge density are quite preferred. It is believed that these select guars impart modified physical properties (ie, rheology) to the formed coacervates. Applicants have found that the characteristics of the polymer in these compositions can affect the bioavailability / range of the antidandruff particulates, these characteristics include molecular weight and charge density of the cationic guar polymer. Guar with low molecular weight are preferred, guar with low charge density are preferred. Guar with low molecular weight and low charge density are quite preferred. It is believed that these select guars impart modified physical properties (ie, rheology) to the formed coacervates. These differences in physical properties are assumed to affect bioavailability / range. The techniques for analyzing the formation of complex coacervates are known in this field. For example, microscopic analyzes of the shampoo compositions, at any selected dilution step, can be used to identify a coacervate phase has been formed. This coacervate phase can be identified as an additional emulsified phase in the composition. The use of dyes can be used to distinguish the coacervate phase from other insoluble phases dispersed in the shampoo composition.
11 Physical properties of cationic guar The average molecular weight of suitable cationic conditioning agents for use herein is usually between about
,000 and 10,000,000, preferably between about 50,000 and 2,000,000, more preferably between about 50,000 and 1,500,000, more preferably between about 50,000 and 700,000, most preferably between about 50,000 and 400,000, most preferably between about 100,000 and 400,000. Guar have a cationic charge density typically between about 0.05 meq / g and 7 meq / g, as measured at the pH of the intended use of the shampoo composition, preferably between about 0.05meq / gm and 5meq / g, of greater preference of between about 0.05 meq / g and 2 meq / g, more preferably between about O.lmeq / g and l.Omeq / g, most preferably between about 0.3meq / g and l.Omeq / g. The pH of the intended use of the shampoo composition normally ranges from about pH 3 to pH 9, preferably from about pH 4 to pH 7.
iii. Counterions used to form the cationic guars Any anionic counterions can be used together with the cationic guars with the proviso that the cationic guars remain soluble in water, in the shampoo composition, or in a coacervate phase of the shampoo composition and with the condition that the counterions be physically and chemically compatible with the essential components of the shampoo composition or otherwise not unduly impair the performance, stability or aesthetics of the product. Non-limiting examples of these counterions include: halides (eg, chloride, fluoride, bromide, iodide), sulfate, methylisulfate, and mixtures thereof.
2. Types of cationic polymers Examples of cationic guars that can be suitably employed in shampoo compositions herein include, but are not limited to: cationic polysaccharides (eg, cationic guar). These cationic polymers are described in detail below.
i. Cationic polysaccharides The preferred cationic polymers for use in the anti-dandruff and conditioning shampoo compositions of the present invention are those known as cationic polysaccharides. Cationic polysaccharides are those polymers based on C5 to C6 sugars and derivatives that have been made cationic by grafting cationic entities into the polysaccharide structure and include homopolymers, copolymers, terpolymers, etc., of quaternary ammonium monomer units or substituted with cationic amine , optionally in combination with non-cation ionic monomers. The polysaccharides can be composed of one type of sugar or more than one type. The cationic amines may be primary, secondary, or tertiary amines (preferably secondary or tertiary), depending on the particular species and the selected pH of the shampoo composition. The monomers may be in straight chain or branched chain geometrical arrangements. All monomer units may have cationic nitrogen containing entities attached thereto, preferably some of the monomer units do not have these entities attached. Non-limiting examples of cationic polysaccharides are described in the CTFA Cosme t i c Ingredi on t Di c t i on a ry, 3a. ed., edited by Estrin, Crosley and Haynes, (The Cosmetic, Toiletry and Fragrance Association, Inc., Washington, DC (1982), the description is incorporated herein by reference.) Polysaccharide cationic polymers include cationic polymers with base in the galactomannan copolymer known as guar gum obtained from the guar bean endosperm.
b. Cationic Guar Derivatives Other cationic polysaccharide polymers suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention they are guar cationic polymers. Guar are derivatives of galactomannan gum (guar) substituted ionically. Guar gum for use in the preparation of these guar gum derivatives is normally obtained as a material that occurs in the nature of the guar plant seeds. The guar molecule itself is a branched straight-chain muran at regular intervals with single-member galactose units in alternative handy units. The mannose units are linked together by means of ß (1-4) glycosidic bonds. The galactose branching arises in the manner of a bond to (1-6). The cationic derivatives of guar gums are obtained by the reaction between the hydroxyl groups of the compounds of polygalactum mannan and reactive quaternary ammonium. The degree of substitution of the cationic groups on the guar structure should be sufficient to provide the necessary cationic charge density described above. Suitable quaternary ammonium compounds for use in the formation of the cationic guar polymers include those which are in accordance with the general Formula (XII):
wherein R1, R2 and R3 are methyl or ethyl groups; R4 is any epoxyalkyl group of the general Formula (XIII):
HjQ CH-R5- \ / O
or R4 is a halohydrin group of the general Formula (XIV):
wherein R is an alkylene of Ci to C3; X is chlorine or bromine and Z is an anion such as, for example, Cl ~, Br ",
I "or HS04". Guar cationic polymers (cationic guar gum derivatives) formed from the reagents described above are represented by the general Formula (XV):
where R is guar gum. Preferably, the guar cationic polymer is hydroxypropyltrimethylammonium guar chloride, which can be more specifically represented by the general formula (XVI):
Specific non-limiting examples of guar cationic polymers that are in accordance with Formula XVI include: Jaguar® C 13S, which has a cationic charge density of 0.8meq / g (available from Rhodia Company) and Jaguar C 17, which have a density cationic charge of 1.6meq / g (available from Rhodia Company). Other suitable guar cationic polymers include hydroxypropylated guar cationic derivatives. Still other suitable cationic polymers include etherified guar copolymers, some examples of which are described in U.S. Patent No. 3,958,581, the disclosure of which is incorporated herein by reference.
E. Water The antidandruff shampoo and conditioner compositions of the present invention comprise between about 20% and 94.75% by weight of the composition, preferably between about 50% and 94.75%, most preferably between about 60% and 85%, of water.
II. OPTIONAL COMPONENTS The anti-dandruff and conditioning shampoo compositions of the present invention may, in some embodiments, also comprise additional optional components known or otherwise effective for use in personal care hair care products. Additional surfactants, additional cationic polymers, suspending agents, polyalkylene glycols, hair growth regulating agents and other optional components are described in detail below.
