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MCB3837 对正常人体微生物群的生态影响。

Ecological impact of MCB3837 on the normal human microbiota.

机构信息

Department of Laboratory Medicine, Karolinska University Hospital, Karolinska Institutet, SE-141 86 Stockholm, Sweden.

University Medical Center Schleswig-Holstein, Institute for Infection Medicine, Brunswiker Str. 4, D-24105 Kiel, Germany.

出版信息

Int J Antimicrob Agents. 2014 Aug;44(2):125-30. doi: 10.1016/j.ijantimicag.2014.03.016. Epub 2014 May 23.

Abstract

MCB3837 is a novel, water-soluble, injectable prodrug that is rapidly converted to the active substance MCB3681 in vivo following intravenous (i.v.) administration. Both MCB3837 and MCB3681 are oxazolidinone-quinolone hybrid molecules. The purpose of the present study was to investigate the effect of MCB3681 on the human skin, nose, oropharyngeal and intestinal microbiota following administration of MCB3837. Twelve healthy male subjects received i.v. MCB3837 (6 mg/kg body weight) once daily for 5 days. Skin, nose, saliva and faecal samples were collected on Day -1 (pre dose), during administration on Days 2 and 5, and post dose on Days 8, 12 and 19. Micro-organisms were identified to genus level. No measurable concentrations of MCB3681 were found in any saliva samples or in the faecal samples on Day -1. On Day 2, 10 volunteers had faecal MCB3681 concentrations between 16.5 mg/kg faeces and 275.1mg/kg faeces; no MCB3681 in faeces could be detected in two of the volunteers. On Day 5, all volunteers had faecal concentrations of MCB3681 ranging from 98.9 to 226.3 mg/kg. MCB3681 caused no ecological changes in the skin, nasal and oropharyngeal microbiota. The numbers of enterococci, bifidobacteria, lactobacilli and clostridia decreased in the intestinal microbiota during administration of the drug. Numbers of Escherichia coli, other enterobacteria and Candida were not affected during the study. There was no impact on the number of Bacteroides. The faecal microbiota was normalised on Day 19. No new colonising aerobic or anaerobic Gram-positive bacteria with MCB3681 minimum inhibitory concentrations of ≥4 mg/L were found.

摘要

MCB3837 是一种新型的、水溶性的、可注射的前药,在静脉注射(i.v.)给药后迅速转化为体内的活性物质 MCB3681。MCB3837 和 MCB3681 都是恶唑烷酮-喹诺酮杂合分子。本研究的目的是研究 MCB3681 给药后对人体皮肤、鼻子、口咽和肠道微生物群的影响。12 名健康男性受试者每天接受一次静脉注射 MCB3837(6mg/kg 体重),连续 5 天。在给药前(第-1 天)、第 2 天和第 5 天,以及给药后第 8 天、第 12 天和第 19 天采集皮肤、鼻子、唾液和粪便样本。微生物鉴定到属水平。在任何唾液样本或第-1 天的粪便样本中均未检测到可测量浓度的 MCB3681。第 2 天,10 名志愿者的粪便 MCB3681 浓度在 16.5mg/kg 粪便和 275.1mg/kg 粪便之间;两名志愿者的粪便中未检测到 MCB3681。第 5 天,所有志愿者的粪便 MCB3681 浓度均在 98.9 至 226.3mg/kg 之间。MCB3681 对皮肤、鼻腔和口咽微生物群没有引起生态变化。在药物给药期间,肠道微生物群中的肠球菌、双歧杆菌、乳杆菌和梭菌数量减少。在研究期间,大肠杆菌、其他肠杆菌和假丝酵母菌的数量没有受到影响。拟杆菌的数量没有受到影响。第 19 天粪便微生物群恢复正常。没有发现对 MCB3681 最低抑菌浓度≥4mg/L 的新定植需氧或厌氧革兰阳性细菌。

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