首页> 外文期刊>Therapeutic Drug Monitoring >High-performance liquid chromatographic analysis of the anticancer drug irinotecan (CPT-11) and its active metabolite SN-38 in human plasma.
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High-performance liquid chromatographic analysis of the anticancer drug irinotecan (CPT-11) and its active metabolite SN-38 in human plasma.

机译:人体血浆中抗癌药物伊立替康(CPT-11)及其活性代谢产物SN-38的高效液相色谱分析。

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摘要

A rapid, sensitive, and specific high-performance liquid chromatography (HPLC) method for the simultaneous determination of irinotecan (CPT-11) and its active metabolite SN-38 in human plasma is described. The analytes are quantified as the totals of their carboxylate and lactone form. The sample pretreatment consisted of a simple protein precipitation with acetonitrile-methanol (1:1, v/v), after which CPT-11 and SN-38 were quantitatively converted to their carboxylate form by adding 0.01 mol/L sodium tetraborate (pH, 9). Chromatography was carried out on a Zorbax SB-C18 column with fluorescence detection. The method has been validated, and stability tests under various clinically relevant conditions have been performed. The lower limit of quantification (LLOQ) was 5.0 ng/mL for CPT-11 and 0.5 ng/mL for SN-38. Standard concentration ranges were linear between 5 and 1,500 ng/mL for CPT-11 and between 0.5 and 100 ng/mL for SN-38. This assay is simple, rapid, and very useful for therapeutic monitoring of CPT-11 and SN-38.
机译:描述了一种快速,灵敏,特异的高效液相色谱(HPLC)方法,用于同时测定人血浆中的伊立替康(CPT-11)及其活性代谢产物SN-38。将分析物定量为其羧酸盐和内酯形式的总和。样品前处理包括用乙腈-甲醇(1:1,v / v)沉淀简单的蛋白质,然后通过添加0.01 mol / L四硼酸钠(pH,pH,pH值)将CPT-11和SN-38定量转化为羧酸盐形式。 9)。在具有荧光检测的Zorbax SB-C18柱上进行色谱。该方法已经过验证,并且已经在各种临床相关条件下进行了稳定性测试。 CPT-11的定量下限(LLOQ)为5.0 ng / mL,SN-38的定量下限(LLOQ)为0.5 ng / mL。对于CPT-11,标准浓度范围是线性的,介于5和1500 ng / mL之间;对于SN-38,标准浓度范围是线性的,在0.5和100 ng / mL之间。该测定法简单,快速,对CPT-11和SN-38的治疗监测非常有用。

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