WO1995023580A1 - Prevention et traitement de la depilation secondaire - Google Patents
Prevention et traitement de la depilation secondaire Download PDFInfo
- Publication number
- WO1995023580A1 WO1995023580A1 PCT/JP1995/000350 JP9500350W WO9523580A1 WO 1995023580 A1 WO1995023580 A1 WO 1995023580A1 JP 9500350 W JP9500350 W JP 9500350W WO 9523580 A1 WO9523580 A1 WO 9523580A1
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- WO
- WIPO (PCT)
- Prior art keywords
- hair loss
- administration
- group
- hair
- copper
- Prior art date
Links
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- 230000035617 depilation Effects 0.000 title abstract 2
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q7/00—Preparations for affecting hair growth
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/06—Tripeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/58—Metal complex; Coordination compounds
Definitions
- the present invention relates to an agent for preventing and treating secondary hair loss characterized by containing a tripeptide monocopper complex having an excellent effect in preventing and treating secondary hair loss induced by administration of an anticancer agent or the like.
- An object of the present invention is to prevent and treat secondary hair loss, which is a side effect of chemotherapy or radiation therapy such as administration of an anticancer drug, more reliably.
- the “secondary hair loss” in the present invention means a hair loss symptom secondary to a side effect caused by chemotherapy such as administration of an anticancer agent or radiation therapy.
- chemotherapy such as administration of an anticancer agent or radiation therapy.
- peptide-copper complexes have a hair growth-promoting effect on male pattern baldness, in which men lose their hair with age, but it has still been demonstrated that they are effective in secondary hair loss. Did not.
- the present inventors thought that the peptide-copper complex was effective in preventing and treating secondary hair loss, and made extensive studies using a rat chemotherapy hair loss model.
- FIG. 1 is a diagram showing the degree of hair loss of the whole body of the test substance-administered group, control group (vehicle-administered group), and normal group (anti-cancer drug-non-administered group) in Example 1 as a hair loss score as a criterion. It is.
- FIG. 2 is a diagram showing animals in a test substance administration group on day 13 after the start of anticancer drug administration in Example 1.
- FIG. 3 is a diagram showing animals in a control group on day 13 after the start of anticancer drug administration in Example 1.
- FIG. 4 is a diagram showing animals in a normal group on day 13 after the start of anticancer drug administration in Example 1.
- FIG. 5 is a diagram showing the degree of hair loss in the whole body of the test substance-administered group, the control group (vehicle-administered group), and the normal group (anti-cancer drug-non-administered group) in Example 2 as a hair loss score as a criterion. It is.
- FIG. 6 is a diagram showing animals in a test substance administration group on day 14 after the start of anticancer drug administration in Example 2.
- FIG. 7 is a diagram showing animals in a control group on day 14 after the start of anticancer drug administration in Example 2.
- FIG. 8 is a diagram showing animals in the normal group on day 14 after the start of anticancer drug administration in Example 2.
- Figure 9 shows the test substance-applied group and the control group (vehicle) on day 21 after hair removal in Example 3.
- Fig. 2 shows the degree of hair loss of the animals in the application group) as a percentage of the area of hair removal relative to the area of hair removal.
- FIG. 10 is a diagram showing the animals in the normal group (the group not administered with an anticancer drug) 21 days after hair removal in Example 3.
- FIG. 11 shows the animals in the test substance application group 21 days after hair removal in Example 3.
- FIG. 12 is a diagram showing animals of a control group (vehicle-applied group) 21 days after hair removal in Example 3.
- the active ingredient of the present invention is a triptide copper complex represented by the general formula X: copper (II) (wherein X represents a tripeptide), and the constituent amino acids of tribetide are glycine, alanine, /, 'Lin, leucine, isoleucine, serine, threonine, cystine, cystine, methine, aspartic acid, glutamic acid, lysine, arginine, phenylalanine, tyrosine, histidine, tryptophan, proline, hydroxyproline, etc.
- These amino acids can be prepared by a method described in JP-A-5-505808 by appropriately combining these three amino acids.
- the amino acid may be either L-form or D-form.