A. Other Surfactants The anti-dandruff and conditioning shampoo compositions of the present invention may, in some embodiments, further comprise between about 0.5% and 25% by weight of the composition, preferably between about 1% and 20%, with the maximum preference of between about 1% and 10%, of a surfactant other than the anionic surfactants described above, suitable for application to hair or skin. These other optional surfactants should be chemically and physically compatible with the essential components of the shampoo composition and should not otherwise unduly damage the performance, aesthetics or stability of the product. The other suitable surfactants include, but are not limited to: amphoteric, zwitterionic, cationic, nonionic and mixtures thereof. Amphoteric detergent surfactants suitable for use herein include, but are not limited to, those surfactants broadly described as derivatives of secondary and tertiary aliphatic amines in which the aliphatic radical can be a straight or branched chain and wherein one of the aliphatic substituents contains between about 8 and 18 carbon atoms and one contains an anionic water solubilizing group such as, for example, carboxy, sulfonate, sulfate, phosphate, or phosphonate. Suitable zwitterionic detergent surfactants for use herein include, but are not limited to, those surfactants broadly described as derivatives of aliphatic, phosphonium and sulfonium quaternary ammonium compounds, in which the aliphatic radicals can be straight or branched chain and wherein one of the aliphatic substituents contain between about 8 and 18 carbon atoms and one contains an anionic group such as, for example, carboxy, sulfonate, sulfate, phosphate or phosphonate. The zwitterionic detergent surfactants are betaines. Cationic detergent surfactants for use herein include, but are not limited to, surfactants containing nitrogen entities with quaternary ammonium. Examples of suitable cationic surfactants are those corresponding to the general formula (XVIII):
wherein R 1 R2, R 3, and R 4 are independently selected from an aliphatic group of Ci to C 22, or an alkoxy, polyoxyalkylene, alkylamido, hydroxyalkyl, aryl or alkylaryl aromatic group, having up to 22 carbon atoms, preferably alkyl Ci to C22; and X is a salt-forming anion, such as those selected from halogen (e.g., chloride, bromide), acetate, citrate, lactate, glycolate, phosphate, nitrate, sulfate, and alkylsulfate radicals. The aliphatic groups may contain, in addition to the carbon and hydrogen atoms, ether linkages and other groups such as, for example, amino groups. The longer chain aliphatic groups (C? 2 and greater) may be saturated or unsaturated. Preferred cationic detergent surfactants are those which contain two long alkyl chains and two short alkyl chains or those which contain a long alkyl chain and three short alkyl chains. These long alkyl chains are preferably Ci2 to C22, more preferably C6 to C22. These short alkyl chains are preferably Ci to C3, more preferably Ci to C2. Suitable nonionic detergent surfactants for use herein include, but are not limited to, those compounds produced by the condensation of alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound, which may be aliphatic or aromatic alkyl in nature. . Non-limiting examples of other amphoteric, zwitterionic, cationic and non-ionic detergent surfactants suitable for use in the anti-dandruff and conditioning shampoo composition of the present invention are described in McCutcheon's, Em ul si fi ers and De t ergen ts, (1989), published by MC Pub. Co. and in U.S. Patent No. 2 2,, 443388,, 009911; U.S. Patent No. 2, 528, 37; U.S. Patent No. 2,658,072;; U.S. Patent No. 3, 155, 591; U.S. Patent No. 3,929,667; U.S. Patent No. 3,959,461;; U.S. Patent No. 4,387,090;; U.S. Patent No. 5, 104, 646; U.S. Patent 5,106,609;; and U.S. Patent No. 5,837,661, all descriptions are incorporated herein by reference.
B. Other types of cationic polymers The anti-dandruff and conditioning shampoo compositions of the present invention may, in some embodiments, also comprise cationic polymers other than the guar described above. Examples of cationic polymers that can be suitably employed in the shampoo compositions herein include, but are not limited to, cationic polysaccharides (e.g., cationic cellulose derivatives), copolymers of vinyl monomers, vinyl pyrrolidone copolymers, modified cationic proteins, and certain Quaternary polymer salts. These cationic polymers are described in detail below.
i. Cationic polysaccharides The preferred cationic polymers for use in the anti-dandruff and conditioning shampoo compositions of the present invention are those known as cationic polysaccharides. Cationic polysaccharides are those polymers based on C5 to C5 sugars and derivatives that have been made cationic by grafting cationic entities into the polysaccharide structure and include homopolymers, copolymers, terpolymers etc., quaternary ammonium or amine substituted monomer units. cationic, optionally in combination with non-cationic monomers. The polysaccharides can be composed of one type of sugar or more than one type. The cationic amines may be primary, secondary, or tertiary amines (preferably secondary or tertiary), depending on the particular species and the selected pH of the shampoo composition. The monomers may be in straight chain or branched chain geometrical arrangements. All monomeric units can have cationic nitrogen containing entities attached to them, preferably some of the monomer units do not have these entities attached. Non-limiting examples of cationic polysaccharides are described in the CTFA Cosmetic Ingredient Dictionary, 3a. ed., edited by Estrin, Crosley and Haynes, (The Cosmetic, Toiletry and Fragrance Association, Inc., Washington, DC (1982), the disclosure of which is incorporated herein by reference.) Polysaccharide cationic polymers include the following: celluloses cationic and hydroxyethylcelluloses; cationic starches and hydroxyalkyl starches; cationic polymers based on arabinose vegetable gums; cationic polymers derived from xylose polymers (such as those found in wool, straw, cottonseed pods and corn ears); cationic polymers derived from fucose polymers (such as those found as a component of cell walls in marine algae); cationic polymers derived from fructose polymers (such as Inulin, which is found in certain plants); cationic polymers based on sugars containing acid (such as galacturonic acid and glucuronic acid); cationic polymers based on amino sugars (such as galactosamine and glucosamine); cationic polymers based on 5 and 6 membered ring polyalcohols; cationic polymers based on galactose monomers (such as those found in gums and plant mucilages); and cationic polymers based on mannose monomers (such as those found in plants, yeasts and red algae), cationic celluloses and hydroxyethylcelluloses, cationic starches and hydroxyalkyl starches, cationic polymers based on guar gum, and mixtures thereof are preferred. .
to. Cationic Cellulose Derivatives Other suitable cationic polymers which are used in the anti-dandruff and conditioning shampoo compositions of the present invention are the cationic cellulose derivatives and cationic starch derivatives. These cationic polymers include those that conform to formula (XI):
wherein A is a residual group of anhydroglucose, (eg, a residual cellulose starch or anhydroglucose, R is an alkylene oxyalkylene, polyoxyalkylene or hydroxyalkylene group, or a combination thereof; R1, R2 and R3 are alkyl, aryl independent , alkylaryl, arylalkyl, alkoxyalkyl or alkoxyaryl, each group contains up to about 18 carbon atoms and the total number of carbon atoms of each cationic entity (ie, the sum of carbon atoms in R1, R2 and R3) is preferably of about 20 or less, and X is an anionic counterion as described above.The preferred cationic cellulose polymers include, but are not limited to, those polymers available from Amerchol Corporation and its polymer series Polymer JR and LR as hydroxyethyl cellulose salts that react with epoxide substituted with trimethyl ammonium, which is referenced in the industry (CTFA) as Polyquaternium 10 (for example, JR 30M®, onible from Amerchol Corporation). Polyquaternium 10 polymers preferred for use herein, typically have a charge density of between about 200,000 and 1,500,000. Another type of preferred cationic cellulose includes the polymeric quaternary ammonium salt of hydroxyethylcellulose which is reacted with lauryl dimethyl ammonium substituted epoxide, known in the industry (CTFA) as Polyquaternium 24, (for example, Polymer LM 200®, available from Amerchol Corporation). Also suitable for use herein are those cellulose copolymers containing quaternary nitrogen of hydroxyethylcellulose which is reacted with diallyldimethylammonium chloride, known in the industry (CTFA) as Polyquaternium 4 (for example, Celquat® H-100 available from National Starch Corporation). The quaternary nitrogen-containing cellulose ethers suitable for use herein are described in U.S. Patent No. 3,962,418, and still other copolymers of etherified cellulose, guar and starch for use herein are disclosed in the US Pat. United States No. 3,958,581, the two descriptions thereof are incorporated herein by reference.
