首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous measurement of amiodarone and desethylamiodarone in human plasma and serum by stable isotope dilution liquid chromatography-tandem mass spectrometry assay.
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Simultaneous measurement of amiodarone and desethylamiodarone in human plasma and serum by stable isotope dilution liquid chromatography-tandem mass spectrometry assay.

机译:稳定同位素稀释液相色谱-串联质谱法同时测定人血浆和血清中的胺碘酮和去乙基胺碘酮。

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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.
机译:稳定的同位素稀释液相色谱-电喷雾串联质谱(LC-MS / MS)测定法可测量胺碘酮(胺碘酮)(维持房颤患者窦性心律的最常用药物)及其在人体血浆和血清中的主要代谢产物去乙基胺碘酮发达。使用胺碘酮-D(4)和去乙基胺碘酮-D(4)作为内标,在4.0分钟的运行时间中进行了胺碘酮和去乙基胺碘酮的测量。用于胺碘酮和去乙基胺碘酮分析的四次重复测量的涵盖12个校准物的校准曲线是线性的,可重现的范围为0.01-40.0 mg / L(r> 0.999)。血浆基质中胺碘酮的检出限为2.7微克/升,去乙基乙胺碘酮为1.9微克/升,血浆基质的定量下限为胺碘酮为7.5微克/升,去乙基胺碘酮为2.5微克/升。两种物质的测定间不准确性和不准确性分别<8%和<9%。胺碘酮的平均提取率为99.6%(范围为92.6-107.7%),而去乙基胺碘酮的平均提取率为90.2%(范围为80.0-94.7%)。在本方法和使用可用于这些药物的HPLC分析的市售试剂组进行UV检测的HPLC方法之间,胺碘酮(n = 162)和去乙基胺碘酮(n = 117)分别适度。 Passing-Bablok回归线为HPLC = 0.98(LC-MS / MS)+0.10 [mg / L];胺碘酮的r = 0.94,HPLC = 1.05(LC-MS / MS)+0.02 [mg / L];对于去乙基胺碘酮,r = 0.90。这种灵敏且无干扰的LC-MS / MS分析方法可快速,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。

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