Charter M K, Gull S F
Mullard Radio Astronomy Observatory, Cavendish Laboratory, Cambridge, England.
J Pharmacokinet Biopharm. 1987 Dec;15(6):645-55. doi: 10.1007/BF01068418.
A new method is presented for calculating the rate at which a drug enters the bloodstream after dosing, given the concentration of the drug in blood at various times. The method is based on the principle of maximum entropy, which has not been applied previously to pharmacokinetic problems. The resulting input rate functions are smooth and physiologically realistic, free of spurious oscillations yet still showing small-scale structure where there is evidence for it in the data. Blood samples do not need to be taken at equal intervals, and no preliminary smoothing or interpolation of the data is required.
提出了一种新方法,用于在已知给药后不同时间血液中药物浓度的情况下,计算药物进入血液循环的速率。该方法基于最大熵原理,此前尚未应用于药代动力学问题。由此产生的输入速率函数是平滑的,符合生理实际,没有虚假振荡,但在数据中有证据表明存在小规模结构的地方仍会显示出来。不需要以相等的时间间隔采集血样,也不需要对数据进行初步平滑或插值。