WO2005105029A1 - Uso de péptidos xikvav en preparación de composiciones cosméticas para mejorar la firmeza de la piel mediante el aumento de la adhesión celular - Google Patents
Uso de péptidos xikvav en preparación de composiciones cosméticas para mejorar la firmeza de la piel mediante el aumento de la adhesión celular Download PDFInfo
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- WO2005105029A1 WO2005105029A1 PCT/ES2005/000175 ES2005000175W WO2005105029A1 WO 2005105029 A1 WO2005105029 A1 WO 2005105029A1 ES 2005000175 W ES2005000175 W ES 2005000175W WO 2005105029 A1 WO2005105029 A1 WO 2005105029A1
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- WIPO (PCT)
- Prior art keywords
- peptides
- cosmetic composition
- skin
- xikvav
- firmness
- Prior art date
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- 108090000765 processed proteins & peptides Proteins 0.000 title claims abstract description 65
- 102000004196 processed proteins & peptides Human genes 0.000 title claims abstract description 56
- 239000000203 mixture Substances 0.000 title claims abstract description 35
- 239000002537 cosmetic Substances 0.000 title claims abstract description 34
- 238000002360 preparation method Methods 0.000 title claims abstract description 7
- 230000021164 cell adhesion Effects 0.000 title description 18
- 210000002469 basement membrane Anatomy 0.000 claims abstract description 17
- 210000003491 skin Anatomy 0.000 claims description 15
- 230000014509 gene expression Effects 0.000 claims description 13
- 102000006495 integrins Human genes 0.000 claims description 13
- 108010044426 integrins Proteins 0.000 claims description 13
- 210000002510 keratinocyte Anatomy 0.000 claims description 13
- 210000004927 skin cell Anatomy 0.000 claims description 10
- 230000035587 bioadhesion Effects 0.000 claims description 9
- -1 amino, hydroxyl Chemical group 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 230000037393 skin firmness Effects 0.000 claims description 5
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Chemical group OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 150000001413 amino acids Chemical class 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical group OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims description 2
- 239000006071 cream Substances 0.000 claims description 2
- 125000003074 decanoyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C(*)=O 0.000 claims description 2
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- 125000003396 thiol group Chemical class [H]S* 0.000 claims 3
- QFOHBWFCKVYLES-UHFFFAOYSA-N Butylparaben Chemical compound CCCCOC(=O)C1=CC=C(O)C=C1 QFOHBWFCKVYLES-UHFFFAOYSA-N 0.000 claims 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 claims 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 claims 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- XPJVKCRENWUEJH-UHFFFAOYSA-N Isobutylparaben Chemical compound CC(C)COC(=O)C1=CC=C(O)C=C1 XPJVKCRENWUEJH-UHFFFAOYSA-N 0.000 claims 1
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- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 1
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- 235000010228 ethyl p-hydroxybenzoate Nutrition 0.000 claims 1
- 239000004403 ethyl p-hydroxybenzoate Substances 0.000 claims 1
- NUVBSKCKDOMJSU-UHFFFAOYSA-N ethylparaben Chemical compound CCOC(=O)C1=CC=C(O)C=C1 NUVBSKCKDOMJSU-UHFFFAOYSA-N 0.000 claims 1
- 235000011187 glycerol Nutrition 0.000 claims 1
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
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- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 3
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Classifications
-
- 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
- A61Q19/08—Anti-ageing preparations
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- compositions for improving skin firmness, increasing the adhesion of skin cells to each other and to the basal lamina.
- Said compositions comprise a cosmetically effective amount of peptides of the general formula X-isoleucyl-lysyl-valyl-alanyl-valine-Y (hereinafter referred to as XIKVAV), of formula I, where X may be H, an amino acid, or a group linear or branched chain acyl (see figure 1) and Y can be amino, hydroxyl or thiol, all of them substituted or not with fatty acids:
- the skin is the largest organ of the human body. Two layers can be distinguished: the epidermis and the dermis. These two layers are joined through the basement membrane, matrix formed by different macromolecules (collagen, laminin, proteoglycans, etc.).
