Basker M J, Comber K R, Sutherland R, Valler G H
Chemotherapy. 1977;23(6):424-35. doi: 10.1159/000222012.
Carfecillin, the alpha-phenyl ester of carbenicillin, hydrolyses rapidly in the presence of serum or body tissues to liberate carbenicillin but hydrolysis is less rapid in aqueous solution. The activity of carfecillin in antibacterial tests in vitro depends upon the extent of hydrolysis to carbenicillin, and in conventional serial dilution tests carfecillin shows an antibacterial spectrum generally similar to that of carbenicillin due to extensive hydrolysis. However, in tests in which the extent of hydrolysis is reduced, carfecillin displays lesser activity than carbenicillin against gram-negative bacilli and greater activity against gram-positive cocci. In the presence of serum carfecillin is hydrolysed rapidly to carbenicillin and the activity shown is solely that of carbenicillin. Unlike carbenicillin, carfecillin is well absorbed in mice after oral administration, producing significant carbenicillin blood concentrations and the compound is as effective by the oral route in the treatment of various experimental mouse infections as is parenteral carbenicillin.
羧苄青霉素苯酯(卡非西林)在血清或身体组织存在的情况下会迅速水解,释放出羧苄青霉素,但在水溶液中水解速度较慢。卡非西林在体外抗菌试验中的活性取决于其水解为羧苄青霉素的程度,在传统的系列稀释试验中,由于广泛水解,卡非西林显示出的抗菌谱通常与羧苄青霉素相似。然而,在水解程度降低的试验中,卡非西林对革兰氏阴性杆菌的活性低于羧苄青霉素,而对革兰氏阳性球菌的活性则高于羧苄青霉素。在血清存在的情况下,卡非西林会迅速水解为羧苄青霉素,所显示的活性完全是羧苄青霉素所具有的活性。与羧苄青霉素不同,卡非西林经口服给药后在小鼠体内吸收良好,可产生显著的羧苄青霉素血药浓度,并且该化合物经口服途径治疗各种实验性小鼠感染时与注射用羧苄青霉素一样有效。