Limbert M, Klesel N, Seeger K, Seibert G, Winkler I, Schrinner E
J Antibiot (Tokyo). 1984 Aug;37(8):892-900. doi: 10.7164/antibiotics.37.892.
Cefodizime possesses a broad antibacterial spectrum including staphylococci, streptococci and Enterobacteriaceae. Neisseria gonorrhoeae and Haemophilus influenzae are also highly susceptible to cefodizime. Because of its beta-lactamase stability cefodizime is active against bacterial strains producing especially plasmid-coded enzymes. The MICs of cefodizime are slightly higher than those of cefotaxime, but with most Gram-negative bacteria they are lower than those of cefazolin, cefotiam and piperacillin. The in vitro activity of cefodizime is not dependent on inoculum size, or on the pH and composition of the test medium. Cefodizime did not induce in vitro resistance of Staphylococcus aureus or Escherichia coli. Because of its binding properties to PBPs 1A/B and 3, cefodizime leads to filamentation of Gram-negative rods and, at only slightly higher concentrations, to bacteriolysis.
头孢地嗪具有广泛的抗菌谱,包括葡萄球菌、链球菌和肠杆菌科细菌。淋病奈瑟菌和流感嗜血杆菌对头孢地嗪也高度敏感。由于其对β-内酰胺酶稳定,头孢地嗪对产生特别是质粒编码酶的细菌菌株具有活性。头孢地嗪的最低抑菌浓度(MIC)略高于头孢噻肟,但对大多数革兰氏阴性菌而言,其MIC低于头孢唑林、头孢替安和哌拉西林。头孢地嗪的体外活性不依赖于接种量,也不依赖于试验培养基的pH值和成分。头孢地嗪未诱导金黄色葡萄球菌或大肠杆菌产生体外耐药性。由于其与青霉素结合蛋白1A/B和3的结合特性,头孢地嗪导致革兰氏阴性杆菌形成丝状体,且在仅略高的浓度下导致细菌溶解。