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舒巴坦对头孢哌酮针对各种临床分离株活性的影响

[Effects of sulbactam on the activity of cefoperazone against various clinical isolates].

作者信息

Uete T, Matsuo K

机构信息

Department of Clinical Investigation, Kitano Hospital, Tazuke Kofukai Medical Research Institute.

出版信息

Jpn J Antibiot. 1989 Apr;42(4):896-909.

PMID:2769941
Abstract

Sulbactam/Cefoperazone (SBT/CPZ) have been used in clinical infusion at ratios of 1:1 and 1:2 in Japan and U.S.A., respectively. After an administration of these drugs as a 1:1 parenteral formulation, the ratio of levels of CPZ and SBT in blood was 1:1/4 to 1:1/5 for 1 to 2 hours, whereas the ratio of free, unbound drug levels was 1:1.4 to 1:1.5. In urine these drugs were excreted at a ratio between 1:1 and 1:4 during 6 hours after the infusion. Antimicrobial interaction studies using various combinations of CPZ and SBT were performed to obtain information with respect to the effect of SBT on the antimicrobial activity of CPZ in vivo and the most appropriate ratio of these drugs for the in vitro test system. Antimicrobial activities were determined using the agar dilution method and the disk diffusion susceptibility test. SBT increased the activity of CPZ against various clinical isolates tested except Enterococcus faecalis. CPZ-SBT at a fixed ratio of 1:1/5 significantly increased the antimicrobial activity of CPZ, resulting in decreases in MIC values and increases in disk inhibitory zone diameters. These drugs at ratios 1:1 to 1:3 maximized the synergistic enhancement of the activity. Therefore, a fixed ratio between 1:1/5 and 1:1 would be appropriate for the in vitro antimicrobial test system using either the agar dilution method or the disk susceptibility test. Based on pharmacokinetic data for CPZ and SBT, results of the present study on antimicrobial activity would support that the parenteral formulation of CPZ-SBT at the fixed ratios of 1:1 and 2:1 for the intravenous infusion used in Japan and U.S.A., respectively, are appropriate. The effect of SBT on the activity of CPZ was more marked against clinical isolates with greater production abilities of beta-lactamase than against those with less production abilities. SBT/CPZ, however, exerted a synergistic effect against methicillin-resistant Staphylococcus aureus without beta-lactamase production. The MIC80 of SBT/CPZ (1:1) against various clinical isolates with 10(6) CFU/ml inoculum size were as follows: S. aureus 12.5 micrograms/ml, Staphylococcus epidermis 3.13 micrograms/ml, and E. faecalis 50 micrograms/ml. Those of Gram-negative bacilli were: Escherichia coli 0.20 microgram/ml, Klebsiella pneumoniae 0.20 micrograms/ml, Proteus mirabilis 0.78 microgram/ml, Proteus vulgaris 0.78 microgram/ml, Pseudomonas aeruginosa 12.5 micrograms/ml, Serratia marcescens 25 micrograms/ml, Enterobacter spp. 3.13 micrograms/ml, Citrobacter spp. 12.5 micrograms/ml and Acinetobacter spp. 0.78 microgram/ml.

摘要

在日本和美国,舒巴坦/头孢哌酮(SBT/CPZ)分别以1:1和1:2的比例用于临床输注。以1:1的肠胃外制剂形式给药这些药物后,血液中CPZ和SBT的水平比例在1至2小时内为1:1/4至1:1/5,而游离、未结合药物水平的比例为1:1.4至1:1.5。在输注后6小时内,这些药物在尿液中的排泄比例为1:1至1:4。进行了使用CPZ和SBT各种组合的抗菌相互作用研究,以获取关于SBT对CPZ体内抗菌活性的影响以及这些药物在体外测试系统中最合适比例的信息。使用琼脂稀释法和纸片扩散药敏试验测定抗菌活性。除粪肠球菌外,SBT增强了CPZ对各种测试临床分离株的活性。固定比例为1:1/5的CPZ-SBT显著增强了CPZ的抗菌活性,导致MIC值降低和纸片抑菌圈直径增加。这些药物比例为1:1至1:3时,活性的协同增强达到最大值。因此,对于使用琼脂稀释法或纸片药敏试验的体外抗菌测试系统,1:1/5至1:1的固定比例是合适的。基于CPZ和SBT的药代动力学数据,本研究关于抗菌活性的结果将支持日本和美国分别用于静脉输注的固定比例为1:1和2:1的CPZ-SBT肠胃外制剂是合适的。SBT对CPZ活性的影响在β-内酰胺酶产生能力较强的临床分离株中比对产生能力较弱的分离株更明显。然而,SBT/CPZ对不产生β-内酰胺酶的耐甲氧西林金黄色葡萄球菌发挥了协同作用。SBT/CPZ(1:1)对接种量为10(6) CFU/ml的各种临床分离株的MIC80如下:金黄色葡萄球菌为12.5微克/毫升,表皮葡萄球菌为3.13微克/毫升,粪肠球菌为50微克/毫升。革兰氏阴性杆菌的MIC80为:大肠杆菌为0.20微克/毫升,肺炎克雷伯菌为0.20微克/毫升,奇异变形杆菌为0.78微克/毫升,普通变形杆菌为0.78微克/毫升,铜绿假单胞菌为12.5微克/毫升,粘质沙雷氏菌为25微克/毫升,肠杆菌属为3.13微克/毫升,柠檬酸杆菌属为12.5微克/毫升,不动杆菌属为0.78微克/毫升。

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