ii. Vinyl monomer copolymers Other cationic polymers suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention are copolymers of vinyl monomers, having protonated cationic amine or quaternary ammonium functional groups, which are reacted with water soluble monomers . Non-limiting examples of these monomers include: acrylamide, methacrylamide, alkyl and dialkyl acrylamides, alkyl and dialkyl methacrylamides, alkyl acrylate, alkyl methacrylate, vinyl caprolactone, vinyl pyrrolidone, and mixtures thereof. The alkyl and dialkyl substituted monomers preferably have Ci to C alkyl groups? , more preferably alkyl groups of Ci to C3. Other suitable monomers include vinyl esters, vinyl alcohol (produced by the hydrolysis of polyvinyl acetate), maleic anhydride, propylene glycol, ethylene glycol and mixtures thereof.
1
The protonated amino cationic and quaternary ammonium monomers, for inclusion in the cationic polymers of the shampoo composition herein, include vinyl compounds substituted with dialkylaminoalkyl acrylate, dialkylaminoalkyl methacrylate, monoalkylaminoalkyl acrylate, monoalkylaminoalkyl methacrylate, trialkyl methacryloxyalkyl ammonium salt, trialkyl acryloxyalkyl ammonium, diallyl ammonium quaternary salts; and vinyl quaternary ammonium monomers having cationic rings containing nitrogen such as for example, quaternized pyridinium, imidazolium and pyrrolidones, such as, for example, alkyl vinyl imidazolium salts, alkyl vinyl pyridinium and alkyl vinyl pyrrolidone. The alkyl portions of these monomers are preferably lower alkyl such as, for example, C1-C3 alkyls. Amine-substituted vinyl monomers suitable for use herein include dialkylaminoalkyl acrylamide and dialkylaminoalkyl methacrylamide, wherein the alkyl groups are preferably hydrocarbyls from Ci to C, more preferably Ci to C3 alkyls.
iii. Vinyl pyrrolidone copolymers Other cationic polymers suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention include: salt copolymers of l-vinyl-2-pyrrolidone and 1-vinyl-3-methylimidazolium (e.g., chloride salt) , known in the industry (CTFA) as Polyquaternium 16 (for example, Luviquat® FC 370, available from BASF Wyandotte Corporation); copolymers of l-vinyl-2-pyrrolidone and dimethylaminoethyl methacrylate, known in the industry (CTFA) as Polyquaternium 11 (for example, Gafquat® 755N, available from ISP Corporation); cationic polymers containing diallyl quaternary ammonium, including, for example, dimethyl ilaldiallylammonium chloride homopolymer, known in the industry (CTFA) as Polyquaternium 6; copolymers of acrylamide and dimethyldiallylammonium chloride, known in the industry (CTFA) as Polyquaternium 7; and mineral acid salts of amino alkyl alkyls of homopolymers and copolymers of C3 to C5 carboxylic acids, such as those described in U.S. Patent No. 4,009,256, the disclosure of which is incorporated herein by reference.
iv. Modified Cationic Proteins and Quaternary Polymeric Salts Still other cationic polymers for use in the anti-dandruff and conditioning shampoo compositions of the present invention are modified cationic proteins, such as lauryldimonium hydroxypropyl collagen (eg, Croquat® L, available from Croda Corporation), keratin of hydrolyzed hair with hydroxypropyl cocodimony (for example, Croquat® HH, available from Croda Corporation). Other cationic polymers include the quaternary polymer salt prepared by the reaction of adipic acid and dimethylaminopropylamin, which is reacted with dichloroethyl ether, known in the industry (CTFA) as polyquaternium 2 (for example, Mirapol® AD-1, available from Rhodia) and the quaternary polymer salt prepared by the reaction of azelaic acid and dimethylaminopropyl ether, known in the industry (CTFA) as polyquaternium 18 (for example, Mirapol® AZ-1, available from Rhodia Corporation).
v. Additional cationic polymers Still other cationic polymers suitable for use herein are those of the Arquad® series of quaternary ammonium salts, available from Akzo Nobel. Other preferred cationic polymers for use herein include: Polymer KG30M (Polyquaternium 10 and quaternized cellulose), Incroquat® behenyl trimonium methosulfate (cetearyl alcohol and behentium methosulfate), available from Croda; Merquat® 5 (quaternary ammonium resin), available from Calgon; Gafquat series 440
(quaternized cationic copolymers), available from ISP; Akypoquat® 131, available from Kao; Saleare® SC 60 (quaternary ammonium resin), or Saleare® SC95 or SC96 (thickeners for cationic liquid dispersion), all available from Ciba; and Meadowquat® HG
(PEG-2-disalviamido-ylmonium methosulfate), available from Fanning.
C. Suspension Agent The anti-dandruff and conditioning shampoo compositions of the present invention can, in some embodiments, comprise between about 0.1% and 10% by weight of the composition, preferably between about 0.3% and 5%, of greater preferably between 0.3% and 2.5%, of a suitable suspending agent for application to hair or skin. It is believed that the suspending agent suspends the water-insoluble dispersed materials in the shampoo compositions. This suspension agent must be physically and chemically compatible with the essential components of the composition and should not otherwise unduly damage the stability, aesthetics or performance of the product. Examples of suspending agents that can be suitably employed in shampoo compositions herein include, but are not limited to: acyl derivatives, long chain amine oxides, xanthan gum, and mixtures thereof. These and other suitable suspending agents are described in greater detail below.
1. Acyl Derivatives and Long Chain Amine Oxides Acyl-derived suspension agents include but are not limited to: glyceryl esters, long chain hydrocarbyls, long chain esters of long chain fatty acids, long chain esters of alkanol chain amides long Another group of suitable suspending agent includes the long chain amine oxides. The acyl derivative and long chain amine oxide suspending agents are described in U.S. Patent No. 4,741,855, the disclosure of which is incorporated herein by reference. The acyl derivative suspension agents for use herein are glyceryl esters, which include ethylene glycol esters of Ci6 to C22 fatty acids. More preferred are ethylene glycol stearates, both mono- and di-stearate, more ethylene glycol di stearate containing less than about 7% of the monostearate is preferred. Also suitable for use in shampoo compositions of the present long chain hydrocarbyls include N, N-dihydrocarbyl benzoic acid and soluble salts thereof (for example Na, K) particularly tallow amido benzoic acid and N, N-di (hydrogenated) Ci6-C? 8 from this family, available from Stepan Company. Non-limiting examples of long chain esters of long chain fatty acids include: stearyl stearate and cetyl palmitate. Non-limiting examples of long chain esters of long chain alkanol amides include: stearamide diethanolamide ida stearate and stearamide monoethanolamide stearate. Non-limiting examples of long chain amine oxides suitable for use as suspending agents herein include alkyl (Ci6-C22) dimethyl amine oxides (for example, stearyl dimethyl amine oxide).
