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新型广谱氟喹诺酮类药物WIN 57273的体外评价

In vitro evaluation of WIN 57273, a new broad-spectrum fluoroquinolone.

作者信息

Jones R N, Barry A L

机构信息

Clinical Microbiology Institute, Tualatin, Oregon 97062.

出版信息

Antimicrob Agents Chemother. 1990 Feb;34(2):306-13. doi: 10.1128/AAC.34.2.306.

DOI:10.1128/AAC.34.2.306
PMID:2327779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC171578/
Abstract

WIN 57273 is a new fluoroquinolone that has an expanded spectrum of activity against Staphylococcus spp. (MIC for 90% of isolates [MIC90], 0.008 microgram/ml), Enterococcus faecalis (MIC90, 0.06 microgram/ml), Bacillus spp. (MIC90, 0.03 micrograms/ml), Listeria monocytogenes (MIC90, 0.06 microgram/ml), Streptococcus spp. (MIC90, 0.03 microgram/ml), and Bacteroides fragilis group strains (MIC90, 0.5 microgram/ml). Like other fluoroquinolone compounds, WIN 57273 was active against members of the family Enterobacteriaceae (97% of strains inhibited by less than or equal to 2 micrograms/ml), Haemophilus, Branhamella, and Neisseria strains (100% susceptible), Acinetobacter spp. (100% susceptible), and Pseudomonas aeruginosa (68% susceptible). We observed that WIN 57273 was very active against cephalosporin- or aminoglycoside-resistant gram-negative strains but shared cross-resistance with other fluoroquinolones. Increasing inoculum concentrations had minimal effects on WIN 57273 MICs, and the drug was considered to be bactericidal based on reference MBC and kill curve analyses. Unlike most previously studied drugs in this class, WIN 57273 had increased activity (three- to fourfold) at low pH. Rates of mutation to WIN 57273 resistance at eight times its MIC were in the range of 5.6 x 10(-8) to greater than 1.4 x 10(-9). This new compound possesses a wide potential spectrum of use, and it should be evaluated further by in vitro and in vivo studies.

摘要

WIN 57273是一种新型氟喹诺酮类药物,对葡萄球菌属(90%分离株的最低抑菌浓度[MIC90]为0.008微克/毫升)、粪肠球菌(MIC90为0.06微克/毫升)、芽孢杆菌属(MIC90为0.03微克/毫升)、单核细胞增生李斯特菌(MIC90为0.06微克/毫升)、链球菌属(MIC90为0.03微克/毫升)以及脆弱拟杆菌群菌株(MIC90为0.5微克/毫升)具有更广的抗菌谱。与其他氟喹诺酮类化合物一样,WIN 57273对肠杆菌科成员(97%的菌株被≤2微克/毫升抑制)、嗜血杆菌属、布兰汉菌属和奈瑟菌属菌株(100%敏感)、不动杆菌属(100%敏感)以及铜绿假单胞菌(68%敏感)有活性。我们观察到WIN 57273对头孢菌素或氨基糖苷类耐药革兰阴性菌株非常有效,但与其他氟喹诺酮类药物存在交叉耐药性。接种物浓度增加对WIN 57273的MIC影响极小,根据参考MBC和杀菌曲线分析,该药物被认为具有杀菌作用。与该类中大多数先前研究的药物不同,WIN 57273在低pH值时活性增加(三到四倍)。在八倍其MIC浓度下对WIN 57273耐药的突变率在5.6×10⁻⁸至大于1.4×10⁻⁹范围内。这种新化合物具有广泛的潜在应用范围,应通过体外和体内研究进一步评估。

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