Smith G H, Levy R H
Drug Intell Clin Pharm. 1982 Sep;16(9):693-5. doi: 10.1177/106002808201600909.
A comparison of two analytical methods of quinidine plasma determination--the modified extraction fluorometric method and the mass spectrometric method--was made. Plasma supplies collected at steady state from normal human volunteers participating in a bioavailability study were analyzed, using both methods. A total of 359 samples were analyzed. Comparison of both sets of values, by linear regression, yielded an r2 value of 0.84. The results of this comparison were consistent with the results reported by others, confirming that the commonly used extraction fluorometric method of quinidine determination is sufficiently accurate for monitoring quinidine plasma concentrations in the patient care setting, as well as for bioavailability comparisons between products.
对两种奎尼丁血浆测定分析方法——改良萃取荧光法和质谱法——进行了比较。使用这两种方法对参与生物利用度研究的正常人类志愿者在稳态下采集的血浆样本进行了分析。总共分析了359个样本。通过线性回归对两组数值进行比较,得出r2值为0.84。该比较结果与其他人报告的结果一致,证实常用的奎尼丁萃取荧光测定法对于监测患者护理环境中的奎尼丁血浆浓度以及产品间生物利用度比较而言足够准确。