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Selective and Accurate Determination Method of Propofol in Human Plasma by Mixed-Mode Cation Exchange Cartridge and GC-MS

机译:混合模式阳离子交换柱和GC-MS选择性准确测定人血浆中异丙酚

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摘要

A gas chromatography-mass spectrometry (GC-MS) method for the determination of propofol in human plasma has been developed and validated. Propofol was extracted from human plasma by using mixed-mode cation exchange/reversed-phase (MCX) cartridges. As propofol easily volatilizes during concentration, 100% methanol was injected directly into GC-MS to elute propofol. Despite avoiding concentration process of the eluted solution, lower limit of quantization (LLOQ) of propofol was 25 ng/mL. The validated method exhibited good linearity (R 2 = 0.9989) with accuracy and precision −5.8%~11.7% and 3.7%~11.6%, respectively. The other validation parameters, recovery and matrix effect, ranged from 96.6% to 99.4% and 95.3% to 101.4%, respectively. Propofol standard was quantified to evaluate possible loss due to the concentration processes, nitrogen gas and centrifugal vacuum. These two concentration processes resulted in notable decrease in the quantity of propofol, signifying avoiding any concentration processes during propofol quantification. Also, to confirm suitability of the developed method, authentic human plasma samples were analyzed. The selective assay method using MCX cartridge and GC-MS facilitated quantification of propofol in plasma sample accurately by preventing any losses due to the concentration processes.
机译:建立并验证了气相色谱-质谱法(GC-MS)测定人血浆中异丙酚的方法。使用混合模式阳离子交换/反相(MCX)色谱柱从人血浆中提取异丙酚。由于丙泊酚在浓缩过程中容易挥发,因此将100%甲醇直接注入GC-MS中以洗脱丙泊酚。尽管避免了洗脱液的浓缩过程,但异丙酚的定量下限(LLOQ)为25μng/ mL。验证的方法具有良好的线性度(R 2 = 0.9989),准确度和精密度分别为-5.8%〜11.7%和3.7%〜11.6%。其他验证参数(回收率和基质效应)分别为96.6%至99.4%和95.3%至101.4%。对异丙酚标准品进行了定量,以评估由于浓缩过程,氮气和离心真空而可能造成的损失。这两个浓缩过程导致了异丙酚量的显着减少,这表明在进行异丙酚定量时避免了任何浓缩过程。另外,为确认所开发方法的适用性,对真实的人血浆样品进行了分析。使用MCX色谱柱和GC-MS进行的选择性测定方法通过防止由于浓缩过程引起的任何损失,有助于准确定量血浆样品中的异丙酚。

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