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Nanomicelle formulation of vinca alkaloid anticancer drug encapsulated in polyethylene glycol derivative of phospholipid

机译:磷脂聚乙二醇衍生物包裹的长春花生物碱抗癌药物的Nanomicelle制剂

摘要

The present invention provides a nano-micellar preparation containing vinca alkaloids antitumor agent for intravenous injection, which cincludes a therapeutically effective amount of vinca alkaloids antitumor agent (vinblastine, vincristine, vindesine and vinorelbine), a phosphatide derivatized with polyethylene glycol, together with pharmaceutically acceptable adjuvants. The preparation is prepared by encapsulating the medicament with a nano-micelle to obtain the nano-micellar preparation containing vinca alkaloids antitumor agent for injection. The vinca alkaloids antitumor agent and the phosphatide derivatized with polyethylene glycol form a nano-micelle with a highly uniform particle size. In the micelle, the hydrophobic core of encapsulated medicament is surrounded by polyethylene glycol molecules to form a hydrophilic protective layer, so that the medicament is prevented from contacting with the enzymes and other protein molecules in blood and being recognized and phagocytozed by reticuloendothelial system in body, and the circulation time in vivo of the micelle is prolonged.
机译:本发明提供了包含用于静脉注射的长春花生物碱抗肿瘤剂的纳米胶束制剂,其包括治疗有效量的长春花生物碱抗肿瘤剂(长春碱,长春新碱,长春地辛和长春瑞滨),用聚乙二醇衍生的磷脂以及药学上可接受的佐剂。通过用纳米胶囊包封药物以获得包含注射用长春花生物碱抗肿瘤剂的纳米胶束制剂来制备制剂。长春花生物碱抗肿瘤剂和用聚乙二醇衍生的磷脂形成具有高度均一粒径的纳米胶束。在胶束中,被包封药物的疏水核心被聚乙二醇分子包围,形成亲水性保护层,从而防止了药物与血液中的酶和其他蛋白质分子接触,并被体内的网状内皮系统识别并吞噬。 ,延长了胶束的体内循环时间。

著录项

  • 公开/公告号JP2009507049A

    专利类型

  • 公开/公告日2009-02-19

    原文格式PDF

  • 申请/专利权人 北京徳科瑞医薬科技有限公司;

    申请/专利号JP20080529454

  • 发明设计人 梁 偉;婁 民 安;司 維;

    申请日2006-09-08

  • 分类号A61K31/475;A61K47/24;A61K9/107;A61K47/12;A61K9/19;A61P35;A61K45;

  • 国家 JP

  • 入库时间 2022-08-21 19:39:17

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