Kuzuya T, Takagi K, Apichartpichean R, Muraoka I, Nadai M, Hasegawa T
Department of Hospital Pharmacy, Nagoya University, School of Medicine, Japan.
J Pharmacobiodyn. 1989 Jul;12(7):405-9. doi: 10.1248/bpb1978.12.405.
The effect of a newly developed quinolone, NY-198, on the pharmacokinetics and metabolism of theophylline was investigated under steady-state conditions in six male healthy volunteers, in a crossover fashion. A sustained-release theophylline formulation (200 mg twice daily at 12 h intervals) was received as monotherapy or coadministration with NY-198 (200 mg twice daily at 12 h intervals). No significant change in the pharmacokinetic parameters of theophylline was observed during coadministration of NY-198. No significant change in urinary excretion of theophylline and its metabolites was also observed. These findings indicate that NY-198 does not influence the pharmacokinetics of theophylline and we can suggest that quinoline derivatives have less effect on theophylline disposition than 1,8-naphthyridine derivatives among quinolones.
在六名男性健康志愿者中,以交叉方式在稳态条件下研究了新开发的喹诺酮类药物NY - 198对茶碱药代动力学和代谢的影响。受试者接受缓释茶碱制剂(每日两次,每次200 mg,间隔12小时)单药治疗或与NY - 198联合给药(每日两次,每次200 mg,间隔12小时)。在联合使用NY - 198期间,未观察到茶碱药代动力学参数有显著变化。茶碱及其代谢物的尿排泄也未观察到显著变化。这些发现表明,NY - 198不影响茶碱的药代动力学,并且我们可以认为在喹诺酮类药物中,喹啉衍生物对茶碱处置的影响小于1,8 - 萘啶衍生物。