- L-alanyl-L-histidyl-L-lysine copper (11)
- glycyl-L-histidyl L-lysine copper (11)
- L-lysyl-L-histidyl-daricin complexes such as copper (II).
- L-alanyl-L-histidyl-L-lysine copper (11)
- glycyl-L-histidyl-L-lysine copper ( ⁇ )
- L-aralanyl-L-histidyl-L —Lysine copper (II).
- “copper ( ⁇ )” means a divalent copper ion, and is a tripeptide-copper (II) Although the molar ratio of tripeptide: copper ( ⁇ ) in the complex can be changed as appropriate, it is particularly preferably 1: 1 to 2: 1.
- Particularly preferred tripeptide-copper (II) complexes include, for example, L-alanyl-L-histidyl L-lysine: copper ( ⁇ ) (1: 1), daricyl-L-histidyl L-lysine: copper (II) ( 1: 1), etc., and these triptotide-copper complexes can be used alone or as a mixture of two or more.
- the agent for preventing or treating secondary hair loss of the present invention can be provided as a pharmaceutical, a quasi-drug, or a cosmetic, and its dosage form can be an intradermal injection or an external preparation.
- bases such as creams, lotions, emulsions, ointments and gels can be used. If necessary, various preservatives, fragrances, stabilizers, coloring agents, humectants, thickeners, etc. Additives can also be added.
- the amount of the secondary hair loss preventing / treating agent of the present invention can be appropriately changed depending on the kind of the drug used in the chemotherapy, the degree of the symptom, the dosage form, etc., but is usually about 0.001 to 10% by weight, preferably. Is incorporated in the preparation in an amount of about 0.01 to 5% by weight.
- the dosage of the agent for preventing and treating secondary hair loss of the present invention usually varies depending on the administration method and dosage form, but is in the range of 0.1 to 4 ml per day for adults. This daily dose is administered once or several times a day. The daily dose may be larger than the above, if necessary.
- the site of administration is preferably on the scalp.
- Example 1 The test results of Example 1 are shown in FIG.
- the whole body of the test substance-administered group, control group, and normal group animals 13 days after the start of anticancer drug administration is shown in FIGS. 2, 3, and 4, respectively.
- Intradermal administration of L-alanyl-L-histidine-L-lysine Copper (II) (1: 1) 0.05 ml of a physiological saline solution containing 0.25% to one place at the center of the back of 8-day-old SD rats I do. From the next day, once a day, intraperitoneally administer Ar a-C at a dose of 25 mgZkg. The determination of the hair loss preventing effect was made by scoring the hair loss status of the whole body and the test substance administration site in the same manner as in Example 1. In the control group, only physiological saline was used.
- Test results> The test results of Example 2 are shown in FIG.
- test substance administration group of the present invention In the 0.25% test substance administration group of the present invention, almost the whole body hair excluding the administration site showed a hair loss pattern similar to that of the control group, but hair loss was prevented around the test substance administration site, and scars due to intradermal administration were observed. Was also not recognized.
- FIGS. 6, 7, and 8 The whole body images of the test substance administration group, control group, and normal group animals on day 14 after the start of anticancer drug administration are shown in FIGS. 6, 7, and 8, respectively.
- Example 1 and Example 2 the effect of preventing intradermal administration of the substance of the present invention for hair loss due to chemotherapy was clarified. Whether or not the application of the substance of the present invention exerts a hair loss preventing effect was examined using a mouse chemotherapy hair loss model.
- FIG. 9 shows the hair removal rate of the test substance-applied group and the control group (vehicle-applied group) on day 21 after hair removal as a percentage of the hair removal area to the hair removal area.
- the whole body images of the normal group (anticancer drug-free group), the test substance-applied group, and the control group (vehicle-applied group) on day 21 after hair removal are shown in FIGS. 10, 11, and 12, respectively.
- the agent for preventing and treating secondary hair loss of the present invention is effective for secondary hair loss.