- the basal lamina is rich in type IV collagen, proteoglycans and entactin and laminin glycoproteins. These molecules provide a structural network as well as bioadhesive properties for cell binding.
- the laminin sequence contains several domains of link: for type IV collagen, for perlecan (heparan sulfate proteoglycan), for entactin and for the receptors found on the surface of cells.
- This basement membrane is a specialized extracellular matrix formed by three layers: - Lucid sheet: this layer is directly in contact with the basal keratinocytes, and its main component is laminin. Dense sheet: it is located below the lucid sheet and extends parallel to it with a similar thickness. It is an amorphous material, in which collagen IV predominates, responsible for the high tensile strength and flexibility of the basement membrane. Reticular lamina: it is below the anterior layers, but its location is more inaccurate, and is caused by the fibroblasts of the dermis. It is formed by anchorage fibrils and elastic microfibrils that are introduced into the dense lamina, thereby attaching to the basement membrane and providing cohesion to the skin tissue.
- Anchoring fibrils are structures formed by collagen Vil.
- the laminin the main component thereof.
- Laminin is a glycoprotein of approximately 850 kDa and, after collagen, it is the most abundant protein in the extracellular matrix (ECM).
- ECM extracellular matrix
- Laminin is found exclusively in the basement membranes and is formed by three long chains of polypeptides (alpha, beta and gamma) distributed in the form of a cross and joined by disulfide bridges. The three chains exist in different subtypes of laminin and their combinations result in a dozen different isoforms of laminin, of which laminin-1 is the most studied.
- integrins the first MEC receptors that were discovered. It is a group of transmembrane cell surface receptors, which is. They are responsible for cell-cell and cell-MEC interactions. The cells recognize the binding domains in the laminin through the receptor integrins, resulting in their binding to the basement membrane, rich in laminins. Likewise, receptor integrins mediate junctions between cells through specific ligands.
- skin aging which is a biological process common to all living beings.
- Adhesive molecules are included to promote endothelialization of the implant and its adhesion to the cells and the implant is made of porous biomaterial that allows the growth of capillaries through the material.
- US Patent 6,428,579 [Implantable prosthetic devices coated with bioactive molecules], refers to a gold-coated implant on which bioactive peptides with properties of different types adhere: cell modulators, chemotactic, anticoagulants, antithrombotic , anti-tumor, anti-infective, growth enhancers, anti-inflammatory, etc.
- SIKVAV is mentioned within the group of peptides that bind to integrin.
- ntegrin substrate peptides are used to improve adhesion of the peptide to bone tissue, for example, SIKVAV.
- US Patent 6,673,108 Transmural concentric multilayer ingrowth matrix within well-defined porosity
- An example of a protein layer is a fibrin layer derivatized with peptides or growth factors, and specifically, a fibrin layer with laminin derived peptides such as SIKVAV. None of these patents refers to the use of peptides of the general formula XIKVAV in cosmetic compositions. Therefore the " so much and foundation " of TM la.
- the present invention ⁇ is ⁇ to provide a cosmetic composition capable of increasing the firmness of the skin, thereby delaying its aging.
- Peptides of the general formula XIKVAV form a chemotactic region in the laminin, that is, a region of cellular attraction. This is the reason why these peptides promote cell adhesion, growth and migration, thus regenerating the basal lamina.
- the stimulation properties of angiogenesis are also known in these peptides, which promotes proliferation and differentiation of endothelial cells [Journal of Cellular Physiol. 1992
- XIKVAV peptides have different functions of cosmetic application, at the level of skin cells, which are the following: - Stimulation of keratinocyte adhesion (see Figure 8) in the presence of XIKVAV peptides, such as IKVAV, SIKVAV or Pal-IKVAV, where X is the radical H, seril or palmitoyl, respectively. Stimulation of ⁇ 6 integrin expression in fibroblasts, as seen in Figure 3, in which fluorescence is observed in the presence of XIKVAV, when ⁇ 6 integrin is expressed as opposed to Figure 2 illustrating what happened in the sample control, in which XIKVAV is not added.
