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At the time for the liposome of dokisorubishin where at the time

机译:当时用于多异异丁星的脂质体

摘要

PROBLEM TO BE SOLVED: To obtain the subject kit capable of being easily prepared, having small particle size of liposome effectively containing agents and containing no aggregates by allowing the kit to include a liposome membrane-forming material comprising a phospholipid composition containing phospholipid, liposome zeta-potential-increasing agent, etc., a cationic agents and an aqueous medium. ;SOLUTION: (A) A phospholipid composition prepared by dissolving (i) a liposome membrane-forming material comprising a phospholipid, e.g. phosphatidyl choline with (ii) a liposome zata-potential-increasing agent, e.g. oleic acid having a negative electric charge, sodium cholesterol sulfate, etc., enclosed in a vessel under an inactive gas atmosphere is added to (B) a cationic agent such as doxorubicin, vincristine, daunorubicin or the like when it is used, and the obtained solution is added to (C) an aqueous medium suitable for intravenus injections, e.g. a sodium chloride solution having 0.9 wt.% concentration, Ringer's solution or the like.;COPYRIGHT: (C)2000,JPO
机译:解决的问题:为了获得易于制备的,具有小粒径的脂质体的有效试剂盒,该脂质体有效地包含试剂并且不包含聚集体,方法是使该试剂盒包括脂质体膜形成材料,该材料包含脂质组合物,所述磷脂组合物包含磷脂,脂质体ζ电位增强剂等,阳离子剂和水性介质。 ;解决方案:(A)通过溶解(i)包含磷脂例如脂质体的脂质体膜形成材料而制备的磷脂组合物。磷脂酰胆碱与(ii)脂质体zata电位增加剂,例如在惰性气体气氛下封闭在容器中的具有负电荷的油酸,胆固醇硫酸钠等被添加到(B)使用时的阿霉素,长春新碱,柔红霉素等阳离子剂中,并且将获得的溶液添加到(C)适用于静脉内注射的水性介质中,例如浓度为0.9 wt。%的氯化钠溶液,林格氏溶液等;版权:(C)2000,JPO

著录项

  • 公开/公告号JP4444385B2

    专利类型

  • 公开/公告日2010-03-31

    原文格式PDF

  • 申请/专利权人 帝人株式会社;

    申请/专利号JP19990048320

  • 发明设计人 米谷 芳枝;永井 恒司;王 俊平;

    申请日1999-02-25

  • 分类号A61K9/127;A61K31/704;A61K47/10;A61K47/12;A61K47/24;A61K47/28;

  • 国家 JP

  • 入库时间 2022-08-21 18:57:29

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