AU2006203095A1 - Methods for improving the health of hair and scalp - Google Patents
Methods for improving the health of hair and scalp Download PDFInfo
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- 210000004209 hair Anatomy 0.000 title claims description 77
- 238000000034 method Methods 0.000 title claims description 68
- 210000004761 scalp Anatomy 0.000 title description 21
- 230000036541 health Effects 0.000 title description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 54
- 230000003698 anagen phase Effects 0.000 claims description 50
- 239000002453 shampoo Substances 0.000 claims description 42
- 230000001965 increasing effect Effects 0.000 claims description 34
- 230000003695 hair diameter Effects 0.000 claims description 32
- XMAYWYJOQHXEEK-OZXSUGGESA-N (2R,4S)-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 27
- 229960004125 ketoconazole Drugs 0.000 claims description 27
- 230000001939 inductive effect Effects 0.000 claims description 25
- 229940043810 zinc pyrithione Drugs 0.000 claims description 24
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 claims description 24
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 18
- 230000003721 exogen phase Effects 0.000 claims description 15
- 239000003638 chemical reducing agent Substances 0.000 claims description 12
- 210000004919 hair shaft Anatomy 0.000 claims description 10
- 230000012010 growth Effects 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 206010035502 Plasmodium ovale infection Diseases 0.000 claims description 7
- VIDTVPHHDGRGAF-UHFFFAOYSA-N selenium sulfide Chemical compound [Se]=S VIDTVPHHDGRGAF-UHFFFAOYSA-N 0.000 claims description 7
- 229960005265 selenium sulfide Drugs 0.000 claims description 7
- 150000003852 triazoles Chemical class 0.000 claims description 7
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 6
- 239000006071 cream Substances 0.000 claims description 6
- 229910052744 lithium Inorganic materials 0.000 claims description 6
- OWEGWHBOCFMBLP-UHFFFAOYSA-N 1-(4-chlorophenoxy)-1-(1H-imidazol-1-yl)-3,3-dimethylbutan-2-one Chemical compound C1=CN=CN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 OWEGWHBOCFMBLP-UHFFFAOYSA-N 0.000 claims description 3
- AFNXATANNDIXLG-SFHVURJKSA-N 1-[(2r)-2-[(4-chlorophenyl)methylsulfanyl]-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound C1=CC(Cl)=CC=C1CS[C@H](C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 AFNXATANNDIXLG-SFHVURJKSA-N 0.000 claims description 3
- QXHHHPZILQDDPS-UHFFFAOYSA-N 1-{2-[(2-chloro-3-thienyl)methoxy]-2-(2,4-dichlorophenyl)ethyl}imidazole Chemical compound S1C=CC(COC(CN2C=NC=C2)C=2C(=CC(Cl)=CC=2)Cl)=C1Cl QXHHHPZILQDDPS-UHFFFAOYSA-N 0.000 claims description 3
- VHVPQPYKVGDNFY-DFMJLFEVSA-N 2-[(2r)-butan-2-yl]-4-[4-[4-[4-[[(2r,4s)-2-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]phenyl]-1,2,4-triazol-3-one Chemical compound O=C1N([C@H](C)CC)N=CN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@@H]3O[C@](CN4N=CN=C4)(OC3)C=3C(=CC(Cl)=CC=3)Cl)=CC=2)C=C1 VHVPQPYKVGDNFY-DFMJLFEVSA-N 0.000 claims description 3
- BYBLEWFAAKGYCD-UHFFFAOYSA-N Miconazole Chemical compound ClC1=CC(Cl)=CC=C1COC(C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 BYBLEWFAAKGYCD-UHFFFAOYSA-N 0.000 claims description 3
- 229960005074 butoconazole Drugs 0.000 claims description 3
- SWLMUYACZKCSHZ-UHFFFAOYSA-N butoconazole Chemical compound C1=CC(Cl)=CC=C1CCC(SC=1C(=CC=CC=1Cl)Cl)CN1C=NC=C1 SWLMUYACZKCSHZ-UHFFFAOYSA-N 0.000 claims description 3
- 229960003344 climbazole Drugs 0.000 claims description 3
- 229960004022 clotrimazole Drugs 0.000 claims description 3
- VNFPBHJOKIVQEB-UHFFFAOYSA-N clotrimazole Chemical compound ClC1=CC=CC=C1C(N1C=NC=C1)(C=1C=CC=CC=1)C1=CC=CC=C1 VNFPBHJOKIVQEB-UHFFFAOYSA-N 0.000 claims description 3
- 125000004188 dichlorophenyl group Chemical group 0.000 claims description 3
- VEVFSWCSRVJBSM-HOFKKMOUSA-N ethyl 4-[4-[[(2r,4s)-2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCN1C(C=C1)=CC=C1OC[C@@H]1O[C@@](CN2C=NC=C2)(C=2C(=CC(Cl)=CC=2)Cl)OC1 VEVFSWCSRVJBSM-HOFKKMOUSA-N 0.000 claims description 3
- 229960004130 itraconazole Drugs 0.000 claims description 3
- 229960002509 miconazole Drugs 0.000 claims description 3
- 229960002607 sulconazole Drugs 0.000 claims description 3
- 229960004214 tioconazole Drugs 0.000 claims description 3
- 241000041995 Pelargonium ovale Species 0.000 claims 3
- 229960004884 fluconazole Drugs 0.000 claims 2
- RFHAOTPXVQNOHP-UHFFFAOYSA-N fluconazole Chemical compound C1=NC=NN1CC(C=1C(=CC(F)=CC=1)F)(O)CN1C=NC=N1 RFHAOTPXVQNOHP-UHFFFAOYSA-N 0.000 claims 2
