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高效液相色谱法测定少量血浆中的拉莫三嗪

Determination of lamotrigine in small volumes of plasma by high-performance liquid chromatography.

作者信息

Cheng Ching-Ling, Chou Chen-Hsi, Hu Oliver Yoa-Pu

机构信息

Department of Pharmacy, Chia-Nan University of Pharmacy and Science, Tainan, Taiwan.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Mar 25;817(2):199-206. doi: 10.1016/j.jchromb.2004.12.004.

Abstract

Lamotrigine is a broad-spectrum antiepileptic agent. This study describes a simple and sensitive high-performance liquid chromatographic method for the determination of lamotrigine in 50 microl of plasma. Lamotrigine and the internal standard guanabenz were extracted with 1.2 ml of diethyl ether, after the samples alkalinized with 10 microl of sodium hydroxide solution (1N). Chromatographic separation was achieved on a silica column with the mobile phase of acetonitrile-water containing 0.2% phosphoric acid and 0.3% triethylamine (pH 2.7) (84:16, v/v), at a flow-rate of 1 ml/min. The eluant was detected at 225 nm. The retention time was about 6 min for lamotrigine and 7 min for guanabenz. No endogenous substances and concomitant anticonvulsants were found to interfere. Calibration curves were linear from 0.1 to 5 microg/ml. The relative recovery of lamotrigine averaged about 80%. The limit of quantitation was 0.1 microg/ml. The intra- and inter-day precision (expressed as coefficient of variation, CV) was 8.1%, or less, and the accuracy was within 11.5% deviation of the nominal concentration. The method is suitable in pharmacokinetic investigation and monitoring lamotrigine concentration.

摘要

拉莫三嗪是一种广谱抗癫痫药。本研究描述了一种简单且灵敏的高效液相色谱法,用于测定50微升血浆中的拉莫三嗪。在用10微升氢氧化钠溶液(1N)将样品碱化后,用1.2毫升乙醚萃取拉莫三嗪和内标胍法辛。在硅胶柱上进行色谱分离,流动相为含0.2%磷酸和0.3%三乙胺(pH 2.7)的乙腈-水(84:16,v/v),流速为1毫升/分钟。在225纳米处检测洗脱液。拉莫三嗪的保留时间约为6分钟,胍法辛的保留时间约为7分钟。未发现内源性物质和同时使用的抗惊厥药有干扰。校准曲线在0.1至5微克/毫升范围内呈线性。拉莫三嗪的相对回收率平均约为80%。定量限为0.1微克/毫升。日内和日间精密度(以变异系数CV表示)为8.1%或更低,准确度在标称浓度偏差的11.5%以内。该方法适用于药代动力学研究和监测拉莫三嗪浓度。

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