Engel G, Hofmann U, Eichelbaum M
Dr. Margarete Fischer-Bosch-Institut für Klinische Pharmakologie, Stuttgart, Germany.
J Chromatogr B Biomed Appl. 1995 Apr 7;666(1):111-6. doi: 10.1016/0378-4347(94)00563-k.
A highly sensitive and specific gas chromatographic-tandem mass spectrometric method was developed for the determination of the antipyrine (INN: phenazone) metabolites, norantipyrine, 4-hydroxyantipyrine and 3-hydroxy-methylantipyrine, in biological material. Deuterated analogues of the metabolites were used as internal standards. The method has a limit of quantitation of 5 ng per sample for the determination of norantipyrine, 4-hydroxy-antipyrine and 3-hyddroxymethylantipyrine with coefficients of variation of 19.4, 14.6 and 20.7%, respectively. Precision and accuracy are good over the whole range measured (5-500 ng/sample) with a coefficient of variation, respectively error of determination < or = 20%. Due to its high sensitivity the method can be used to study the formation of these metabolites in microsomal preparations containing only 100 micrograms of protein.
建立了一种高灵敏度和高特异性的气相色谱 - 串联质谱法,用于测定生物材料中的安替比林(国际非专利药品名称:非那宗)代谢物,去甲安替比林、4 - 羟基安替比林和3 - 羟基甲基安替比林。代谢物的氘代类似物用作内标。该方法测定去甲安替比林、4 - 羟基安替比林和3 - 羟基甲基安替比林的定量限为每个样品5 ng,变异系数分别为19.4%、14.6%和20.7%。在整个测量范围内(5 - 500 ng/样品),精密度和准确度良好,变异系数分别为测定误差≤20%。由于其高灵敏度,该方法可用于研究仅含100微克蛋白质的微粒体制剂中这些代谢物的形成。