Sutherland R, Beale A S, Boon R J, Griffin K E, Slocombe B, Stokes D H, White A R
Am J Med. 1985 Nov 29;79(5B):13-24. doi: 10.1016/0002-9343(85)90124-x.
The antibacterial effects produced by ticarcillin disodium plus clavulanate potassium, a combination of the broad-spectrum penicillin ticarcillin, and the beta-lactamase inhibitor clavulanic acid as the potassium salt, have been measured in vitro and in experimental infection studies. The presence of clavulanic acid resulted in a significant enhancement of the activity of ticarcillin against a wide range of beta-lactamase-producing bacteria. These included ticarcillin-resistant strains of Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, P. vulgaris, Yersinia enterocolitica, and the anaerobe Bacteroides fragilis. In addition, beta-lactamase-producing isolates of Hemophilus influenzae, Branhamella catarrhalis, Neisseria gonorrhoeae, and Staphylococcus aureus were susceptible to ticarcillin and clavulanate. Clavulanic acid did not influence the activity of ticarcillin against ticarcillin-susceptible bacteria. The bactericidal effects of the antibiotic combination were measured in an in vitro kinetic model in which the drug concentrations were varied to simulate those measured in humans after intravenous dosing with ticarcillin (3.0 g) and clavulanate potassium (100 mg clavulanic acid). In these tests, ticarcillin plus clavulanic acid had pronounced bactericidal activity against ticarcillin-resistant bacteria. The protection of ticarcillin by clavulanic acid from inactivation by bacterial beta-lactamases in vivo was demonstrated in experimental infection models in which the efficacy of the ticarcillin plus clavulanic acid combination against infections caused by beta-lactamase-producing bacteria was correlated with the presence of effective concentrations of both antibiotic and inhibitor at the site of infection.
替卡西林钠与克拉维酸钾(一种由广谱青霉素替卡西林和β-内酰胺酶抑制剂克拉维酸的钾盐组成的联合制剂)的抗菌效果已在体外及实验性感染研究中进行了测定。克拉维酸的存在显著增强了替卡西林对多种产β-内酰胺酶细菌的活性。这些细菌包括对替卡西林耐药的大肠杆菌、肺炎克雷伯菌、奇异变形杆菌、普通变形杆菌、小肠结肠炎耶尔森菌以及厌氧菌脆弱拟杆菌。此外,产β-内酰胺酶的流感嗜血杆菌、卡他布兰汉菌、淋病奈瑟菌和金黄色葡萄球菌分离株对替卡西林和克拉维酸敏感。克拉维酸不影响替卡西林对其敏感细菌的活性。在体外动力学模型中测定了该抗生素联合制剂的杀菌效果,在该模型中改变药物浓度以模拟静脉注射替卡西林(3.0 g)和克拉维酸钾(100 mg克拉维酸)后在人体中测得的浓度。在这些试验中,替卡西林加克拉维酸对耐替卡西林细菌具有显著的杀菌活性。在实验性感染模型中证实了克拉维酸在体内对替卡西林的保护作用,使其免受细菌β-内酰胺酶的灭活,在这些模型中,替卡西林加克拉维酸联合制剂对产β-内酰胺酶细菌所致感染的疗效与感染部位同时存在有效浓度的抗生素和抑制剂相关。