- the preventive / therapeutic agent for secondary hair loss of the present invention is useful as a preventive and therapeutic agent for secondary hair loss that exhibits an excellent effect.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Gastroenterology & Hepatology (AREA)
- Inorganic Chemistry (AREA)
- Dermatology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Prévention et traitement de la dépilation secondaire consécutive à une chimiothérapie à base de carcinostatiques ou à une radiothérapie, au moyen d'un complexe de tripeptide de cuivre de formule générale X:Cu(II) où X est un tripeptide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU18614/95A AU1861495A (en) | 1994-03-03 | 1995-03-03 | Preventive and remedy for secondary depilation |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6/58188 | 1994-03-03 | ||
JP5818894 | 1994-03-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1995023580A1 true WO1995023580A1 (fr) | 1995-09-08 |
Family
ID=13077053
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1995/000350 WO1995023580A1 (fr) | 1994-03-03 | 1995-03-03 | Prevention et traitement de la depilation secondaire |
Country Status (2)
Country | Link |
---|---|
AU (1) | AU1861495A (fr) |
WO (1) | WO1995023580A1 (fr) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005504063A (ja) * | 2001-09-03 | 2005-02-10 | リシャール・ヴェルミー | 化学療法誘導性脱毛の予防に関連する組成物および方法 |
JP2006504448A (ja) * | 2002-07-02 | 2006-02-09 | プロサイト コーポレイション | ペプチド銅錯体および軟組織充填物を含有する組成物 |
JP2007516209A (ja) * | 2003-07-18 | 2007-06-21 | アンスティテュ・ヨーロペアン・ドゥ・ビョロジ・セリュレール | 脱毛症の予防および治療的処置用組成物の製造のためのペプチド複合体の使用 |
WO2021247531A1 (fr) * | 2020-06-01 | 2021-12-09 | Balchem Corporation | Chélates métalliques de diaminoacide ou chélates métalliques de triaminoacide |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH05501567A (ja) * | 1989-11-13 | 1993-03-25 | プロサイト コーポレーション | 毛髪成長を刺激するための金属―ペプチド組成物及び方法 |
JPH06305941A (ja) * | 1993-04-15 | 1994-11-01 | Procyte Corp | 毛の成長を促進する医薬及び化粧品 |
-
1995
- 1995-03-03 AU AU18614/95A patent/AU1861495A/en not_active Abandoned
- 1995-03-03 WO PCT/JP1995/000350 patent/WO1995023580A1/fr active Application Filing
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH05501567A (ja) * | 1989-11-13 | 1993-03-25 | プロサイト コーポレーション | 毛髪成長を刺激するための金属―ペプチド組成物及び方法 |
JPH06305941A (ja) * | 1993-04-15 | 1994-11-01 | Procyte Corp | 毛の成長を促進する医薬及び化粧品 |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005504063A (ja) * | 2001-09-03 | 2005-02-10 | リシャール・ヴェルミー | 化学療法誘導性脱毛の予防に関連する組成物および方法 |
JP2006504448A (ja) * | 2002-07-02 | 2006-02-09 | プロサイト コーポレイション | ペプチド銅錯体および軟組織充填物を含有する組成物 |
JP2007516209A (ja) * | 2003-07-18 | 2007-06-21 | アンスティテュ・ヨーロペアン・ドゥ・ビョロジ・セリュレール | 脱毛症の予防および治療的処置用組成物の製造のためのペプチド複合体の使用 |
JP2013010769A (ja) * | 2003-07-18 | 2013-01-17 | Inst Europeen De Biologie Cellulair | 脱毛症の予防および治療的処置用組成物の製造のためのペプチド複合体の使用 |
JP2015134777A (ja) * | 2003-07-18 | 2015-07-27 | アンスティテュ・ヨーロペアン・ドゥ・ビョロジ・セリュレールInstitut Europeen De Biologie Cellulaire | 脱毛症の予防および治療的処置用組成物の製造のためのペプチド複合体の使用 |
WO2021247531A1 (fr) * | 2020-06-01 | 2021-12-09 | Balchem Corporation | Chélates métalliques de diaminoacide ou chélates métalliques de triaminoacide |
Also Published As
Publication number | Publication date |
---|---|
AU1861495A (en) | 1995-09-18 |
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