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新型注射用广谱头孢菌素E1077的体外和体内抗菌活性

In vitro and in vivo antibacterial activities of E1077, a novel parenteral cephalosporin with a broad antibacterial spectrum.

作者信息

Hata K, Otsuki M, Nishino T

机构信息

Department of Microbiology, Kyoto Pharmaceutical University, Japan.

出版信息

Antimicrob Agents Chemother. 1992 Sep;36(9):1894-901. doi: 10.1128/AAC.36.9.1894.

DOI:10.1128/AAC.36.9.1894
PMID:1416879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC192206/
Abstract

E1077 is a new injectable cephalosporin with a broad spectrum of antibacterial activity against gram-positive and gram-negative bacteria, including staphylococci and Pseudomonas aeruginosa. The in vitro activities of E1077 against clinical isolates of methicillin-susceptible Staphylococcus aureus (MIC of E1077 for 90% of the strains tested [MIC90], 0.78 microgram/ml) and methicillin-resistant S. aureus (MIC90, 50 micrograms/ml) were similar to those of cefpirome and flomoxef. Against Enterococcus faecalis (MIC90, 6.25 micrograms/ml), E1077 was the most active of the drugs tested and four times more active than cefpirome. The MIC90S of E1077 for streptococci, Haemophilus influenzae, and Neisseria gonorrhoeae ranged from 0.05 to 0.78 microgram/ml; E1077 was similar in activity to cefpirome. E1077 inhibited 90% of most species of the family Enterobacteriaceae at concentrations of less than or equal to 1.56 micrograms/ml, with the exception of Serratia marcescens and Proteus vulgaris (12.5 micrograms/ml). The activity of E1077 against P. aeruginosa (MIC90, 6.25 micrograms/ml) was comparable to that of ceftazidime. In vivo activity was evaluated with systemic infections in mice. E1077 showed a protective effect against systemic infections by gram-positive or gram-negative bacteria, as reflected by its in vitro activity. The protective effects of E1077 were higher than those of cefpirome against S. aureus and P. aeruginosa infections and similar to those of cefpirome against other bacterial infections. Morphological studies using differential interference and phase-contrast microscopy showed that low concentrations of E1077 caused swelling of S. aureus and spheroplast and bulge formation in P. aeruginosa. In general, the antibacterial profile of E1077 is similar to that of cefpirome.

摘要

E1077是一种新型注射用头孢菌素,对革兰氏阳性菌和革兰氏阴性菌具有广谱抗菌活性,包括葡萄球菌和铜绿假单胞菌。E1077对甲氧西林敏感金黄色葡萄球菌临床分离株的体外活性(90%受试菌株的E1077最低抑菌浓度[MIC90],0.78微克/毫升)和耐甲氧西林金黄色葡萄球菌(MIC90,50微克/毫升)与头孢匹罗和氟氧头孢相似。对于粪肠球菌(MIC90,6.25微克/毫升),E1077是受试药物中活性最高的,其活性比头孢匹罗高4倍。E1077对链球菌、流感嗜血杆菌和淋病奈瑟菌的MIC90范围为0.05至0.78微克/毫升;E1077的活性与头孢匹罗相似。E1077在浓度小于或等于1.56微克/毫升时能抑制90%的大多数肠杆菌科菌种,但粘质沙雷氏菌和普通变形杆菌除外(12.5微克/毫升)。E1077对铜绿假单胞菌的活性(MIC90,6.25微克/毫升)与头孢他啶相当。通过小鼠全身感染评估了其体内活性。E1077对革兰氏阳性菌或革兰氏阴性菌引起的全身感染显示出保护作用,这与其体外活性一致。E1077对金黄色葡萄球菌和铜绿假单胞菌感染的保护作用高于头孢匹罗,对其他细菌感染的保护作用与头孢匹罗相似。使用微分干涉和相差显微镜进行的形态学研究表明,低浓度的E1077会导致金黄色葡萄球菌肿胀以及铜绿假单胞菌形成原生质球和凸起。总体而言,E1077的抗菌谱与头孢匹罗相似。

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本文引用的文献

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Comparison of in vitro activity of GR 20263, a novel cephalosporin derivative, with activities of other beta-lactam compounds.新型头孢菌素衍生物GR 20263的体外活性与其他β-内酰胺类化合物活性的比较。
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The Antibacterial activity in vitro and beta-lactamase stability of the new cephalosporin HR 810 in comparison with five other cephalosporins and two aminoglycosides.新型头孢菌素HR 810与其他五种头孢菌素及两种氨基糖苷类药物相比的体外抗菌活性及β-内酰胺酶稳定性
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Comparison of a new cephalosporin, BMY 28142, with other broad-spectrum beta-lactam antibiotics.
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Production of low-affinity penicillin-binding protein by low- and high-resistance groups of methicillin-resistant Staphylococcus aureus.耐甲氧西林金黄色葡萄球菌低抗性组和高抗性组产生低亲和力青霉素结合蛋白。
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In-vitro antibacterial activity of L-105, a new cephalosporin.新型头孢菌素L-105的体外抗菌活性
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Beta-lactamase stability of cefpirome (HR 810), a new cephalosporin with a broad antimicrobial spectrum.头孢匹罗(HR 810)的β-内酰胺酶稳定性,一种具有广谱抗菌活性的新型头孢菌素。
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Chromosomal cephalosporinases responsible for multiple resistance to newer beta-lactam antibiotics.对新型β-内酰胺类抗生素具有多重耐药性的染色体头孢菌素酶。
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