Koch A, Federspil P, Hartmetz G
Laryngol Rhinol Otol (Stuttg). 1985 Dec;64(12):649-51.
Since metronidazole is very effective against anaerobic bacteria, we studied its pharmacokinetics in perilymph, cerebrospinal fluid, aqueous humour, and serum. 1, 2, 4, 6, 10 and 16.5 hours after intraperitoneal injection of 200 mg/kg metronidazole to six groups of six guinea pigs each, we determined the drug concentrations by high-pressure liquid chromatography. In the serum, 1, 2 and 16.5 hours after application, drug levels of 194 +/- 22 mg/l, 127 +/- 54 mg/l and 2 +/- 1 mg/l respectively were found. Half-life was 6 hours. Similar high and long-lasting concentrations could be determined in the aqueous humour, cerebrospinal fluid and perilymph. In contrast to our findings with aminoglycoside antibiotics, beta lactam antibiotics and fosfomycin, we could not observe any retention of metronidazole in the perilymph.
由于甲硝唑对厌氧菌非常有效,我们研究了其在淋巴液、脑脊液、房水和血清中的药代动力学。给六组每组六只豚鼠腹腔注射200mg/kg甲硝唑后1、2、4、6、10和16.5小时,我们通过高压液相色谱法测定药物浓度。在血清中,给药后1、2和16.5小时,分别发现药物水平为194±22mg/L、127±54mg/L和2±1mg/L。半衰期为6小时。在房水、脑脊液和淋巴液中可测定到相似的高浓度且持久的浓度。与我们使用氨基糖苷类抗生素、β-内酰胺类抗生素和磷霉素的研究结果不同,我们在淋巴液中未观察到甲硝唑有任何潴留现象。