Watson W A, McKinney P E
Department of Emergency Medicine, School of Pharmacy, University of Missouri-Kansas City.
DICP. 1991 Oct;25(10):1081-4. doi: 10.1177/106002809102501012.
Studies determining the effects of activated charcoal on drug absorption frequently use area under the plasma drug concentration versus time curve or drug and metabolite recovery in the urine as endpoints. The considerations in using these endpoints is presented using studies that have evaluated the effects of activated charcoal on acetylcysteine absorption. Acetylcysteine's pharmacokinetics, quantitation of plasma concentrations, and the lack of an identifiable pharmacokinetic-pharmacodynamic relationship all contribute to the difficulties in determining whether activated charcoal inhibits the oral absorption of acetylcysteine, or alters acetylcysteine's efficacy in treating acetaminophen overdoses. The results of these studies should be interpreted cautiously, with consideration of internal and external study validity.
确定活性炭对药物吸收影响的研究通常将血浆药物浓度-时间曲线下面积或尿液中药物及代谢物回收率作为终点指标。通过评估活性炭对乙酰半胱氨酸吸收影响的研究来阐述使用这些终点指标时的考量因素。乙酰半胱氨酸的药代动力学、血浆浓度定量以及缺乏可识别的药代动力学-药效学关系,都使得难以确定活性炭是否抑制乙酰半胱氨酸的口服吸收,或改变其在治疗对乙酰氨基酚过量时的疗效。这些研究结果应谨慎解读,并考虑研究的内部和外部有效性。