- XIKVAV peptides are capable of favoring keratinocyte adhesion on their own, and stimulating synthesis by laminin V fibroblasts and ⁇ 6 integrin (bioadhesion peptides), both involved with hemidesmosomes that are essential structures for dermo-epidermal junction.
- laminin V fibroblasts and ⁇ 6 integrin bioadhesion peptides
- the stimulation of the microcirculation mentioned above, together with the good condition of the basement membrane, will help the adequate transport of oxygen and metabolites, as well as the elimination of excretion products, thus improving the functional capacity of epidermal cells and at the same time their resistance and firmness.
- XIKVAV peptides incorporated into a cosmetic composition of topical application have a direct effect on the prevention of skin aging, delaying the loss of contact between the dermis and the epidermis and avoiding the structural and functional changes that form Part of the aging process.
- this refers to the use of peptides of the general formula XIKVAV (see Figure 1), where X is selected from the group consisting of H, an amino acid, or an acyl chain group linear or branched, and Y may be amino, hydroxyl or thiol, all of them substituted or not with fatty acids, for stimulation of skin cell bioadhesion by increasing the expression of bioadhesion peptides.
- X is hydrogen, serine, palmitoyl or decanoyl and Y may be amino, hydroxyl or thiol, all of them substituted or not with fatty acids.
- X is serine and Y is hydroxyl, that is, the SIKVAV peptide.
- X is hydrogen and Y is hydroxyl, that is, the IKVAV peptide.
- the cutaneous cells in which bioadhesion are keratinocytes' and proceedingspt ⁇ dos ⁇ of ⁇ s ⁇ rrlntegrina b ⁇ oadhes ⁇ ón ⁇ 6 and laminin V.
- a cosmetic composition comprising, in a cosmetically acceptable medium, a cosmetically effective amount of peptides of the general formula XIKVAV for the stimulation of skin cell bioadhesion by increasing the expression of bioadhesion peptides
- said composition is of dermal application
- said composition increases the firmness of the skin and this effect is produced by increasing adhesion of the skin cells to each other and to the base plate.
- the XIKVAV peptides are incorporated into a cosmetic composition in a concentration of up to 12%.
- the XIKVAV peptides are incorporated into a cosmetic composition in a concentration preferably of 5%.
- Preferred excipients are those commonly used in cosmetics: water, alcohols, lecithins, natural or artificial polymers, surfactants and surfactants, preservatives, etc.
- Preferred cosmetic forms are those commonly used: creams, lotions, emulsions, shampoos, serums, gels, etc.
- the composition comprises the following ingredients in the following weight percentages:
- the present invention relates to the use of peptides of the general formula XIKVAV in the preparation of a cosmetic composition that increases skin firmness. Since cells use integrins to recognize laminins, and laminins bind cells through integrins, the cosmetic composition according to the present invention will enhance cell adhesion and its binding to the basement membrane, since XIKVAV peptides are capable of increasing the production of integrins and laminins and is compatible to be used as ingredients in a cosmetic composition.
- the assay uses a primary antibody (monoclonal) that binds to the protein to be detected (integrin or laminin), and a secondary antibody (polyclonal) that binds to the complex between the protein and the primary antibody.
- the secondary antibody is coupled to a fluorescent compound (FITC-Fluorescein Isothiocyanate-Fluorescein Isothiocyanate).
- the FITC is illuminated with a light filtered at 495 nm (absorption wavelength) and the light emitted by the dye is detected at 528 nm (emission wavelength).
- Figure 2 shows, by immunofluorescence emission, the expression of integrin ⁇ 6 in human fibroblasts untreated with SIKVAV.
- Figure 3 shows, by immunofluorescence emission, the expression of integrin ⁇ 6 in human fibroblasts untreated with SIKVAV.
- Figure 3 also by immunofluorescence emission.
- the difference in the expression of laminin in the presence and absence of SIKVAV has been identified. This difference in expression can be observed in Figures 4 and 5.
