Hanna S, Rosen M, Eisenberger P, Rasero L, Lachman L
J Pharm Sci. 1978 Jan;67(1):84-6. doi: 10.1002/jps.2600670121.
A specific and quantitative GLC method for warfarin in human plasma is described. The procedure uses papaverine as the internal standard and involves a dichloroethane extraction of the acidified specimen. The organic extract is evaporated, and the evaporated extract is dissolved in 50 microliter of chloroform. Aliquots of 2-3 microliter are injected into a gas chromatograph equipped with a flame-ionization detector. The sensitivity of the method is such that 0.3 microgram of intact warfarin can be detected in 1 ml of plasma. Statistical analyses indicate a recovery of 97.26 +/- 1.89% SD. The procedure was successfully applied to plasma drug level studies in humans.
本文描述了一种用于测定人血浆中华法林的特异性定量气相色谱法。该方法使用罂粟碱作为内标,对酸化后的样本进行二氯乙烷萃取。将有机萃取液蒸发,蒸发后的萃取物溶于50微升氯仿中。取2 - 3微升的等分试样注入配有火焰离子化检测器的气相色谱仪中。该方法的灵敏度足以在1毫升血浆中检测出0.3微克的完整华法林。统计分析表明回收率为97.26 +/- 1.89%(标准差)。该方法已成功应用于人体血浆药物浓度研究。