2. Xanthan gum Xanthan gum is also suitable as a suspending agent herein. The concentration of xanthan gum will normally vary between about 0.1% and 3% by weight of the composition, preferably between about 0.4% and 1.2%. The use of xanthan gum as a suspending agent in silicone-containing shampoo compositions is described, for example, in U.S. Patent No. 4,788,006, the disclosure of which is incorporated herein by reference. The combination of long chain acyl derivatives and xanthan gum can also be used as a suspending agent in shampoo compositions, as described in U.S. Patent No. 4,704,272, the disclosure of which is incorporated herein by reference. reference.
and. Other suspending agents Still other suspending agents suitable for use in the anti-dandruff and conditioning shampoo compositions of the present invention include carboxyvinyl polymers. Among these polymers, copolymers of acrylic acid crosslinked with polysilyl saccharose are preferred as described in U.S. Patent No. 2,798,053, the disclosure of which is incorporated herein by reference. Examples of these polymers include Carbopol 934, 940, 941 and 956, available from B.F. Goodrich Company. Other suitable suspending agents include primary amines having a fatty alkyl entity having at least about 16 carbon atoms (e.g., palmitamine and stearamine), and secondary amines having two fatty alkyl entities, each having less about 12 carbon atoms (eg, dipalmitoylamine and di (hydrogenated tallow) amine). Also suitable are the amide of di (hydrogenated tallow) phthalic acid and the crosslinked copolymer of maleic anhydride and methyl vinyl ether. Still other suitable suspending agents can be used in shampoo compositions, including those which can impart a gel-like viscosity to the composition, for example as water-soluble or colloidally water-soluble polymers similar to cellulose ethers (eg methylcellulose), hydroxybutyl methylcellulose, hydroxypropylcellulose, hydroxypropyl methylcellulose, hydroxyethyl ethylcellulose and hydroxyethylcellulose), guar gum, polyvinyl alcohol, polyvinyl pyrrolidone, hydroxypropyl guar gum, starch and starch derivatives and other thickeners, viscosity modifiers, gelling agents and mixtures thereof. A preferred viscosity modifier useful as a suspending agent is trihydroxystearin, (for example, Trixin RMR, available from Rheox Company).
D. Polyalkylene glycol The anti-dandruff and conditioning shampoo compositions of the present invention may, in some embodiments, further comprise between about 0.005% and 1.5% by weight of the composition, preferably between about 0.05% and 1%, of greater preference between about 0.1% and 0.5%, most preferably between about 0.1% and 0.3% polyalkylene glycols suitable for application to hair or skin. It is believed that the selected polyalkylene glycols provide performance for improved foam generation, ability to spread the improved shampoo and, importantly, improved anti-dandruff particulate efficiency for the compositions described herein. These polyalkylene glycols should be physically and chemically compatible with the essential components described herein and should not otherwise unduly damage the stability, aesthetics or performance of the product. It has been found that these polyalkylene glycols, when added to the shampoo compositions described herein, enhance the foam generation performance by providing a richer and denser foam generation and that correlates with consumer perception of the foam. performance conditioner for hair. It has also been found that, in those embodiments which contain silicone conditioning agents, the selected polyalkylene glycols can reduce the concentration of the anionic detergent surfactant necessary to provide hair cleansing. In these reduced surfactant compositions, the cleaning and conditioning performance for the hair is still good, while the performance for foam generation is intensified. Polyethylene glycols, for example, are known to be used in improving foam generation performance in cleaning compositions, as described in U.S. Patent No. 5,837,661, the disclosure of which is incorporated herein by reference. It has also been found that these selected polyalkylene glycols, when added to the silicone-containing shampoo composition, enhance the spreadability of the shampoo compositions in the hair. This spreading ability of the shampoo composition during the application also provides consumers with an improved performance conditioning perception. This particular performance is surprising from these selected polyalkylene glycols which are known as thickening agents and to the extent that these thickening agents could be expected to damage rather than enhance the spreadability of the shampoo compositions in the hair.
Polyalkylene glycols suitable for use in the shampoo compositions herein are characterized by the general Formula (XVII): H (OCH 2 CH) n OH
R wherein R is hydrogen, methyl and mixtures thereof, preferably hydrogen, and n is an integer having an average value of between about 1,500 and 120,000, preferably between about 1,500 and 50,000, more preferably between about 2,500 and 25,000 and most preferably between 3,500 and 15,000. When R is hydrogen, these materials are polymers of ethylene oxide, which are also known as polyethylene oxides. When R is methyl, these materials are polypropylene oxide polymers, which are also known as polypropylene glycols. When R is methyl, it is also understood that the various positional isomers of the resulting polymers may exist. Polyethylene glycols, polypropylene glycols and mixtures thereof are preferred for use herein.
Specific non-limiting examples of polyethylene glycol polymers for use in the antidandruff shampoo and conditioner compositions of the present invention include: PEG-2M, wherein R is hydrogen and n has an average value of about 2,000 (eg, Polyox WSR® N -10, available from Union Carbide); PEG-5M, wherein R is hydrogen and n has an average value of about 5,000 (for example, Polyox WSR® N-35 and Polyox WSR® N-80, both available from Union Carbide); PEG-7M wherein R is hydrogen and n has an average value of about 7,000 (for example, Polyox WSR® N-750 available from Union Carbide); PEG-9M wherein R is hydrogen and n has an average value of about 9,000 (for example, Polyox WSR® N-3333 available from Union Carbide); PEG-14M wherein R is hydrogen and n has an average value of about 14,000 (for example, Polyox WSR® N-3000 available from Union Carbide); PEG-23M wherein R is hydrogen and n has an average value of about 23,000 (for example, Polyox WSR® N-12k, available from Union Carbide); PEG-90M wherein R is hydrogen and n has an average value of about 90,000 (for example, Polyox WSR® 301, available from Union Carbide); and PEG-100M wherein R is hydrogen and n has an average value of about 100,000 (eg, Carbowax PEG 4600MR, available from Union Carbide). Preferred polyethylene glycols include PEG 7M, PEG 14M, PEG 25M, PEG 90M and mixtures thereof.
