WO2013178065A1 - Amino acid copper complex with effects of preventing alopecia, growing hair and protecting skin, preparation method and application - Google Patents
Amino acid copper complex with effects of preventing alopecia, growing hair and protecting skin, preparation method and application Download PDFInfo
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- WO2013178065A1 WO2013178065A1 PCT/CN2013/076407 CN2013076407W WO2013178065A1 WO 2013178065 A1 WO2013178065 A1 WO 2013178065A1 CN 2013076407 W CN2013076407 W CN 2013076407W WO 2013178065 A1 WO2013178065 A1 WO 2013178065A1
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- 0 C*C(*)(C(O*(C)(C(C)C)OC(C(*)(*(C)c1c(*)nc(*)[n]1*)N(*)*)=O)=O)N(C)C Chemical compound C*C(*)(C(O*(C)(C(C)C)OC(C(*)(*(C)c1c(*)nc(*)[n]1*)N(*)*)=O)=O)N(C)C 0.000 description 5
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/28—Compounds containing heavy metals
- A61K31/30—Copper compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/555—Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
-
- 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
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- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C279/04—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton
- C07C279/14—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton being further substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- 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
- Amino acid copper complex for preventing hair loss, hair growth and skin care, preparation method and application thereof
- the invention relates to the field of biomedicine, in particular to an amino acid copper complex, a preparation method thereof and application thereof in preventing hair loss and skin care.
- Hair loss as a common disease of modern people, has been paid more and more attention. According to a survey by the World Health Organization, there are hundreds of millions of patients with hair loss in the world, and hair loss has become a social problem that plagues the world. The moment of hair loss affects people, makes people's pressure more and more, and enters the vicious circle of stress->hair loss->more stress. Book
- Hair growth is inseparable from hair follicles, and the presence of hair follicles is a prerequisite for hair growth replacement. Hair growth is divided into three periods: growth period, regression period and rest period. The growth period of the hair follicles, hair bulbs and dermal papillae are also large, at this time the hair matrix cells are actively dividing, causing hair growth. From the growth phase to the degenerative phase, the hair follicles become shorter, the hair bulbs shrink, the dermal papillas gather into a small group, and at the lower end of the hair bulb, the hair germ cells stop dividing and keratinize, and the hair and hair follicles are not firmly connected. Hair is easy to fall off.
- new hair bulbs and dermal papillae are formed at the lower end of the hair follicle, and new hair is grown.
- the new hair grows into the original hair follicle, and the old hair is pushed out, and the new hair reaches out to the skin.
- DHT 5-alpha reductase
- SLS skin firmness
- DHT 5-alpha reductase
- DHT is the main cause of male degeneration. DHT is produced by testosterone by 5-alpha reductase. After DHT binds to receptors on cells in hair follicles ( The number of receptors is related to heredity, which triggers a series of hair loss reactions that cause baldness.
- Copper inhibits the action of 5-alpha reductase, re-converts dihydrotestosterone to testosterone, and solves the problem of hair loss from the root. Copper ions also have Enlarging hair follicles, accelerating hair growth, inhibiting the discovery of hair growth, regulating the production of melanin in hair, regulating the energy metabolism of hair follicle cells, and eliminating free radicals on the skin. After a large number of safety tests, no toxicity problems were found, and It also does not cause an increase in copper in the blood during use.
- the first technical problem to be solved by the present invention is to provide an amino acid copper complex having anti-hair loss, hair growth and skin care effects.
- the second technical problem to be solved by the present invention is to provide a method for preparing an amino acid copper complex having anti-hair loss, hair growth and skin care effects.
- a third technical problem to be solved by the present invention is to provide an amino acid copper complex as an anti-hair loss and hair growth preparation.
- a fourth technical problem to be solved by the present invention is to provide an application of an amino acid copper complex as a skin care product.
- the technical solution of the present invention is:
- An amino acid copper complex for preventing hair loss, hair growth and skin care which is composed of a divalent copper ion and an amino acid having a structure of a base acid and/or an amino acid structure:
- R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R u , R 12 and R 13 are different kinds of side chain functional groups or the same side chain functional group, n is an integer greater than or equal to zero.
- the divalent copper ion and the amino acid of the two structures may be complexed in any ratio, wherein the amino acid is a variety of amino acids conforming to the listed amino acid structure 1 and the amino acid structure 2, and the coordination network with the divalent copper ion in a different manner.
- the preferred molar ratio of the divalent copper ion to the amino acid in the amino acid copper complex is 1: 0. 1 ⁇ 10.
- amino acid copper complex prepared by the present invention For convenience of explanation of the amino acid copper complex prepared by the present invention, the following several complex structures of different structures are listed for illustration.
- the amino acid and the divalent copper ion can be complexed in different ways, and are not limited to the three complex structures listed below, and include other modes of short chain, long chain and other spatial orbital multiple angle coordination. Coordination complexation.
- R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R u , R 12 , R 13 represent different kinds of side chain functional groups or the same side chain functional group , n is an integer greater than or equal to 0.
- the technical solution of the present invention is:
- a method for preparing an amino acid copper complex having anti-hair loss, hair growth and skin care effects comprising the steps of: mixing a solution of divalent copper ions with at least one of amino acids satisfying the following structure, and concentrating the reaction solution after complexation reaction Crystallizing or precipitating the complex in the form of crystals using an organic solvent, that is, obtaining the amino acid copper complex for preventing hair loss, hair growth, and skin care;
- R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R u , R 12
- n is an integer greater than or equal to zero.
- the organic solvent is methanol, ethanol or isopropanol.
- the preferred molar ratio of the divalent copper ion to the amino acid in the amino acid copper complex is 1: 0. 1 ⁇ 10.
