Karbwang J, Na Bangchang K, Molunto P, Bunnag D
Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Southeast Asian J Trop Med Public Health. 1989 Mar;20(1):65-9.
A simple, specific, rapid and sensitive High Performance Liquid Chromatography (HPLC) method has been developed to measure plasma level of quinine and quinidine. The drugs were extracted successively from plasma at basic pH with chloroform and quantified on a revers-phase Z-module C18 HPLC column with fluorescence detector (excitation 340 nm, emission 425 nm). The isocratic mobile phase used was the mixture of 0.05 M ammonium formate and acetonitrile (93.5:6.5, v/v), adjusted pH to 2.0 with ortho-phosphoric acid. The limits of quantitation for these compounds were as low as 4 ng/ml of plasma, using a 0.25 ml specimen. Calibration curves were linear (R squared = 0.9994) in the range 0-7,000 ng/ml. An interassay reproducibility was 6.8%, 0.3% and 1.2% at the concentrations of 250 ng, 4,000 ng and 8,000 ng of quinine, respectively. Inter-assay coefficient of variation of quinidine was 1.8%, 2.7% and 3.7% at the concentrations of 250 ng, 1,500 ng and 3,000 ng, respectively. Recovery of quinine and quinidine were 76% and 81%, respectively. The method has been used in the analysis of quinine and quinidine in healthy volunteers receiving quinine or quinidine intravenously. The method is now being used to assay samples from field studies with satisfactory results.
已开发出一种简单、特异、快速且灵敏的高效液相色谱(HPLC)方法来测定血浆中奎宁和奎尼丁的水平。在碱性pH条件下,用氯仿从血浆中依次提取药物,并在配备荧光检测器(激发波长340nm,发射波长425nm)的反相Z模块C18 HPLC柱上进行定量分析。所用的等度流动相是0.05M甲酸铵和乙腈的混合物(93.5:6.5,v/v),用正磷酸将pH调至2.0。使用0.25ml样本时,这些化合物的定量限低至血浆4ng/ml。校准曲线在0 - 7000ng/ml范围内呈线性(决定系数R² = 0.9994)。在奎宁浓度为250ng、4000ng和8000ng时,批间重复性分别为6.8%、0.3%和1.2%。在奎尼丁浓度为250ng、1500ng和3000ng时,批间变异系数分别为1.8%、2.7%和3.7%。奎宁和奎尼丁的回收率分别为76%和81%。该方法已用于分析静脉注射奎宁或奎尼丁的健康志愿者体内的奎宁和奎尼丁。目前该方法正用于现场研究样本的检测,结果令人满意。