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钆四吡嗪(Gd-Tex)-丙二酸盐-铂缀合物:在正常和铂耐药细胞系中的合成及与卡铂的比较。

Gadolinium texaphyrin (Gd-Tex)-malonato-platinum conjugates: synthesis and comparison with carboplatin in normal and Pt-resistant cell lines.

机构信息

Department of Chemistry and Biochemistry, Texas Institute for Diagnostics and Drug Development, 1 University Station-A5300, The University of Texas, Austin, TX 78712-0165, USA.

出版信息

Dalton Trans. 2009 Dec 28(48):10834-40. doi: 10.1039/b912089k. Epub 2009 Oct 7.

Abstract

The synthesis of a new PEG-solubilized gadolinium texaphyrin (Gd-Tex) conjugate containing a malonate-Pt(NH(3))(2) moiety is described. The effect of the tumor localizing Gd-Tex macrocycle on platinum activity was evaluated in cell culture. The malonate moiety, analogous to that present in carboplatin, is expected to release an aquated Pt(NH(3))(2) species under physiological conditions. The half-life in phosphate-buffered saline was found to be ca. 3 days at room temperature, and the hydrolytic product released from the conjugate was collected and confirmed as Pt-based by flameless atomic absorption spectrophotometry. Anti-proliferative activity was tested using A549 human lung cancer and A2780 human ovarian cancer cell lines. In both cell lines, the activity of the Gd-Tex conjugate was found to be similar to that of carboplatin. Efficacy against a Pt-resistant ovarian cell line greater than that displayed by carboplatin was also observed.

摘要

一种新型的聚乙二醇(PEG)增溶的钆四吡咯(Gd-Tex)缀合物的合成,其中含有丙二酸酯-Pt(NH(3))(2)部分。在细胞培养中评价了肿瘤定位的 Gd-Tex 大环对铂活性的影响。丙二酸酯部分类似于卡铂中的部分,预计在生理条件下释放出一个水合的 Pt(NH(3))(2)物种。在室温下,在磷酸盐缓冲液中的半衰期约为 3 天,从缀合物中释放出的水解产物通过无火焰原子吸收分光光度法被确认为基于铂的产物。使用 A549 人肺癌和 A2780 人卵巢癌细胞系测试了抗增殖活性。在这两种细胞系中,Gd-Tex 缀合物的活性与卡铂相似。还观察到对铂耐药的卵巢癌细胞系的疗效大于卡铂的疗效。

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