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甲硝唑和替硝唑的比较药代动力学及其组织穿透性。

Comparative pharmacokinetics of metronidazole and tinidazole and their tissue penetration.

作者信息

Bergan T, Solhaug J H, Søreide O, Leinebø O

出版信息

Scand J Gastroenterol. 1985 Oct;20(8):945-50. doi: 10.3109/00365528509088853.

DOI:10.3109/00365528509088853
PMID:4081633
Abstract

Since metronidazole and tinidazole are used prophylactically against infections after colorectal surgery, their pharmacokinetics and that of hydroxy-metronidazole were compared in 34 such patients. Seventeen patients received a single dose of 1.5 g (50-min infusion) of either agent 1 h before the operation. The concentrations of serum and tissue homogenates (subcutaneous fat, omentum, peritoneum, ileum, appendix, colon) were assayed by high-pressure liquid chromatography. The serum concentrations 1 h after start of infusion were 34.1 +/- 6.7 mg/l of metronidazole, 2.3 +/- 1.2 mg/l of OH-metronidazole, and 35.2 +/- 6.3 mg/l of tinidazole. OH-metronidazole and tinidazole were detectable for 72 h and metronidazole for 48 h. The ranges of serum and tissue concentrations (subcutaneous fat, omentum, peritoneum, ileum, appendix, colon) overlapped (within one single standard deviation). The tissue concentrations were high, particularly in intestinal tissues, except that the levels were low in subcutaneous tissue. The serum half-life of metronidazole was 9.0 +/- 1.6 h, of OH-metronidazole 14.8 +/- 7.4 h, and of tinidazole 16.4 +/- 3.8 h. The terminal-phase distribution volume was 35.8 +/- 10.01 for metronidazole and 40.6 +/- 9.91 for tinidazole, and the total body clearance 2.7 +/- 1.2 l/h and 1.8 +/- 0.5 l/h, respectively. The slower disposition of OH-metronidazole, which inhibits anaerobic bacteria, prolongs the duration of bioactivity in the body after metronidazole to that reached by tinidazole. OH-tinidazole was not detected in patient specimens (assay standards ensured that it could be assayed).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

由于甲硝唑和替硝唑用于结直肠手术后感染的预防,对34例此类患者的甲硝唑、羟基甲硝唑和替硝唑的药代动力学进行了比较。17例患者在手术前1小时接受单剂量1.5g(50分钟输注)的其中一种药物。通过高压液相色谱法测定血清和组织匀浆(皮下脂肪、大网膜、腹膜、回肠、阑尾、结肠)的浓度。输注开始后1小时血清浓度分别为:甲硝唑34.1±6.7mg/l,羟基甲硝唑2.3±1.2mg/l,替硝唑35.2±6.3mg/l。羟基甲硝唑和替硝唑可检测72小时,甲硝唑可检测48小时。血清和组织浓度范围(皮下脂肪、大网膜、腹膜、回肠、阑尾、结肠)有重叠(在一个标准差范围内)。组织浓度较高,尤其是在肠道组织中,除皮下组织中的水平较低外。甲硝唑的血清半衰期为9.0±1.6小时,羟基甲硝唑为14.8±7.4小时,替硝唑为16.4±3.8小时。甲硝唑的终末相分布容积为35.8±10.01,替硝唑为40.6±9.91,全身清除率分别为2.7±1.2l/h和1.8±0.5l/h。抑制厌氧菌的羟基甲硝唑较慢的处置过程,使甲硝唑在体内的生物活性持续时间延长至替硝唑达到的水平。在患者标本中未检测到羟基替硝唑(检测标准确保其可被检测)。(摘要截短于250字)

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