Bergan T, Lolekha S, Cheong M K, Poh C L, Patancharoen S
Department of Microbiology, Faculty of Medicine, National University of Singapore.
Scand J Infect Dis Suppl. 1988;56:11-3.
The pharmacokinetics of 400 mg norfloxacin administered orally were studied in 19 patients both during the acute phase of bacterial gastroenteritis and during convalescence, after normalization of bowel movements. The peak serum concentrations, total area under the serum concentration curve, rate of elimination and serum half-life in the beta-phase were all similar during the acute phase of the disease as well as after normalization of the intestinal function. The only difference was that the time to peak concentrations was longer (p less than 0.01) during the acute phase of the disease. That finding suggests that the faster intraintestinal transport of the drug during the acute stage of the disease leads to a reduced efficiency of early absorption. However, since the bioavailability was not affected, norfloxacin is obviously absorbed at a lower intestinal level and no dose adjustment should be necessary in patients with diarrhoea.
对19例细菌性肠胃炎急性期及恢复期(排便正常后)的患者口服400mg诺氟沙星后的药代动力学进行了研究。疾病急性期及肠道功能恢复正常后,血清峰浓度、血清浓度曲线下总面积、消除率及β相血清半衰期均相似。唯一的差异是疾病急性期达峰浓度时间较长(p<0.01)。这一发现表明,疾病急性期药物在肠道内转运较快,导致早期吸收效率降低。然而,由于生物利用度未受影响,诺氟沙星显然在较低肠道水平被吸收,腹泻患者无需调整剂量。