Unlock instant, AI-driven research and patent intelligence for your innovation.

Cosmetic composition material containing exogenous ligand-receptor system and its application

A technology for cosmetic compositions and coordination compounds, which can be applied to cosmetics, cosmetic preparations, and medical preparations containing active ingredients, etc., can solve the problems of adhesion of cosmetic active agents, fiber degradation, toxicity, etc., which are difficult to resist shampoo.

Inactive Publication Date: 2004-05-12
LOREAL SA
View PDF29 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, it is difficult to achieve the attachment of shampoo-resistant cosmetic active agents to the surface of the hair
In currently used technologies, the effect produced by the simple adsorption of the active agent on the fiber is eliminated by the initial wash of the shampoo, and the chemical binding can cause toxicity problems or lead to degradation of the fiber

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Cosmetic composition material containing exogenous ligand-receptor system and its application
  • Cosmetic composition material containing exogenous ligand-receptor system and its application
  • Cosmetic composition material containing exogenous ligand-receptor system and its application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0296] Example 1: Shampoo resistance of anti-FITC-dextran complexes

[0297]In this example, anti-FITC (anti-fluorescein isothiocyanate) was adsorbed on the hair, and then the FITC-dextran complex was attached to the hair.

[0298] a) Anti-FITC adsorbed to the hair surface

[0299] Five hairs (ie, about 10 mg) from one strand of washed natural hair were placed as individual samples in siliconized glass flasks.

[0300] A 50 μg / ml anti-FITC (Sigma F-5636) solution was prepared in PBS buffer (0.1 M, pH 7.2). 800 μl of anti-FITC solution was brought into contact with the hair sample. The mixture was stirred at room temperature for 24 hours.

[0301] The sample was rinsed once with 1ml 0.05% Tween 20 PBS solution, then rinsed once with 1ml PBS solution, rinsed three times with distilled water (3×1ml distilled water vortexed for 1 minute)

[0302] b) Adsorption and immobilization of the FITC-dextran complex on the treated hair surface

[0303] A 100 µg / ml FITC-dextran (Sigma, ...

Embodiment 2

[0305] Example 2: Shampoo Resistance of Anti-FITC-Biotin Complexes

[0306] In this example, anti-FITC was adsorbed to the hair, and then the FITC-biotin complex was attached to the hair.

[0307] a) Anti-FITC adsorbed to the hair surface

[0308] (see Example 1)

[0309] b) Adsorption and immobilization of FITC-biotin complex on the treated hair surface

[0310] A 100 µg / ml FITC-biotin (Molecular Probes, ref: B-1370) solution was prepared in phosphate buffer (pH 7.2). Untreated hair and anti-FITC-treated hair were incubated in 1 ml of this solution for 2 hours at room temperature. Samples were rinsed 3 times with distilled water (3 x 1 ml distilled water vortexed for 1 min). Controls prepared in parallel corresponded to hair treated with anti-FITC but not exposed to FITC-biotin.

[0311] 50 μg / ml of avidin-peroxidase (Sigma, ref: A3151) was prepared in phosphate buffer (pH 7.2). The samples were incubated in 1 ml of this solution for 1 hour at room temperature and then ...

Embodiment 3

[0314] Example 3: Shampoo Resistance of Anti-FITC-Pigment Complexes

[0315] In this example, PEI-FITC (polyethyleneimine-FITC) was adsorbed to the hair, and then the anti-FITC-pigment complex was attached to the hair.

[0316] a) Preparation of PEI-FITC solution

[0317] 500 [mu]l of 100 mg / ml FITC (Pierce 46110) was prepared in DMF. 400 μl of FITC solution was gradually added to a small beaker containing 2 ml of 5% PEI (pH 8.5). The mixture was stirred at room temperature for 2 hours under the protection of an aluminum foil and then purified on a PD10 column (Amersham 17-0851-01) (mobile phase: 3.5 ml deionized water).

[0318] b) Adsorption of anti-FITC to the pigment surface

[0319] 100 mg ocher pigment (iron oxide) was washed with 1 ml PBS pH 7.2. 1 ml of anti-FITC solution at a concentration of 500 μg / ml in PBS pH 7.2 was added to the pigment. The mixture was stirred at room temperature for 2 hours and then centrifuged. Pigment-anti-FITC was washed 6 times with 1 ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
melting pointaaaaaaaaaa
boiling pointaaaaaaaaaa
Login to View More

Abstract

Cosmetic composition comprises a compound (I) and a complexing agent capable of forming a complex with (I), the complex having a dissociation constant of 0.1 or less at 25 degrees C. Cosmetic composition comprises a compound of formula (I) and a complexing agent capable of forming a complex with (I), the complex having a dissociation constant of 0.1 or less at 25 degrees C: L(A)n(Y)m(alpha)p (I) m, p = 0-100; n = 0 or 1; alpha = an anchoring group for covalent bonding to keratinic materials; L = a complexable group other than biotin; A = a 1-100C linear or branched divalent group optionally interrupted by heteroatoms and optionally substituted with OH, amino, halo, aryl, phosphate, phosphonate, sulfate, sulfonate, COOH, alkoxycarbonyl and alkoxy; Y = Z or BW; Z = COOH, SH, alkoxycarbonyl, amino, ammonio, phosphite, phosphate, phosphonate, sulfate, sulfite, sulfonate; W = a cosmetically active residue, e.g. derived from UV filters, moisturizers, emollients, conditioners, antistatic agents, antiperspirants, fragrances, reducing or oxidizing agents, colorants, antimicrobial agents, antidandruff agents, (in)organic particles, polymer(s) adsorbed on (in)organic particles, film-forming agents or (in)organic particles adsorbed on film-forming agents; B = an entity for attaching W to L or A, e.g. an amine, imine, amide, ester, disulfide, thioester, urethane, urea, ether, thioether, azo, methine, epoxy, aromatic, heterocyclic or dialkylpolysiloxane group. Independent claims are also included for: (1) composition comprising at least one compound (I); (2) composition comprising at least one complexing agent of formula (II); treatment of keratinic materials by sequential or simultaneous application of selected compounds (I) and (II); (3) kits comprising selected compounds (I) and (II) in separate compartments. D(A')n'(X)m'(alpha')p' (II) alpha' = an anchoring group for covalent bonding to keratinic materials.

Description

technical field [0001] The present invention relates to a cosmetic composition comprising at least one compound a) in combination with at least one complexing agent b), wherein compound a) or complexing agent b) optionally carries at least one cosmetically active group , and / or a binding group capable of covalently attaching to the keratin material. [0002] The invention also relates to several methods of hair treatment based on these compounds, the object of which is to produce on the fibers a deposit of a layer of material imparting novel cosmetic properties. Background technique [0003] It would be beneficial to be able to attach active agents that provide long-lasting benefit to keratinous materials, especially the hair. However, it is difficult to achieve the attachment of shampoo-resistant cosmetic active agents to the surface of the hair. In currently used technologies, the effect of simple adsorption of the active agent on the fiber is eliminated by the initial w...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): A61K8/00A61K8/64A61K8/66A61K8/73A61Q5/00
CPCA61K2800/57A61K2800/94A61Q5/00A61K8/73
Inventor G·维克A·利沃瑞尔B·贝尔纳
Owner LOREAL SA