- the technical solution of the present invention is:
- the amino acid copper complex for preventing hair loss, hair growth and skin care is used as an anti-hair loss and hair growth preparation.
- the amino acid copper complex is prepared into a water, ointment, liniment, gel, cream, lotion or spray dosage form, and is adjusted to a suitable pH value for the human body.
- the technical solution of the present invention is:
- Amino acid copper complex for preventing hair loss, hair growth and skin care as a skin care product.
- the amino acid copper complex is prepared into a water, ointment, liniment, gel, cream, lotion or spray dosage form, and is adjusted to a suitable pH value for the human body.
- the amino acid copper complex prepared by complexing divalent copper ions with an amino acid has the same effect as the copper polypeptide, and not only has a repairing effect on the skin, but also has anti-hair loss and hair growth effects.
- the amino acid copper complex can be formulated into a liquid preparation, a paste, a liniment, a gel, a cream, an emulsion, a spray, etc., and can be adjusted to a suitable pH value of the human body, and the skin can be effectively prevented from the normal skin free factor.
- the invention does not cause the rise of copper element in the blood during use, is safe and has no toxic side effects, and is a A more efficient and safer product enriched with a new generation of active copper repair factors that can be used as an alternative to expensive copper peptides.
- the preparation method has the advantages of simple preparation method and low cost, and is a great discovery in anti-hair loss, hair growth and skin care research, and is also a breakthrough in application, can meet the demand for anti-hair loss products, and solve the troubles caused by hair loss to modern people. At the same time, the application and promotion of the invention can create considerable economic benefits.
- Copper sulfate pentahydrate is used as a source of divalent copper ions, and an amino acid material which is a complex of L-histidine which conforms to the amino acid structure-1 is used.
- amino acid copper complex Take 9. 00g of water in a beaker, and then weigh 0. 35g of copper sulfate pentahydrate, 0. 65g of L-histidine, added under stirring, fully stirred and completely dissolved That is, a solution of 10.00 g of a structure containing an amino acid copper complex was prepared.
- Copper chloride dihydrate is used as a source of divalent copper ions, and an amino acid raw material which is a complex of L-arginine which conforms to the amino acid structure II is used.
- Preparation of the amino acid copper complex Take 9.20g of water in a beaker, and then weigh 0. 15g of copper chloride dihydrate, 0. 65g of L-arginine, add under stirring, fully stirred and fully dissolved After that, a solution of 10.00 g of a structure containing an amino acid copper complex was prepared.
- the copper sulfate pentahydrate is used as a source of divalent copper ions, and the amino acid materials of the complex amino acid structure L-histidine and L-arginine are used as the complex.
- the agglomerate of the amino acid copper complex Take 9. 00g of water in a beaker, and then weigh 0. 35g of copper sulfate pentahydrate, 0. 28g L-histidine, 0. 37g L-arginine, under stirring 00 ⁇ The solution containing the structure of the amino acid copper complex was prepared.
- Copper hydroxide is used as a source of divalent copper ions, and an amino acid raw material which is a complex of L-histidine which conforms to amino acid structure 1 and L-arginine of structure II is used.
- amino acid copper complex 0.18g Copper hydroxide was added to a beaker, and 1.00 mol/L of dilute hydrochloric acid was added dropwise to completely dissolve it. After dissolution, water was added to the total mass of the reaction liquid of 9.35 g, and then 0.28 g of histidine and 0.37 g of arginine were weighed separately. After adding, it is fully stirred and uniformly dissolved to prepare a solution of 100.00 g of a structure containing an amino acid copper complex.
- Copper chloride dihydrate is used as a source of divalent copper ions, and an amino acid raw material which is a complex of L-arginine which conforms to the amino acid structure II is used.
- amino acid copper complex a copper chloride solution and an L-arginine solution according to a molar ratio of copper chloride dihydrate to L-arginine of 1:1, stirred and mixed uniformly, and then complexed, and then Ethanol was added dropwise to the obtained reaction solution, and the complex was precipitated in the form of crystals with ethanol to obtain the amino acid copper complex which was resistant to hair loss, hair growth and skin care.
- Copper sulfate pentahydrate is used as a source of divalent copper ions, and an amino acid material which is a complex of L-arginine which conforms to the amino acid structure II is used.
- amino acid copper complex The copper sulfate solution and the L-arginine solution are stirred and mixed according to the molar ratio of copper sulfate to L-arginine of 1:8, and then the complex reaction is carried out, and then the reaction is obtained. Methanol was added dropwise to the solution, and the complex was precipitated in the form of crystals with methanol to obtain the amino acid copper complex for preventing hair loss, hair growth and skin care.
- the copper nitrate trihydrate is used as the source of the divalent copper ion, and the amino acid raw materials of the complex amino acid structure L-histidine and L-arginine are used as the complex.
- Preparation of amino acid copper complex The solution of copper nitrate and L-histidine, L-arginine according to copper nitrate trihydrate and L-histidine, L-arginine is 1: 0.05 mole The mixture is stirred and mixed uniformly, and the complexation reaction is carried out. Then, isopropanol is added dropwise to the obtained reaction solution, and the complex is precipitated in the form of crystals with isopropanol to obtain the amino acid for preventing hair loss, hair growth and skin care. Copper complex.
- Copper acetate monohydrate is used as a source of divalent copper ions
- L-histidine and L-arginine which are in accordance with amino acid structure 1 and structure 2 are used as amino acid raw materials of the complex.
- Preparation of amino acid copper complex a solution of copper acetate monohydrate and L-histidine, L-arginine solution according to copper acetate monohydrate and L-histidine, L-arginine is 1: 3 mole
- the mixture is stirred and mixed uniformly to carry out a complexation reaction, and then the reaction solution is concentrated and crystallized to obtain the amino acid copper complex which is anti-hair loss, hair growth and skin care.
