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载甲氨蝶呤的还原降解性 PEG-b-PAA-b-PEG 三嵌段共聚物胶束用于癌症化疗。

Reduction-degradable PEG-b-PAA-b-PEG triblock copolymer micelles incorporated with MTX for cancer chemotherapy.

机构信息

National Engineering Research Center for Biomaterials, Sichuan University, 29 Wangjiang Road, Chengdu 610064, China.

出版信息

Colloids Surf B Biointerfaces. 2013 Dec 1;112:197-203. doi: 10.1016/j.colsurfb.2013.07.056. Epub 2013 Aug 8.

DOI:10.1016/j.colsurfb.2013.07.056
PMID:23981981
Abstract

Reduction-breakable core-shell type polymeric micelles from reduction-degradable amphiphilic polyethylene glycol-b-polyamide amine-b-polyethylene glycol triblock copolymers (PEG-b-PAA-b-PEG) were prepared as new drug carriers of methotrexate (MTX) for cancer chemotherapy. The PEG-b-PAA-b-PEG copolymers were synthesized in a simple one-step process under mild condition through Michael addition. Spherical micelles with diameters ranging from 65 to 123nm were successfully fabricated from the copolymers. These micelles could effectively encapsulate the anti-cancer drug MTX in the core with drug loading content around 13%. The incorporation of MTX resulted in a little size increase but did not influence the morphology of micelles. The drug was hardly released from the micelles in normal condition without DDT as the reductant, but fast released up to 100% within 24h when the structure of micelle core was broken in the presence of DTT, thus provided a potential tool for tumor targeting delivery of MTX using the higher concentration of reductant in tumor tissues. The proliferation inhibition experiments demonstrate that MTX-encapsulated micelles show significant cytotoxicity to KB, HepG2 and 4T1 tumor cells, especiallythe 4T1 cells.

摘要

采用还原可断裂核壳型两亲性聚乙二醇-b-聚酰胺胺-b-聚乙二醇三嵌段共聚物(PEG-b-PAA-b-PEG)制备了作为甲氨蝶呤(MTX)用于癌症化疗的新药物载体的聚合物胶束。PEG-b-PAA-b-PEG 共聚物通过迈克尔加成在温和条件下以简单的一步法合成。成功地从共聚物制备了直径为 65 至 123nm 的球形胶束。这些胶束可以有效地将抗癌药物 MTX 封装在核心中,载药量约为 13%。掺入 MTX 导致稍微增加了尺寸,但不影响胶束的形态。在没有 DDT 作为还原剂的正常条件下,药物几乎不会从胶束中释放,但当在 DTT 的存在下破坏胶束的核结构时,在 24 小时内快速释放高达 100%,因此为使用肿瘤组织中更高浓度的还原剂对 MTX 进行肿瘤靶向递送提供了一种潜在的工具。增殖抑制实验表明,包封 MTX 的胶束对 KB、HepG2 和 4T1 肿瘤细胞表现出显著的细胞毒性,特别是 4T1 细胞。

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