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VISCOELASTIC GELS AS NOVEL FILLERS

机译:粘弹性凝胶作为新型填料

摘要

FIELD: medicine.;SUBSTANCE: group of inventions relates to a method of producing and purifying a derivative (HBC) of hyaluronic acid, involving the following steps: a) dissolving an alkaline solution of diepoxide of diglycidyl ether 1,4-butanediol (BDDE) in stoichiometric ratio of 2.5 to 25 % mole of repeating links of hyaluronic acid, followed by b) dispersing hyaluronic acid (HA) in the solution specified in subparagraph (a) at room temperature, c) starting the reaction by thermal activation of the solution specified in subparagraph (b), heated at temperature of 35 to 55 °C for 2 to 36 hours, d) extruding the obtained mass through a metal sieve to reduce its particles to a size of approximately 600 mcm, e) hydrating the obtained gel by diluting with water 3 to 20 times, f) adjusting pH to neutral with an aqueous solution of HCl, g) depositing a water-soluble organic solvent, such as ethanol, methanol, isopropanol, n-propanol, dioxane, acetonitrile, acetone and/or mixtures thereof, until a product in form of a precipitated powder is obtained, h) washing with organic solvents, such as ethanol, methanol, isopropanol, n-propanol, dioxane, acetonitrile, acetone and/or mixtures thereof, containing water, i) drying in vacuum until removal of residual solvents below 400 ppm and obtaining white HBC powder; method of producing a biomaterial consisting of a mixture of hyaluronic acid hexadecylamide (HYADD) with HBC; to a method of producing and purifying an HBC derivative, comprising steps of: a) dissolving BDDE diepoxide in alkaline solution in stoichiometric ratio of 2.5 to 25 mole of repeating links of hyaluronic acid, followed by b) dispersing HA in the solution specified in the previous subparagraph a) at room temperature, c) triggering the reaction by thermal activation, wherein the solution specified in subparagraph (b) is heated at 35 to 55 °C for 2 to 36 hours, d) bringing the pH to neutral with an aqueous solution of HCl, e) hydrating the obtained gel by diluting with water 3 to 20 times; method of producing a biomaterial consisting of a mixture of HYADD and HBC; to a biomaterial consisting of a mixture of HYADD with HBC, cross-linked with BDDE in weight ratio of 10:90 to 90:10, as a new filler and/or as a body profiling product; to application of biomaterial as new filler and/or new product for body profiling in treatment of skin defects, in dermatology, in dermatocosmetology and/or aesthetic surgery.;EFFECT: group of inventions provides possibility of immediate regeneration/recovery of dermal/skin tissue, which lost its initial density.;14 cl, 2 dwg, 16 ex
机译:发明领域本发明涉及一种透明质酸衍生物(HBC)的制备和纯化方法,涉及以下步骤:a)溶解二缩水甘油醚1,4-丁二醇(BDDE)的二环氧的碱性溶液。 )以2.5至25%摩尔的透明质酸重复键的化学计量比,然后b)在室温下将透明质酸(HA)分散在(a)项中指定的溶液中,c)通过热活化(b)项中指定的溶液,在35至55°C的温度下加热2至36小时,d)通过金属筛将获得的物料挤出以使其颗粒减小至约600 mcm,e)将获得的物料水化用水稀释3至20倍以形成凝胶; f)用HCl水溶液将pH调节至中性; g)沉积水溶性有机溶剂,例如乙醇,甲醇,异丙醇,正丙醇,二恶烷,乙腈,丙酮和/或其混合物,直到获得沉淀粉末形式的产物,h)用含水的有机溶剂如乙醇,甲醇,异丙醇,正丙醇,二恶烷,乙腈,丙酮和/或它们的混合物洗涤,i)真空干燥直到除去低于400 ppm的残留溶剂并获得白色HBC粉末;生产由透明质酸十六烷基酰胺(HYADD)与HBC的混合物组成的生物材料的方法;制备和纯化HBC衍生物的方法,包括以下步骤:a)将BDDE二环氧化物以化学计量比为2.5至25摩尔的透明质酸重复键溶解在碱性溶液中,然后b)将HA分散在前面的a)项在室温下,c)通过热活化触发反应,其中将(b)项中指定的溶液在35至55°C下加热2至36小时,d)用水溶液将pH调至中性HCl溶液,e)通过用水稀释3至20倍而使获得的凝胶水合;生产由HYADD和HBC的混合物组成的生物材料的方法;制成由HYADD和HBC的混合物与BDDE交联而成的生物材料,其重量比为10:90至90:10,作为一种新的填充剂和/或作为人体轮廓产品;用作生物材料的新填充物和/或新产品,用于人体轮廓治疗皮肤缺陷,皮肤病学,皮肤美容和/或美容手术。;效果:一组发明提供了立即再生/恢复皮肤/皮肤组织的可能性,它失去了初始密度。; 14 cl,2 dwg,16 ex

著录项

  • 公开/公告号RU2692800C2

    专利类型

  • 公开/公告日2019-06-27

    原文格式PDF

  • 申请/专利权人 FIDIA FARMACHEUTICHI S.P.A.;

    申请/专利号RU20140149799

  • 发明设计人 DESTE MATTEO (IT);RENER DAVIDE (IT);

    申请日2014-12-09

  • 分类号A61L27/26;A61L27/52;A61L27/58;C08L5/08;

  • 国家 RU

  • 入库时间 2022-08-21 11:46:07

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