- Example 9 The amino acid copper complex solution prepared in Example 1 was diluted and prepared into a water agent, and adjusted to a suitable pH value of the human body for use as an anti-hair loss and hair growth product.
- the crystals of the amino acid copper complex prepared in Example 5 were respectively added to the anti-hair loss product to allow the use of an auxiliary agent and a carrier to prepare a gelling agent, which was adjusted to a suitable pH value of the human body for use as an anti-hair loss and hair growth product.
- the amino acid copper complex solution prepared in Example 3 is added to a skin care product to allow the use of an auxiliary agent and a carrier to prepare a cream, which is used as a skin care product under a suitable pH value of the human body.
- the crystal of the amino acid copper complex prepared in Example 6 was added to the skin care product to allow the use of an auxiliary agent and a carrier to prepare a spray dosage form, which was adjusted to a suitable pH value of the human body as a skin care product.
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Description
一种防脱发、 生发、 护肤作用的氨基酸铜络合物、 制备方法及应用 技术领域 Amino acid copper complex for preventing hair loss, hair growth and skin care, preparation method and application thereof
本发明涉及生物医药领域, 尤其涉及氨基酸铜络合物、 其制备方法及其在 防脱发和护肤方面的应用。 The invention relates to the field of biomedicine, in particular to an amino acid copper complex, a preparation method thereof and application thereof in preventing hair loss and skin care.
背景技术 Background technique
脱发作为现代人的一种普遍病症, 已经得到越来越多的人的重视。 根据世 界卫生组织的一项调查数据显示:说全世界已经有几亿脱发患者, 脱发问题已经 成为困扰全世界的社会难题。 脱发时刻影响着人们, 使人们的压力越来越大, 进入压力-〉脱发-〉压力更大的恶性循环。 书 Hair loss, as a common disease of modern people, has been paid more and more attention. According to a survey by the World Health Organization, there are hundreds of millions of patients with hair loss in the world, and hair loss has become a social problem that plagues the world. The moment of hair loss affects people, makes people's pressure more and more, and enters the vicious circle of stress->hair loss->more stress. Book
头发的生长是与毛囊分不开的, 毛囊的存在是保证头发生长更换的前提。 头发的生长分为生长期、 退行期及休止期三个周期。 生长期的毛囊长、 毛球和 毛乳头也大, 此时毛母质细胞分裂活跃, 使头发生长。 由生长期转入退化期, 此时毛囊变短, 毛球缩小, 毛乳头聚成一个小团, 连在毛球低端, 毛母质细胞 停止分裂并发生角化, 头发与毛囊连接不牢, 毛发易脱落。 在下一个生长周期 开始时, 在毛囊低端形成新的毛球和毛乳头, 开始生长新头发, 新发长入原有 的毛囊内, 将旧发推出, 新发伸到皮肤外面。 Hair growth is inseparable from hair follicles, and the presence of hair follicles is a prerequisite for hair growth replacement. Hair growth is divided into three periods: growth period, regression period and rest period. The growth period of the hair follicles, hair bulbs and dermal papillae are also large, at this time the hair matrix cells are actively dividing, causing hair growth. From the growth phase to the degenerative phase, the hair follicles become shorter, the hair bulbs shrink, the dermal papillas gather into a small group, and at the lower end of the hair bulb, the hair germ cells stop dividing and keratinize, and the hair and hair follicles are not firmly connected. Hair is easy to fall off. At the beginning of the next growth cycle, new hair bulbs and dermal papillae are formed at the lower end of the hair follicle, and new hair is grown. The new hair grows into the original hair follicle, and the old hair is pushed out, and the new hair reaches out to the skin.
西医上治疗脱发被美国 FDA认证的药品只有非那雄胺和米诺地尔, 但这两 种药物均有比较严重的副作用。 除了这两种药以外, 治疗脱发的方法还有被西 方医学界承认的植发。 药物治疗与植发虽已经取得极大的进展, 但仍然有着极 大的局限性。 Western medicine for the treatment of hair loss The United States FDA-certified drugs are only finasteride and minoxidil, but both drugs have serious side effects. In addition to these two drugs, methods for treating hair loss include hair transplants recognized by the Western medical community. Although medical treatment and hair transplantation have made great progress, they still have great limitations.
