Suppr超能文献

采用高效液相色谱法分析抗癌药物VP 16 - 213和VM 26及其代谢产物。

Analysis of the anticancer drugs VP 16-213 and VM 26 and their metabolites by high-performance liquid chromatography.

作者信息

Strife R J, Jardine I, Colvin M

出版信息

J Chromatogr. 1980 May 9;182(2):211-20. doi: 10.1016/s0378-4347(00)81625-4.

Abstract

A rapid and convenient high-performance liquid chromatographic procedure for the analysis of the clinically useful anticancer agents VP 16-213 and VM 26 is described. The drugs, which are semi-synthetic derivatives of the natural product podophyllotoxin, are extracted from plasma with chloroform. The extracts are evaporated to dryness, reconstituted in methanol, and chromatographed on a reversed-phase microparticle C18 column using isocratic elution with a mixture of methanol--water (60:40). Each drug is used as the internal standard for the other. Quantitation to 500 ng/ml (0.85 nmole/ml) plasma is based on peak height ratios using UV detection at 254 nm. Patient plasma concentration versus time data agree well with previously published data obtained using radiolabelled drug. Investigations into the nature of the hydroxy acid metabolite of VP 16-213, carried out using paired-ion chromatography with tetrabutylammonium bromide and fluorescence detection, are described. Also, a unique separation of VP 16-213 and a possible metabolite, the isomer, picro VP 16-213, is described.

摘要

本文描述了一种快速便捷的高效液相色谱法,用于分析临床上有用的抗癌药物VP 16 - 213和VM 26。这两种药物是天然产物鬼臼毒素的半合成衍生物,用氯仿从血浆中提取。提取物蒸发至干,用甲醇复溶,然后在反相微粒C18柱上进行色谱分析,采用甲醇 - 水(60:40)混合液等度洗脱。每种药物都作为另一种药物的内标。基于在254 nm处使用紫外检测的峰高比,可对血浆中500 ng/ml(0.85 nmole/ml)的药物进行定量。患者血浆浓度与时间的数据与先前使用放射性标记药物获得的数据吻合良好。本文还描述了使用四丁基溴化铵和荧光检测的配对离子色谱法对VP 16 - 213的羟基酸代谢物性质进行的研究。此外,还描述了VP 16 - 213与其可能的代谢物——异构体picro VP 16 - 213的独特分离。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验