首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of azelastine and its major metabolite desmethylazelastine in human plasma using high performance liquid chromatography-tandem mass spectrometry
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Simultaneous determination of azelastine and its major metabolite desmethylazelastine in human plasma using high performance liquid chromatography-tandem mass spectrometry

机译:高效液相色谱-串联质谱法同时测定人血浆中的氮卓斯汀及其主要代谢物去甲基氮卓斯汀

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摘要

A selective and sensitive high performance liquid chromatography-tandem mass spectrometric method was developed for the analysis of azelastine and its major metabolite, desmethylazelastine, in human plasma. Azelastine- ~(13)C, d _3 was used as internal standard. Azelastine, desmethylazelastine and the internal standard were extracted by a liquid-liquid extraction method and separation was performed under isocratic chromatographic condition. An abnormal signal loss issue for desmethylazelastine during method development was investigated and resolved. The developed method was precise and reproducible as shown by good intraday assay and interday assay precision (CV%≤12.8%). The calibration curve was linear over a range of 10.0/10.0-1000/200pg/mL for azelastine/desmethylazelastine. The method was successfully applied to a pilot bioequivalence study subsequently.
机译:建立了一种选择性和灵敏的高效液相色谱-串联质谱法,用于分析人血浆中的氮卓斯汀及其主要代谢产物去甲基氮卓斯汀。氮卓斯汀-(13)C,d_3用作内标。用液-液萃取法萃取氮卓斯汀,去甲基氮卓斯汀和内标,并在等度色谱条件下进行分离。研究并解决了方法开发过程中去甲基氮卓斯汀的异常信号丢失问题。良好的日内检测和日间检测精度(CV%≤12.8%)表明,所开发的方法精确且可重现。氮卓斯汀/去甲基氮卓斯汀的校准曲线在10.0 / 10.0-1000 / 200pg / mL范围内呈线性。该方法已成功地应用于随后的生物等效性试验研究。

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