国际化妆品公司已开始兴起一阵铜元素旋风, 因为最新证据表明铜是抗衰 老的最新秘密武器。 当所有的埃及人将铜作为修复伤口之用后, 铜对皮肤有好 处这一观点便盛行了很长一段时间, 但是当 70年代一位美国生物化学家 Loren Pickart博士发现铜多肽时, 人们才开始在科学上对其做进一步的研究。 他的 早期工作表明, 当铜元素与蛋白质结合在一起, 一些特殊的铜多肽会对伤口的 愈合、 发囊的修复和皮肤病有很好的疗效。 通过促进胶原 、 弹性蛋白, 以及与 其他必要的皮肤构成要素之合成, 美国一项独立皮肤医师研究发现, 铜多肽能 够有效防止对普通皮肤自由因子和受刺激的胶原之损害。 事实上, 在提升皮 肤紧致性方面它们比世界领先的抗衰老产品 Retin A更有效。 另一项研究表明, 铜多肽也有助于在暴露于 SLS (—种在许多洗发水、清洁、 洗涤和洗衣产品中很 普遍的一种清洁剂) 之后对皮肤完整性的恢复。 大量科研表明: 5— alpha还原 酶 (二氢睾酮(Dihydrotestosterone , DHT)是造成雄脱的主因。 DHT 由睾酮经 5-alpha还原酶作用而产生。 DHT与毛囊内细胞上的受体结合后(受体多寡与遗 传有关), 引发一连串的毛发凋落反应而引起秃头。 铜抑制 5-alpha还原酶的作 用, 将二氢睾酮重新转化为睾酮, 从根源上解决了脱发的问题。 铜离子还具有 扩大毛囊, 加速毛发生长, 抑制脱发现象促进毛发黑色素的生成、 调节毛囊细 胞的能量代谢、 清除皮肤上的自由基的作用。 在经过了大量的安全测试后, 并 未发现任何毒性问题, 且在使用过程中也不会引起血液中铜元素的升高。 International cosmetics companies have begun to create a whirlwind of copper, because the latest evidence shows that copper is the latest secret weapon for anti-aging. When all the Egyptians used copper as a repairing wound, the idea that copper is good for the skin has been popular for a long time, but when the American biochemist Dr. Loren Pickart discovered the copper peptide in the 1970s, Begin to study it further in science. His early work showed that when copper is combined with protein, some special copper peptides have a good effect on wound healing, hair repair and skin diseases. By promoting the synthesis of collagen, elastin, and other essential skin components, an independent dermatologist in the United States found that copper peptides are effective in preventing damage to common skin free factors and stimulated collagen. In fact, in the lift skin They are more effective than the world's leading anti-aging product, Retin A, in terms of skin firmness. Another study showed that copper peptides also contribute to the recovery of skin integrity after exposure to SLS, a cleaner commonly found in many shampoo, cleaning, washing and laundry products. A large number of scientific studies have shown that: 5-alpha reductase (Dihydrotestosterone (DHT) is the main cause of male degeneration. DHT is produced by testosterone by 5-alpha reductase. After DHT binds to receptors on cells in hair follicles ( The number of receptors is related to heredity, which triggers a series of hair loss reactions that cause baldness. Copper inhibits the action of 5-alpha reductase, re-converts dihydrotestosterone to testosterone, and solves the problem of hair loss from the root. Copper ions also have Enlarging hair follicles, accelerating hair growth, inhibiting the discovery of hair growth, regulating the production of melanin in hair, regulating the energy metabolism of hair follicle cells, and eliminating free radicals on the skin. After a large number of safety tests, no toxicity problems were found, and It also does not cause an increase in copper in the blood during use.
铜多肽的这一系列的研究, 充分的展示出了铜多肽的优势, 但铜多肽系列 成分价格相当昂贵, 这在满足市场需求上又成为了一大障碍, 而我们通过大量 的实验, 惊奇的发现了一种新型防脱发、 生发、 护肤作用的氨基酸铜络合物, 该氨基酸铜络合物与铜多肽具有相同功效, 该氨基酸铜络合物能够有效防止普 通皮肤自由因子和胶原所受到的刺激损害, 对皮肤进行完整性的恢复, 作用在 头皮表层, 则从毛发的根源毛囊上做护理修复, 让毛囊逐步恢复健康, 使头发 恢复正常的生长周期, 从而实现防脱发、 生发、 护肤作用效果, 并且该氨基酸 铜络合物在成本上远低于铜多肽, 在使用上方便且安全而无毒副作用, 这不仅 在防脱发、 生发、 护肤研究上是一大发现, 而且在应用上是一大突破, 实现为 有防脱发、 生发、 护肤需要的人们解决烦恼, 同时可以创造可观的经济效益。 发明内容 This series of studies on copper peptides fully demonstrates the advantages of copper peptides, but the price of copper peptide series is quite expensive, which has become a major obstacle in meeting market demand, and we have been surprised by a large number of experiments. A novel copper complex of amino acids against hair loss, hair growth and skin care has been discovered. The copper complex of the amino acid has the same effect as the copper polypeptide, and the copper complex of the amino acid can effectively prevent the normal skin free factor and collagen from being affected. Stimulating damage, restoring the integrity of the skin, acting on the surface of the scalp, then repairing and repairing from the hair follicles of the hair, allowing the hair follicles to gradually return to health, returning the hair to a normal growth cycle, thereby preventing hair loss, hair growth, and skin care. The effect, and the amino acid copper complex is much lower in cost than the copper polypeptide, and is convenient and safe in use without toxic side effects, which is not only a major discovery in anti-hair loss, hair growth, skin care research, but also in application. A big breakthrough, to solve the problem of people who have anti-hair loss, hair growth, skin care needs Annoyed, at the same time can create considerable economic benefits. Summary of the invention
本发明所要解决的第一个技术问题是: 提供一种具有防脱发、 生发、 护肤 作用的氨基酸铜络合物。 The first technical problem to be solved by the present invention is to provide an amino acid copper complex having anti-hair loss, hair growth and skin care effects.
本发明所要解决的第二个技术问题是: 提供一种具有防脱发、 生发、 护肤 作用的氨基酸铜络合物的制备方法。 The second technical problem to be solved by the present invention is to provide a method for preparing an amino acid copper complex having anti-hair loss, hair growth and skin care effects.
本发明所要解决的第三个技术问题是: 提供氨基酸铜络合物作为防脱发、 生发制剂的应用。 A third technical problem to be solved by the present invention is to provide an amino acid copper complex as an anti-hair loss and hair growth preparation.
本发明所要解决的第四个技术问题是: 提供氨基酸铜络合物作为护肤产品 的应用。 为解决上述第一个技术问题, 本发明的技术方案是: A fourth technical problem to be solved by the present invention is to provide an application of an amino acid copper complex as a skin care product. In order to solve the above first technical problem, the technical solution of the present invention is:
一种防脱发、 生发、 护肤作用的氨基酸铜络合物, 由二价铜离子与具有以 基酸结构一和 /或氨基酸结构二的氨基酸络合而成: An amino acid copper complex for preventing hair loss, hair growth and skin care, which is composed of a divalent copper ion and an amino acid having a structure of a base acid and/or an amino acid structure:
其中, R2、 R3、 R4、 R5、 R6、 R7、 R8、 R9、 R10, Ru、 R12、 R13为不同种侧链官 能团或者同一种侧链官能团, n为大于等于 0的整数。 Wherein R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R u , R 12 and R 13 are different kinds of side chain functional groups or the same side chain functional group, n is an integer greater than or equal to zero.