E. Hair Regulating Agents for Hair Growth The compositions herein may also optionally comprise, in addition to zinc pyrithione, other hair regrowing agents. These agents can be selected from a wide variety of molecules that can function in different ways to enhance the hair growth effects of a compound of the present invention. These optional agents, when present, are normally employed in the compositions herein at a level ranging from about 0.001% to 15%, preferably from about 0.1% to 10%, most preferably from about 0.5. % and 5% by weight of the composition. As used herein, the term "hair growth regulation" should be understood as including: stimulating hair growth and / or hair thickening; prevent, reduce, suspend and / or delay hair loss and / or hair thinning; increase the speed of hair growth; induce the formation of a greater number of strands of hair; increase the diameter of the strand of hair; lengthen the strand of hair; change the hair follicle from hair to terminal; convert the follicles from the telogen phase to the anagen phase (thereby increasing the total proportion of follicles in the anagen phase relative to the follicles in the telogen phase); treat alopecias; and any combination thereof. Vasodilators such as, for example, potassium channel agonists including, for example, minoxidil and minoxidil derivatives such as, for example, aminaxil and those described in U.S. Patent 3,382,247, U.S. Patent 5,756,092, issued the May 26, 1998, U.S. Patent 5,772,990, issued June 30, 1998, U.S. Patent 5,760,043, issued June 2, 1998; U.S. Patent 328,914, issued on June 12, 1998; July 1994, U.S. Patent 5,466,694, issued November 14, 1995, 5,438,058, granted August 1, 1995 and U.S. Patent 4,973,474, issued November 27, 1990, (all of which are incorporated herein by reference). incorporated herein by reference) and chromacalin and diazoxide can be used as optional hair growth regulating agents in the compositions herein. A suitable class of optional activity enhancer for use herein are the anti-androgens. Examples of suitable ant i-androgens may include, but are not limited to, 5-a-reductase inhibitors, such as, for example, finasteride and those described in U.S. Patent 5,516,779, issued May 14, 1996 (incorporated herein by reference). reference) and in Nnane et al, Cancer Research 58, "Effects of Some Novel Inhibitors of C17.20-Lyase and 5a-Reductase in Vi tro and in Vi ve and Their Potential Role in the Treatment of Prostate Cancer. cyproterone acetate, azelaic acid and its derivatives and those compounds described in U.S. Patent 5,480,913, issued January 2, 1996, flutamide and those described in U.S. Patent 5,411,981, issued May 2, 1995 , U.S. Patent 5,565,467, issued October 15, 1996 and U.S. Patent 4,910,226, issued March 20, 1990, all are incorporated herein by reference. of agents to regulate the growth of > optional hair types are immunosuppressants such as, for example, 1) cyclosporin and cyclosporin analogs including those described in U.S. Provisional Patent Application No. 60 / 122,925, Fulmer et al., "Method of Treating Hair Loss Using Non- Immunosuppress ive Compounds ", filed on March 5, 1999, incorporated herein by reference and 2) analogs of FK506 such as for example, those described in U.S. Provisional Patent Application No. 60 / 102,449, Mclver et al., "Heterocyclic 2-Substituted Ketoamides", filed on September 30, 1998, the United States provisional patent application No 60 / 102,448, Mclver et al., "2-Substituted Ketoamides", filed September 30, 1998, U.S. Provisional Patent Application No. 60 / 102,539, Mclver et al., "2-Subs ituted Heterocyclic Sulfonamides ", filed on September 30, 1998, U.S. Provisional Patent Application No. 60 / 102,458, Tiesman et al.," Method of Treating Hair Loss Using Ketoamides ", filed September 30, 1998 and U.S. Provisional Patent Application No. 60 / 102,437, Mclver et al., "Method of Treating Hair Loss Using Sulfonamides", filed September 30, 1998, all are incorporated herein by reference. Another suitable class of optional agents for regulating hair growth are antimicrobials such as, for example, selenium sulfide, ketoconazole, triclocarbide, triclosan, zinc pyrithione, itraconazole, Asian acid, hinokitiol, mipirocin and those described in EPA 0,680,745 (incorporated in the present as reference), clinacicin hydrochloride, benzoyl peroxide, benzyl peroxide and minocycline. Anti- inflammatories can also be incorporated into the compositions herein as an optional activity enhancer. Examples of suitable anti-inflammatories may include glucocorticoids such as, for example, hydrocortisone, mometasone furoate and predni solone, non-spheroidal anti-inflammatories including cyclooxygenase or lipoxygenase inhibitors such as, for example, those described in the patent. of the United States 5,756,092 and benzydamine, salicylic acid and those compounds described in EPA 0,770,399, published May 2, 1997, WO 94/06434, published March 31, 1994 and FR 2,268,523 published November 21, 1975, all they are incorporated herein by reference. Another suitable class of optional agents for regulating hair growth are thyroid hormones and derivatives and analogues thereof. Examples of thyroid hormones suitable for use herein may include triiodothythrine. Examples of thyroid hormone analogues which may be suitable for use herein include those described in U.S. Provisional Patent Application No. 60 / 136,996, Zhang et al., "Method of Treating Hair Loss", presented on June 1
1999, the provisional patent application of the
^ United States No. 60 / 137,024, Zhang et al., "Method of Treating Hair Loss Using Biphenyl Compounds", filed on June 1, 1999, the provisional patent application of the United States No.
