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头孢匹胺和阿帕西林单独及联合使用时的体外比较活性

Comparative in vitro activities of cefpiramide and apalcillin individually and in combination.

作者信息

Allan J D, Eliopoulos G M, Ferraro M J, Moellering R C

出版信息

Antimicrob Agents Chemother. 1985 May;27(5):782-90. doi: 10.1128/AAC.27.5.782.

Abstract

The in vitro activities of cefpiramide and apalcillin were compared with those of other third-generation cephalosporins and extended-spectrum penicillins against over 1,000 clinical bacterial isolates. The activity of cefpiramide against Pseudomonas aeruginosa was comparable to those of piperacillin and cefoperazone, inhibiting 90% of strains at concentrations less than or equal to 16.0 micrograms/ml. This drug was also active against a broad range of gram-negative organisms but was generally less active than many of the other cephalosporins tested against members of the family Enterobacteriaceae. The activity of cefpiramide against gram-positive organisms was comparable to that of cefoperazone. Apalcillin, along with ceftazidime, was the most active agent tested against P. aeruginosa and Acinetobacter calcoaceticus subsp. anitratus, inhibiting 90% of these strains at concentrations less than or equal to 8 micrograms/ml. Against other gram-negative and gram-positive organisms, its activity was similar to that of piperacillin. The activities of both cefpiramide and apalcillin were significantly reduced by the presence of several plasmid-mediated beta-lactamases in a series of otherwise isogenic strains of P. aeruginosa in comparison with their activities against a parent strain which lacks these enzymes. Many strains of Enterobacter cloacae were synergistically inhibited by the combination of gentamicin with either cefpiramide (5 of 10 strains) or apalcillin (6 of 10 strains). Most strains of P. aeruginosa were synergistically inhibited by the combination of gentamicin with either cefpiramide (8 of 10 strains) or apalcillin (10 of 10 strains). However, cefoxitin antagonized the activity of both cefpiramide and apalcillin against most of these same strains.

摘要

将头孢匹胺和阿帕西林的体外活性与其他第三代头孢菌素及广谱青霉素针对1000多株临床分离细菌的活性进行了比较。头孢匹胺对铜绿假单胞菌的活性与哌拉西林和头孢哌酮相当,在浓度小于或等于16.0微克/毫升时可抑制90%的菌株。该药物对多种革兰氏阴性菌也有活性,但总体上比对肠杆菌科成员进行测试的许多其他头孢菌素活性低。头孢匹胺对革兰氏阳性菌的活性与头孢哌酮相当。阿帕西林与头孢他啶一样,是针对铜绿假单胞菌和醋酸钙不动杆菌亚种鲍曼不动杆菌测试的最具活性的药物,在浓度小于或等于8微克/毫升时可抑制90%的这些菌株。针对其他革兰氏阴性和革兰氏阳性菌,其活性与哌拉西林相似。与它们对缺乏这些酶的亲本菌株的活性相比,在一系列其他方面同基因的铜绿假单胞菌菌株中,几种质粒介导的β-内酰胺酶的存在显著降低了头孢匹胺和阿帕西林的活性。庆大霉素与头孢匹胺(10株中的5株)或阿帕西林(10株中的6株)联合使用可协同抑制许多阴沟肠杆菌菌株。庆大霉素与头孢匹胺(10株中的8株)或阿帕西林(10株中的10株)联合使用可协同抑制大多数铜绿假单胞菌菌株。然而,头孢西丁拮抗头孢匹胺和阿帕西林对大多数这些相同菌株的活性。

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本文引用的文献

6
Pharmacokinetics of cefpiramide (SM-1652) in humans.头孢匹胺(SM-1652)在人体内的药代动力学。
Antimicrob Agents Chemother. 1984 Feb;25(2):221-5. doi: 10.1128/AAC.25.2.221.
7
Comparative pharmacokinetics of apalcillin and piperacillin.阿帕西林与哌拉西林的比较药代动力学
Antimicrob Agents Chemother. 1984 Jan;25(1):105-8. doi: 10.1128/AAC.25.1.105.

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