- Figure 6 shows cell adhesion in untreated human fibroblasts and Figure 7 shows cell adhesion in fibroblasts treated with SIKVAV.
- Figures 6 and 7 show a uniform coating of the test well and the growth and distribution of fibroblasts that are related to cell adhesion rather than cell proliferation.
- the cosmetic preparation with SIKVAV favors the formation of blood vessels, improving microcirculation.
- Example 3 In this embodiment, the "in vitro" evaluation of keratinocyte cell adhesion to peptides of general formula XIKVAV and comparative among them is shown.
- HEKa Human Epidermal Keratinocytes
- control assays are performed with micro-wells coated with 40 ⁇ M of BSA (bovine serum albumin) to evaluate non-specific cell adhesion. All microwells have been washed with 200 ⁇ L of PBS (phosphate buffered saline) and blocked for 1 hour with 1% BSA in PBS at 37 ° C.
- BSA bovine serum albumin
- human cutaneous keratinocitbs were added trypsin, labeled for 30 minutes at 37 ° C in Calcein-AM at a concentration of 5 ⁇ M and finally washed three times in the EpiLife ® medium.
- the labeled cells (4.5 x 10 4 / micro well) were added to the plate previously coated with the XIKVAV peptide and incubated for 2 hours at 37 ° C in a humidified atmosphere with 5% CO 2 .
- Cell adhesion was assessed by measuring calcein flowering before and after washing. The percentage of cell adhesion was determined by dividing the flowering of adhered cells by the total flowering of cells added to each micro well.
- the cell adhesion promoted by the XIKVAV peptides was calculated with respect to the non-specific adhesion of the cells to BSA.
- the results show that XIKVAV peptides are capable of promoting keratinocyte adhesion in a dose-dependent manner (see Figs. 8, 9 and 10).
- the cell fixation caused by XIKVAV peptides was 65% with respect to non-specific adhesion at the highest concentration studied.
- These results show that XIKVAV peptides are recognized by specialized receptors on the cell surface.
- Figure 10 shows the levels of cell adhesion of the SIKVAV-OH and SIKVAV-NH 2 peptides where it is seen that at small doses (0.5 ⁇ g / ml) the adhesion produced by SIKVAV-NH 2 is greater and at higher doses Increased adhesion of SIKVAV-OH peptides is generated.
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Abstract
Description
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Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2005237268A AU2005237268B2 (en) | 2004-04-28 | 2005-04-05 | Use of XIKVAV peptides in the preparation of cosmetic compositions which are intended to improve the firmness of the skin by increasing cell adhesion |
BRPI0510257-0A BRPI0510257B1 (pt) | 2004-04-28 | 2005-04-05 | Uso de peptídeos xikvav na preparação de composições cosméticas para melhoria da firmeza da pele através do aumento da adesão celular |
MXPA06012495A MXPA06012495A (es) | 2004-04-28 | 2005-04-05 | Uso de peptidos xikvav en preparacion de composiciones cosmeticas para mejorar la firmeza de la piel mediante el aumento de la adhesion celular. |
PL05731868T PL1741421T3 (pl) | 2004-04-28 | 2005-04-05 | Stosowanie peptydów XIKVAV do przygotowywania kompozycji kosmetycznych, które są przeznaczone do poprawy jędrności skóry dzięki zwiększeniu adhezji komórek |
