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Imipenem/cilastatin. A review of its antibacterial activity, pharmacokinetic properties and therapeutic efficacy.亚胺培南/西司他丁。对其抗菌活性、药代动力学特性及治疗效果的综述。
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In vitro susceptibility of Mycobacterium tuberculosis, Mycobacterium fortuitum and Mycobacterium chelonei to augmentin.结核分枝杆菌、偶然分枝杆菌和龟分枝杆菌对阿莫西林克拉维酸钾的体外敏感性
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本文引用的文献

1
In vitro susceptibility of Mycobacterium fortuitum to cefoxitin.偶然分枝杆菌对头孢西丁的体外敏感性
Antimicrob Agents Chemother. 1981 Jan;19(1):205-7. doi: 10.1128/AAC.19.1.205.
2
Susceptibility of organisms in the Mycobacterium fortuitum complex to antituberculous and other antimicrobial agents.偶然分枝杆菌复合群中各微生物对抗结核及其他抗菌药物的敏感性。
Antimicrob Agents Chemother. 1977 Aug;12(2):295-7. doi: 10.1128/AAC.12.2.295.
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Description and classification of the newer cephalosporins and their relationships with the established compounds.新型头孢菌素的描述、分类及其与现有化合物的关系。
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偶然分枝杆菌对N-甲酰亚胺基硫霉素及几种头孢霉素的体外敏感性

In vitro susceptibility of Mycobacterium fortuitum to N-formimidoyl thienamycin and several cephamycins.

作者信息

Cynamon M H, Palmer G S

出版信息

Antimicrob Agents Chemother. 1982 Dec;22(6):1079-81. doi: 10.1128/AAC.22.6.1079.

DOI:10.1128/AAC.22.6.1079
PMID:6961887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC185727/
Abstract

The comparative in vitro activity of N-formimidoyl thienamycin, cefmetazole, cefoxitin, cefotetan (YM-09330), and moxalactam against 13 isolates of Mycobacterium fortuitum was evaluated by agar dilution susceptibility testing. N-Formimidoyl thienamycin inhibited 10 to 12 strains at 6.25 micrograms/ml, cefmetazole inhibited 12 of 13 strains at 12.5 micrograms/ml, cefoxitin inhibited 11 of 13 strains at 25 micrograms/ml, and cefotetan inhibited 11 of 13 strains at 50 micrograms/ml. Moxalactam was less active than the other compounds tested, inhibiting only 9 of 13 strains at 50 micrograms/ml.

摘要

通过琼脂稀释药敏试验评估了N-甲酰亚胺硫霉素、头孢美唑、头孢西丁、头孢替坦（YM-09330）和拉氧头孢对13株偶然分枝杆菌的体外比较活性。N-甲酰亚胺硫霉素在6.25微克/毫升时抑制10至12株菌，头孢美唑在12.5微克/毫升时抑制13株菌中的12株，头孢西丁在25微克/毫升时抑制13株菌中的11株，头孢替坦在50微克/毫升时抑制13株菌中的11株。拉氧头孢的活性低于其他受试化合物，在50微克/毫升时仅抑制13株菌中的9株。