Uri J V, Actor P, Zajac I, Pitkin D H, Phillips L, Guarini J R, Bartus H F, Polansky T J, Dunn G L, Hoover J R, Weisbach J A
J Antibiot (Tokyo). 1979 Nov;32(11):1161-7. doi: 10.7164/antibiotics.32.1161.
Three cephalosporins with 7-(2-hydroxyiminophenylacetamido) side chains (SK&F 79433, 80000 and 80303), differing in their 3-substituents, exhibited similar broad-spectrum antibacterial activity in vitro against strains of Staphylococcus aureus, Streptococcus faecalis and various Gram-negative bacilli. All three were active in vivo (s.c., mouse) against S. aureus, Escherichia coli or Klebsiella pneumoniae, but they differed significantly in serum pharmacokinetic profiles. SK&F 80303 produced high and extremely prolonged serum levels and protected mice when administered up to 24 hours prior to challenge with beta-lactamase-producing S. aureus or K. pneumoniae. It was resistant to hydrolysis by beta-lactamases from S. aureus, and variably so to beta-lactamases from E. coli strains. SK&F 80303 was bacteriolytic to logarithmically growing S. aureus, E. coli, Proteus mirabilis, K. pneumoniae and Enterobacter cloacae (partially). SK&F 80303 illustrates further the effect of the 3-sulfoalkyltetrazole substituent on the pharmacokinetic properties of cephalosporins. Its combined biological properties make it a possible candidate for therapeutic and long-term prophylactic use.
三种带有7-(2-羟基亚氨基苯乙酰胺)侧链的头孢菌素(SK&F 79433、80000和80303),其3-取代基不同,在体外对金黄色葡萄球菌、粪肠球菌和各种革兰氏阴性杆菌菌株表现出相似的广谱抗菌活性。这三种药物在体内(皮下注射,小鼠)对金黄色葡萄球菌、大肠杆菌或肺炎克雷伯菌均有活性,但它们的血清药代动力学特征有显著差异。SK&F 80303产生高且持续时间极长的血清水平,并且在对产β-内酰胺酶的金黄色葡萄球菌或肺炎克雷伯菌进行攻击前24小时给药时能保护小鼠。它对来自金黄色葡萄球菌的β-内酰胺酶有抗性,对来自大肠杆菌菌株的β-内酰胺酶的抗性则有所不同。SK&F 80303对对数生长期的金黄色葡萄球菌、大肠杆菌、奇异变形杆菌、肺炎克雷伯菌和阴沟肠杆菌(部分)具有溶菌作用。SK&F 80303进一步说明了3-磺烷基四唑取代基对头孢菌素药代动力学性质的影响。其综合生物学特性使其有可能成为治疗和长期预防用途的候选药物。