Vandamme T F, Demoustier M, Rollmann B
Université Catholique de Louvain, Unité de Pharmacie Galénique, Bruxelles, Belgium.
Eur J Drug Metab Pharmacokinet. 1995 Apr-Jun;20(2):145-9. doi: 10.1007/BF03226369.
A rapid and sensitive procedure is described for the quantitation of levamisole in plasma using high-performance liquid chromatography (HPLC). The procedure involves sample preparation using a reverse-phase C18 cartridge prior to chromatography and quantitation using peak area ratios (UV absorbance detection, 225 nm) of levamisole to the internal standard, quinine. The limit of detection was 21 ng/ml and the limit of quantification was 72 ng/ml, both contained in 1 ml of plasma. The recoveries were sufficiently high (73.1%) and overall coefficient of variation of the procedure was 0.25%. This procedure has been used to determine levamisole levels in human and cattle plasma. A comparison of using two C18 columns (Nova-pak, Puresil) was also studied and discussed.
描述了一种使用高效液相色谱(HPLC)定量血浆中左旋咪唑的快速灵敏方法。该方法包括在色谱分析前使用反相C18柱进行样品制备,并使用左旋咪唑与内标物奎宁的峰面积比(紫外吸光度检测,225nm)进行定量。检测限为21ng/ml,定量限为72ng/ml,均包含在1ml血浆中。回收率足够高(73.1%),该方法的总体变异系数为0.25%。此方法已用于测定人和牛血浆中的左旋咪唑水平。还研究并讨论了使用两种C18柱(Nova-pak、Puresil)的比较情况。