Suppr超能文献

甲硝唑及其羟基代谢物对拟杆菌属的体外活性

In vitro activities of metronidazole and its hydroxy metabolite against Bacteroides spp.

作者信息

Pendland S L, Piscitelli S C, Schreckenberger P C, Danziger L H

机构信息

Department of Pharmacy Practice, University of Illinois, Chicago 60612.

出版信息

Antimicrob Agents Chemother. 1994 Sep;38(9):2106-10. doi: 10.1128/AAC.38.9.2106.

Abstract

Metronidazole is metabolized to two major oxidative products: an acid metabolite and a hydroxy metabolite. While the activity of the acid metabolite is negligible, the activity of the hydroxy metabolite is approximately 65% of the activity of the parent drug. Pharmacokinetic studies of metronidazole and its hydroxy metabolite have shown that the MICs of both compounds remain above the MICs for most anaerobic organisms over an 8-h dosing interval. By a checkerboard assay, the combined activities of metronidazole and the hydroxy metabolite were examined against 4 quality control strains of Bacteroides species. Macrobroth tube dilutions were set up with Wilkins-Chalgren broth. Serial twofold dilutions of each agent were performed to achieve final concentrations ranging from 0.06 to 4.0 micrograms/ml. The MICs for Bacteroides fragilis and B. distasonis were 1.0 microgram/ml for both parent drug and metabolite. For B. thetaiotamicron and B. ovatus, the MICs of metronidazole and the hydroxy metabolite were 1.0 and 2.0 micrograms/ml, respectively. Synergy was determined by calculating the fractional inhibitory concentration (FIC) index. The interpretative criteria for the FIC index were as follows: synergy, FIC < or = 0.5; partial synergy, 0.51 to 0.75; indifference, FIC 0.76 to 4.0; and antagonism, FIC > 4.0. Partial synergy was observed for the four anaerobes tested, with FIC indices ranging from 0.63 to 0.75. On the basis of this data, in vitro susceptibilities to agents such as metronidazole may ultimately require reevaluation to account for active metabolites.

摘要

甲硝唑代谢为两种主要的氧化产物

一种酸性代谢物和一种羟基代谢物。虽然酸性代谢物的活性可忽略不计,但羟基代谢物的活性约为母体药物活性的65%。甲硝唑及其羟基代谢物的药代动力学研究表明,在8小时给药间隔内,这两种化合物的最低抑菌浓度(MIC)对大多数厌氧菌仍高于其MIC。通过棋盘法,检测了甲硝唑和羟基代谢物对4株拟杆菌属质量控制菌株的联合活性。用威尔金斯-查尔格伦肉汤进行大管稀释。对每种药物进行连续两倍稀释,以达到最终浓度范围为0.06至4.0微克/毫升。脆弱拟杆菌和狄氏拟杆菌对母体药物和代谢物的MIC均为1.0微克/毫升。对于多形拟杆菌和卵形拟杆菌,甲硝唑和羟基代谢物的MIC分别为1.0和2.0微克/毫升。通过计算分数抑菌浓度(FIC)指数来确定协同作用。FIC指数的解释标准如下:协同作用,FIC≤0.5;部分协同作用,0.51至0.75;无作用,FIC 0.76至4.0;拮抗作用,FIC>4.0。对所测试的4种厌氧菌观察到部分协同作用,FIC指数范围为0.63至0.75。基于这些数据,对甲硝唑等药物的体外敏感性可能最终需要重新评估,以考虑活性代谢物的影响。

相似文献

引用本文的文献

9
Diosmin pretreatment affects bioavailability of metronidazole.地奥司明预处理会影响甲硝唑的生物利用度。
Eur J Clin Pharmacol. 2003 Apr;58(12):803-7. doi: 10.1007/s00228-002-0543-5. Epub 2003 Mar 1.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验