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可逆聚乙二醇化纳米载体递送达卡巴铂。

Reversibly PEGylated nanocarrier for cisplatin delivery.

机构信息

Institute of Polymers, Bulgarian Academy of Sciences, Acad. Georgi Bonchev Str. Bl.103, 1113 Sofia, Bulgaria.

出版信息

J Inorg Biochem. 2013 Mar;120:54-62. doi: 10.1016/j.jinorgbio.2012.12.005. Epub 2012 Dec 21.

Abstract

A star-shaped copolymer bearing a shell of poly(ethylene glycol) (PEG) chains was designed as a carrier of cisplatin. The proposed strategy was based on synthesis of a PEGylating agent and the incorporation of cisplatin as a reversible linker for PEG modification of the star macromolecules. The attachment of PEG chains to the stars and their release under physiological conditions, as well as the changes in particle size and mobility upon drug loading, was evidenced by diffusion ordered NMR spectroscopy (DOSY). The results demonstrated that PEGylation reduced inter-stars cross-linking and increased the stability of the nanocolloidal solution. The formation of PEG shell resulted in higher drug payload and improved drug release profile of the nanoconjugates. The in vitro bioassay in a panel of human tumor cell lines confirmed that the PEGylated conjugates exhibited superior growth inhibitory activity compared to the cisplatin-loaded nonPEGylated carrier.

摘要

一种具有聚乙二醇(PEG)链外壳的星形共聚物被设计为顺铂的载体。该策略基于合成一种 PEG 化试剂,并将顺铂作为 PEG 修饰星形大分子的可逆连接物。通过扩散排序 NMR 光谱(DOSY)证实了 PEG 链与星形物的连接以及在生理条件下 PEG 的释放,以及载药后颗粒大小和迁移率的变化。结果表明,PEG 化降低了星型物之间的交联,提高了纳米胶体溶液的稳定性。PEG 壳的形成导致更高的药物载量和改善了纳米复合物的药物释放特性。在一系列人肿瘤细胞系中的体外生物测定证实,与负载顺铂的非 PEG 化载体相比,PEG 化的缀合物表现出优异的生长抑制活性。

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