Zaman M M, Landman D, Burney S, Quale J M
Department of Medicine (111E), Department of Veterans Affairs Medical Center at Brooklyn, New York 11209, USA.
J Antimicrob Chemother. 1996 Jan;37(1):127-32. doi: 10.1093/jac/37.1.127.
Clinafloxacin, a new quinolone antibiotic with enhanced activity against Gram-positive bacteria, has demonstrated in-vitro activity against multidrug-resistant Enterococcus faecium, particularly when combined with penicillin. Rabbits with experimental endocarditis due to a multidrug-resistant strain of E. faecium were treated with clinafloxacin and/or penicillin. After three days of therapy, significant reduction of bacterial concentrations were found in vegetations, kidneys, and spleens of animals treated with clinafloxacin. The combination of clinafloxacin and penicillin was significantly better in reducing vegetation bacterial concentrations compared to the other groups (-4.4 log10 cfu/g compared with control). Serum levels of clinafloxacin consistently exceeded the MIC of the strain, and clinafloxacin-resistant isolates could not be detected. Clinafloxacin demonstrated promising activity in vivo against multidrug-resistant E. faecium, and further studies are warranted.
克林沙星是一种对革兰氏阳性菌活性增强的新型喹诺酮类抗生素,已显示出对多重耐药性粪肠球菌的体外活性,尤其是与青霉素联合使用时。患有由多重耐药性粪肠球菌菌株引起的实验性心内膜炎的兔子,接受了克林沙星和/或青霉素治疗。治疗三天后,在用克林沙星治疗的动物的赘生物、肾脏和脾脏中发现细菌浓度显著降低。与其他组相比,克林沙星和青霉素联合使用在降低赘生物细菌浓度方面明显更好(与对照组相比,降低了-4.4 log10 cfu/g)。克林沙星的血清水平始终超过该菌株的最低抑菌浓度,且未检测到耐克林沙星的分离株。克林沙星在体内对多重耐药性粪肠球菌显示出有前景的活性,值得进一步研究。