Greenwood D, Pearson N, Eley A, O'Grady F
Antimicrob Agents Chemother. 1980 Mar;17(3):397-401. doi: 10.1128/AAC.17.3.397.
Cefotaxime and its desacetoxymethyl derivative, ceftizoxime (previously known as FK749), are both extremely active against a wide spectrum of bacteria. In the present comparative study, the activity of ceftizoxime exceeded that of cefotaxime by a factor of four or more for strains of Klebsiella, Enterobacter, Providencia, Serratia, and Bacteroides; the only species for which the activity of cefotaxime exceeded that of ceftizoxime by a factor of four was Vibrio cholerae. Against other species, the activity of the two drugs was roughly comparable. Both showed outstanding activity against Haemophilus influenzae and Neisseria gonorrhoeae. Comparative turbidimetric and morphological studies revealed that ceftizoxime was able to induce spheroplast formation and rapid lysis in Escherichia coli strains at lower concentrations than cefotaxime. This difference was not found, however, when E. coli strains resistant to ampicillin by an intrinsic (nonenzymic) mechanism were tested.
头孢噻肟及其去乙酰氧甲基衍生物头孢唑肟(以前称为FK749)对多种细菌都具有极强的活性。在本比较研究中,对于克雷伯菌属、肠杆菌属、普罗威登斯菌属、沙雷菌属和拟杆菌属的菌株,头孢唑肟的活性比头孢噻肟高出四倍或更多;头孢噻肟活性比头孢唑肟高出四倍的唯一菌种是霍乱弧菌。对于其他菌种,两种药物的活性大致相当。二者对流感嗜血杆菌和淋病奈瑟菌均表现出出色的活性。比较比浊法和形态学研究表明,头孢唑肟在比头孢噻肟更低的浓度下就能诱导大肠杆菌菌株形成原生质球并快速裂解。然而,当测试对氨苄西林具有固有(非酶促)耐药机制的大肠杆菌菌株时,未发现这种差异。