Wijnands W J, Janssen T J, Guelen P J, Vree T B, De Witte T M
Department of Pulmonary Disease, Foundation Deventer Hospitals, The Netherlands.
Pharm Weekbl Sci. 1988 Dec 9;10(6):272-6. doi: 10.1007/BF02219667.
The pharmacokinetic parameters of theophylline and its major metabolites were measured in two healthy volunteers, after the administration of theophylline alone and during co-medication with ofloxacin, 200 mg twice daily, or enoxacin, 200 mg twice daily. During enoxacin co-medication, elimination half-lives of theophylline increased from 8.7 h to 17.4 h and from 6.1 to 12.3 h, respectively. As the renal clearance of theophylline did not change, the decreased elimination of theophylline during enoxacin co-medication must result from a reduced metabolic clearance. Enoxacin co-medication caused a clearly decreased formation of the metabolites 1-methyluric acid and 3-methylxanthine, formed by N-demethylation, whereas the C-8 oxidation of theophylline was less influenced compared to the blank. Enoxacin's interference with the theophylline disposition is predominantly based on the inhibition of the microsomal N-demethylation. Ofloxacin co-medication did not induce a change in the plasma parameters or renal excretion of theophylline and its metabolites.
在两名健康志愿者中,分别测定了单独给予茶碱以及与每日两次200毫克氧氟沙星或每日两次200毫克依诺沙星合用时茶碱及其主要代谢产物的药代动力学参数。在与依诺沙星合用时,茶碱的消除半衰期分别从8.7小时增加到17.4小时以及从6.1小时增加到12.3小时。由于茶碱的肾清除率未发生变化,因此在与依诺沙星合用时茶碱消除减少必定是由于代谢清除率降低所致。与依诺沙星合用时,由N - 去甲基化形成的代谢产物1 - 甲基尿酸和3 - 甲基黄嘌呤的生成明显减少,而与空白相比,茶碱的C - 8氧化受影响较小。依诺沙星对茶碱处置的干扰主要基于对微粒体N - 去甲基化的抑制。与氧氟沙星合用时,茶碱及其代谢产物的血浆参数或肾排泄未发生变化。