在线固相萃取和柱切换法测定尿样中的异丙嗪及其代谢物

Q Song , L Putcha
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引用次数: 16

摘要

建立了在线固相萃取-切换柱色谱法定量测定尿液中异丙嗪及其三种代谢物的方法。这里描述的柱转换系统使用提取柱从尿液基质中纯化PMZ及其代谢物。用梯度洗脱法冲洗萃取柱,去除外来基质干扰。然后将感兴趣的分析物洗脱到分析柱上,使用更大溶剂强度的流动相进行进一步的色谱分离。该方法特异性强,灵敏度高,对PMZ的检测范围为3.75 ~ 1400 ng/ml,对代谢物异丙嗪亚砜、单去甲异丙嗪亚砜和单去甲异丙嗪的检测范围为2.5 ~ 1400 ng/ml。PMZ的定量下限为3.75 ng/ml, C.V.小于6.2%;代谢物的定量下限为2.50 ng/ml, C.V.小于11.5%,信噪比为10:1或更高。PMZ和代谢物的准确度和精密度偏差在±11.8%以内,测定内和测定间精密度不大于5.5% C.V.。方法采用Plackett-Burman试验设计进行稳健性研究。说明了分析方法在人体药代动力学研究中的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitation of promethazine and metabolites in urine samples using on-line solid-phase extraction and column-switching

A chromatographic method for the quantitation of promethazine (PMZ) and its three metabolites in urine employing on-line solid-phase extraction and column-switching has been developed. The column-switching system described here uses an extraction column for the purification of PMZ and its metabolites from a urine matrix. The extraneous matrix interference was removed by flushing the extraction column with a gradient elution. The analytes of interest were then eluted onto an analytical column for further chromatographic separation using a mobile phase of greater solvent strength. This method is specific and sensitive with a range of 3.75–1400 ng/ml for PMZ and 2.5–1400 ng/ml for the metabolites promethazine sulfoxide, monodesmethyl promethazine sulfoxide and monodesmethyl promethazine. The lower limits of quantitation (LLOQ) were 3.75 ng/ml with less than 6.2% C.V. for PMZ and 2.50 ng/ml with less than 11.5% C.V. for metabolites based on a signal-to-noise ratio of 10:1 or greater. The accuracy and precision were within ±11.8% in bias and not greater than 5.5% C.V. in intra- and inter-assay precision for PMZ and metabolites. Method robustness was investigated using a Plackett–Burman experimental design. The applicability of the analytical method for pharmacokinetic studies in humans is illustrated.

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