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罗红霉素单独及与乙胺丁醇、利福平、阿米卡星、氧氟沙星和氯法齐明联合使用对鸟分枝杆菌复合群的活性。

Activities of roxithromycin used alone and in combination with ethambutol, rifampin, amikacin, ofloxacin, and clofazimine against Mycobacterium avium complex.

作者信息

Rastogi N, Goh K S, Bryskier A

机构信息

Unité de la Tuberculose et des Mycobactéries, Institut Pasteur, Morne Jolivière, Pointe-à-Pitre, Guadeloupe, French West Indies.

出版信息

Antimicrob Agents Chemother. 1994 Jun;38(6):1433-8. doi: 10.1128/AAC.38.6.1433.

Abstract

Preliminary studies showed that roxithromycin possessed significant in vitro activity against a variety of atypical mycobacteria such as the Mycobacterium avium complex, M. scrofulaceum, M. szulgai, M. malmoense, M. xenopi, M. marinum, and M. kansasii and rare pathogens such as M. chelonae and M. fortuitum. In this investigation, radiometric MICs of roxithromycin, ethambutol, rifampin, amikacin, ofloxacin, and clofazimine for 10 clinical isolates of the M. avium complex (5 each from human immunodeficiency virus [HIV]-positive and HIV-negative patients) were determined. Roxithromycin MICs against all the isolates were below the reported maximum concentration of drug in serum at the routine pH of 6.8, and the MICs were further lowered by 1 to 2 dilutions at a pH of 7.4. In vitro enhancement of roxithromycin activity against all strains was further investigated by the previously established Bactec 460-TB method by combining the drugs at sub-MIC levels. Antibacterial activity of roxithromycin was enhanced in all 10 strains by ethambutol, in 3 strains each by rifampin and clofazimine, in 2 strains by amikacin, and in 1 strain by ofloxacin. In vitro screening of three-drug combinations showed that combinations of roxithromycin, ethambutol, and a third potential anti-M. avium drug (rifampin, amikacin, ofloxacin, or clofazimine) resulted in further enhancement of activity in 13 out of 20 drug combinations screened.

摘要

初步研究表明,罗红霉素对多种非典型分枝杆菌具有显著的体外活性,如鸟分枝杆菌复合群、瘰疬分枝杆菌、苏尔加分枝杆菌、马尔默分枝杆菌、偶发分枝杆菌、海分枝杆菌和堪萨斯分枝杆菌,以及罕见病原体,如龟分枝杆菌和偶然分枝杆菌。在本研究中,测定了罗红霉素、乙胺丁醇、利福平、阿米卡星、氧氟沙星和氯法齐明对10株鸟分枝杆菌复合群临床分离株(5株来自人类免疫缺陷病毒[HIV]阳性患者,5株来自HIV阴性患者)的放射测量最低抑菌浓度(MIC)。罗红霉素对所有分离株的MIC均低于在常规pH值6.8时血清中报道的药物最高浓度,并且在pH值为7.4时,MIC进一步降低1至2倍稀释度。通过先前建立的Bactec 460-TB方法,以亚MIC水平联合药物,进一步研究了罗红霉素对所有菌株的体外活性增强情况。乙胺丁醇使罗红霉素在所有10株菌株中的抗菌活性增强,利福平和氯法齐明分别使3株菌株的抗菌活性增强,阿米卡星使2株菌株的抗菌活性增强,氧氟沙星使1株菌株的抗菌活性增强。对三联药物组合的体外筛选表明,在筛选的20种药物组合中,罗红霉素、乙胺丁醇和第三种潜在抗鸟分枝杆菌药物(利福平、阿米卡星、氧氟沙星或氯法齐明)的组合使13种组合的活性进一步增强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d73/188227/92e186e568cf/aac00020-0244-a.jpg

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