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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Validation of a sensitive LC/MS/MS method for simultaneous quantitation of flupentixol and melitracene in human plasma.
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Validation of a sensitive LC/MS/MS method for simultaneous quantitation of flupentixol and melitracene in human plasma.

机译:灵敏的LC / MS / MS方法可同时定量测定人血浆中的氟哌噻吨和美曲汀的有效性。

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摘要

A sensitive method has been developed and validated, using LC/ESI-MS/MS, for simultaneous quantitation of flupentixol and melitracen--antidepressant drugs, in human plasma. The quantitation of the target compounds was determined in a positive ion mode and multiple reaction monitoring (MRM). The method involved a repeated liquid-liquid extraction with diethyl ether and analytes were chromatographed on a C(8) chromatographic column by elution with acetonitrile-water-formic acid (36:64:1, v/v/v) and analyzed by tandem mass spectrometry. The method was validated over the concentration ranges of 26.1-2090 pg/ml for flupentixol and 0.206-4120 ng/ml for melitracen. The correlation coefficients of both analyst were >0.998 for six sets of calibration curves. The recovery was 60.9-75.1% for flupentixol, melitracen and internal standard. The lower limit of quantitation (LLOQ) detection was 26.1 pg/ml for flupentixol and 0.206 ng/ml for melitracen. Intra- and inter-day precision of the assay at three concentrations were 2.15-5.92% with accuracy of 97.6-103.0% for flupentixol and 0.5-6.36% with accuracy of 98.7-101.7% for melitracen. Stability of compounds was established in a battery of stability studies, i.e., bench-top, autosampler and long-term storage stability as well as freeze/thaw cycles. The method proved to be suitable for bioequivalence study of flupentixol and melitracen in healthy human male volunteers.
机译:使用LC / ESI-MS / MS已开发并验证了一种灵敏的方法,可同时定量测定人血浆中的氟喷替醇和美曲辛-抗抑郁药。目标离子的定量以阳离子模式和多反应监测(MRM)确定。该方法涉及用乙醚重复液-液萃取,分析物在C(8)色谱柱上进行色谱分离,用乙腈-水-甲酸(36:64:1,v / v / v)进行洗脱,并进行串联分析质谱。该方法在氟喷替洛的浓度范围为26.1-2090 pg / ml的范围内,而对美曲舒的浓度范围为0.206-4120 ng / ml的范围内进行了验证。六组校准曲线的两位分析师的相关系数均> 0.998。氟喷托索,美利曲辛和内标物的回收率为60.9-75.1%。氟喷噻醇的定量下限(LLOQ)检测值为26.1 pg / ml,美利曲辛的定量检测下限为0.206 ng / ml。在三种浓度下,日间和日间测定的精密度分别为2.15-5.92%和氟哌丁醇的准确度为97.6-103.0%,而0.5-6.36%的药物测定结果为美利康的准确度为98.7-101.7%。在一系列稳定性研究中确定了化合物的稳定性,即台式,自动进样器和长期储存稳定性以及冻融循环。该方法被证明适用于健康人类男性志愿者中的氟喷他醇和美曲汀的生物等效性研究。

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