- 241000282412 Homo Species 0.000 claims 1
- 201000004384 Alopecia Diseases 0.000 description 24
- 230000003676 hair loss Effects 0.000 description 20
- 208000024963 hair loss Diseases 0.000 description 20
- 208000001840 Dandruff Diseases 0.000 description 14
- 230000008859 change Effects 0.000 description 14
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- 206010039793 Seborrhoeic dermatitis Diseases 0.000 description 12
- 230000029142 excretion Effects 0.000 description 12
- 238000011282 treatment Methods 0.000 description 7
- 150000002460 imidazoles Chemical class 0.000 description 6
- 206010061218 Inflammation Diseases 0.000 description 5
- 241000555688 Malassezia furfur Species 0.000 description 5
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- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 4
- 229960002026 pyrithione Drugs 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- 210000003491 skin Anatomy 0.000 description 4
- 206010015150 Erythema Diseases 0.000 description 3
- 241000101040 Pityriasis Species 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 231100000640 hair analysis Toxicity 0.000 description 3
- 230000002757 inflammatory effect Effects 0.000 description 3
- WAHQBNXSPALNEA-UHFFFAOYSA-L lithium succinate Chemical compound [Li+].[Li+].[O-]C(=O)CCC([O-])=O WAHQBNXSPALNEA-UHFFFAOYSA-L 0.000 description 3
- 229960004254 lithium succinate Drugs 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
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- 210000001732 sebaceous gland Anatomy 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 208000003251 Pruritus Diseases 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 201000002996 androgenic alopecia Diseases 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
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- ZFMITUMMTDLWHR-UHFFFAOYSA-N Minoxidil Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 description 1
- WPNJAUFVNXKLIM-UHFFFAOYSA-N Moxonidine Chemical compound COC1=NC(C)=NC(Cl)=C1NC1=NCCN1 WPNJAUFVNXKLIM-UHFFFAOYSA-N 0.000 description 1
- 206010039792 Seborrhoea Diseases 0.000 description 1
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- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
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Landscapes
- Cosmetics (AREA)
Description
.0 -1
AUSTRALIA
SPATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT cORIGINAL Name of Applicant/s: Johnson Johnson Consumer Companies, Inc.
Actual Inventor/s: Gerard Frans Maria Jan Cauwenbergh Address for Service is: SHELSTON IP Margaret Street Telephone No: (02) 9777 1111 SYDNEY NSW 2000 Facsimile No. (02) 9241 4666 CCN: 3710000352 Attorney Code: SW Invention Title: METHODS FOR IMPROVING THE HEALTH OF HAIR AND SCALP Details of Original Application No. 2003203846 dated 23 Apr 2003 The following statement is a full description of this invention, including the best method of performing it known to me/us:- File: 38721AUP01 500925383_1 .DOC/5844 METHODS FOR IMPROVING THE HEALTH OF HAIR AND SCALP CROSS-REFERENCE TO RELATED APPLICATION This Application claims the benefit of United States Provisional O Application Number 60/069,993 filed on 18 December 1997, which is Sincorporated by reference in its entirety.
NO
SBACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to methods of improving the health of hair and the scalp. More particularly, this invention relates to methods for reducing hair shedding, methods for increasing hair diameter, and methods for maintaining hair in the anagen phase for a prolonged period of time.
2. Descrotion of Prior Art Dandruff ("pityriasis capitis sicca") and seborrheic dermatitis ("pityriasis capitis oleosa") are two related clinical manifestations of one common dermatological disorder that involves the scalp as well as other areas of the body having a high density of sebaceous glands. While dandruff is primarily a scaling condition, it is often also associated with some inflammation. See e.g. Dawber, "The Scaly and Itchy Scalp," Hair and Scalo Disorders 191-227 (1995). Typically dandruff is expressed on the scalp, but other areas of the body that are predisposed to seborrheic dermatitis also often show mild scaling without obvious signs of inflammation. In seborrheic dermatitis, the inflammatory counterpart of the same disorder, erythema is always present, and the inflammatory infiltrate is more pronounced. See e.g. Ford, G. et al., 111 Br. J. Dermatol 603-07 (1984)("Ford").
