Cleeland R, Squires E
Am J Med. 1984 Oct 19;77(4C):3-11.
Ceftriaxone possesses potent activity, both in vitro and in vivo, against a broad range of bacteria. MIC50 and MIC90 geometric means were calculated using the results of broth and agar dilution assays performed worldwide. The MIC90 for ceftriaxone overall was 8 micrograms/ml or less for Enterobacteriaceae and 0.024 microgram/ml or less for Neisseria and Hemophilus species. Moderate activity was noted against Pseudomonas and Acinetobacter species (MIC50 12 to 28 micrograms/ml). Ceftriaxone was extremely active against nonenterococcal streptococci (MIC90 0.07 microgram/ml or less) and quite active against methicillin-susceptible Staphylococcus aureus (MIC90 5 micrograms/ml or less). Ceftriaxone generally was inactive against enterococci and methicillin-resistant staphylococci. Activity against anaerobes was good, except for many strains of Bacteroides fragilis and B. thetaiotaomicron (MIC greater than 64 micrograms/ml). Ceftriaxone exhibited excellent stability to beta-lactamases. The effect of medium and inoculum on in vitro testing was minimal. Excellent activity was demonstrated in vivo. Against Enterobacteriaceae, nonenterococcal streptococci, and H. influenzae, the PD50 in mice generally was less than 1 mg/kg. S. aureus strains responded moderately (mean PD50 6.5 mg/kg), whereas against most P. aeruginosa strains, PD50s ranged from 5 to greater than 250 mg/kg. The superior pharmacokinetic profile of ceftriaxone compared with that of other new cephalosporins was demonstrated by use of a prophylactic treatment schedule. The ability of ceftriaxone to penetrate the cerebrospinal fluid and provide excellent therapeutic coverage was confirmed in experimental meningitis models.
头孢曲松在体外和体内对多种细菌均具有强大的活性。使用全球范围内肉汤稀释法和琼脂稀释试验的结果计算MIC50和MIC90几何均值。对于大肠埃希菌属,头孢曲松总体MIC90为8微克/毫升或更低;对于奈瑟菌属和嗜血杆菌属,MIC90为0.024微克/毫升或更低。对铜绿假单胞菌属和不动杆菌属可见中度活性(MIC50为12至28微克/毫升)。头孢曲松对非肠球菌性链球菌具有极强活性(MIC90为0.07微克/毫升或更低),对甲氧西林敏感金黄色葡萄球菌活性较强(MIC90为5微克/毫升或更低)。头孢曲松通常对肠球菌和耐甲氧西林葡萄球菌无活性。除许多脆弱拟杆菌和多形拟杆菌菌株外(MIC大于64微克/毫升),对厌氧菌活性良好。头孢曲松对β-内酰胺酶表现出极佳的稳定性。培养基和接种量对体外试验的影响极小。在体内表现出优异的活性。对于大肠埃希菌属、非肠球菌性链球菌和流感嗜血杆菌,小鼠体内的PD50通常小于1毫克/千克。金黄色葡萄球菌菌株反应中等(平均PD50为6.5毫克/千克),而对于大多数铜绿假单胞菌菌株,PD50范围为5至大于250毫克/千克。通过预防性治疗方案证明了头孢曲松与其他新型头孢菌素相比具有更优越的药代动力学特征。在实验性脑膜炎模型中证实了头孢曲松穿透脑脊液并提供优异治疗覆盖的能力。