本发明中二价铜离子与两种结构的氨基酸可以以任意比例络合, 其中氨基 酸为符合所列氨基酸结构一和氨基酸结构二的各种氨基酸, 与二价铜离子以不 同方式的配位络合, 能游离出二价铜离子的、 或者能跟符合所列结构的氨基酸 结构一和氨基酸结构二的各种氨基酸反应生成该氨基酸铜络合物的原料, 都可 作为二价铜离子的来源。 In the present invention, the divalent copper ion and the amino acid of the two structures may be complexed in any ratio, wherein the amino acid is a variety of amino acids conforming to the listed amino acid structure 1 and the amino acid structure 2, and the coordination network with the divalent copper ion in a different manner. A raw material capable of freeing out divalent copper ions or reacting with various amino acids conforming to the amino acid structure 1 and amino acid structure 2 of the listed structure to form a copper complex of the amino acid, which can be used as a source of divalent copper ions. .
作为一种优选, 所述氨基酸铜络合物中的二价铜离子与所述氨基酸优选的 络合摩尔比为 1 : 0. 1〜10。 1〜10。 The preferred molar ratio of the divalent copper ion to the amino acid in the amino acid copper complex is 1: 0. 1~10.
为方便说明本发明制备的氨基酸铜络合物, 现列举以下几个不同结构的络 合物以作说明。 本发明中氨基酸与二价铜离子可以以不同方式的配位络合, 不 局限于以下所列三种络合结构, 还包括其他方式的短链、 长链以及其他空间轨 道多个角度配位的配位络合。 For convenience of explanation of the amino acid copper complex prepared by the present invention, the following several complex structures of different structures are listed for illustration. In the present invention, the amino acid and the divalent copper ion can be complexed in different ways, and are not limited to the three complex structures listed below, and include other modes of short chain, long chain and other spatial orbital multiple angle coordination. Coordination complexation.
其中, 、 R2、 R3、 R4、 R5、 R6、 R7、 R8、 R9、 R10, Ru、 R12、 R13代表不同种侧链 官能团或者同一种侧链官能团, n为大于等于 0的整数。 Wherein, R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R u , R 12 , R 13 represent different kinds of side chain functional groups or the same side chain functional group , n is an integer greater than or equal to 0.
为解决上述第二个技术问题, 本发明的技术方案是: In order to solve the above second technical problem, the technical solution of the present invention is:
制备具有防脱发、 生发、 护肤作用的氨基酸铜络合物的方法, 包括以下步 骤: 将二价铜离子的溶液与符合以下结构的氨基酸中的至少一种混合均匀, 络 合反应后浓缩反应液结晶或使用有机溶剂将络合物以晶体形式析出, 即得到所 述防脱发、 生发、 护肤作用的氨基酸铜络合物; 其中, R2、 R3、 R4、 R5、 R6、 R7、 R8、 R9、 R10、 Ru、 R12、 A method for preparing an amino acid copper complex having anti-hair loss, hair growth and skin care effects, comprising the steps of: mixing a solution of divalent copper ions with at least one of amino acids satisfying the following structure, and concentrating the reaction solution after complexation reaction Crystallizing or precipitating the complex in the form of crystals using an organic solvent, that is, obtaining the amino acid copper complex for preventing hair loss, hair growth, and skin care; Wherein R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R u , R 12 ,
能团或者同一种侧链官能团, n为大于等于 0的整数。 An energy group or the same side chain functional group, n is an integer greater than or equal to zero.
优选的, 所述有机溶剂为甲醇、 乙醇或异丙醇。 Preferably, the organic solvent is methanol, ethanol or isopropanol.
作为一种优选, 所述氨基酸铜络合物中的二价铜离子与所述氨基酸优选的 络合摩尔比为 1 : 0. 1〜10。 1〜10。 The preferred molar ratio of the divalent copper ion to the amino acid in the amino acid copper complex is 1: 0. 1~10.
为解决上述第三个技术问题, 本发明的技术方案是: In order to solve the above third technical problem, the technical solution of the present invention is:
防脱发、 生发、 护肤作用的氨基酸铜络合物作为防脱发、 生发制剂的应用。 优选的, 将所述氨基酸铜络合物制备成水剂、 膏剂、 擦剂、 凝胶剂、 霜剂、 乳液剂或喷剂剂型, 调到人体适宜的 pH值下使用。 The amino acid copper complex for preventing hair loss, hair growth and skin care is used as an anti-hair loss and hair growth preparation. Preferably, the amino acid copper complex is prepared into a water, ointment, liniment, gel, cream, lotion or spray dosage form, and is adjusted to a suitable pH value for the human body.
为解决上述第四个技术问题, 本发明的技术方案是: In order to solve the above fourth technical problem, the technical solution of the present invention is:
防脱发、 生发、 护肤作用的氨基酸铜络合物作为护肤产品的应用。 Amino acid copper complex for preventing hair loss, hair growth and skin care as a skin care product.
优选的, 将所述氨基酸铜络合物制备成水剂、 膏剂、 擦剂、 凝胶剂、 霜剂、 乳液剂或喷剂剂型, 调到人体适宜的 pH值下使用。 Preferably, the amino acid copper complex is prepared into a water, ointment, liniment, gel, cream, lotion or spray dosage form, and is adjusted to a suitable pH value for the human body.
