Guy R H, Hadgraft J
J Pharmacokinet Biopharm. 1983 Apr;11(2):189-203. doi: 10.1007/BF01061849.
Theoretical expressions are derived to predict the amount of a drug reaching the dermal capillaries as a function of simple physicochemical parameters. The mathematical approach involves the solution of the diffusion equation for the drug in the skin using the technique of Laplace transformation. First-order kinetics are assumed for the absorption of drug from the vehicle into the skin and for uptake into the capillaries. The relative importance of these different processes (absorption from vehicle, diffusion through the skin, and capillary removal) involved in the percutaneous penetration of a drug is discussed, and their influence upon the time course of the absorption phenomenon is illustrated.
推导了理论表达式,以预测到达真皮毛细血管的药物量与简单物理化学参数的函数关系。数学方法涉及使用拉普拉斯变换技术求解皮肤中药物的扩散方程。假设药物从载体吸收到皮肤以及进入毛细血管的过程为一级动力学。讨论了药物经皮渗透过程中这些不同过程(从载体吸收、通过皮肤扩散和毛细血管清除)的相对重要性,并说明了它们对吸收现象时间进程的影响。