Bingen E, Lambert-Zechovsky N, Doit C, Duvignaud P, Georges D, Mariani-Kurkdjian P
Service de Microbiologie, Hôpital Robert Debré, Paris, France.
J Antimicrob Chemother. 1991 Oct;28(4):533-6. doi: 10.1093/jac/28.4.533.
We have used a dynamic in-vitro model to determine the killing kinetics of two formulations of cefuroxime axetil against 18 clinical strains of Haemophilus influenzae. The concentration of cefuroxime axetil was adjusted dynamically to simulate the mean serum profile in healthy volunteers following the administration of a single 250 mg dose in oral suspension or tablet form. Bacterial numbers were reduced by 3 log10 cfu/mL during the eight-hour experimental period with both dosage form simulations. Our results suggest that cefuroxime axetil, 250 mg in oral suspension or tablet form, may protect against the dissemination of H. influenzae during episodes of bacteraemia.
我们使用了一种动态体外模型来确定两种头孢呋辛酯制剂对18株临床分离的流感嗜血杆菌的杀菌动力学。动态调整头孢呋辛酯的浓度,以模拟健康志愿者单次口服250mg口服混悬液或片剂后血清中的平均药物浓度曲线。在两种剂型模拟的八小时实验期间,细菌数量均减少了3 log10 cfu/mL。我们的结果表明,250mg口服混悬液或片剂形式的头孢呋辛酯可能在菌血症发作期间预防流感嗜血杆菌的传播。