由于采用了上述技术方案, 本发明的有益效果是: Due to the adoption of the above technical solutions, the beneficial effects of the present invention are:
本发明将二价铜离子与氨基酸络合制备的氨基酸铜络合物, 与铜多肽具有 相同功效, 不仅对皮肤具有修复作用, 而且具有防脱发和生发作用。 可以将氨 基酸铜络合物制成水剂、 膏剂、 擦剂、 凝胶、 面霜、 乳液、 喷剂等剂型, 调到 人体适宜的 pH值下使用, 作用在皮肤上则有效防止普通皮肤自由因子和胶原所 受到的刺激损害, 对皮肤进行完整性的恢复, 将其作用在头皮毛囊表层, 使修 复因子直接作用在头皮毛囊, 有效渗透于毛发根部, 则起到活化毛囊组织、 促 进血液循环、 促进毛囊对养分充分吸收的作用, 从而对头皮进行完整性修复, 最终达到防脱发、 生发、 护肤效果。 The amino acid copper complex prepared by complexing divalent copper ions with an amino acid has the same effect as the copper polypeptide, and not only has a repairing effect on the skin, but also has anti-hair loss and hair growth effects. The amino acid copper complex can be formulated into a liquid preparation, a paste, a liniment, a gel, a cream, an emulsion, a spray, etc., and can be adjusted to a suitable pH value of the human body, and the skin can be effectively prevented from the normal skin free factor. And the stimulation damage caused by collagen, the restoration of the integrity of the skin, the action on the surface of the scalp hair follicle, so that the repair factor directly acts on the scalp hair follicle, effectively penetrate the root of the hair, then activate the hair follicle tissue, promote blood circulation, Promote the full absorption of nutrients by the hair follicles, thus repairing the integrity of the scalp, and finally achieving anti-hair loss, hair growth and skin care effects.
本发明在使用中, 不会引起血液中铜元素的升高, 安全无毒副作用, 是一 种富含新一代活性铜修复因子的更有效、 更安全的产品, 可作为价格昂贵的铜 多肽的替代产品。 本发明制备方法简单、 成本低廉, 在防脱发、 生发、 护肤研 究上是一大发现, 在应用上也是一大突破, 可以满足人们对防脱发产品的需求, 解决脱发给现代人带来的烦恼, 同时本发明的应用推广又可以创造可观的经济 效益。 The invention does not cause the rise of copper element in the blood during use, is safe and has no toxic side effects, and is a A more efficient and safer product enriched with a new generation of active copper repair factors that can be used as an alternative to expensive copper peptides. The preparation method has the advantages of simple preparation method and low cost, and is a great discovery in anti-hair loss, hair growth and skin care research, and is also a breakthrough in application, can meet the demand for anti-hair loss products, and solve the troubles caused by hair loss to modern people. At the same time, the application and promotion of the invention can create considerable economic benefits.
具体实施方式 detailed description
下面结合具体的实施例, 进一步阐述本发明。 应理解, 这些实施例仅用于 说明本发明而不用于限制本发明的范围。 此外应理解, 在阅读了本发明讲授的 内容之后, 本领域技术人员可以对本发明作各种改动或修改, 这些等价形式同 样落于本申请所附权利要求书所限定的范围。 The invention is further illustrated below in conjunction with specific embodiments. It is to be understood that the examples are not intended to limit the scope of the invention. It is to be understood that the invention may be modified or modified by those skilled in the art in the light of the scope of the present invention.
实施例 1 Example 1
以五水硫酸铜作为二价铜离子的来源, 以符合氨基酸结构一的 L-组氨酸作 为络合物的氨基酸原料。 氨基酸铜络合物的制备: 取 9. 00g水于烧杯中, 再分 别称取 0. 35g 五水硫酸铜、 0. 65g L-组氨酸, 在搅拌下加入, 待充分搅拌均匀 全部溶解后即制成 10. 00g含有氨基酸铜络合物结构的溶液。 Copper sulfate pentahydrate is used as a source of divalent copper ions, and an amino acid material which is a complex of L-histidine which conforms to the amino acid structure-1 is used. Preparation of amino acid copper complex: Take 9. 00g of water in a beaker, and then weigh 0. 35g of copper sulfate pentahydrate, 0. 65g of L-histidine, added under stirring, fully stirred and completely dissolved That is, a solution of 10.00 g of a structure containing an amino acid copper complex was prepared.
实施例 2 Example 2
以二水氯化铜作为二价铜离子的来源, 以符合氨基酸结构二的 L-精氨酸作 为络合物的氨基酸原料。 氨基酸铜络合物的制备: 取 9. 20g水于烧杯中, 再分 别称取 0. 15g 二水氯化铜、 0. 65g L-精氨酸, 在搅拌下加入, 待充分搅拌均匀 全部溶解后即制成 10. 00g含有氨基酸铜络合物结构的溶液。 Copper chloride dihydrate is used as a source of divalent copper ions, and an amino acid raw material which is a complex of L-arginine which conforms to the amino acid structure II is used. Preparation of the amino acid copper complex: Take 9.20g of water in a beaker, and then weigh 0. 15g of copper chloride dihydrate, 0. 65g of L-arginine, add under stirring, fully stirred and fully dissolved After that, a solution of 10.00 g of a structure containing an amino acid copper complex was prepared.
实施例 3 Example 3
以五水硫酸铜作为二价铜离子的来源, 以符合氨基酸结构一及结构二的 L- 组氨酸、 L-精氨酸作为络合物的氨基酸原料。氨基酸铜络合物的制备: 取 9. 00g 水于烧杯中, 再分别称取 0. 35g 五水硫酸铜、 0. 28g L-组氨酸、 0. 37g L-精氨 酸, 在搅拌下加入, 待充分搅拌均匀全部溶解后即制成 10. 00g含有氨基酸铜络 合物结构的溶液。 The copper sulfate pentahydrate is used as a source of divalent copper ions, and the amino acid materials of the complex amino acid structure L-histidine and L-arginine are used as the complex. The agglomerate of the amino acid copper complex: Take 9. 00g of water in a beaker, and then weigh 0. 35g of copper sulfate pentahydrate, 0. 28g L-histidine, 0. 37g L-arginine, under stirring 00克溶液。 The solution containing the structure of the amino acid copper complex was prepared.
