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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of irinotecan (CPT-11) and SN-38 in human whole blood and red blood cells by liquid chromatography with fluorescence detection
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Determination of irinotecan (CPT-11) and SN-38 in human whole blood and red blood cells by liquid chromatography with fluorescence detection

机译:液相色谱-荧光检测法测定人全血和红细胞中的伊立替康(CPT-11)和SN-38

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摘要

An analytical method was developed for the anticancer agent irinotecan (CPT-11) and its main metabolite SN-38 in human whole blood and in red blood cells (RBCs). Sample pretreatment involved deproteinization of whole blood or plasma-diluted RBCs isolated by MESED instruments, with a mixture of aqueous perchloric acid and methanol (1:1, v/v). Separation was carried out using isocratic elution on a Hypersil ODS stationary phase, with detection at excitation and emission wavelengths of 355 and 515 nm, respectively. The lower limit of quantitation (LLQ) in blood was established at 5.00 ng/ml for both compounds, with values for within-run precision (WRP) and between-run precision (BPR) of less than 10%. The method is currently being applied to investigate the blood distribution of (CPT-11) and SN-38 in cancer patients.
机译:开发了一种抗癌剂伊立替康(CPT-11)及其主要代谢产物SN-38在人全血和红细胞(RBC)中的分析方法。样品预处理涉及使用高氯酸水溶液和甲醇(1:1,v / v)的混合物将全血或血浆稀释的红细胞(由MESED仪器分离)脱蛋白。在Hypersil ODS固定相上使用等度洗脱进行分离,分别在355和515 nm的激发和发射波长下进行检测。两种化合物的血液定量下限(LLQ)均为5.00 ng / ml,批内精密度(WRP)和批间精密度(BPR)的值均小于10%。该方法目前正用于研究癌症患者中(CPT-11)和SN-38的血液分布。

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