前药
化学
配体(生物化学)
电化学
渗透(战争)
铂金
共轭体系
顺铂
组合化学
生物物理学
立体化学
核化学
有机化学
生物化学
电极
物理化学
受体
催化作用
化疗
运筹学
生物
工程类
外科
聚合物
医学
作者
Daniil Spector,Alexander S. Erofeev,Petr V. Gorelkin,Alexander N. Vaneev,Roman Akasov,Nikolay V. Ul’yanovskiy,Вита Н. Никитина,Alevtina S. Semkina,Kseniya Yu. Vlasova,Mikhail A. Soldatov,Alexander L. Trigub,Dmitry A. Skvortsov,Alexander V. Finko,Н. В. Зык,Dmitry Sakharov,Alexander G. Majouga,Елена К. Белоглазкина,Olga O. Krasnovskaya
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-09-01
卷期号:61 (37): 14705-14717
被引量:14
标识
DOI:10.1021/acs.inorgchem.2c02062
摘要
We report herein a Pt(IV) prodrug with metronidazole in axial positions Pt-Mnz. The nitroaromatic axial ligand was conjugated with a cisplatin scaffold to irreversibly reduce under hypoxic conditions, thereby retaining the Pt(IV) prodrug in the area of hypoxia. X-ray near-edge adsorption spectroscopy (XANES) on dried drug-preincubated tumor cell samples revealed a gradual release of cisplatin from the Pt-Mnz prodrug instead of rapid intracellular degradation. The ability of the prodrug to penetrate into three-dimensional (3D) spheroid cellular cultures was evaluated by a novel electrochemical assay via a platinum-coated carbon nanoelectrode, capable of single-cell measurements. Using a unique technique of electrochemical measurements in single tumor spheroids, we were able to both detect the real-time response of the axial ligand to hypoxia and establish the depth of penetration of the drug into the tumor model.
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