Synthesis, characterization and in vitro and in vivo anticancer activity of Pt(IV) derivatives of [Pt(1S,2S-DACH)(5,6-dimethyl-1,10-phenanthroline)]

被引:44
|
作者
Harper, Benjamin W. J. [1 ]
Petruzzella, Emanuele [1 ]
Sirota, Roman [1 ]
Faccioli, Fernanda Fabiola [2 ]
Aldrich-Wright, Janice R. [3 ]
Gandin, Valentina [2 ]
Gibson, Dan [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Pharm, Inst Drug Res, IL-91120 Jerusalem, Israel
[2] Univ Padua, Dipartimento Sci Farmaco, Via Marzolo 5, I-35131 Padua, Italy
[3] Western Sydney Univ, Sch Sci & Hlth, Penrith, NSW 1797, Australia
基金
以色列科学基金会;
关键词
PLATINUM COMPLEXES; DRUG DEVELOPMENT; CANCER-CELLS; CYTOTOXICITY; LIGANDS; PRODRUGS; AGENTS; METALLOINTERCALATORS; OXALIPLATIN; CHEMISTRY;
D O I
10.1039/c7dt01054k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This report describes the synthesis, characterization and biological activity of a series of platinum(IV) derivatives of [Pt(1S,2S-DACH)(5,6-dimethyl-1,10-phenanthroline)] (Pt56MeSS) with non-bioactive, lipophilic and bioactive axial ligands. In an attempt to explore the anticancer activity potential of the Pt(IV) derivatives, 2D and 3D cytotoxic screening and a preliminary in vivo study were performed. The average IC50 values of the platinum(IV) derivatives ranged from 1.26 to 5.39 mu M, compared with 1.24 mu M for Pt56MeSS, suggesting that the axial ligands have a relatively minor effect on the potency of the compounds. Preliminary in vivo studies indicate that the platinum(IV) derivatives of Pt56MeSS are active in vivo and can reduce the tumor to a similar extent to cisplatin.
引用
收藏
页码:7005 / 7019
页数:15
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