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首页> 外文期刊>Chromatographia >Simultaneous Analysis of Zofenopril and Its Active Metabolite Zofenoprilat in Human Plasma by LC–ESI-MS Using Pre-Column Derivatization with p-Bromophenacyl Bromide
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Simultaneous Analysis of Zofenopril and Its Active Metabolite Zofenoprilat in Human Plasma by LC–ESI-MS Using Pre-Column Derivatization with p-Bromophenacyl Bromide

机译:使用对溴苯甲酰溴的柱前衍生化LC-ESI-MS同时分析人血浆中的佐非诺普利及其活性代谢物左芬诺拉特

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Zofenoprilat is an active metabolite of zofenopril, which is very unstable in plasma because of oxidative degradation of its thiol group. In this method, p-bromophenacyl bromide was used as derivatization reagent, immediately after plasma separation, to react with the free thiol group of zofenoprilat and form the derivative zofenoprilat-p-BPB. After acidification with 50% acetic acid, the derivatized plasma samples were extracted with methyl tert-butyl ether and separated on a C18 column with 40:60 (v/v) 10 mM ammonium acetate buffer solution containing 0.1% formic acid–acetonitrile as mobile phase. Calibration plots were linear over the concentration range 1–500 ng mL−1 for zofenopril and 2–1,800 ng mL−1 for zofenoprilat. The method was successfully used to study the bioavailability of zofenopril calcium capsules relative to that of zofenopril calcium tablets in healthy Chinese volunteers.
机译:Zofenoprilat是zofenopril的活性代谢产物,由于其硫醇基的氧化降解,其在血浆中非常不稳定。在该方法中,血浆分离后立即将对溴苯甲酰基溴用作衍生试剂,使其与左芬诺拉特的游离硫醇基反应并形成衍生物左芬诺拉特-p-BPB。用50%乙酸酸化后,将衍生的血浆样品用甲基叔丁基醚萃取,并在C 18 柱上进行分离,并用40:60(v / v)10 mM乙酸铵缓冲溶液0.1%甲酸-乙腈作为流动相。校准曲线在zofenopril浓度范围为1–500 ng mL -1 和zofenoprilat浓度范围为2–1,800 ng mL -1 范围内是线性的。该方法已成功用于研究在健康的中国志愿者中zofenopril钙胶囊相对于zofenopril钙片的生物利用度。

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