Those of skill in the art have come to the consensus that both 0 10 dandruff and seborrheic dermatitis are two aspects of the same disease.
See Ford; Sabouraud, "Maladies Due Cuir Chevelu II," Les Maladies Desquamatives, 207-327 (1904); and Van Vloten, et al., "Eczeem," B Dermatologie and Venereologie 90 109 (1996). It is well known that individuals who have dandruff will, if the condition is not treated, often develop the more inflammatory aspect seborrheic dermatitis, while those having seborrheic dermatitis might show scaling only during the periods of less pronounced inflammation. Although those skilled in the art generally agree that the lipophylic yeast, Pityrosporum ovale ovae"), is a key contributor in the pathogenesis of seborrheic dermatitis and dandruff, it is likewise accepted that both conditions should not be regarded as an infection. Rather, it is the yeast's overcolonization of the scalp and other body areas having a high density of sebaceous glands that causes a very mild inflammatory reaction, i.e. dandruff, or a moderate inflammatory reaction, i.e. seborrheic dermatitis, redness, as well as an accelerated turnover of the epidermis. See Ford and Arese, et al., "Effect of Ketoconazole Medicated Shampoos on Squamometry and Malassezia Ovalis Load in Pityriasis Capitis," 58 Cutis 235-37 (1996).
Typical primary symptoms of dandruff and seborrheic dermatitis include scaling, redness, and itching; however, several other clinical manifestations such as seborrhea (oiliness), telogen effluvium (shedding), thin shaft diameter, androgenic alopecia, and reduction in percent anagen hairs have also been reported in conjunction with this disorder. See Shuster, "Psoriatic Alopecia," 87 Br. J. Dermatol. 74 77 (1972); 0 3 O 5 Rushton, et al., "Natural Progression of Male Pattern Baldness in Young Men," 16 Clin. Exp. Dermatol. 188 192 (1991); Bergfeld, F.W., "Hair Disorders" Dermatology 1541 1560 (1992); and Pierard-Franchimort, et al., "Approche Physiopathologique de la Seborrhee Du Cuir Chevelu,' 115 Ann. Dermatol. Venereol. 451 53 (1988).
Various methods have been employed to stimulate the growth of hair 0 and/or increase its diameter; however, these methods are not without their 0shortcomings. One known method employs the application of minoxidil to areas such as the scalp for purposes for stimulating hair growth and Sprolonging the period of time that hair is in the anagen phase.
Unfortunately, this method has been found to be effective in only a small proportion of users. Another known method for increasing hair diameter involves the application of silicone-containing treatments to areas such as the scalp. Disadvantageously, this method produces a "build-up" of silicone on the hair that tends to dull its physical appearance.
It would be desirable to provide a method of treating seborrheic dermatitis and dandruff by improving these alternative manifestations indicative of an unhealthy scalp.
SUMMARY OF THE INVENTION In accordance with this invention, there is provided a method of increasing the amount of anagen hair in a human comprising, consisting essentially of, andlor consisting of applying an effective amount of an agent which inhibits the growth of P. ovale or a mixture thereof to an area of a human where an increase in the amount of anagen hair is desired.
In another embodiment of this invention, there is provided a method of reducing the sheiding of hair in a human comprising, consisting essentially of, and/or consisting of topically applying an effective amount of an agent which inhibits the growth of P. ovale or a mixture thereof to an area of the human where a decrease in the shedding is desired.
In yet another embodiment of this invention, there is provided a method of increasing the diameter of a hair shaft comprising, consisting essentially of, and/or consisting of topically applying an effective amount of 0 10 an imidazole, a triazole, selenium sulfide, a lithium-containing product, or Smixtures thereof to an area of a human wherein an increase in the diameter N0 is desired.
0 The methods of this invention not only are effective in alleviating symptoms indicative of unhealthy hair and scalp, but also are effective in treating two underlying, related clinical manifestations, dandruff and seborrheic dermatitis.
BRIEF DESCRIPTION OF THE DRAWINGS The invention will be more fully understood and further advantages will be come apparent when reference is made to the following detailed description of the invention and the accompanying drawings in which: FIG. 1 is a graph of the percent change in amount of anagen hair from baseline in a 6 month period versus the amount of panelists.
FIG. 2 is a graph of the percent change in hair diameter from baseline in a 6 month period versus the amount of panelists.
FIG. 3 is a scattergram of the baseline sebum excretion rate (pg/cmr /hr) versus the sebum excretion rate (p.g/cm2/hr) six months later for subjects using a ketoconazole -containing shampoo (FIG. 3A) and a zinc pyrithione shampoo (FIG. 3B).