ES05731868.5T ES2501941T3 (es) | 2004-04-28 | 2005-04-05 | Uso de péptidos XIKVAV en preparación de composiciones cosméticas para mejorar la firmeza de la piel mediante el aumento de la adhesión celular |
CA2564312A CA2564312C (en) | 2004-04-28 | 2005-04-05 | Use of xikvav peptides in the preparation of cosmetic compositions which are intended to improve the firmness of the skin by increasing cell adhesion |
JP2007510051A JP5384824B2 (ja) | 2004-04-28 | 2005-04-05 | 細胞接着を増加させることにより皮膚の弾力を改善させる化粧品の組成物の調整におけるxikvavペプチドの使用 |
US11/587,878 US7943156B2 (en) | 2004-04-28 | 2005-04-05 | Use of peptides of general formula I X-SEQ ID No.1-Y in the preparation of cosmetic compositions which are intended to improve the firmness of the skin by increasing cell adhesion |
EP05731868.5A EP1741421B1 (en) | 2004-04-28 | 2005-04-05 | Use of xikvav peptides in the preparation of cosmetic compositions which are intended to improve the firmness of the skin by increasing cell adhesion |
KR1020067022761A KR101353748B1 (ko) | 2004-04-28 | 2005-04-05 | 셀 접착성 증가에 의한 피부 경도 향상용 화장용 조성물준비에의 엑스-이솔레우실-리실-바릴-알라닐-바린-와이펩타이드의 용도 |
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---|---|---|---|
ES200401018A ES2293753B1 (es) | 2004-04-28 | 2004-04-28 | Uso de peptidos xikvav en preparacion de composiciones cosmeticas para mejorar la firmeza de la piel mediante el aumento de la adhesion celular. |
ESP200401018 | 2004-04-28 |
Publications (1)
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WO2005105029A1 true WO2005105029A1 (es) | 2005-11-10 |
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PCT/ES2005/000175 WO2005105029A1 (es) | 2004-04-28 | 2005-04-05 | Uso de péptidos xikvav en preparación de composiciones cosméticas para mejorar la firmeza de la piel mediante el aumento de la adhesión celular |
Country Status (14)
Country | Link |
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US (1) | US7943156B2 (es) |
EP (1) | EP1741421B1 (es) |
JP (1) | JP5384824B2 (es) |
KR (1) | KR101353748B1 (es) |
CN (1) | CN1964694A (es) |
AU (1) | AU2005237268B2 (es) |
BR (1) | BRPI0510257B1 (es) |
CA (1) | CA2564312C (es) |
ES (2) | ES2293753B1 (es) |
MX (1) | MXPA06012495A (es) |
PL (1) | PL1741421T3 (es) |
RU (1) | RU2371167C2 (es) |
WO (1) | WO2005105029A1 (es) |
ZA (1) | ZA200608996B (es) |
Cited By (4)
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WO2009005151A1 (ja) * | 2007-07-05 | 2009-01-08 | Nissan Chemical Industries, Ltd. | 新規脂質ペプチド並びにヒドロゲル |
EP2123673A1 (en) * | 2006-10-25 | 2009-11-25 | Lipotec, S.A. | Neuronal exocytosis inhibiting peptides |
CN102203115A (zh) * | 2008-10-03 | 2011-09-28 | 利普泰股份公司 | 用于皮肤、粘膜、头皮和/或头发的治疗和/或护理的肽及它们在美容组合物或药物组合物中的用途 |
CN103314005A (zh) * | 2011-03-25 | 2013-09-18 | 利普泰股份公司 | 在皮肤和/或粘膜的治疗和/或护理中有用的肽以及它们在化妆品组合物或药用组合物中的用途 |
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WO2015063613A2 (en) | 2013-11-01 | 2015-05-07 | Spherium Biomed S.L. | Inclusion bodies for transdermal delivery of therapeutic and cosmetic agents |
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AU2017215476B2 (en) | 2016-02-04 | 2022-12-08 | ALASTIN Skincare, Inc. | Compositions and methods for invasive and non-invasive procedural skincare |
