首页> 外国专利> METHOD FOR OBTAINING NON-TOXIC GELS BASED ON MODIFIED CARBOXYMETHYLCELLULOSE AND THEIR USE IN MEDICINE

METHOD FOR OBTAINING NON-TOXIC GELS BASED ON MODIFIED CARBOXYMETHYLCELLULOSE AND THEIR USE IN MEDICINE

机译:基于改性羧甲基纤维素获得无毒凝胶的方法及其在医学中的应用

摘要

FIELD: medicine. ;SUBSTANCE: group of inventions relates to the field of medicine, namely to a gel based on modified carboxymethylcellulose or its pharmaceutically acceptable salt for use as a filler for medical implants, a carrier substance, a lubricant and/or an anti-adhesion barrier, an anti-adhesive gel or an intradermal filler and to a method for producing a gel based on modified carboxymethylcellulose or its pharmaceutically acceptable salt, including the following stages: a) the creation of covalent bonds between the molecules of carboxymethylcellulose or its pharmaceutically acceptable salt by interacting in solution with carboxymethylcellulose or its pharmaceutically acceptable salt with a crosslinking agent, which is a substituted oxyrane selected from 1,4-butanedioldiglycidyl ether, polyethylene glycoldiglycidyl ether or polypropylene glycoldiglycidyl ether; b) neutralization of free epoxy groups in modified carboxymethylcellulose or its pharmacologically acceptable salt obtained at stage a), and neutralization of the crosslinking agent residues by adding an amino acid or a combination of at least two amino acids to the reaction mixture obtained at stage a); c) removal of the amino acid and/or crosslinking agent residues by dialysis of the gel obtained after stage b) in a sodium-phosphate physiological buffer solution or water for injection. ;EFFECT: group of inventions provides for the development of a new effective method for producing a gel by modifying carboxymethylcellulose or its pharmacologically acceptable salt, which has low toxicity, and this method for production is well scalable and makes it possible to obtain low-toxic and biocompatible gels with a high degree of purity. ;22 cl, 9 dwg, 2 tbl, 15 ex
机译:领域:医学。 ;物质:发明组涉及药物领域,即基于改性羧甲基纤维素的凝胶或其药学上可接受的盐作为用于医用植入物的填料,载体物质,润滑剂和/或抗粘附屏障,抗粘性凝胶或皮内填料以及基于改性的羧甲基纤维素或其药学上可接受的盐的制备凝胶的方法,包括以下阶段:a)羧甲基纤维素分子或其药学上可接受的盐之间的共价键的产生用羧甲基纤维素溶液或其药学上可接受的盐与交联剂相互作用,其是选自1,4-丁二烯酰基醚,聚乙基甘油酯酰基醚或聚丙烯甘油氧化乙烯醚的取代氧氧烷。 b)在阶段a)中,中和改性的羧甲基纤维素中的游离环氧基团或其药理学上可接受的盐,并通过将氨基酸或至少两个氨基酸的组合加入到阶段A中获得的反应混合物中和的交联剂残留物中和); c)通过在B)中在磷酸钠生理缓冲溶液或注射水中透析通过阶段B)中获得的凝胶的透析除去氨基酸和/或交联剂残留物。 ;效果:发明组通过改变羧甲基纤维素或其药理学上可接受的盐,其具有含有低毒性的制造凝胶的新的有效方法,并且这种生产方法是良好的可扩展性,使其可以获得低毒性和具有高纯度的生物相容性凝胶。 ; 22 cl,9 dwg,2 tbl,15 ex

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号