Lesko L J
Clin Pharmacokinet. 1979 Nov-Dec;4(6):449-59. doi: 10.2165/00003088-197904060-00004.
There are an increasing number of clinical and experimental studies appearing in the literature suggesting that the elimination kinetics of theophylline may be dose-dependent in man. Evidence of nonlinearity includes observations that steady-state serum theophylline concentrations may increase disproportionately with increases in dose and that the elimination half-life of theophylline after multiple doses is longer than after single doses. Theophylline is apparently eliminated by parallel Michaelis-Menten and first-order kinetics. Although no specific studies of theophylline metabolism have been carried out to determine the causes of nonlinearity, it would appear that 1-demethylation of theophylline is a potentially saturable metabolic pathway. Dietary methylxanthines or their metabolites may influence the rate of elimination of theophylline and contribute to the causes of nonlinearity. Until the elimination kinetics of theophylline have been studied in more detail as a function of dose, it would seem prudent to increase doses of theophylline cautiously to minimise the risks of adverse side effects which might be associated with unexpected accumulation of theophylline.
文献中出现的临床和实验研究越来越多,表明茶碱在人体内的消除动力学可能与剂量有关。非线性的证据包括观察到稳态血清茶碱浓度可能随剂量增加而非比例增加,以及多剂量给药后茶碱的消除半衰期比单剂量给药后更长。茶碱显然是通过平行的米氏动力学和一级动力学消除的。尽管尚未进行关于茶碱代谢的具体研究以确定非线性的原因,但茶碱的1-去甲基化似乎是一条潜在的可饱和代谢途径。饮食中的甲基黄嘌呤或其代谢产物可能会影响茶碱的消除速率,并导致非线性的原因。在更详细地研究茶碱作为剂量函数的消除动力学之前,谨慎增加茶碱剂量以尽量减少可能与茶碱意外蓄积相关的不良副作用风险似乎是明智的。