实施例 4 Example 4
以氢氧化铜作为二价铜离子的来源, 以符合氨基酸结构一的 L-组氨酸及结 构二的 L-精氨酸作为络合物的氨基酸原料。氨基酸铜络合物的制备: 取 0.18g 氢氧化铜于烧杯中, 滴加 1.00mol/L稀盐酸使其完全溶解, 溶解后加水到反应液 总质量 9.35g, 再分别称取 0.28g组氨酸、 0.37g精氨酸, 在搅拌下加入, 待充分 搅拌均匀全部溶解后即制成 lO.OOg含有氨基酸铜络合物结构的溶液。 Copper hydroxide is used as a source of divalent copper ions, and an amino acid raw material which is a complex of L-histidine which conforms to amino acid structure 1 and L-arginine of structure II is used. Preparation of amino acid copper complex: 0.18g Copper hydroxide was added to a beaker, and 1.00 mol/L of dilute hydrochloric acid was added dropwise to completely dissolve it. After dissolution, water was added to the total mass of the reaction liquid of 9.35 g, and then 0.28 g of histidine and 0.37 g of arginine were weighed separately. After adding, it is fully stirred and uniformly dissolved to prepare a solution of 100.00 g of a structure containing an amino acid copper complex.
实施例 5 Example 5
以二水氯化铜作为二价铜离子的来源, 以符合氨基酸结构二的 L-精氨酸作 为络合物的氨基酸原料。 氨基酸铜络合物的制备: 将氯化铜溶液与 L-精氨酸溶 液按照二水氯化铜与 L-精氨酸为 1 : 1的摩尔比, 搅拌混合均匀, 进行络合反应, 然后向得到的反应溶液中滴加乙醇, 用乙醇将络合物以晶体形式析出, 即得到 所述防脱发、 生发、 护肤作用的氨基酸铜络合物。 Copper chloride dihydrate is used as a source of divalent copper ions, and an amino acid raw material which is a complex of L-arginine which conforms to the amino acid structure II is used. Preparation of amino acid copper complex: a copper chloride solution and an L-arginine solution according to a molar ratio of copper chloride dihydrate to L-arginine of 1:1, stirred and mixed uniformly, and then complexed, and then Ethanol was added dropwise to the obtained reaction solution, and the complex was precipitated in the form of crystals with ethanol to obtain the amino acid copper complex which was resistant to hair loss, hair growth and skin care.
实施例 6 Example 6
以五水硫酸铜作为二价铜离子的来源, 以符合氨基酸结构二的 L-精氨酸作 为络合物的氨基酸原料。 氨基酸铜络合物的制备: 将硫酸铜溶液与 L-精氨酸溶 液按照硫酸铜与 L-精氨酸为 1 : 8的摩尔比, 搅拌混合均匀, 进行络合反应, 然 后向得到的反应溶液中滴加甲醇, 用甲醇将络合物以晶体形式析出, 即得到所 述防脱发、 生发、 护肤作用的氨基酸铜络合物。 Copper sulfate pentahydrate is used as a source of divalent copper ions, and an amino acid material which is a complex of L-arginine which conforms to the amino acid structure II is used. Preparation of amino acid copper complex: The copper sulfate solution and the L-arginine solution are stirred and mixed according to the molar ratio of copper sulfate to L-arginine of 1:8, and then the complex reaction is carried out, and then the reaction is obtained. Methanol was added dropwise to the solution, and the complex was precipitated in the form of crystals with methanol to obtain the amino acid copper complex for preventing hair loss, hair growth and skin care.
实施例 7 Example 7
以三水硝酸铜作为二价铜离子的来源, 以符合氨基酸结构一及结构二的 L- 组氨酸、 L-精氨酸作为络合物的氨基酸原料。 氨基酸铜络合物的制备: 将硝酸 铜溶液与 L-组氨酸、 L-精氨酸溶液按照三水硝酸铜与 L-组氨酸、 L-精氨酸为 1 : 0. 05 的摩尔比, 搅拌混合均匀, 进行络合反应, 然后向得到的反应溶液中滴 加异丙醇, 用异丙醇将络合物以晶体形式析出, 即得到所述防脱发、 生发、 护 肤作用的氨基酸铜络合物。 The copper nitrate trihydrate is used as the source of the divalent copper ion, and the amino acid raw materials of the complex amino acid structure L-histidine and L-arginine are used as the complex. Preparation of amino acid copper complex: The solution of copper nitrate and L-histidine, L-arginine according to copper nitrate trihydrate and L-histidine, L-arginine is 1: 0.05 mole The mixture is stirred and mixed uniformly, and the complexation reaction is carried out. Then, isopropanol is added dropwise to the obtained reaction solution, and the complex is precipitated in the form of crystals with isopropanol to obtain the amino acid for preventing hair loss, hair growth and skin care. Copper complex.
