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可生物降解聚合物-顺铂(IV)缀合物作为顺铂(II)的前药。

Biodegradable polymer - cisplatin(IV) conjugate as a pro-drug of cisplatin(II).

机构信息

State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People's Republic of China.

出版信息

Biomaterials. 2011 Oct;32(30):7732-9. doi: 10.1016/j.biomaterials.2011.06.072. Epub 2011 Jul 23.

Abstract

A Pt(IV) complex was covalently conjugated to a new biodegradable amphiphilic tri-block copolymer, MPEG-b-PCL-b-PLL, which contains pendant amino groups, to form a polymeric pro-drug of cisplatin(II), MPEG-b-PCL-b-PLL/Pt(IV). The conjugate was assembled into nano-micelles. The Pt(IV) complex, the polymer carrier and the conjugate were characterized systematically. In vitro release experiments showed that drug release from the polymer-Pt(IV) micelles follows an acid responsive and oxidation-reduction sensitive kinetics. HPLC-ICP-MS analysis revealed that cisplatin(II) can be released from the conjugate under an acidic plus a reductive condition which is available inside a cancerous cell. In vitro MTT assay demonstrated that the polymer-Pt(IV) micelles display higher cytotoxicity against SKOV-3 tumor cells than both cisplatin(II) and Pt(IV) complex. This enhanced cytotoxicity is attributed to effective internalization of the micelles by the cells via endocytosis mechanism, which was observed by fluorescence imaging and by direct determination of the platinum uptake by the cells. This polymer-Pt(IV) conjugate is a promising polymeric pro-drug of cisplatin in micellar form. It can protect the Pt(IV) complex against blood clearance. It can enter cancerous cells via endocytosis mechanism and then cisplatin(II) can be released. Therefore, this polymeric pro-drug of cisplatin is expected to find clinical applications in the future.

摘要

一种 Pt(IV) 配合物通过共价键与一种新的可生物降解的两亲性三嵌段共聚物 MPEG-b-PCL-b-PLL 相连,该共聚物含有侧链氨基,形成顺铂(II)的聚合物前药 MPEG-b-PCL-b-PLL/Pt(IV)。该缀合物被组装成纳米胶束。对 Pt(IV) 配合物、聚合物载体和缀合物进行了系统的表征。体外释放实验表明,聚合物-Pt(IV) 胶束中的药物释放遵循酸响应和氧化还原敏感动力学。HPLC-ICP-MS 分析表明,顺铂(II)可以从缀合物中在酸性加还原条件下释放,该条件在癌细胞内是可用的。体外 MTT 测定表明,聚合物-Pt(IV) 胶束对 SKOV-3 肿瘤细胞的细胞毒性高于顺铂(II)和 Pt(IV) 配合物。这种增强的细胞毒性归因于胶束通过内吞作用机制被细胞有效内化,这可以通过荧光成像和通过直接测定细胞摄取的铂来观察到。这种聚合物-Pt(IV) 缀合物是顺铂的一种有前途的胶束形式的聚合物前药。它可以保护 Pt(IV) 配合物免受血液清除。它可以通过内吞作用机制进入癌细胞,然后释放顺铂(II)。因此,这种顺铂的聚合物前药有望在未来找到临床应用。

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