Fass R J
Antimicrob Agents Chemother. 1983 Aug;24(2):156-62. doi: 10.1128/AAC.24.2.156.
Minimal inhibitory concentrations (MICs) or two alpha-carboxypenicillins (carbenicillin and ticarcillin) and three acylaminopenicillins (azlocillin, mezlocillin, and piperacillin) for 300 aerobic and facultative gram-negative bacilli were determined by a microdilution method and compared by parametric statistical tests. Within each group of penicillins, MICs were highly interrelated; MICs of one antibiotic were readily predictable based on knowledge of MICs of another antibiotic. Ticarcillin was consistently more active than carbenicillin by approximately one dilution step, but the relative activities of the acylaminopenicillins varied by bacterial species. The acylaminopenicillins were generally more active than the alpha-carboxypenicillins, particularly against alpha-carboxypenicillin-resistant organisms. There were exceptions, however, and antibiotic MICs in one group were not readily predictable on the basis of the knowledge of antibiotic MICs in the other group. The enhanced antibacterial potencies and spectra of the acylaminopenicillins against gram-negative bacilli make these antibiotics potentially useful therapeutic agents. It is not necessary for clinical laboratories to routinely perform susceptibility tests with all five antibiotics.
采用微量稀释法测定了300株需氧和兼性革兰氏阴性杆菌对两种α-羧基青霉素(羧苄西林和替卡西林)以及三种酰氨基青霉素(阿洛西林、美洛西林和哌拉西林)的最低抑菌浓度(MIC),并通过参数统计检验进行比较。在每组青霉素中,MIC高度相关;基于另一种抗生素的MIC值,很容易预测一种抗生素的MIC值。替卡西林始终比羧苄西林活性高约一个稀释度,但酰氨基青霉素的相对活性因细菌种类而异。酰氨基青霉素通常比α-羧基青霉素活性更高,尤其是对α-羧基青霉素耐药的菌株。然而,也有例外情况,一组抗生素的MIC值不能根据另一组抗生素的MIC值轻易预测。酰氨基青霉素对革兰氏阴性杆菌增强的抗菌效力和谱使其成为潜在有用的治疗药物。临床实验室没有必要常规对所有五种抗生素进行药敏试验。