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人血浆中安非他酮及其主要代谢物的高效液相色谱测定法。

HPLC assay for bupropion and its major metabolites in human plasma.

作者信息

Loboz Katarzyna K, Gross Annette S, Ray John, McLachlan Andrew J

机构信息

Faculty of Pharmacy, University of Sydney, NSW 2006, Australia.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Sep 5;823(2):115-21. doi: 10.1016/j.jchromb.2005.06.009.

Abstract

Bupropion is used clinically as an antidepressant and in smoking cessation. As it is metabolised to hydroxybupropion specifically by CYP2B6, bupropion has also been used as a probe to assess CYP2B6 activity. A specific and reproducible HPLC assay has been developed to simultaneously quantify bupropion and its major metabolites hydroxybupropion, threohydrobupropion and erythrohydrobupropion in human plasma. The analysis was performed on an Aqua C18 HPLC column, with a mobile phase consisting of 45:55 of methanol:0.05 M phosphate buffer (pH 5.5) and simultaneous UV detection at 214 nm (bupropion metabolites) and 254 nm (bupropion, internal standard timolol maleate). The assay showed a linear response for bupropion (2.5-250 ng/mL), threohydrobupropion (5-250 ng/mL), erythrohydrobupropion (10-250 ng/mL) and hydroxybupropion (10-1000 ng/mL). Extraction recovery was reproducible and greater than 55% for each analyte. The inter- and intra-day assay variability (measured as percent coefficient of variation; %CV) was less than 15% for all analytes. Limit of quantification was 2.5 ng/mL for bupropion, 5 ng/mL for threohydrobupropion and 10 ng/mL for hydroxybupropion and erythrohydrobupropion. This assay is more sensitive than currently published methods using HPLC with UV detection for the simultaneous quantitation of bupropion and metabolites and can be used for assessing CYP2B6 activity in vivo following a single dose of bupropion.

摘要

安非他酮在临床上用作抗抑郁药和戒烟药。由于它主要通过CYP2B6代谢为羟基安非他酮,安非他酮也被用作评估CYP2B6活性的探针。已开发出一种特异性和可重复性的高效液相色谱法(HPLC),用于同时定量人血浆中的安非他酮及其主要代谢物羟基安非他酮、苏式羟基安非他酮和赤式羟基安非他酮。分析在Aqua C18 HPLC柱上进行,流动相由45:55的甲醇:0.05 M磷酸盐缓冲液(pH 5.5)组成,同时在214 nm(安非他酮代谢物)和254 nm(安非他酮、内标马来酸噻吗洛尔)处进行紫外检测。该方法对安非他酮(2.5 - 250 ng/mL)、苏式羟基安非他酮(5 - 250 ng/mL)、赤式羟基安非他酮(10 - 250 ng/mL)和羟基安非他酮(10 - 1000 ng/mL)呈线性响应。每种分析物的提取回收率可重复且大于55%。所有分析物的日间和日内分析变异性(以变异系数百分比;%CV衡量)均小于15%。安非他酮的定量限为2.5 ng/mL,苏式羟基安非他酮为5 ng/mL,羟基安非他酮和赤式羟基安非他酮为10 ng/mL。该方法比目前已发表的使用紫外检测的HPLC同时定量安非他酮及其代谢物的方法更灵敏,可用于评估单剂量安非他酮后体内的CYP2B6活性。

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