Preston D A
Postgrad Med J. 1979;55 Suppl 4:22-9.
Laboratory aspects of cefaclor, a new orally-effective cephalosporin antibiotic, are summarized. On the basis of data from a variety of studies, the useful antibacterial spectrum of cefaclor is shown to include all classes of bacteria that are generally susceptible to cephalothin and cephalexin. Against many Enterobacteriaceae, Haemophilus sp. and Streptococcus pneumoniae, cefaclor has a significant potency advantage over cephalexin. Bacteria that are susceptible to cefaclor are killed by concentrations at or near the inhibitory concentration. In vitro enzymatic hydrolysis experiments have shown that cefaclor is a relatively good substrate for several beta-lactamases. Orally administered cefaclor is effective in protection of mice from the lethal effects of intraperitoneal challenges with cefaclor-susceptible bacteria. The chemical instability of cefaclor, test medium composition and inoculum density influence the results of in vitro susceptibility tests with cefaclor. Methods for routine susceptibility testing are described.
本文总结了新型口服有效头孢菌素抗生素头孢克洛的实验室研究情况。基于多项研究数据,头孢克洛的有效抗菌谱显示包括所有通常对头孢噻吩和头孢氨苄敏感的各类细菌。针对许多肠杆菌科细菌、嗜血杆菌属和肺炎链球菌,头孢克洛相较于头孢氨苄具有显著的效力优势。对头孢克洛敏感的细菌在达到或接近抑制浓度时即被杀死。体外酶水解实验表明,头孢克洛是几种β-内酰胺酶的相对良好底物。口服头孢克洛可有效保护小鼠免受腹腔注射头孢克洛敏感菌致死效应的影响。头孢克洛的化学不稳定性、测试培养基成分和接种物密度会影响头孢克洛体外药敏试验结果。文中描述了常规药敏试验方法。