Neu J C
Antimicrob Agents Chemother. 1976 Sep;10(3):535-42. doi: 10.1128/AAC.10.3.535.
Mecillinam, a beta-amidinopenicillanic acid derivative, was combined with ampicillin, amoxicillin, carbenicillin, cephalothin, cefamandole, and cefoxitin and tested against most members of the Enterobacteriaceae and Pseudomonas. Synergy was demonstrated with selected isolates of most of the organisms tested. Isolates highly susceptible to mecillinam (minimum inhibitory concentration, <0.8 mug/ml) were not synergistically inhibited by addition of another beta-lactam antibiotic. Synergy of mecillinam and a beta-lactamase-resistant penicillin, cloxacillin, was demonstrated. In media of osmolality >10 mOsm or of conductivity >6 mS, mecillinam and beta-lactam antibiotics showed synergy in most instances, whereas at low osmolality and conductivity the activity of mecillinam is so great that synergy cannot be demonstrated. The proportion of mecillinam to beta-lactam antibiotic that will be synergistic ranged from 100:1 to 1:1 to 1:100. Mecillinam did not increase the activity, minimum inhibitory concentration or minimum bactericidal concentration values, of beta-lactam compounds against streptococci, staphylococci, clostridia, listeria, or bacteroides. Synergy was not demonstrated with combinations of mecillinam and aminoglycosides (kanamycin, gentamicin, tobramycin, amikacin), chloramphenicol, tetracycline, or polymyxins.
美西林,一种β-脒基青霉素酸衍生物,与氨苄西林、阿莫西林、羧苄西林、头孢噻吩、头孢孟多和头孢西丁联合使用,并针对肠杆菌科和假单胞菌的大多数成员进行了测试。在所测试的大多数生物体的选定分离株中显示出协同作用。对美西林高度敏感(最低抑菌浓度,<0.8μg/ml)的分离株不会因添加另一种β-内酰胺抗生素而受到协同抑制。美西林与一种耐β-内酰胺酶的青霉素氯唑西林显示出协同作用。在渗透压>10mOsm或电导率>6mS的培养基中,美西林和β-内酰胺抗生素在大多数情况下显示出协同作用,而在低渗透压和电导率下,美西林的活性非常高,以至于无法证明协同作用。美西林与β-内酰胺抗生素产生协同作用的比例范围为100∶1至1∶1至1∶100。美西林不会增加β-内酰胺化合物对链球菌、葡萄球菌、梭菌、李斯特菌或拟杆菌的活性、最低抑菌浓度或最低杀菌浓度值。美西林与氨基糖苷类(卡那霉素、庆大霉素、妥布霉素、阿米卡星)、氯霉素、四环素或多粘菌素的组合未显示出协同作用。