Upton R N, Mather L E, Runciman W B, Nancarrow C, Carapetis R J
Department of Anaesthesia and Intensive Care, Flinders University of South Australia, Adelaide.
J Pharmacokinet Biopharm. 1988 Feb;16(1):13-29. doi: 10.1007/BF01061860.
Mass balance principles were used to derive a number of terms that are helpful in describing the rate and extent of regional drug uptake. Regional drug uptake was defined as the net movement of drug from the blood perfusing a region into the extravascular space of the region due to the distribution and/or elimination of the drug. By analogy with the traditional physiological definition of flux, net drug flux was defined as the difference in mass per unit time of drug respectively entering and leaving a region via the arterial and venous blood vessels. The time-integral of net drug flux, net drug mass, was defined as the mass of drug that has entered a region via the arterial blood vessels but has not left the region via the venous blood vessels. For regions in which no drug elimination occurs, the mean regional drug concentration was defined as the net drug mass divided by the mass of the region. When a number of criteria are satisfied, the net drug flux is approximately the rate of drug uptake and the net drug mass is approximately the extent of drug uptake. Several examples are given to demonstrate the broad range of applications of mass balance principles. First, the method was used to characterize the differences between drug distribution and elimination in a hypothetical region using drug concentrations simulated from compartmental models of either distribution alone or distribution with elimination. Second, the whole body distribution net flux was described during a constant rate infusion of iodohippurate (IOH) into a sheep from the difference between the whole body net flux and renal net flux of IOH. Third, the time course of the mean myocardial lignocaine (lidocaine) concentrations in a sheep after an intravenous bolus of lignocaine were described. The time course of the lignocaine-induced depression of myocardial contractility followed more closely the mean myocardial lignocaine concentrations than that of either the arterial or coronary sinus blood concentrations. It is concluded that the use of mass balance principles provides a simple, empirical, and physiologically based method for the determination of the rate and extent of both drug distribution and elimination in regions as simple as single organs or as complex as the whole body.
质量平衡原理被用于推导一些有助于描述局部药物摄取速率和程度的术语。局部药物摄取被定义为由于药物的分布和/或消除,药物从灌注某一区域的血液进入该区域血管外间隙的净移动。类似于通量的传统生理学定义,净药物通量被定义为单位时间内分别通过动脉和静脉血管进入和离开某一区域的药物质量之差。净药物通量的时间积分,即净药物质量,被定义为通过动脉血管进入某一区域但尚未通过静脉血管离开该区域的药物质量。对于不发生药物消除的区域,平均局部药物浓度被定义为净药物质量除以该区域的质量。当满足若干标准时,净药物通量近似于药物摄取速率,净药物质量近似于药物摄取程度。给出了几个例子以说明质量平衡原理的广泛应用。首先,该方法被用于利用仅由分布模型或分布与消除模型模拟得到的药物浓度,来表征一个假设区域内药物分布和消除的差异。其次,通过碘马尿酸(IOH)全身净通量与肾净通量之差,描述了向绵羊恒速输注碘马尿酸期间的全身分布净通量。第三,描述了静脉注射利多卡因后绵羊心肌利多卡因平均浓度的时间进程。利多卡因诱导的心肌收缩力抑制的时间进程比动脉血或冠状窦血浓度更紧密地跟随心肌利多卡因平均浓度。得出的结论是,使用质量平衡原理为确定药物在像单个器官一样简单或像全身一样复杂的区域内的分布和消除速率及程度提供了一种简单、经验性且基于生理学的方法。