Journal of Chromatographic Science Advance Access published December 5, 2014 Journal of Chromatographic Science 2014;1– 6 doi:10.1093/chromsci/bmu100

Article

Determination of Clevidipine and Its Primary Metabolite in Rat Plasma by a Dispersive Liquid – Liquid Microextraction Method Yuxia Zhou, Qiaogen Zou*, Lili Sun, Ping Wei and Pingkai Ouyang College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 210009, P.R. China *Author to whom correspondence should be addressed. Email: [email protected] Received 17 December 2013; revised 22 July 2014

Dispersive liquid– liquid microextraction based on the solidification of a floating organic droplet combined with high-performance liquid chromatography with ultraviolet detection (HPLC-UV) was developed for the determination of clevidipine and its primary metabolite in Sprague-Dawley rat plasma samples. During the extraction procedure, to facilitate an efficient procedure, the plasma protein was precipitated first by using a mixture of a zinc sulfate solution and acetonitrile. Several extraction parameters were carefully evaluated and optimized, including the type and volume of the extraction solvent, salt effect, pH and extraction time. Under the optimum conditions, the limits for quantification were 2.5 and 5.0 ng mL21 for clevidipine and its primary metabolite, respectively. Sufficient linearity of clevidipine or its primary metabolite was observed with the coefficient of correlation (r) above 0.9979. The method showed good precision and accuracy, with intra- and inter-assay coefficients of variation

Determination of clevidipine and its primary metabolite in rat plasma by a dispersive liquid-liquid microextraction method.

Dispersive liquid-liquid microextraction based on the solidification of a floating organic droplet combined with high-performance liquid chromatograph...
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