FIG. 4 is a graph of the percent change in hair loss reduction from baseline versus the length of treatment from baseline at one, three and six month intervals.
DESCRIPTION OF THE PREFERRED EMBODIMENTS SAs used herein, "anagen hair" shall mean hair that is in the growth phase.
V) 10 In all embodiments of the present invention, the active ingredients 0 may be applied to a desired area via any inert vehicle or carrier suitable for 0topical applications including, but not limited to a shampoo, a soap, a gel, a IN cream, a lotion, a solution, and the like (hereinafter collectively "Medium').
SThe Medium, which can either be oil-based or preferably water-based, may be designed to be left on the skin and not washed shortly after application.
In an alternative, preferred embodiment, the Medium may be designed to be rinsed off within a given amount of time after application. In the latter embodiment wherein the active ingredients are incorporated into a shampoo, the shampoo is applied to wet hair, and the hair is washed in accordance with known practices.
The areas to which the active ingredients may be applied include one or more of those areas typically affected by seborrheic dermatitis and dandruff, which include but are not limited to the scalp and other hairy areas, body folds, behind the ears, areas of the body having a high density of sebaceous glands, and/or areas having an increased presence of P.
ovale.
In the first embodiment of this invention, an anagen hair-inducing agent is comprised of any agent capable of inhibiting the growth of P. ovale.
Examples of suitable anagen hair-inducing agents include, but are not limited to, imidazoles, triazoles, zinc pyrithione (including zinc pyrithione in its ultramicronized form), selenium sulfide, lithium-containing products such as lithium salts including but not limited to lithium succinate, or mixtures thereof, which are topically applied in an effective amount to an area of a human where an increase in the amount of anagen hair is desired.
Preferred areas include those which possess or had possessed hair such as, for example, the scalp.
While various imidazoles may be employed, the preferred IN compounds include, but are not limited to ketoconazole; dichlorophenyl imidazolodioxalan, which is commercially available from Janssen Pharmaceutica, under the tradename, "Elubiol"; clotrimazole; itraconazole; miconazole; climbazole; tioconazole; sulconazole; butoconazole; fluconazoie; and any possible stereo isomers thereof and mixtures thereof. Ketoconazole and ultra-micronized zinc pyrithione are preferred anagen hair-inducing agents.
The topical application of the anagen hair-inducing agent is performed by applying a dilute,solution of the anagen hair-inducing agent to a desired area. The amount of anagen hair-inducing agent used in this embodiment shall be an amount effective for increasing the amount of anagen hair in a desired area of a human. As used herein "amount effective" shall mean an amount sufficient to cover the region of skin surface where an indication exists as well as to ameliorate the indication. Although the amount of anagen hair-inducing agent used will depend upon, for example, the amount of anagen hair desired and a human's tolerance and/or receptiveness to the particular anagen hair-inducing agent selected, typically from about 0.001 mg/sq. mm to about 1000 mg/ sq. mm, and preferably from about 0.1 mg/sq. mm to about 50 mg/ sq. mm of anagen hair-inducing agent is typically applied to the skin's surface. Such appropriate amounts of anagen hair-inducing agent may be delivered to a desired area when the amount of the anagen hair-inducing agerts- present.
in the desired Medium in an amount, based upon the total weight of the Medium, of from about 0.01 percent to about 20 percent, and preferably from about 0.5 percent to about 5 percent.
The anagen hair-inducing agent is preferably applied topically to the desired areas of the body at regular intervals, and more preferably from about 1 to about 7 times per week. In one embodiment, the anagen hairinducing agent may be applied more frequently during the initial stages of treatment, e.g. from about 4 to about 7 times per week-r ritiihe desired effect is achieved, then less frequently when maintenance is desired, e.g.
from about 1 to about 2 times per week. It is preferable to continue use of the agent in order to maintain the resulting increase in amount of anagen Shair, that is to keep the hair growing for a longer period of time.
The anagen hair-inducing agent should remain on the desired area of the human at least for about 15 seconds, preferably from about 15 seconds to about 5 minutes, and more preferably from about 60 seconds to about 3 minutes.
Media containing the anagen hair-inducing agent may be prepared by combining the anagen hair-inducing agent with the other components commonly present in the Media under ambient conditions via any mixing devices commonly used in the art. When ketoconazole is used as the anagen hair-inducing agent, it is preferable to incorporate an antioxidant component in the Media as set forth in U.S. Patent No. 5,456,851, which is incorporated by reference herein. Butylated hydroxytotuene (BHT) and butylated hydroxyanisole (BHA) are the antioxidants of choice. Details of how to prepare a cream containing the anagen hair-inducing compound are disclosed in U.S. Patent No. 4,942,162, which is incorporated by reference herein; and details of how to prepare a shampoo containing the anagen hair-inducing compound are disclosed in U.S. Patent No. 5,456,851.
