Buck R E, Price K E
Antimicrob Agents Chemother. 1977 Feb;11(2):324-30. doi: 10.1128/AAC.11.2.324.
Cefadroxil is a new semisynthetic cephalosporin with a broad antibacterial spectrum and a high chemotherapeutic potential when administered orally. The inhibitory activity of this compound was similar to that of cephalexin and cephradine when tested against 602 clinical isolates on Mueller-Hinton medium. In the oral treatment of experimental infections of mice, cefadroxil was more effective than cephalexin against Streptococcus pyogenes, and comparably effective against Streptococcus pneumoniae, Staphylococcus aureus, and several gram-negative species. Administered orally to mice, at doses ranging from 25 to 100 mg/kg, cefadroxil attained peak concentrations in the blood similar to those of cephalexin. At a dose of 200 mg/kg, however, higher peak levels were noted with cefadroxil than with cephalexin. In regard to other properties which were investigated, the behavior of cefadroxil compared favorably to that of cephalexin.
头孢羟氨苄是一种新型半合成头孢菌素,口服时具有广谱抗菌谱和高化疗潜力。在穆勒-欣顿培养基上对602株临床分离株进行测试时,该化合物的抑制活性与头孢氨苄和头孢拉定相似。在小鼠实验性感染的口服治疗中,头孢羟氨苄对化脓性链球菌的疗效比头孢氨苄更好,对肺炎链球菌、金黄色葡萄球菌和几种革兰氏阴性菌的疗效相当。以25至100mg/kg的剂量口服给小鼠,头孢羟氨苄在血液中达到的峰值浓度与头孢氨苄相似。然而,在200mg/kg的剂量下,头孢羟氨苄的峰值水平高于头孢氨苄。关于所研究的其他特性,头孢羟氨苄的表现优于头孢氨苄。