Gaspari F, Bonati M
J Pharm Pharmacol. 1987 Apr;39(4):252-60. doi: 10.1111/j.2042-7158.1987.tb06262.x.
A method to establish the correlation between the reverse phase high performance liquid chromatographic retention of caffeine and its metabolites and their n-octanol/water partition coefficients is described. The log (P) values were always below zero, ranging from -0.02 to -2.03. The capacity factor quadratically back-extrapolated to 100% water eluent (k'w) was used as the index of lipophilicity. The compounds examined gave a good correlation (r greater than 0.99) with log (k'w) if considered in separate series, depending on the substituent position. For a structure-pharmacokinetic relationship study, correlations were found between the partition coefficient and some pharmacokinetic parameters, suggesting that for drugs that are widely metabolized, any predictions of their disposition from physicochemical characteristics are hazardous.
描述了一种建立咖啡因及其代谢物的反相高效液相色谱保留与其正辛醇/水分配系数之间相关性的方法。log(P)值始终低于零,范围为-0.02至-2.03。将容量因子二次外推至100%水洗脱液(k'w)用作亲脂性指标。所研究的化合物如果按取代基位置分成不同系列考虑,则与log(k'w)具有良好的相关性(r大于0.99)。对于结构-药代动力学关系研究,发现分配系数与一些药代动力学参数之间存在相关性,这表明对于广泛代谢的药物,根据其物理化学特性对其处置进行任何预测都是有风险的。