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WO2020028694A1 (en) | 2018-08-02 | 2020-02-06 | ALASTIN Skincare, Inc. | Liposomal compositions and methods of use |
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- 2005-04-05 CN CNA2005800184945A patent/CN1964694A/zh active Pending
- 2005-04-05 AU AU2005237268A patent/AU2005237268B2/en active Active
- 2005-04-05 EP EP05731868.5A patent/EP1741421B1/en active Active
- 2005-04-05 KR KR1020067022761A patent/KR101353748B1/ko active IP Right Grant
- 2005-04-05 US US11/587,878 patent/US7943156B2/en active Active
- 2005-04-05 CA CA2564312A patent/CA2564312C/en not_active Expired - Fee Related
- 2005-04-05 BR BRPI0510257-0A patent/BRPI0510257B1/pt active IP Right Grant
- 2005-04-05 RU RU2006137956/15A patent/RU2371167C2/ru not_active IP Right Cessation
- 2005-04-05 ES ES05731868.5T patent/ES2501941T3/es active Active
- 2005-04-05 WO PCT/ES2005/000175 patent/WO2005105029A1/es active Application Filing
- 2005-04-05 JP JP2007510051A patent/JP5384824B2/ja active Active
- 2005-04-05 PL PL05731868T patent/PL1741421T3/pl unknown
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EP2123673A1 (en) * | 2006-10-25 | 2009-11-25 | Lipotec, S.A. | Neuronal exocytosis inhibiting peptides |
EP2123673A4 (en) * | 2006-10-25 | 2011-01-12 | Lipotec Sa | NEURONAL EXOCYTOSIS-INHIBITING PEPTIDES |
AU2007310796B2 (en) * | 2006-10-25 | 2013-10-10 | Bcn Peptides, S.A. | Neuronal exocytosis inhibiting peptides |
WO2009005151A1 (ja) * | 2007-07-05 | 2009-01-08 | Nissan Chemical Industries, Ltd. | 新規脂質ペプチド並びにヒドロゲル |
JP5441693B2 (ja) * | 2007-07-05 | 2014-03-12 | 日産化学工業株式会社 | 新規脂質ペプチド並びにヒドロゲル |
US8816049B2 (en) | 2007-07-05 | 2014-08-26 | Nissan Chemical Industries, Ltd. | Lipid peptide and hydrogel |
US8916682B2 (en) | 2007-07-05 | 2014-12-23 | Nissan Chemical Industries, Ltd. | Lipid peptide and hydrogel |
CN102203115A (zh) * | 2008-10-03 | 2011-09-28 | 利普泰股份公司 | 用于皮肤、粘膜、头皮和/或头发的治疗和/或护理的肽及它们在美容组合物或药物组合物中的用途 |
CN102203115B (zh) * | 2008-10-03 | 2015-05-13 | 利普泰股份公司 | 用于皮肤、粘膜、头皮和/或头发的治疗和/或护理的肽及它们在美容组合物或药物组合物中的用途 |
CN103314005A (zh) * | 2011-03-25 | 2013-09-18 | 利普泰股份公司 | 在皮肤和/或粘膜的治疗和/或护理中有用的肽以及它们在化妆品组合物或药用组合物中的用途 |
CN103314005B (zh) * | 2011-03-25 | 2016-08-10 | 利普泰股份公司 | 在皮肤和/或粘膜的治疗和/或护理中有用的肽以及它们在化妆品组合物或药用组合物中的用途 |
Also Published As
Publication number | Publication date |
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BRPI0510257A (pt) | 2008-01-02 |
ZA200608996B (en) | 2008-07-30 |
US20080085852A1 (en) | 2008-04-10 |
ES2293753A1 (es) | 2008-03-16 |
ES2293753B1 (es) | 2009-03-16 |
BRPI0510257B1 (pt) | 2014-12-02 |
RU2371167C2 (ru) | 2009-10-27 |
KR20070095752A (ko) | 2007-10-01 |
MXPA06012495A (es) | 2007-01-31 |
CA2564312C (en) | 2014-03-25 |
AU2005237268A1 (en) | 2005-11-10 |
US7943156B2 (en) | 2011-05-17 |
JP5384824B2 (ja) | 2014-01-08 |
EP1741421B1 (en) | 2014-06-25 |
KR101353748B1 (ko) | 2014-01-21 |
ES2501941T3 (es) | 2014-10-02 |
CA2564312A1 (en) | 2005-11-10 |
CN1964694A (zh) | 2007-05-16 |
PL1741421T3 (pl) | 2014-11-28 |
AU2005237268B2 (en) | 2010-12-23 |
RU2006137956A (ru) | 2008-06-10 |
EP1741421A1 (en) | 2007-01-10 |
JP2007534727A (ja) | 2007-11-29 |
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