Roberts M S, Fraser S, Wagner A, McLeod L
Department of Pharmacy, Otago Medical School, Dunedin, New Zealand.
J Pharmacokinet Biopharm. 1990 Jun;18(3):209-34. doi: 10.1007/BF01062200.
The residence time distributions of sucrose and taurocholate have been determined from the outflow concentration-time profiles after bolus input into an in situ perfused rat liver preparation. The normalized variance (and the dispersion number) appeared to be independent of perfusate flow rate (10 to 37 ml/min) and perfusate albumin concentration (0.5%). The apparent volume of distribution for sucrose appeared to increase with flow rate but was unaffected by the concentration of albumin (0-5%) present in the perfusate. The changes in taurocholate availability with flow rate were adequately accounted for by the dispersion model, whereas taurocholate availability-protein binding changes required an albumin-mediated transport model to be used in conjunction with the dispersion model.
在将蔗糖和牛磺胆酸盐大剂量注入原位灌注大鼠肝脏制剂后,根据流出液浓度-时间曲线确定了它们的停留时间分布。归一化方差(和分散数)似乎与灌注液流速(10至37毫升/分钟)和灌注液白蛋白浓度(0.5%)无关。蔗糖的表观分布容积似乎随流速增加,但不受灌注液中白蛋白浓度(0-5%)的影响。分散模型充分解释了牛磺胆酸盐可用性随流速的变化,而牛磺胆酸盐可用性-蛋白质结合变化则需要将白蛋白介导的转运模型与分散模型结合使用。