In another aspect of the present invention, a hair shedding reductant comprised of any agent capable of inhibiting the growth of P. ovale is topically applied in an effective amount to an area of a human where a decrease in the amount of hair shedding is desired. Preferred areas include those which possess hair such as, for example, the scalp. Examples of Ssuitable hair shedding reductants include, but are not limited to, imidazoles, 0 triazoles, elubiol, zinc pyrithione (including zinc pyrithione in its Sultramicronized form), selenium sulfide, lithium-containing products such as Slithium salts including but not limited to lithium succinate, or mixtures thereof.
Examples of suitable imidazoles include, but are not limited to those set-forth above. Ketoconazole and ultra-micronized zinc pyrithione are preferred hair shedding reductant agents.
The amount of hair shedding reductant used in this embodiment shall be an amount effective for decreasing the amount of shedding hair in a desired area of the human. This amount, as wellf as the method for preparing the Media containing the hair shedding reductant and the method for using such Media are similar to those respective amounts and methods provided above for the Media containing the anagen hair-inducing agent.
In another aspect of the present invention, a hair diameter increasing agent comprised of imidazoles, triazoles, selenium sulfide, lithiumcontaining products such as lithium salts including but not limited to lithium succinate, or mixtures thereof (including mixtures with zinc pyrithione) is topically applied in an effective amount to an area of a human where in an increase in hair diameter is desired. Preferred areas include those which possess hair such as, for example, the scalp.
Examples of suitable imidazoles include, but are not limited to those set forth above. Ketoconazole is the preferred hair diameter increasing agent. In embodiments wherein zinc pyrithione is used in combination with a hair diameter increasing agent, the zint pyrithione is present in an amount, based upon the total weight of the solution comprised of the hair diameter increasing agent, of from about 0.25 percent to about 2 percent The amount of hair diameter increasing agent used in this Sembodiment shall be an amount effective for increasing the diameter of hair shafts in a desired area of the human. This amount, as well as the method for preparing the Media containing the hair diameter increasing agent and the method for using such Media are similar to those respective amounts tf 10 and methods provided above for the Media containing the anagen hair- Sinducing agent.
0 In nearly all embodiments of the present invention, positive results \0 were apparent as early as about 2 weeks after the first use. However, after 0using the anagen hair inducing agent for about 6 months in accordance with the process of the present invention, we have unexpectedly found that the number of anagen hairs in the treated area increased by a percentage of up to about 40 percent. Further, we have also unexpectedly found that the number of hairs shed in the treated area after 6 months of use of the hair shedding reductant in accordance with the process of this invention decreased by a percentage of up to about 20 percent.
tn addition, we have unexpectedly found that after using the hair diameter increasing agent for about 6 months in accordance with the process of the present invention, the diameter of the hair shafts in the treated area increased by up to a percentage of about 50 percent Similarly, we have found that the oiliness of these treated areas also decreased by about 9% during this period. In view of these results, we have discovered a correlation between sebum excretion rate and hair diameter, i.e. that those who experienced a greater than 20% increase in hair diameter also experience about a 6% decrease in sebum excretion rate. Conversely, those who did not use the hair diameter increasing agent and who experienced about a 5% decrease in hair diameter also had about a increase in scalp oiliness. We believe that the use of products which are capable of reducing the oil of the treated area, e.g. scalp, will also enhance Sthe thickness of hair when used on a regular basis.
The invention illustratively disclosed herein suitably may be practiced in the absence of any component, ingredient, or step which is not specifically disclosed herein. Several examples are set forth below to further illustrate the nature of the invention and the manner of carrying it out However, the invention should not be considered as being limited to the details thereof.
O
EXAMPLES
The following shampoos were used in the Examples below- Shamooo A: a 1% ketoconazole shampoo available from Neutrogena Corporation under the tradename, "Long Lasting Dandruff Shampoo." Shamooo B: a 1 zinc pyrithione shampoo available from the Procter Gamble Company under the tradename, "New Head Shoulders." The following test methods were performed in the Examples below: 1) Pilarv Index urm) he piary index was calculated as the product of the percent of anagen hair and the hair shaft diameter (Jim).
For the baseline assessment, hair samples were identified on the venex area then plucked out with a rubber-tipped tweezer. The removed hair sample was placed under a microscope in order to count the hair strands and to identify the hair cycle stage for each respective strand, i.e.
anagen (growing), telogen (ending), or catagen (resting). From these resulting trichograms the proportion of hairs in the anagen phase was obtained.
A computerized image analysis of the same hair samples was performed using a MOP Videoplan analyzer manufactured by Kontron GmbH in order to measure the average diameter of the hair shafts in accordance with the directions provided therewith.
