Destache C J, Pakiz C B, Stoysich A M
Creighton University School of Pharmacy and Allied Health Professions and Medicine, Omaha, NE 68178, USA.
J Antimicrob Chemother. 1996 Dec;38(6):977-85. doi: 10.1093/jac/38.6.977.
Using microdialysis in a rabbit model of Streptococcus pneumoniae meningitis, the pharmacokinetics and pharmacodynamics of a new fluoroquinolone, A-80556, were determined. A-80556 (10 mg/kg iv) was administered to four rabbits. Saline was given to four separate control animals. A microdialysis probe perfused the CSF (2 microL/min) and effluent was collected at 0-0.25, 0.25-1, 1-2, 2-4, and 4-6 h after injection of A-80556. Seven blood samples were collected and analyzed by HPLC. At 0, 2, 4 and 6 h 300 microL of CSF was withdrawn for pharmacodynamic measurements. Plasma A-80556 concentrations demonstrated AUC0-infinity 2.40 +/- 0.272 micrograms.h/mL; T1/2 beta 1.07 +/- 0.011 h; Vd 6.35 +/- 0.50 L/kg; and Cl1 4.23 +/- 0.48 L/h.kg. Penetration into the CSF was 18.21%. Pharmacodynamics using time-kill curves showed a 3-log reduction in bacterial counts in CSF at 2 h after administration continuing for the remaining four hours of the experiment. These results demonstrate that microdialysis can be used for determination of drug penetration and efficacy in experimental S. pneumoniae meningitis.
在肺炎链球菌性脑膜炎的兔模型中使用微透析技术,测定了一种新型氟喹诺酮类药物A - 80556的药代动力学和药效学。给4只兔子静脉注射A - 80556(10 mg/kg)。给另外4只对照动物注射生理盐水。一个微透析探针以2微升/分钟的速度灌注脑脊液,并在注射A - 80556后的0 - 0.25、0.25 - 1、1 - 2、2 - 4和4 - 6小时收集流出液。采集7份血样并用高效液相色谱法进行分析。在0、2、4和6小时抽取300微升脑脊液进行药效学测量。血浆中A - 80556浓度显示AUC0 - ∞为2.40±0.272微克·小时/毫升;T1/2β为1.07±0.011小时;Vd为6.35±0.50升/千克;Cl1为4.23±0.48升/小时·千克。药物进入脑脊液的渗透率为18.21%。使用时间 - 杀菌曲线的药效学研究表明,给药后2小时脑脊液中的细菌计数下降了3个对数,并在实验剩余的4小时内持续下降。这些结果表明,微透析可用于测定实验性肺炎链球菌性脑膜炎中药物的渗透率和疗效。