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Skin preparations for extenal use

A technology for skin and topical preparations, used in skin care preparations, skin diseases, cosmetic preparations, etc., and can solve problems such as unsatisfactory effects, thermal and oxidative instability, and instability

Inactive Publication Date: 2003-05-21
PENTAPHARM AG +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] However, vitamin C, hydroquinone, and kojic acid are unstable to heat and oxidation, especially in water, and have some problems such as decomposition and coloring when used in skin topical formulations
[0005] Vitamin C derivatives such as magnesium L-ascorbyl phosphate and beta-arbutin are more stable to heat and oxidation, but their effects are less satisfactory

Method used

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  • Skin preparations for extenal use
  • Skin preparations for extenal use

Examples

Experimental program
Comparison scheme
Effect test

preparation Embodiment 1

[0050] In order to prepare the compositions shown in Table 1, the α-arbutin prepared in the above examples (hereinafter, the term "α-arbutin" should always indicate the α-arbutin), methyl p-hydroxybenzoate The ester and butyl p-hydroxybenzoate are added to a mixture of purified water and propylene glycol, and the above mixture is heated to 80°C to dissolve.

[0051] The mixture of other ingredients shown in Table 1 was uniformly dissolved by heating to 80° C., gradually added to the above solution, and the obtained mixture was emulsified at high speed using a homogenizer-mixer.

[0052] After emulsification, the mixture was gradually cooled to 30°C with stirring to prepare an ointment.

[0053] Table 1

[0054] weight ratio%

[0055] Alpha-Arbutin 2.0

[0056] Vaseline 4.0

[0057] Stearyl Alcohol 5.0

[0058] Liquid paraffin 17.0

[0059] POE(20) cetyl ether 4.0

[0060] Glyceryl Monos...

preparation Embodiment 2

[0065] To prepare the composition formulations shown in Table 2, α-arbutin was added to purified water and dissolved at 70°C. The resulting solution was maintained at this temperature.

[0066] On the other hand, the other ingredients in Table 2 were mixed, maintaining a temperature of 70°C. The above-mentioned mixture of α-arbutin and purified water at 70°C was added to the mixture of other ingredients maintained at 70°C, and the resulting mixture was cooled under stirring to prepare a cream.

[0067] Table 2

[0068] weight ratio%

[0069] Alpha-Arbutin 1.0

[0070] Polyethylene glycol isostearate 7.5

[0071] Cetyl Alcohol 1.0

[0072] Liquid paraffin 7.5

[0073] Isopropyl myristate 7.5

[0074] Diethylene glycol monoethyl ether 10.5

[0075] Parabens 0.5

[0076] Propylene Glycol 5.0

[0077] purified water balance

preparation Embodiment 3

[0079] To prepare the compositions in Table 3, α-arbutin was added to purified water, dissolved at a temperature of 70°C, and the solution was maintained at this temperature.

[0080] On the other hand, the other ingredients in Table 3 except locust bean gum were mixed and maintained at 70°C.

[0081] The above mixture of α-arbutin and purified water maintained at 70°C was added to the mixture of other ingredients maintained at 70°C. The resulting mixture was stirred well, cooled to 50°C, homogenized, and continued cooling to 30°C.

[0082] Add locust bean gum to the above mixture, cool to 30°C, stir the resulting mixture, and prepare an emulsion after cooling.

[0083] table 3

[0084] Percent by weight α-Arbutin 0.05 Polyoxyethylene sorbitan monostearate 5.0 Sorbitan monostearate 3.0 Glycerol monostearate 2.0 Cetyl alcohol 2.5 Isopropyl myristate 8.0 Parabens 0.5 Propylene Glycol 2.0 Locust Bean Gum 2.0 Pu...

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Abstract

Skin preparations for external use containing a melanin formation inhibitor which is highly stable to heat and oxidation and thus suffers from no degradation / coloration in the preparations with the passage of time, as observed in the existing melanin formation inhibitors. These preparations contain, as the melanin formation inhibitor, hydroquinone- alpha -glucopyranoside having an excellent effect of inhibiting human tyrosinase activity.

Description

technical field [0001] The present invention relates to topical skin preparations containing hydroquinone-α-D-glucopyranoside obtained by alpha-bonding glucose to one of the hydroxyl groups of hydroquinone. [0002] Skin topical formulations include: basic skin care products such as creams, lotions, essences, facial masks, cold creams and makeup bases, cosmetics such as foundations, blushers, eyeshadows, eyeliners and fingernails. Nail polishes, hair care products such as shampoos and tonics, body care products such as facial scrubs, body soaps, body washes, soaps and fragrances. Background technique [0003] Various melanogenesis inhibitors have been used for skin whitening (preventing skin darkening), and for preventing or improving melasma, freckles, and other skin problems caused by excessive ultraviolet light exposure. For example, representative examples thereof may include hydroquinone, arbutin which is obtained by β-bonding glucose with a phe...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07H15/203A61K8/00A61K8/60A61K31/7028A61K31/7034A61P17/16A61Q19/00A61Q19/02
CPCA61K8/602A61K8/60A61Q19/02A61P17/16A61K8/35
Inventor 中山宏基冈田茂孝米谷俊西村隆久
Owner PENTAPHARM AG