Nitti V, Virgilio R, Patricolo M R, Iuliano A
Chemotherapy. 1977;23(1):1-6. doi: 10.1159/000221963.
The time course of the serum and urine concentrations of rifampicin were evaluated during and after administration of an intravenous preparation of the antibiotic. 300, 450 and 600 mg dose levels of the antibiotic were evaluated, all being given as intravenous infusion after solution in 500 ml of glucose, the infusion lasting 3 h. The results have shown that the serum level curves and the kinetic parameters calculated on them do not differ to any major extent from those corresponding to the same doses given orally. No changes of relevance in the half-life values were observed between doses. Changes in serum bilirubin levels were observed with a pattern similar to that commonly seen with oral administration of rifampicin.
在静脉注射该抗生素制剂期间及之后,对利福平的血清和尿液浓度的时间进程进行了评估。评估了300、450和600毫克剂量水平的抗生素,所有剂量均在溶于500毫升葡萄糖后通过静脉输注给药,输注持续3小时。结果表明,血清水平曲线以及据此计算的动力学参数与口服相同剂量时的相应参数在任何主要方面均无差异。各剂量之间未观察到半衰期值有相关变化。观察到血清胆红素水平的变化模式与口服利福平常见的模式相似。