Basker M J, Merrikin D J, Ponsford R J, Slocombe B, Tasker T C
J Antimicrob Chemother. 1986 Sep;18(3):399-405. doi: 10.1093/jac/18.3.399.
BRL 20330 is the o-methyl phenyl ester of temocillin which is well absorbed after oral administration and converted to temocillin in the body. BRL 20330 was administered to healthy subjects in a three-part cross-over study with single doses equivalent to 400, 600 and 800 mg of temocillin. Peak serum concentrations of temocillin were 9.8, 12.8 and 15.8 mg/l respectively and concentrations of 3.0-6.0 mg/l were measured at 12 h after dosing. High and prolonged concentrations of temocillin were measured in the urine. The mean urinary recovery was 22-25% and only 0.2% of unhydrolyzed BRL 20330 was detected in the urine. Little difference in the extent of absorption was noted when BRL 20330 was administered with food although the peak levels of temocillin were delayed and reduced slightly. Urinary concentrations of temocillin, even after 24 h, were bactericidal for a number of Gram-negative bacteria including multi-resistant strains. BRL 20330 was well tolerated and there was no evidence of gastro-intestinal adverse effects.
BRL 20330是替莫西林的邻甲基苯酯,口服后吸收良好,并在体内转化为替莫西林。在一项三部分交叉研究中,对健康受试者给予BRL 20330,单剂量分别相当于400、600和800毫克替莫西林。替莫西林的血清峰值浓度分别为9.8、12.8和15.8毫克/升,给药后12小时测得的浓度为3.0 - 6.0毫克/升。在尿液中检测到高浓度且持续时间长的替莫西林。平均尿回收率为22 - 25%,尿液中仅检测到0.2%未水解的BRL 20330。当BRL 20330与食物一起给药时,吸收程度差异不大,尽管替莫西林的峰值水平有所延迟且略有降低。即使在24小时后,替莫西林的尿液浓度对多种革兰氏阴性菌包括多重耐药菌株仍具有杀菌作用。BRL 20330耐受性良好,没有胃肠道不良反应的证据。