60 / 137,022, Zhang et al., "Method of Treating Hair Loss Using Carboxyl Derivatives", filed June 1, 1999, U.S. Provisional Patent Application No. 60 / 137,023, Zhang et al. , "Method of Treating Hair Loss Using Sulfonyl Thyromimetic Compounds", filed on June 1, 1999, U.S. Provisional Patent Application No. 60 / 137,052, Youngquist et al., "Biaryl Compounds", filed on 1 June 1999, U.S. Provisional Patent Application No. 60 / 137,063, Youngquist et al., "Sulfur-Bridged Compounds", filed June 1, 1999 and the provisional patent application of the United States No. 60 / 136,958, Youngquist et al., "Substituted Biaril Ether Compounds", filed June 1, 1999. Prostaglandin agonists or antagonists may also be used as optional agents to regulate hair growth in the compositions herein. Suitable examples of prostaglandin agonists or antagonists include latanoprost and those described in WO 98/33497, Johnstone, published August 6, 1998, WO 95/11003, Stj ernschant z, published April 27, 1995, JP 97- 100091 and Ueno, JP 96-134242, Nakamura. Another class of optional agents for regulating hair growth for use herein are retinoids. Suitable retinoids may include isotret inoin, acitretin, tazarotene. Non-limiting examples of penetration intensifiers that can be used as optional agents to regulate hair growth in the present include, for example, 2-methyl propan-2-ol, propan-2-ol, ethyl-2-hydroxypropanoate, hexan-2,5-diol, POE (2) ethyl ether, di (2-hydroxypropyl) ether, pent an-2,4-diol, acetone, POE (2) methyl ether, 2-hydroxypropionic acid, 2-hydroxyoctonic acid, propan-l-ol, 1,4-dioxane, tetrahydrofuran, but an-1,4-diol, propylene glycol dipelargonate, polyoxypropylene stearyl ether 15, octyl alcohol, oleyl alcohol ester POE, oleyl alcohol, lauryl alcohol, dioctyl adipate , dicapril adipate, di-isopropyl adipate, di-isopropyl sebacate, dibutyl sebacate, diethyl sebacate, dimethyl sebacate, dioctyl sebacate, dibutyl suberate, dioctyl azelate, dibenzyl sebacate, dibutyl phthalate, dibutyl azelate, ethyl myristate, dimethyl azelate, butyl myristate, dibutyl succinate, didecyl phthalate, decyl oleate, ethyl caproate to, ethyl salicylate, iso-propyl palmitate, ethyl laurate, 2-ethyl-hexyl pelargonate, isopropyl isostearate, butyl laurate, benzyl benzoate, butyl benzoate, hexyl laurate, ethyl caprate, ethyl caprylate, butyl stearate, benzyl salicylate, acid 2-hydroxypropanoic acid, 2-hydroxyoctanoic acid, methylsulfoxide, N, N-dimethyl acetamide, N, N-dimethyl formamide, 2-pyrrolidone, 1-metyl-2-pyrrolidone, 5-yl-2-pyrrolidone, 1, 5 -dimethyl-2-pyrrolidone, 1-ethyl-2-pyrrolidone, phosphine oxides, sugar esters, tetrahydrofurfuronic alcohol, urea, diethyl-ffi-toluamide ", 1-dodecyl-zacyloheptan-2 -one and those described in the patent of the United States 5,015,470, issued May 14, 1991 and United States Patent 5,496,827, issued July 15, 1994 (both are hereby incorporated by reference in their entirety). Other classes of optional agents for regulating hair growth for use herein include flavinoids, ascomycin derivatives and analogues, histamine antagonists such as, for example, diphenhydramine hydrochloride, other triterpenes such as, for example, oleanolic acid and ursolic acid and those described in U.S. Patent 5,529,769, JP 10017431, WO 95/35103, U.S. Patent 5,468,888. JP 09067253, WO 92/09262, JP 62093215, U.S. Patent 5,631,282, U.S. Patent 5,679,705, JP 08193094, Saponins such as, for example, those described in EP 0,558,509 to Bonte et al, published on September 8, 1993 and WO 97/01346 of Bonte et al, published on January 16, 1997 (both are hereby incorporated by reference in their entirety), proeoglycanase or glycosaminoglycanase inhibitors such as, for example, those described in the US Pat. No. 5,015,470, issued May 14, 1991, United States Patent 5,300,284, issued April 5, 1994, and United States Patent 5,185,325, issued February 9, 1993 (all are incorporated herein by reference). whole as reference) estrogen agonists and antagonists, pseudoterines, cytokines and growth factor promoters, analogs or inhibitors such as, for example, interleukin inhibitors, interleukin-6 inhibitors, pro interleukin-10 motors and tumor necrosis factor inhibitors, vitamins such as, for example, vitamin D analogues and parathyroid hormone antagonists, Vitamin B12 analogs and panthenol, interfuagonists and antagonists, hydroxy acids such as for example , those described in U.S. Patent 5,550,158, benzophenones and hydantoin anticonvulsants such as, for example, phenytoin. Other agents for hair growth are described in detail in, for example, JP 09-157,139 of Tsuji et al, published on June 17, 1997.; EP 0277455 Al de Mirabeau, published on August 10, 1988; WO 97/05887 of Cabo Soler et al, published on February 20, 1997; WO 92/16186 to Bonte et al, published March 13, 1992; JP 62-93215 of Okazaki et al, published April 28, 1987; U.S. Patent 4,987,150 to Kurono et al, issued January 22, 1991, JP 290811 to Ohba et al, published October 15, 1992; JP 05-286,835 of Tanaka et al, published on November 2, 1993, FR 2,723,313 of Greff, published on August 2, 1994, the United States patent of Gibson, granted on May 14, 1991, the patent of United States 5,559,092, issued September 24, 1996, United States Patent 5,536,751, issued July 16, 1996, United States Patent 5,714,515, issued February 3, 1998, EPA 0,319,991, published on June 14, 1989, EPA 0,357,630, published October 6, 1988, EPA 0,573,253, published December 8, 1993, JP 61-260010, published November 18, 1986, United States Patent 5,772,990, issued on June 30, 1998, U.S. Patent 5,053,410, issued October 1, 1991, and U.S. Patent 4,761,401, issued August 2, 1988, are all incorporated herein by reference. Some preferred agents for regulating hair growth for use herein are zinc salts of carboxylic acids, saponins, triterpenes, oleanolic acid, ursolic acid, betulinic acid, betulonic acid, crataegolic acid, celastrol, asian acid, 5- a-reduct asa, progesterone, l, 4-methyl-4-azasteroids, 17-ß-N, N-diethylcarbamoyl-4-methyl-4-aza-5-a-andros tan-3-one, receptor antagonists of androgen, cyproterone acetate, minoxidil, azelaic acid and derivatives thereof, cyclosporin, triiodothyronine, diazoxide, potassium channel openers, chromacalin, phenytoin, ketoconazole, finasteride, dutasteride, coal tar, zinc gluconate, glucocortisoids, macrolides, aminaxyl and mixtures thereof.
F. Other Optional Ingredients The anti-dandruff and conditioning shampoo compositions of the present invention may, in some embodiments, also comprise additional optional components known or otherwise effective for use in hair care or personal care products. The concentration of these optional ingredients generally ranges from zero to about 25%, more typically from about 0.05% to 25%, still more typically from about 0.1% to 15% by weight of the composition. These optional components must also be physically and chemically compatible with the essential components described herein and should not otherwise unduly damage the stability, aesthetics or performance of the product. Non-limiting examples of optional components for use in the shampoo composition include anti-static agents, foam boosters, soluble antidandruff agents, viscosity adjusting agents and thickeners, pH adjusting agents (eg, sodium citrate) , citric acid, succinic acid, phosphoric acid, sodium hydroxide and sodium carbonate), preservatives (for example DMDM hydantoin), ant i-microbial agents (eg, triclosan or triclocarbide), dyes, organic solvents or diluents, auxiliaries pearls, perfumes, fatty alcohols, proteins, active agents for the skin, sunscreens, vitamins and pediculocides. Optional optional anti-static agents such as, for example, water insoluble cationic surfactants, typically at concentrations ranging from about 0.1% to 5% by weight of the composition, can be used. These anti-static agents should not unduly interfere with the performance in use and final benefits of the shampoo composition; in particular, the antistatic agent must not interfere with the anionic surfactant. A specific non-limiting example of a suitable anti-static agent is tricetyl methyl ammonium chloride. Optional foam promoters for use in the shampoo compositions described herein include fatty ester (for example, of CB-C22) mono- and di (C1-C5, especially C? -C3) alkanolamides. Specific non-limiting examples of these foam boosters include coconut monoethanolamide, coconut diethanolamide and mixtures thereof. Optional antidandruff agents may be used in addition to the particulate antidandruff active agents of the present invention, typically at concentrations ranging from about 0.1% to 4% by weight of the composition, preferably between about 0.2% and 2%. These optional antidandruff agents include soluble anti-dandruff agents, specific non-limiting examples thereof include: pyroctone olamine, ketoconazole and mixtures thereof. Viscosity thickeners and modifiers can be used, usually in effective amounts for the anti-dandruff and conditioning shampoo compositions of the present invention to generally have a total viscosity of between about 1,000 csk and 20,000 csk, preferably between about 3,000 csk and 10,000 csk. Specific non-limiting examples of these viscosity modifiers and thickeners include: sodium chloride, sodium sulfate and mixtures thereof.