By using a 3-point midline and facial coordinate system with nose tip, ear and fontanelle coordinates, precise relocation of the sample site was achieved for measurements taken after the baseline assessment.
2) Hair shedding: The amount of hairs shed was evaluated by a semi-quantitative count of the hairs collected immediately after the last shampoo usage by the subject, which typically was about 24 hours before a subject visited the laboratory for evaluation. The hairs were collected in a 0 small transparent envelope and then compared with a series of similar Sreference envelopes kept at the laboratory. Each reference envelope Scontained a multiple of 10 hairs. The number of hairs shed in the subject's envelope was matched to a reference standard.
3) Sebum excretion (ua/cm 2 /hour): A sample site near the hairline was located using the above 3-point midline and facial coordinate system.
One hour after cleaning the skin of the site with a 70% ethanol solution, the amount of sebum excreted at that area was measured by holding a probe of a computerized Model SM810 Courage sebumeter from Khazaka, GmbH to the site until an excretion value was provided on the sebumeter.
Using the above-mentioned 3-point system, precise relocation of the sample site was achieved for measurements taken after the baseline assessment.
Examole 1 Comoarative Testina: Percent Hairs in Anaoen Phase Forty-four adult males who ranged in age from 18 to 65 years old, had mild to moderate dandruff, and had mild androgenic alopecia of the vertex, were assigned to shampoo 2 to 3 times per week with Shampoo A, and forty-three other males having the same characteristics were similarly assigned to shampoo with Shampoo B. Before beginning to shampoo with their assigned shampoo, the baseline pilary index value was calculated for each male. After 6 months of shampooing according to this regime, the pilary index value for each male was recalculated.
As evidenced in Table 1 below and in FIG. 1, both the ketoconazolecontaining shampoo and the zinc pyrithione -containing shampoo Sbeneficially improved the percent of anagen hairs by 8.3% and 10.3%, respectively.
TABLE 1: EFFECT OF KETOCONAZOLE AND ZINC PYRITHIONE ON PERCENT HAIRS IN ANAGEN PHASE CHANGE IN AMOUNT OF KETOCONAZOLE ZINC ANAGEN HAIRS N 44 PYRITHIONE N =43 3 8 to 19 13 11 Oto9 20 14 -1 to -10 8 8 -11 to -20* 0 2 a negative value reflects a decrease in the amount of hairs in anagen phase This Example shows that ketoconazole and zinc pyrithione are effective in increasing the number of anagen hairs, i.e. in keeping the hair growing for a longer period of time.
Example 2: Comoarative Testina: Chance in Hair Diameter Example-1 was repeated but the baseline and 6 month values for hair diameter were measured.
As evidenced in Table 2 and in FIG. 2, the ketoconazole-containing shampoo beneficially increased the hair shaft diameter by about 11%, whereas the diameter was slightly decreased by about 3% in those subjects using the zinc pyrithione -containing shampoo.
TABLE 2: EFFECT OF KETOCONAZOLE AND ZINC PYRITHIONE ON CH-ANGE IN HAIR IiAM-T-R CHANGE IN HAIR DIAMETER KETOCONAZOLE
ZINC
N=44
PYRITHIONE
N= 43 20 6 2 to 19 10 2 0to9 19 6 -1 to -10" 9 29 -11 to -20 0 4 a negative value reflects a decrease in the hair diameter This Example shows that ketoconazole, as opposed to zinc pyrithione, is more effective in increasing the diameter of a hair shaft.
Examole 3: Comoarative Testing: Chanoe in Sebum Excretion Rate Example 2 was repeated, except the baseline and 6 month sebum excretion rate was measured.
As evidenced in FIG. 3A and FIG. 3B, the sebum excretion rate for those subjects using the ketoconazole-containing shampoo decreased over the 6 month period by about while the sebum excretion rate for those subjects using the zinc pyrithione-containing shampoo increased by about Since this correlation addressed two biological parameters in relation to each other, the correlation is apparent independent from the type of shampoo used as illustrated in Table 3 and Table 4 below, which shows that the greater the reduction in the amount of sebum excretion, the greater the change in hair diameter.
