High-performance liquid chromatographic methods for the determination of topoisomerase II inhibitors

Chun-Lin Chen , Kami K Thoen , Fatih M Uckun
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引用次数: 24

Abstract

Various methods for separating eleven different types of topoisomerase II (TOPO-2) inhibitors, including epipodophyllotoxins, anthracyclines, anthracenediones, anthrapyrazoles, anthracenebishydrazones, indole derivatives, aminoacridines, benzisoquinolinediones, isoflavones, bisdioxopiperazines and thiobarbituric acids, are summarized. Proper sample preparation and storage is critical to the successful analysis of some TOPO-2 inhibitors due to difficulties associated with adsorption, instability and complex biological components. Solid-phase and liquid–liquid extractions are widely used to separate TOPO-2 inhibitors from biological samples, although simple deproteinization followed by direct analysis of the supernatant is preferable to extraction based on its speed and simplicity. High-performance liquid chromatography (HPLC) is the favored method for the bioanalysis of TOPO-2 inhibitors. UV or diode array detection is generally employed for early pharmacokinetic studies, while fluorescence or electrochemical detection is used more frequently for analytes with fluorescent or oxidative–reductive properties. For analyses requiring highly sensitive and/or specific detection, electrospray mass spectrometry (ESI-MS or ESI-MS–MS) provides a suitable alternative. A comprehensive compilation of the HPLC techniques currently used to separate TOPO-2 inhibitors will aid the future development of analytical methods for new TOPO-2 inhibitors.

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高效液相色谱法测定拓扑异构酶II抑制剂。
综述了11种不同类型拓扑异构酶抑制剂(TOPO-2)的分离方法,包括:表臼毒素、蒽环类、蒽二酮类、蒽吡唑类、蒽醌类、吲哚衍生物、氨基吖啶类、苯并喹啉二酮类、异黄酮类、双氧哌嗪类和硫代巴比妥酸类。适当的样品制备和储存对于一些TOPO-2抑制剂的成功分析至关重要,因为吸附困难,不稳定性和复杂的生物成分。固相萃取和液-液萃取被广泛用于从生物样品中分离TOPO-2抑制剂,尽管基于其速度和简单性,简单的脱蛋白后直接分析上清液比萃取更好。高效液相色谱(HPLC)是TOPO-2抑制剂生物分析的首选方法。紫外或二极管阵列检测通常用于早期药代动力学研究,而荧光或电化学检测更常用于具有荧光或氧化还原性质的分析物。对于需要高灵敏度和/或特异性检测的分析,电喷雾质谱(ESI-MS或ESI-MS - ms)提供了合适的替代方案。对目前用于分离TOPO-2抑制剂的高效液相色谱技术进行综合整理,将有助于新的TOPO-2抑制剂分析方法的未来发展。
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