Regamey C, Libke R D, Engelking E R, Clarke J T, Kirby M M
J Infect Dis. 1975 Mar;131(3):291-4. doi: 10.1093/infdis/131.3.291.
Cefazolin was more susceptible than cephaloridine and cephalothin to in vitro inactivation by coagulase-positive, penicillinase-producing strains of Staphylococcus aureus. Inactivation (which was greater with methicillin-resistant than with methicillin-sensitive strains) was demonstrated by assay of the antibiotics in broth cultures with simultaneous colony counts and by exposure of the antibiotics to penicillinase powders extracted from S. aureus. Cefazolin was destroyed to a greater extent than was cephaloridine, whereas cephalothin underwent little, if any, destruction. The clinical implications of this degradation, thought by some to be of importance for cephaloridine, might also apply to cefazolin.
对于凝固酶阳性、产青霉素酶的金黄色葡萄球菌菌株,头孢唑林比头孢噻啶和头孢噻吩更易在体外被灭活。通过对肉汤培养物中的抗生素进行测定并同时进行菌落计数,以及将抗生素暴露于从金黄色葡萄球菌中提取的青霉素酶粉末,证实了灭活作用(耐甲氧西林菌株的灭活作用比甲氧西林敏感菌株更强)。头孢唑林比头孢噻啶被破坏的程度更大,而头孢噻吩即使有破坏也很少。这种降解的临床意义,一些人认为对头孢噻啶很重要,可能也适用于头孢唑林。