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西诺沙星、氨苄西林和氯霉素对志贺氏菌和非伤寒沙门氏菌的体外活性。

In vitro activity of cinoxacin, ampicillin, and chloramphenicol against Shigella and nontyphoid Salmonella.

作者信息

Rubinstein E, Shainberg B

出版信息

Antimicrob Agents Chemother. 1977 Apr;11(4):577-9. doi: 10.1128/AAC.11.4.577.

DOI:10.1128/AAC.11.4.577
PMID:856008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC352030/
Abstract

The in vitro antibacterial activity of cinoxacin was compared with that of ampicillin and chloramphenicol against 26 strains of nontyphoid Salmonella and 44 strains of Shigella. Cinoxacin was found to have a lower minimal inhibitory concentration than ampicillin and chloramphenicol against all Salmonella and Shigella sonnei strains. Cinoxacin had minimal inhibitory concentrations similar to those of chloramphenicol but lower than those of ampicillin against Shigella flexneri and S. boydii strains.

摘要

将西诺沙星与氨苄西林和氯霉素对26株非伤寒沙门氏菌和44株志贺氏菌的体外抗菌活性进行了比较。结果发现,西诺沙星对所有沙门氏菌和宋内志贺氏菌菌株的最低抑菌浓度均低于氨苄西林和氯霉素。对于弗氏志贺氏菌和鲍氏志贺氏菌菌株,西诺沙星的最低抑菌浓度与氯霉素相似,但低于氨苄西林。

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引用本文的文献

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Cinoxacin. A review of its pharmacological properties and therapeutic efficacy in the treatment of urinary tract infections.西诺沙星。其药理学特性及治疗尿路感染疗效的综述。
Drugs. 1983 Jun;25(6):544-69. doi: 10.2165/00003495-198325060-00002.

本文引用的文献

1
Treatment of sonne dysentery.宋内氏痢疾的治疗
Br Med J. 1965 Oct 16;2(5467):913-5. doi: 10.1136/bmj.2.5467.913.
2
Compound 64716, a new synthetic antibacterial agent.化合物64716,一种新型合成抗菌剂。
Antimicrob Agents Chemother. 1973 Oct;4(4):415-20. doi: 10.1128/AAC.4.4.415.
3
Comparative efficacy of nalidixic acid and ampicillin for severe shigellosis.萘啶酸和氨苄西林治疗重症志贺菌病的疗效比较
Arch Dis Child. 1973 Apr;48(4):305-12. doi: 10.1136/adc.48.4.305.
4
Efficacy of cinoxacin in urinary tract infections.西诺沙星在尿路感染中的疗效。
Antimicrob Agents Chemother. 1976 Mar;9(3):502-5. doi: 10.1128/AAC.9.3.502.
5
Oxolinic acid in the treatment of typhoid fever due to chloramphenicol-resistant strains of Salmonella typhi.恶喹酸治疗对氯霉素耐药的伤寒杆菌引起的伤寒热。
Antimicrob Agents Chemother. 1976 Mar;9(3):387-92. doi: 10.1128/AAC.9.3.387.