首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous quantification of alpha-/beta-diastereomers of arteether, sulphadoxine and pyrimethamine: A promising anti-relapse antimalarial therapeutic combination, by liquid chromatography tandem mass spectrometry
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Simultaneous quantification of alpha-/beta-diastereomers of arteether, sulphadoxine and pyrimethamine: A promising anti-relapse antimalarial therapeutic combination, by liquid chromatography tandem mass spectrometry

机译:同时定量鉴定甲醚,磺胺多辛和乙胺嘧啶的α-/β-非对映异构体:液相色谱串联质谱法用于抗复发的抗疟疾治疗组合

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摘要

A rapid, sensitive, selective and specific HPLC/ESI-MS/MS assay method was developed and validated for the simultaneous quantitation of alpha/beta-diastereomers of arteether (AE), sulphadoxine (SDX) and pyrimethamine (PYR) in rat blood plasma using propyl ether analogue of P-arteether as internal standard. The method involved a single-step, liquid-liquid extraction with ethyl acetate and the analytes were chromatographed on a C-18 chromatographic column by isocratic elution with methanol: ammonium acetate buffer (10 mM, pH 4) (90:10%, v/v) and analyzed by tandem mass spectrometry. The run time was 4.5 min and the weighted (1/x(2)) calibration curves were linear over a range of 0.78-400 ng ml(-1). The method was validated fully and the lower limit of quantification (LLOQ) in plasma was 0.78 ng ml(-1) for all the analytes. The intra- and inter-day precision and accuracy were found to be well within the acceptable limits (< 15%) and the analytes were stable after three freeze-thaw (f-t) cycles. The absolute recoveries were consistent and reproducible. The assay method was applied to pre-clinical pharmacokinetic interaction studies of alpha-/beta-AE, SDX and PYR in rats. (c) 2006 Elsevier B.V. All rights reserved.
机译:建立了一种快速,灵敏,选择性和特异的HPLC / ESI-MS / MS测定方法,并验证了该方法可同时定量大鼠血浆中甲醚(AE),磺胺多辛(SDX)和乙胺嘧啶(PYR)的α/β-非对映异构体用对-甲醚的丙醚类似物作为内标。该方法涉及一步一步的乙酸乙酯液-液萃取,分析物在C-18色谱柱上通过甲醇,乙酸铵缓冲液(10 mM,pH 4)(90:10%,v)等度洗脱进行色谱分离。 / v),并通过串联质谱分析。运行时间为4.5分钟,加权(1 / x(2))校准曲线在0.78-400 ng ml(-1)范围内呈线性。该方法已得到充分验证,所有分析物的血浆下限(LLOQ)为0.78 ng ml(-1)。发现日内和日间精度和准确度均在可接受的范围内(<15%),并且在三个冻融(f-t)循环后,分析物稳定。绝对回收率是一致且可重现的。该测定方法应用于大鼠中α-/β-AE,SDX和PYR的临床前药代动力学相互作用研究。 (c)2006 Elsevier B.V.保留所有权利。

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