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通过多种体外方法评估环丙沙星与其他药物的协同作用。

Evaluation of ciprofloxacin's synergism with other agents by multiple in vitro methods.

作者信息

Moody J A, Gerding D N, Peterson L R

出版信息

Am J Med. 1987 Apr 27;82(4A):44-54.

PMID:3107380
Abstract

The efficacies of ciprofloxacin, ceftizoxime, azlocillin, mezlocillin, and amikacin (minimal inhibitory concentration and minimal bactericidal concentration) against six Pseudomonas aeruginosa, six Enterobacteriaceae, and six group D streptococcal strains were evaluated using both agar and broth susceptibility methods, two inoculum sizes (5.7 log10 colony-forming units (cfu)/ml and 7.7 log10 cfu/ml), and aerobic and anaerobic incubation conditions. The results showed agreement between broth and agar methods of susceptibility determination; inoculum effects with beta-lactam antimicrobials; and decreased susceptibility to amikacin under anaerobiasis. Ciprofloxacin combined with azlocillin, ceftizoxime, or aminoglycosides in broth microdilution checkerboards against 100 gram-negative bacilli and gram-positive cocci demonstrated that ciprofloxacin combined with azlocillin or ceftizoxime was synergistic against at least 50 percent of P. aeruginosa and Serratia marcescens isolates and that ciprofloxacin combined with amikacin was synergistic against at least 50 percent of S. marcescens and Staphylococcus aureus isolates. Ciprofloxacin and azlocillin in combination were evaluated by microdilution checkerboard, agar dilution, and broth macrodilution time-kill methods at two inoculum sizes to assess antibacterial activity. Comparison between in vitro combination methods showed the following: the presence or absence of checkerboard synergism (as defined by the fractional inhibitory concentration index and the fractional bactericidal concentration index) with ciprofloxacin and azlocillin did not correlate with time-kill results; and good agreement between methods when comparing broth macrodilution time-kill (3 log10 cfu/ml or more decrease) with antimicrobial combinations at a single concentration in both agar and microdilution broth for ciprofloxacin and azlocillin. Rabbit studies using subcutaneous dialysis membrane chambers inoculated with six P. aeruginosa, six Enterobacteriaceae, and six group D streptococcal strains were performed using ciprofloxacin, azlocillin, ceftizoxime, and amikacin alone and in combination as therapy. In vitro testing of antibiotic combinations that provided the best prediction of in vivo outcome were combination antibacterial activity (3 log10 cfu/ml or more decrease) at 24 hours using either broth macrodilution time-kill or antimicrobial combinations at a single concentration in either agar or broth (microdilution). For the most efficacious in vivo combination, ciprofloxacin plus azlocillin, there was in vitro correlation with in vivo outcome for 17 of 18 isolates.

摘要

采用琼脂和肉汤药敏试验方法、两种接种量(5.7 log10菌落形成单位(cfu)/ml和7.7 log10 cfu/ml)以及需氧和厌氧培养条件,评估了环丙沙星、头孢唑肟、阿洛西林、美洛西林和阿米卡星(最小抑菌浓度和最小杀菌浓度)对6株铜绿假单胞菌、6株肠杆菌科细菌和6株D组链球菌的抗菌效果。结果表明,肉汤法和琼脂法药敏测定结果一致;β-内酰胺类抗菌药物存在接种量效应;在厌氧条件下对阿米卡星的敏感性降低。在肉汤微量稀释棋盘法中,环丙沙星与阿洛西林、头孢唑肟或氨基糖苷类联合应用于100株革兰阴性杆菌和革兰阳性球菌,结果显示环丙沙星与阿洛西林或头孢唑肟联合应用对至少50%的铜绿假单胞菌和粘质沙雷菌分离株具有协同作用,环丙沙星与阿米卡星联合应用对至少50%的粘质沙雷菌和金黄色葡萄球菌分离株具有协同作用。通过微量稀释棋盘法、琼脂稀释法和肉汤常量稀释时间杀菌法,在两种接种量下评估环丙沙星和阿洛西林联合应用的抗菌活性。体外联合用药方法的比较结果如下:环丙沙星和阿洛西林联合应用时棋盘法协同作用的有无(由部分抑菌浓度指数和部分杀菌浓度指数定义)与时间杀菌结果无关;在比较肉汤常量稀释时间杀菌法(降低3 log10 cfu/ml或更多)与环丙沙星和阿洛西林在琼脂和微量稀释肉汤中单一浓度的抗菌联合用药时,各方法之间具有良好的一致性。使用环丙沙星、阿洛西林、头孢唑肟和阿米卡星单独及联合作为治疗方法,对接种了6株铜绿假单胞菌、6株肠杆菌科细菌和6株D组链球菌的家兔皮下透析膜腔进行了研究。对体内结果预测效果最佳的抗生素联合用药的体外试验是使用肉汤常量稀释时间杀菌法或琼脂或肉汤(微量稀释)中单一浓度的抗菌联合用药,在24小时时的联合抗菌活性(降低3 log10 cfu/ml或更多)。对于最有效的体内联合用药环丙沙星加阿洛西林,18株分离株中有17株的体外结果与体内结果具有相关性。

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