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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 >Development of a HPLC-MS/MS method for the simultaneous determination of nifedipine and lidocaine in human plasma
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Development of a HPLC-MS/MS method for the simultaneous determination of nifedipine and lidocaine in human plasma

机译:一种HPLC-MS / MS方法,用于同时测定人血浆中硝苯地平和利多卡因的方法

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摘要

The method for simultaneous determination of nifedipine (NIF) and lidocaine (LID) in human plasma by one-step sample preparation has been developed for the first time. Due to the photosensitivity of nifedipine and its low plasma concentrations a precise and reliable method was required. The method involved liquid-liquid extraction (methyl tert-butyl ether, MTBE), and 10 mu l. of the resulting sample was analyzed by HPLC-MS/MS. Chromatographic separation was achieved on an YMC-Triart C18 HPLC column (100 x 2.0 mm; S-5 mu m 12 nm). The mobile phase was methanol:water, 60:40 (v/v) and contained 0.15% acetic acid. The linearity of the method was established in the concentration ranges of 0.5-50 ng/mL for NW and 1.0-500 ng/mL for LID. Photodestruction of NIF under ambient light was evaluated. The validated method was successfully applied to analyze human plasma samples after rectal application of the drug (1 g) containing 2.0% LID and 03% NIF. (C) 2016 Elsevier B.V. All rights reserved.
机译:首次开发了通过单步样品制备在人血浆中同时测定硝苯地平(NIF)和Lidocaine(盖子)的方法。 由于硝苯地平的光敏性及其低血浆浓度,需要一种精确可靠的方法。 该方法涉及液 - 液萃取(甲基叔丁基醚,MTBE)和10μl。 通过HPLC-MS / MS分析所得样品。 在YMC-Triart C18 HPLC柱上实现色谱分离(100×2.0mm; s-5μm12nm)。 流动相是甲醇:水,60:40(v / v),含有0.15%乙酸。 该方法的线性度在0.5-50ng / ml的浓度范围内,对于NW和1.0-500ng / ml进行盖子。 评价NIF在环境光下的光脱模。 经过验证的方法被成功地应用于含有2.0%盖子和03%NIF的药物(1g)直肠施加后分析人血浆样品。 (c)2016 Elsevier B.v.保留所有权利。

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