首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Development of a liquid-liquid extraction procedure for five 1,4-dihydropyridines calcium channel antagonists from human plasma using experimental design
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Development of a liquid-liquid extraction procedure for five 1,4-dihydropyridines calcium channel antagonists from human plasma using experimental design

机译:使用实验设计开发一种从人血浆中提取5种1,4-二氢吡啶类钙通道拮抗剂的液-液萃取程序

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A liquid-liquid extraction method using diethyl ether as organic solvent was optimized simultaneously for five 1,4-dihydropyridines (amlodipine,nitrendipine,felodipine,lacidipine and lercanidipine) belonging to the group of calcium channel blockers.Some experimental tools such as a full factorial design,a central composite design and the Multisimplex program were used to optimise the concentration of NaOH,volume of organic solvent and shaking time as main factors that influence the liquid-liquid extraction procedure.Following the extraction,the quantitation of the 1,4-dihydropyridines concentrations were performed by high-performance liquid chromatography with diode-array detector.Therefore,the studied compounds were separated quantitatively on a Supelcosil ABZ+Plus,25 cm x 4.6mm i.d.,5 mum column which was set at 30 deg C,using as mobile phase,a mixture of acetonitrile-water (70:30,v/v) containing 10 mM acetate buffer (pH 5) and setting the detector at a wavelength value of 360 nm.It was concluded that the main factors that influence in the extraction process were the volume of organic solvent and the shaking time.The Multisimplex program suggested as optimal conditions an average of 6 ml of organic solvent and 23 min of shaking time.For these values,the optimised liquid-liquid extraction method showed good values of recoveries (80% for amlodipine and higher than 90% for the rest of the compounds) and low values of R.S.D.(<10%) in the reproducibility of the extraction what makes it reliable for the quantification of all the studied compounds in human plasma.
机译:同时针对两种属于钙通道阻滞剂的1,5,4-二氢吡啶(氨氯地平,硝苯地平,非洛地平,拉地平和拉卡地平)优化了以乙醚为有机溶剂的液-液萃取方法。一些实验工具,例如全析因设计,中心复合设计和Multisimplex程序用于优化NaOH的浓度,有机溶剂的量和振荡时间,这是影响液-液萃取过程的主要因素。在萃取之后,对1,4-进行定量使用高效液相色谱仪和二极管阵列检测器对二氢吡啶进行浓缩,因此,将所研究的化合物在Supelcosil ABZ + Plus,25 cm x 4.6mm内径,30摄氏度的5毫米色谱柱上进行定量分离。作为流动相,是含有10 mM乙酸盐缓冲液(pH 5)的乙腈-水(70:30,v / v)的混合物,并将检测器的波长设置为360 nm。结论是影响萃取过程的主要因素是有机溶剂的量和振荡时间。Multisimplex程序建议平均条件为6 ml有机溶剂和23 min振荡时间作为最佳条件。优化的液-液萃取方法显示出良好的回收率值(氨氯地平为80%,其余化合物的回收率高于90%),而萃取的重现性方面的RSD值较低(<10%),这使得分离的可靠性高。人体血浆中所有研究化合物的定量分析。

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