Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Bad Oeynhausen, Germany.
J Pharm Biomed Anal. 2010 Jan 5;51(1):210-6. doi: 10.1016/j.jpba.2009.08.004. Epub 2009 Aug 12.
A stable isotope dilution liquid chromatography-electrospray ionization tandem mass spectrometry (LC-MS/MS) assay to measure amiodarone, the most frequently used agent for maintaining sinus rhythm in patients with atrial fibrillation, and its major metabolite desethylamiodarone in human plasma and serum was developed. Measurement of amiodarone and desethylamiodarone was performed during a 4.0-min run-time using amiodarone-D(4) and desethylamiodarone-D(4) as internal standards. Calibration curves covering 12 calibrators measured in four replicates each for the analysis of both amiodarone and desethylamiodarone were linear and reproducible in the range of 0.01-40.0 mg/L (r>0.999). Limits of detection in plasma matrix were 2.7 microg/L for amiodarone and 1.9 microg/L for desethylamiodarone, and lower limits of quantification in plasma matrix were 7.5 microg/L for amiodarone and 2.5 microg/L for desethylamiodarone. Interassay imprecision and inaccuracy were <8% and <9% for both substances. Mean extraction yield was 99.6% (range 92.6-107.7%) for amiodarone and 90.2% (range 80.0-94.7%) for desethylamiodarone. Agreement was moderate for amiodarone (n=162) and desethylamiodarone (n=117), respectively, between the present method and a HPLC method with UV detection using a commercially available reagent set for the HPLC analysis of these drugs. The Passing-Bablok regression line was HPLC=0.98 (LC-MS/MS)+0.10 [mg/L]; r=0.94 for amiodarone and HPLC=1.05 (LC-MS/MS)+0.02 [mg/L]; r=0.90 for desethylamiodarone. This sensitive and interference-free LC-MS/MS assay permits rapid and accurate determination of amiodarone and desethylamiodarone in human plasma and other body fluids.
建立了一种稳定同位素稀释液相色谱-电喷雾串联质谱(LC-MS/MS)测定法,用于测量胺碘酮,这是房颤患者维持窦性心律最常用的药物,以及其主要代谢物去乙基胺碘酮在人血浆和血清中的浓度。在 4.0 分钟的运行时间内,使用胺碘酮-D(4)和去乙基胺碘酮-D(4)作为内标,对胺碘酮和去乙基胺碘酮进行测量。胺碘酮和去乙基胺碘酮的分析均采用 12 个校准品,每个校准品重复 4 次,其校准曲线在 0.01-40.0mg/L 范围内呈线性且可重现(r>0.999)。在血浆基质中,胺碘酮的检测限为 2.7μg/L,去乙基胺碘酮的检测限为 1.9μg/L,在血浆基质中,胺碘酮的定量下限为 7.5μg/L,去乙基胺碘酮的定量下限为 2.5μg/L。两种物质的批内精密度和准确度均<8%和<9%。胺碘酮的平均提取回收率为 99.6%(范围为 92.6%-107.7%),去乙基胺碘酮的平均提取回收率为 90.2%(范围为 80.0%-94.7%)。本方法与使用市售试剂盒的 HPLC 法(UV 检测)测定胺碘酮和去乙基胺碘酮的结果相比,对于胺碘酮(n=162)和去乙基胺碘酮(n=117)的测定,两者之间的相关性为中等程度。胺碘酮的 Passing-Bablok 回归直线为 HPLC=0.98(LC-MS/MS)+0.10[mg/L];r=0.94;去乙基胺碘酮的回归直线为 HPLC=1.05(LC-MS/MS)+0.02[mg/L];r=0.90。该灵敏且无干扰的 LC-MS/MS 测定法可用于快速准确地测定人血浆和其他体液中的胺碘酮和去乙基胺碘酮。