III. METHODS OF MANUFACTURE The anti-dandruff and conditioning shampoo compositions of the present invention can be prepared by any known or otherwise effective technique suitable for providing a shampoo composition with the proviso that the resulting composition provides the excellent benefits of hair feeling described in the present. The methods for preparing the antidandruff shampoos and conditioners of the present invention include conventional formulation and mixing techniques. A method such as, for example, that described in U.S. Patent No. 5,837,661, the disclosure of which is incorporated herein by reference, wherein the anti-dandruff particulate of the present invention could normally be added in the same step. as the silicone premix is added, in the description '661.
IV. METHODS OF USE The anti-dandruff and conditioning shampoo compositions of the present invention can be used in a conventional manner to clean and condition hair or skin. They are used in particular in a conventional manner to treat the condition commonly known as dandruff. An effective amount of the composition for cleansing and conditioning the hair or skin is applied to the hair, or other region of the body, which has preferably been moistened, in general with water and then the composition is rinsed. Effective amounts generally range from about lg to 50gm, preferably from about lg to 20gm. The application to hair usually involves operating the composition through the hair in such a way that most or all of the hair is brought into contact with the composition. This method for providing anti-dandruff efficacy and conditioning of the hair comprises the steps of: (a) wetting the hair with water, (b) applying an effective amount of the shampoo composition to the hair, (c) rinsing the shampoo composition to remove it of the hair using water. These steps can be repeated as many times as desired to achieve the desired cleaning, conditioning and antidandruff benefits. It is also contemplated that when the anti-dandruff particulate employed is zinc pyrithione, and / or if other optional hair growth regulating agents are employed, the shampoo compositions of the present invention can be provided for "the regulation of hair growth. The method for regularly using these shampoo compositions comprises steps a, b and c (above).
EXAMPLES The following are non-limiting examples of the anti-dandruff and conditioning shampoo compositions of the present invention. The examples are provided solely for purposes of illustration and are not intended to be limitations of the present invention, as many variations thereof are possible without departing from the spirit and scope of the invention, which could be recognized by one of ordinary skill in the art. in the examples, all concentrations are listed as a percentage by weight, unless otherwise specified. In the sense that is used herein, "others" refers to those optional components such as, for example, preservatives, viscosity modifiers, pH modifiers, fragrances, foam boosters and the like. As is apparent to one of ordinary skill in the art, the selection of these others will depend on the physical and chemical characteristics of the particular ingredients selected to carry out the present invention as described herein. A suitable method for preparing the anti-dandruff and conditioning shampoo compositions described in the following Examples I-XV (below): about one-third of all is added to the ammonium laureth sulfate (added as 25% by weight solution) to a deposit for jacketed and heated mixture between about 60 ° C and 80 ° C with slow stirring to form a surfactant solution. Cocamide MEA and fatty alcohols are added (where appropriate) to the tank and dispersed. Salts (eg, sodium chloride) and pH modifiers (eg, citric acid, sodium citrate) are added to the tank and allowed to disperse. Ethylene glycol distearate ("EGDS") is added to the mixing vessel and allowed to melt. After the EGDS is melted and dispersed, the preservative is added to the surfactant solution. The resulting mixture is cooled to between about 25 ° C and 40 ° C and collected in a finishing tank. As a result of this cooling step, the EGDS crystallizes to form a crystalline lattice in the product. The rest of the ammonium laureth sulfate and other components, including silicone and antidandruff particulate, are added to the tank to finish with agitation to ensure homogeneous mixing. The cationic polymer is dispersed in water as an aqueous solution of between about 0.1% and 10% and then added to the final mixture. Once all the components have been added, the viscosity and pH modifiers can be added, as necessary, to the mixture to adjust the viscosity and pH of the product to the desired degree.
Example number, 1 II. in IV V
Laureth. Ammonium sulfate 11 10 10 10 10
Ammonium lauryl sulfate 5.5 6 6 8 6
Hydroxypropyltrimonium chloride 0.25 0.75 0.4 0.5 0.5 Guar1 PEG90M2 0.1 0.05 0.05 0.01
Zinc pyrithione3 1 1 1 1 1
Homopolymer of 1-decene4 0.5 0.6 0.4 0.2 -
Trimethylpropane Caprilate Capyl5 0.2 0.2 0.1
Dimeticone6 1.5 1.35 1.5 0.55 0.7
Ethylene glycol distearate 1.0 1.0 1.0 1.5 1.5
Cocamida MEA 0.8 0.6 0.6 1.0 1.0
Cetyl alcohol 0.9 0.4 0.6 1.0 1.2
Water and others, - bread id ad snfi ri pnt "p- 1. Guar having a molecular weight of about 200,000 and having a charge density of about 0.71 meq / g, available from Aqualon 2. Polyox WSR 301, available from Union Carbide 3. ZPT having an average particle size of approximately 2.5μm, available from Arch / Olin 4. Puresyn 6, available from Mobil 5. Mobil P4_3, available from Mobil 6. Visasil 330,000 csk, available from General Electric Silicones.
Sample number VI VII VIII IX X
Ammonium Laureth Sulfate 12 12 10 12 12
Ammonium lauryl sulfate 5 6 6 5 4
Polyquaternium-101 0.25 0.25 0.3
Hydroxypropyltrimonium Chloride? .25 0.75 0.4 0.5 0.5 Guar2 PEG1Q0M3 0.15 PEG7M4 0.1 0.2
PEG23M5 0.15 Pyrithione zinc6 1 1 1 1 1
Homopolymer of 1-decene7 0.4 0.2 0.4 0.4 0.1
Trimethylpropane Caprilate Capyl8 0.1 0.2 0.1 0.1
Dimethicone9 1.5 1.5 1.35 1.25 1.15
Ethylene glycol distearate 2.0 1.5 1.5 1.5 1.0
Cocamida MEA 0.6 0.8 0.8 1.5 0.6
Cetyl alcohol 0.6 1.1 0.9 1.0 0.7
Water and others - panf i dari snfi rH pnt-p- 1. UCARE Polymer LR400, available from Amerchol 2. Guar having a molecular weight of about 200,000 and having a charge density of about 0.71 meq / g, available from Aqualon. 3. Carbowax PEG4600, available from Union Carbide. 4. Polyox WSR N-750, available from Union Carbide. 5. Polyox WSR N-12K, available from Union Carbide. 6. ZPT having an average particle size of approximately 2.5μm, available from Arch / Olin. 7. Puresyn 6, available from Mobil. 8. Mobil P43, available from Mobil. 9. Visasil 330,000 csk, available from General Electric Silicones.
