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Amphiphilic block copolymer, method for preparing the same, and micellar drug encapsulation system formed of the copolymer and an antitumor agent

机译:两亲性嵌段共聚物,其制备方法以及由该共聚物和抗肿瘤剂形成的胶束药物包封系统

摘要

The present invention relates to a novel amphiphilic block copolymer, a method for preparing the same, and a micellar drug encapsulation system formed of the copolymer and an antitumor drug. The amphiphilic block copolymer includes a hydrophilic segment and a hydrophobic segment, and the end group of the hydrophobic segment is end-capped with a hydrophobic group. A methoxypolyethylene glycol (or polyethylene glycol) -polyester block copolymer that has been recognized as safe is used as a basic material of the amphiphilic block copolymer of the present invention, and the terminal hydroxyl group of the polyester segment is modified with a hydrophobic group. Therefore, the compatibility between the drug molecule and the hydrophobic segment of the block copolymer is improved, and the interaction therebetween is enhanced. In addition, a larger space is provided for accommodating drug molecules. The micelle has a higher effect of regulating drug molecules inside the micelle core and prevents the drug from dissolving out of the micelle. Therefore, highly stable drug-encapsulated micelles can be obtained.
机译:本发明涉及新型两亲性嵌段共聚物,其制备方法以及由该共聚物和抗肿瘤药形成的胶束药物包封系统。两亲性嵌段共聚物包括亲水性链段和疏水性链段,并且疏水性链段的端基被疏水性基团封端。已经被认为是安全的甲氧基聚乙二醇(或聚乙二醇)-聚酯嵌段共聚物被用作本发明的两亲嵌段共聚物的基础材料,并且聚酯链段的末端羟基被疏水基团改性。因此,改善了药物分子与嵌段共聚物的疏水链段之间的相容性,并且增强了它们之间的相互作用。另外,提供了更大的空间来容纳药物分子。胶束具有更高的调节胶束核心内部药物分子的作用,并防止药物从胶束中溶出。因此,可以获得高度稳定的药物包封的胶束。

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