TABLE 3: CHANGES IN HAIR DIAMETER IN RELATION TO SCALP OIL CHANGE (CATEGORIES INDEPENDENT FROM TYPE OF SHAMPOO
-USED)
CATEGORY: CHANGE IN MEAN CHANGE IN HAIR SCALP OILINESS ()DIAMETER(% 10DECREASE41 (Mean 14.4) from 5 DECREASE TO 5 3.7
INCREASE
(Mean 6) 10INCREASE a negative value reflects a decrease in hair diameter TABLE 4: CHANGES IN SCALP OILINESS IN RELATION TO HAIR DIAMETER CHANGE (CATEGORIES INDEPENDENT FROM TYPP i SHAMODp icr
INO
CATEGORY: CHANGE IN MEAN CHANGE IN SCALP HAIR DIAMETER OIL 20 INCREASE 6.25 (Mean 30.5) FROM 10 TO 19 INCREASE -2.2 (Mean 13.6) FROM -4 TO 9 (Mean .7) FROM 5 TO 10 DECREASE 5.4 (Mean -6.4) 10% DECREASE .6 (Mean -12) %l Lmjl a negative value reflects a decrease in the amount of oil produced This Example shows that ketoconazole is effective in both reducing the amount of sebum excretion while also increasing the diameter of hair shafts. By contrast, zinc pyrithione is comparatively less effective in reducing the amount of sebum excreted and further appears to contribute to a decrease in the diameter of hair shafts. Thus, the Example suggests a relationship between reducing the production of sebum in order to increase hair diameter.
ExamDle 4' Comoarative Testing: Hair Shedding Fifty males who ranged in age from 26 to 56 years old, had mild to moderate dandruff, and had mild androgenic aiopecia of the vertex were assigned to shampoo 2 to 3 times per week with Shampoo A, and fifty other males having the same characteristics were similarly assigned to shampoo with Shampoo B.
Before beginning to shampoo with their assigned shampoo, the baseline shedding value was calculated for each male. At baseline, about 0 10 1/3 of the subjects in both groups had low hair loss, i.e. about 20 to about shafts, 1/3 of the subjects had moderate hair loss, i.e. about 30 to about and 1/3 qf the subjects had high hair loss, i.e. more than about shafts.
After 1, 3, and 6 months of shampooing according to this regime, the shedding value for each male was recalculated. As illustrated in FIG. 4, the subjects who used the ketoconazole shampoo exhibited a significant reduction in hair loss in after only one month of treatment, and a highly significant reduction after three and six months of treatment. At six months of treatment, both groups exhibited significant reductions from base line levels of hair loss.
As further illustrated in Table 5 below, we found that the change in hair loss at six months was related to the baseline hair loss measurement Table Six Month Change in Hair Loss Degree of Hair Loss of Reduction in Hair Reduction in Hair Subjects (Baseline) Loss from Baseline by Loss from Baseline by Subjects Using Subjects Using Zinc Ketoconazole Pyrithione Shampoo B _Shampoo A Low 1 -2 Moderate 9 6 High 17 9 At baseline, the degree of hair loss in the two groups was nearly identical. However, Table 5 shows that as the degree of baseline hair loss was increased, the difference in the reduction of hair loss at six months became more pronounced. Moreover, of those participants who dropped out of the study, 4 of the 6 dropouts'ri the group using Shampoo A had high baseline levels of hair loss, while 5 of the 7 dropouts in the group using Shampoo B had low baseline levels of hair toss. Therefore, the group using Shampoo A lost subjects expected to have a superior result, while the group Susing Shampoo B lost subjects who were expected to have a relatively low improvement in hair loss reduction.
Although this Example shows that ketoconazole and zinc pyrithione are both effective in hair loss reduction, it is apparent that ketoconazole is the preferred agent for hair loss reduction. This Example also shows that the improvement in hair loss reduction occurs relatively soon after using ketoconazole. Further, this -Example shows that the reduction in hair loss is more dramatic in those subjects exhibiting a relatively excessive hair loss before treatment.
While preferred embodiments have been described in the foregoing detailed description, it will be recognized that there is no intent to limit the invention by such disclosure, but rather it is intended to cover all modifications and variations falling within the spirit and scope of the invention as defined in the appended claims.
Claims (30)
1. A method of increasing the amount of anagen hair in a human comprised of topically applying an effective amount of an agent which inhibits the growth of P. ovale or mixture thereof to an area of the human wherein an increase in the amount of anagen hair is desired.
2. The method of claim 1 wherein the agent is comprised of an Simidazole, a triazole, zinc pyrithione, selenium sulfide, a lithium-containing NO 0product, or mixtures thereof. (1 3. The method of claim 1 wherein the imidazole is ketoconazole; dichlorophenyl imidazolodioxalan; clotrimazole; itraconazole; miconazole; climbazole; tioconazole; sulconazole; butoconazole; fluconazole; or any possible stereo isomers thereof and mixtures thereof.
4. The method of claim 1 wherein the agent is ketoconazole, zinc pyrithione, or mixtures thereof. The method of claim 1 wherein the anagen hair inducing agent is topically applied in an amount of from about 0.001 mg/sq. mm to about 1000 mg/ sq. mm to the area.
6. The method of claim 1 wherein the anagen hair inducing agent is applied in a water-based medium or an oil-based medium.