实施例 8 Example 8
以一水醋酸铜作为二价铜离子的来源, 以符合氨基酸结构一及结构二的 L- 组氨酸、 L-精氨酸作为络合物的氨基酸原料。 氨基酸铜络合物的制备: 将一水 醋酸铜溶液与 L-组氨酸、 L-精氨酸溶液按照一水醋酸铜与 L-组氨酸、 L-精氨酸 为 1 : 3 的摩尔比, 搅拌混合均匀, 进行络合反应, 然后将反应溶液浓缩结晶, 即得到所述防脱发、 生发、 护肤作用的氨基酸铜络合物。 Copper acetate monohydrate is used as a source of divalent copper ions, and L-histidine and L-arginine which are in accordance with amino acid structure 1 and structure 2 are used as amino acid raw materials of the complex. Preparation of amino acid copper complex: a solution of copper acetate monohydrate and L-histidine, L-arginine solution according to copper acetate monohydrate and L-histidine, L-arginine is 1: 3 mole The mixture is stirred and mixed uniformly to carry out a complexation reaction, and then the reaction solution is concentrated and crystallized to obtain the amino acid copper complex which is anti-hair loss, hair growth and skin care.
实施例 9 将实施例 1 制备的氨基酸铜络合物溶液, 稀释制备成水剂, 调到人体适宜 的 pH值下作为防脱发、 生发用品使用。 Example 9 The amino acid copper complex solution prepared in Example 1 was diluted and prepared into a water agent, and adjusted to a suitable pH value of the human body for use as an anti-hair loss and hair growth product.
实施例 10 Example 10
分别将实施例 5制备的氨基酸铜络合物晶体, 加入防脱发产品允许使用的 助剂、载体制备成凝胶剂, 调到人体适宜的 pH值下作为防脱发、生发用品使用。 The crystals of the amino acid copper complex prepared in Example 5 were respectively added to the anti-hair loss product to allow the use of an auxiliary agent and a carrier to prepare a gelling agent, which was adjusted to a suitable pH value of the human body for use as an anti-hair loss and hair growth product.
实施例 11 Example 11
将实施例 3 制备的氨基酸铜络合物溶液, 加入护肤产品允许使用的助剂、 载体制备成霜剂, 调到人体适宜的 pH值下作为护肤产品使用。 The amino acid copper complex solution prepared in Example 3 is added to a skin care product to allow the use of an auxiliary agent and a carrier to prepare a cream, which is used as a skin care product under a suitable pH value of the human body.
实施例 12 Example 12
将实施例 6制备的氨基酸铜络合物晶体, 加入护肤产品允许使用的助剂、 载体制备成喷剂剂型, 调到人体适宜的 pH值下作为护肤产品使用。 The crystal of the amino acid copper complex prepared in Example 6 was added to the skin care product to allow the use of an auxiliary agent and a carrier to prepare a spray dosage form, which was adjusted to a suitable pH value of the human body as a skin care product.
以上显示和描述了本发明的基本原理、 主要特征和本发明的优点。 本行业 的技术人员应该了解, 本发明不受上述实施例的限制, 上述实施例和说明书中 描述的只是说明本发明的原理, 在不脱离本发明精神和范围的前提下, 本发明 还会有各种变化和改进, 这些变化和改进都落入要求保护的本发明范围内。 本 发明要求保护范围由所附的权利要求书及其等效物界定。 The basic principles, main features and advantages of the present invention are shown and described above. It should be understood by those skilled in the art that the present invention is not limited by the foregoing embodiments, and that the present invention is only described in the foregoing embodiments and the description of the present invention, without departing from the spirit and scope of the invention. Various changes and modifications are intended to fall within the scope of the invention as claimed. The scope of the invention is defined by the appended claims and their equivalents.
一切从本发明的构思出发, 不经过创造性劳动所作出的结构变换均落在本 发明的保护范围之内。 All changes from the concept of the invention, and structural changes made without creative labor, fall within the scope of the invention.
Claims
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| EP3162367A4 (en) * | 2014-06-27 | 2018-04-18 | Postech Academy-Industry Foundation | Composition for skin penetration, containing cationic molecule transporter and anionic bioactive material |
| EP4279131A1 (en) * | 2022-05-20 | 2023-11-22 | Bioithas S.L. | Probiotic compositions for the treatment of alopecia |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006060548A2 (en) * | 2004-12-02 | 2006-06-08 | Ebersytes, Llc | Novel dermatological composition using bio-activating organocatalysts |
| CN1993106A (en) * | 2003-06-04 | 2007-07-04 | 埃伯赛特斯公司 | Novel dermatological composition |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5470876A (en) * | 1985-07-18 | 1995-11-28 | Proctor; Peter H. | Topical sod for treating hair loss |
| CN101503415A (en) * | 2009-03-10 | 2009-08-12 | 深圳市危险废物处理站有限公司 | Preparation and use of amino acid chelated hydroxy copper chloride crystal |
-
2012
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-
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN1993106A (en) * | 2003-06-04 | 2007-07-04 | 埃伯赛特斯公司 | Novel dermatological composition |
| WO2006060548A2 (en) * | 2004-12-02 | 2006-06-08 | Ebersytes, Llc | Novel dermatological composition using bio-activating organocatalysts |
Non-Patent Citations (4)
| Title |
|---|
| DATABASE REGISTRY 16 November 1984 (1984-11-16), accession no. 3870-80-9 * |
| DATABASE REGISTRY 16 November 1984 (1984-11-16), accession no. 3870-82-1 * |
| DATABASE REGISTRY 2 May 1996 (1996-05-02), accession no. 75889-03-9 * |
| HU ET AL.: "Study on the Stability of Cu(II), Co(II) Complexes with Histidine", CHEMISTRY & BIOENGINEERING, vol. 24, no. 11, 2007, pages 24 - 25, 30 * |
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| EP3162367A4 (en) * | 2014-06-27 | 2018-04-18 | Postech Academy-Industry Foundation | Composition for skin penetration, containing cationic molecule transporter and anionic bioactive material |
| EP4279131A1 (en) * | 2022-05-20 | 2023-11-22 | Bioithas S.L. | Probiotic compositions for the treatment of alopecia |
| WO2023222856A1 (en) * | 2022-05-20 | 2023-11-23 | Bioithas S.L. | Probiotic compositions for the treatment of alopecia |
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