Example number XI XII XIII XIV XV
Ammonium Laureth Sulfate 14 10 10 10 12.5
Ammonium lauryl sulfate 6 6 8 2 4.5
Polyquaternium-101 0.15 0.2 0.1 0.35 Hydroxypropyltrimonium Chloride 0.25 0.4 0.4 0.15 0.5 Guar2 PEG7M3 0.2 PEG90M '' 0.025 0.15
Zinc pyrithione5 1 1 1 1 1
Homopolymer of 1-decene6 0.2 0.3 0.3 0.4 0.4
Trimethylpropane Caprilate Capyl7 0.2 0.1 0.0 0.1 0.1
Dimethicone8 1.0 3.25 3.25 0.5 0.8
Ethylene glycol distearate 1.5 1.0 1.0 2.0 2.0
Cocamida MEA 0.9 0.9 1.5 1.0 1.0
Cetyl alcohol 0.9 0.8 1.0 0.5 0.5
Water and others -nan i arl Rpfi i? pnt-p- 1. UCARE Polymer LR400, available from Amerchol 2. Guar having a molecular weight of about 200,000 and having a charge density of about 0.71 meq / g, available from Aqualon. 3. Polyox WSR N-750, available from Union Carbide. 4. Polyox WSR-301, available from Union Carbide. 5. ZPT having an average particle size of approximately 2.5μm, available from Arch / Olin. 6. Puresyn 6, available from Mobil. 7. Mobil P43, available from Mobil. 8. Visasil 330,000 csk, available from General Electric Silicories.
Claims (13)
- CLAIMS 1. A shampoo composition characterized in that it comprises: a) from 5% to 50% by weight of the composition, of an anionic surfactant; b) from 0.01% to 10% by weight of the composition, of a non-volatile conditioning agent; c) from 0.1% to 4% by weight of the composition, of an antidandruff particulate; d) from 0.02% to 5% by weight of the composition, of a cationic guar derivative; i) wherein the cationic guar derivative has a molecular weight of 50,000 to 700,000; and ii) wherein the cationic guar derivative has a charge density of 0.05 meq / g at 1.0 meq / g; e) water.
- 2. The shampoo composition according to Claim 1, wherein the composition further comprises 0.1% to 10% by weight of the composition, of a suspending agent, wherein the suspending agent is preferably ethylene glycol distearate.
- 3. The shampoo composition according to any preceding claim, wherein the non-volatile conditioning agent is a dispersed silicone.
- 4. The shampoo composition according to any preceding claim, wherein the anti-dandruff particulate is a zinc salt of l-hydroxy-2-pyridinethione and preferably wherein the zinc salt of l-hydroxy-2-pyridinone is in the form of a particle in platelet.
- 5. The shampoo composition according to any preceding claim, wherein the cationic guar derivative has a charge density of 0.1 meq / g at 1.0 meq / g and a molecular weight of 50,000 to 300,000.
- 6. The shampoo composition according to any preceding claim, characterized in that it comprises from 0.1% to 1.0% of the cationic guar derivative.
- 7. The shampoo composition according to any preceding claim, wherein the composition further comprises 0.1% to 5% by weight of the composition, of a cationic polymer according to the general formula: a) wherein A is a residual group of anhydroglucose; b) wherein R is selected from the group consisting of alkylene oxyalkylene, polyoxyalkylene, hydroxyalkylene and mixtures thereof; c) R1, R2 and R3 are independently selected from the group consisting of alkyl, aryl, alkylaryl, arylalkyl, alkoxyalkyl or alkoxyaryl, each group contains up to about 18 carbon atoms and the sum of carbon atoms in R1, R2 and R3 is less than 20; and d) wherein X is selected from the group consisting of chloride, fluoride, bromide, iodide, sulfate, methylisulfate and mixtures thereof; preferably, wherein the cationic polymer is polyquaternium-10.
- 8. The shampoo composition according to any preceding claim, wherein the cationic polymer has a charge density of 0.1 meq / g to 1.0 meq / g, preferably 0.2 meq / g to 0.6 meq / g and a molecular weight of 250,000 to 850,000 preference of 350,000 to 500,000.
- 9. The shampoo composition according to any preceding claim, wherein the composition further comprises 0.005% to 1.5% by weight of the composition, preferably 0.05% to 1.0%, of a polyalkylene glycol corresponding to the formula: H (OCH 2 CH) n OH R a) wherein R is selected from the group consisting of hydrogen, methyl and mixtures thereof, and b) wherein n is an integer having an average value of between about 1,500 and 120,000, preferably between about 3,500 and 15,000.
- 10. A shampoo composition characterized in that it comprises: a) from 10% to 25% by weight of the composition, of an anionic surfactant; b) from 0.01% to 10% by weight of the composition, of a non-volatile, insoluble silicone conditioning agent; c) from 0.3% to 2% by weight of the composition, of a zinc salt of l-hydroxy-2-pyridinone; d) from 0.1% to 5% by weight of the composition, of a cationic guar derivative, i) wherein the cationic guar derivative has a molecular weight of 100,000 to 400,000; and ii) wherein the cationic guar derivative has a charge density of 0.4 meq / g at 1.0 meq / g; e) water.
- 11. A method for providing anti-dandruff efficacy and for conditioning hair characterized in that it comprises: a) moistening the hair with water; b) applying to the hair an effective amount of a shampoo composition according to any preceding claim; and c) rinsing the hair shampoo composition using water.
- 12. The shampoo composition according to any preceding claim, further characterized in that it comprises from 0.001% to 15% by weight of the composition, of a hair growth regulating agent selected from the group consisting of zinc salts of carboxylic acids, saponins, triterpenes , oleanolic acid, ursolic acid, betulinic acid, betulonic acid, crataegolic acid, celastrol, asian acid, 5-oc-reductase inhibitors, progesterone, 1, 4 -met i 1- 4 -a zaes teroides, 17-ß-N , N-diethylcarbamoyl-4-methyl-4-aza-5-a-andros tan-3-one, androgen receptor antagonists, cyproterone acetate, minoxidil, azelaic acid and derivatives thereof, cyclosporin, t riyodot ironin , diazoxide, potassium channel openers, chromacalin, phenytoin, ketoconazole, finasteride, dutasteride, coal pitch, zinc gluconate, glucocortisoids, macrolides, aminaxyl, and mixtures thereof.
- 13. A method for regulating hair growth characterized in that it comprises: a) wetting the hair with water; b) applying to the hair an effective amount of a shampoo composition according to any preceding claim; and c) rinsing the hair shampoo composition using water.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60/132,868 | 1999-05-03 |
Publications (1)
Publication Number | Publication Date |
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MXPA01011219A true MXPA01011219A (en) | 2002-06-05 |
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