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本文引用的文献

1
The in-vitro activity of Bay y 3118, a new chlorofluoroquinolone.新型氯氟喹诺酮类药物Bay y 3118的体外活性
J Antimicrob Chemother. 1993 Jan;31(1):73-80. doi: 10.1093/jac/31.1.73.
2
Susceptibilities of 428 gram-positive and -negative anaerobic bacteria to Bay y3118 compared with their susceptibilities to ciprofloxacin, clindamycin, metronidazole, piperacillin, piperacillin-tazobactam, and cefoxitin.428株革兰氏阳性和阴性厌氧菌对Bay y3118的敏感性及其对环丙沙星、克林霉素、甲硝唑、哌拉西林、哌拉西林-他唑巴坦和头孢西丁的敏感性比较。
Antimicrob Agents Chemother. 1993 Aug;37(8):1649-54. doi: 10.1128/AAC.37.8.1649.
3
Comparative activity of the quinolones against anaerobic bacteria isolated at community hospitals.喹诺酮类药物对社区医院分离出的厌氧菌的比较活性。
Antimicrob Agents Chemother. 1985 Apr;27(4):657-9. doi: 10.1128/AAC.27.4.657.
4
In-vitro and in-vivo potency of five new fluoroquinolones against anaerobic bacteria.五种新型氟喹诺酮类药物对厌氧菌的体外和体内抗菌效能
J Antimicrob Chemother. 1986 Dec;18(6):693-701. doi: 10.1093/jac/18.6.693.
5
The comparative in-vitro activity of eight newer quinolones and nalidixic acid.八种新型喹诺酮类药物与萘啶酸的体外活性比较
J Antimicrob Chemother. 1986 Nov;18 Suppl D:1-20. doi: 10.1093/jac/18.supplement_d.1.
6
Activity of pefloxacin and thirteen other antimicrobial agents in vitro against isolates from hospital and genitourinary infections.培氟沙星及其他13种抗菌药物对医院感染和泌尿生殖系统感染分离菌株的体外活性。
J Antimicrob Chemother. 1986 Jun;17(6):739-46. doi: 10.1093/jac/17.6.739.
7
Comparative activity of ciprofloxacin against anaerobic bacteria.环丙沙星对厌氧菌的比较活性。
Antimicrob Agents Chemother. 1985 Mar;27(3):427-8. doi: 10.1128/AAC.27.3.427.
8
Is ciprofloxacin active against clinically important anaerobes?
J Antimicrob Chemother. 1986 May;17(5):605-13. doi: 10.1093/jac/17.5.605.
9
Comparative in vitro activity of lomefloxacin, a new difluoroquinolone.新型二氟喹诺酮洛美沙星的体外活性比较
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10
Comparative in vitro activities of a new quinolone, WIN 57273, and piperacillin plus tazobactam against anaerobic bacteria.新型喹诺酮类药物WIN 57273与哌拉西林加他唑巴坦对厌氧菌的体外比较活性
Antimicrob Agents Chemother. 1990 Sep;34(9):1858-61. doi: 10.1128/AAC.34.9.1858.

Bay Y3118对厌氧菌的体外活性。

In vitro activity of Bay Y3118 against anaerobic bacteria.

作者信息

Wexler H M, Molitoris E, Finegold S M

机构信息

Research Service, Veterans Administration Medical Center, West Los Angeles, California 90073.

出版信息

Antimicrob Agents Chemother. 1993 Nov;37(11):2509-13. doi: 10.1128/AAC.37.11.2509.

DOI:10.1128/AAC.37.11.2509
PMID:8285647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC192422/
Abstract

The antimicrobial activity of a new quinolone, Bay Y3118, was determined against 326 strains of anaerobic bacteria and compared with the activities of ampicillin-sulbactam, cefotetan, clindamycin, imipenem, metronidazole, and sparfloxacin. The National Committee for Clinical Laboratory Standards-approved Wadsworth agar dilution technique with Brucella-laked blood agar was used throughout the study. Breakpoints used to determine the percent susceptible were 2 micrograms/ml for Bay Y3118 and sparfloxacin, 4 micrograms/ml for clindamycin, 8 micrograms/ml for imipenem, 16 micrograms/ml for metronidazole and ampicillin-sulbactam, and 32 micrograms/ml for cefotetan. Species tested included Bacteroides fragilis (57 strains), other B. fragilis group species (79 strains), Bacteroides gracilis (10 strains), other Bacteroides spp. (9 strains), Prevotella spp. (30 strains), Porphyromonas spp. (9 strains), Fusobacterium spp. (36 strains), Bilophila wadsworthia (14 strains), Clostridium spp. (36 strains), Peptostreptococcus spp. (20 strains), and gram-positive non-spore-forming rods (26 strains). Bay Y3118 inhibited all but 1 of 326 anaerobic bacteria tested at the breakpoint level or lower.

摘要

测定了一种新型喹诺酮类药物Bay Y3118对326株厌氧菌的抗菌活性,并与氨苄西林-舒巴坦、头孢替坦、克林霉素、亚胺培南、甲硝唑和司帕沙星的活性进行了比较。在整个研究过程中,采用了美国国家临床实验室标准委员会批准的、以布鲁氏菌溶解血琼脂为培养基的沃兹沃思琼脂稀释技术。用于确定敏感百分比的断点浓度分别为:Bay Y3118和司帕沙星为2微克/毫升,克林霉素为4微克/毫升,亚胺培南为8微克/毫升,甲硝唑和氨苄西林-舒巴坦为16微克/毫升,头孢替坦为32微克/毫升。检测的菌种包括脆弱拟杆菌(57株)、其他脆弱拟杆菌属菌种(79株)、纤细拟杆菌(10株)、其他拟杆菌属菌种(9株)、普雷沃菌属菌种(30株)、卟啉单胞菌属菌种(9株)、梭杆菌属菌种(36株)、沃兹沃思嗜胆菌(14株)、梭菌属菌种(36株)、消化链球菌属菌种(20株)和革兰氏阳性无芽孢杆菌(26株)。在断点浓度或更低浓度下,Bay Y3118抑制了所检测的326株厌氧菌中的325株。