7. The method of claim 6 wherein the medium is water-based.
8. The method of claim 6 wherein the medium contains, based upon the total weight of the medium, from about 0.01 percent to about 20 percent anagen hair inducing agent.
9. The method of claim 6 wherein the medium contains, based upon the total weight of the medium, from about 0.5 percent to about 5 percent anagen hair inducing agent. The method of claim 6 wherein the medium is a cream.
11. The method of claim 5 wherein the medium is a shampoo.
12. The method of claim 1 wherein the anagen hair inducing agent is applied from about 1 to about 7 times per week.
13. A method of reducing the shedding of hair in a human comprised of topically applying an effective amount of an agent which (0 inhibits the growth of P. ovale or mixture thereof to an area of the human C^ 10 wherein a decrease in the amount of shedding is desired. NC-
14. The method of claim 13 wherein the agent is comprised of an 0 imidazole, a triazole. zinc pyrithione, selenium sulfide, a lithium-containing product, or mixtures thereof. The method of claim 13 wherein the imidazole is ketoconazole; dichlorophenyl imidazolodioxalan; clotrimazole; itraconazole; miconazole; climbazole; tioconazole; sulconazole; butoconazole; fluconazole; or any possible stereo isomers thereof and mixtures thereof.
16. The method of claim 13 wherein the agent is ketoconazole, zinc pyrithione, or mixtures thereof.
17. The method of claim 13 wherein the hair shedding reductant is topically applied in an amount of from about 0.001 mg/sq. mm to about 1000 mg/ sq. mm to the area.
18. The method of claim 13 wherein the hair shedding reductant is applied in a water-based medium or an oil-based medium.
19. The method of claim 18 wherein the medium is a water-based medium. The method of claim 18 wherein the medium contains, based upon the total weight of the medium, from about 0.01 percent to about percent hair shedding reductant.
21. The method of claim 20 wherein the medium contains, based upon the total weight of the medium, from about 0.5 percent to about percent hair shedding reductant.
22. The method of claim 18 wherein the medium is a cream.
23. The method of claim 18 wherein the medium is a shampoo. S24. The method of claim 13 wherein the hair shedding reductant is applied from about 1 to about 7 times per week. A method of increasing the diameter of a hair shaft in a human comprised of topically applying an effective amount of a hair diameter increasing agent comprised of an imidazole, a triazole, selenium sulfide, lithium-containing product or mixtures thereof to an area of the human wherein a decrease in the amount of shedding is desired
26. The method of claim 25 wherein the imidazole is ketoconazole, elubiol, or mixtures thereof.
27. The method of claim 25 wherein the hair diameter increasing agent is topically applied in an amount of from about 0.001 mg/sq. mm to about 1000 mg/ sq. mm to the area.
28. The method of claim 25 wherein the hair diameter increasing agent is applied in a water-based medium or an oil-based medium.
29. The method of claim 28 wherein the medium is a water-based medium. The method of claim 28 wherein the medium contains, based upon the total weight of the medium, from about 0.01 percent to about percent hair diameter increasing agent.
31. The method of claim 28 wherein the medium contains, based upon the total weight of the medium, from about 0.5 percent to about percent hair diameter increasing agent.
32. The method of claim 28 wherein the medium is a cream.
33. The method of claim 29 wherein the medium is a shampoo.
34. The method of claim 25 wherein the hair diameter increasing agent is applied from about 1 to about 7 times per week. The method of claim 25 wherein said hair diameter increasing agent is combined with zinc pyrithione. S21
36. A method for increasing the thickness of hair in humans Scomprising topically applying an oil reducing agent to a desired area.
37. The method of claim 36 wherein the agent is applied in an oil- based or a water-based medium.
38. The method of claim 37 wherein the medium is in the form of a S shampoo.
39. The method of claim 37 wherein the medium is in the form of a cream. A method for increasing the period of time during which hair grows in a human comprised of topically applying an effective amount of an agent which inhibits the growth of P. ovale or mixture thereof to a desired area of the human. DATED this 19th day of July 2006 Shelston IP Attorneys for: Johnson Johnson Consumer Companies, Inc.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60069993 | 1997-12-18 | ||
| AU2003203846A AU2003203846A1 (en) | 1997-12-18 | 2003-04-23 | Methods for improving the health of hair and scalp |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2003203846A Division AU2003203846A1 (en) | 1997-12-18 | 2003-04-23 | Methods for improving the health of hair and scalp |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2006203095A1 true AU2006203095A1 (en) | 2006-10-05 |
Family
ID=37084798
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2006203095A Abandoned AU2006203095A1 (en) | 1997-12-18 | 2006-07-19 | Methods for improving the health of hair and scalp |
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| Country | Link |
|---|---|
| AU (1) | AU2006203095A1 (en) |
-
2006
- 2006-07-19 AU AU2006203095A patent/AU2006203095A1/en not_active Abandoned
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