Boswell F J, Andrews J M, Wise R
Department of Medical Microbiology, City Hospital NHS Trust, Birmingham, UK.
J Antimicrob Chemother. 1998 Feb;41(2):149-53. doi: 10.1093/jac/41.2.149.
The pharmacodynamic properties of a novel ketolide (a new class of macrolide), HMR 3647, were investigated by studying time-kill kinetics and postantibiotic effect (PAE). The time-kill kinetics were studied at two inocula against three strains each of Staphylococcus aureus, Haemophilus influenzae, Moraxella catarrhalis, Streptococcus pneumoniae, Streptococcus pyogenes, Enterococcus faecalis, Enterococcus faecium and Bacteroides fragilis. The PAEs of HMR 3647 were also investigated on these organisms at concentrations equivalent to 1, 4 and 10 x MIC. The time-kill kinetic data demonstrated that HMR 3647 is predominantly bacteriostatic and only slowly bactericidal at higher concentrations. HMR 3647 exhibited a significant PAE with all strains studied, ranging from 1.2 h to 8.2 h at 10 x MIC. The bacteriostatic activity and significant PAE demonstrated by HMR 3647 are similar to those previously obtained with other macrolides.
通过研究时间杀菌动力学和抗生素后效应(PAE),对新型酮内酯(一类新型大环内酯类药物)HMR 3647的药效学特性进行了研究。在两种接种量下,针对金黄色葡萄球菌、流感嗜血杆菌、卡他莫拉菌、肺炎链球菌、化脓性链球菌、粪肠球菌、屎肠球菌和脆弱拟杆菌这三种菌株各研究了时间杀菌动力学。还在相当于1、4和10倍最低抑菌浓度(MIC)的浓度下,研究了HMR 3647对这些微生物的PAE。时间杀菌动力学数据表明,HMR 3647主要具有抑菌作用,仅在较高浓度下才缓慢杀菌。HMR 3647对所有研究菌株均表现出显著的PAE,在10倍MIC时,PAE范围为1.2小时至8.2小时。HMR 3647表现出的抑菌活性和显著PAE与先前使用其他大环内酯类药物所获得的结果相似。