Shah S, Vasantharaju S G, Arumugam K, Muddukrishna B S, Desai N
Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, India.
Arzneimittelforschung. 2012 May;62(5):243-6. doi: 10.1055/s-0032-1301911. Epub 2012 Mar 1.
A sensitive and selective high performance liquid chromatographic (HPLC) method was developed and validated for quantification of lacosamide in rat plasma. A liquid-liquid extraction procedure was optimized to extract lacosamide from rat plasma. Chromatographic separation was accomplished using a reversed phase C18 Hichrom (250×4.6 mm, 5 µm) column with the mobile phase consisting of acetonitrile-phosphate buffer (pH 3.2±0.1; 20 mM) (21:79, v/v) at a flow rate of 1 mL/min. Both intra- and inter day assay precision and accuracy were lower than 15% CV. The lower limit of quantitation was 25 ng/mL for lacosamide and the response was linear in a concentration range from 25 to 10 000 ng/mL. The developed method was successfully used for the preclinical pharmacokinetic study of lacosamide in rats.
建立了一种灵敏且具选择性的高效液相色谱(HPLC)法,并对其进行验证,用于定量大鼠血浆中的拉科酰胺。优化了液-液萃取程序以从大鼠血浆中提取拉科酰胺。采用反相C18 Hichrom(250×4.6 mm,5 µm)色谱柱进行色谱分离,流动相为乙腈-磷酸盐缓冲液(pH 3.2±0.1;20 mM)(21:79,v/v),流速为1 mL/min。日内和日间测定的精密度和准确度的变异系数(CV)均低于15%。拉科酰胺的定量下限为25 ng/mL,在25至10000 ng/mL的浓度范围内响应呈线性。所建立的方法成功用于拉科酰胺在大鼠体内的临床前药代动力学研究。