Slocombe B, Basker M J, Bentley P H, Clayton J P, Cole M, Comber K R, Dixon R A, Edmondson R A, Jackson D, Merrikin D J, Sutherland R
Antimicrob Agents Chemother. 1981 Jul;20(1):38-46. doi: 10.1128/AAC.20.1.38.
BRL 17421 is a new semisynthetic beta-lactam antibiotic with an unusual spectrum of antibacterial activity. The compound exhibits exceptional stability to a wide range of bacterial beta-lactamases and is active against the majority of Enterobacteriaceae, including strains highly resistant to many of the penicillins and cephalosporins currently available. Among the clinical isolates of Enterobacteriaceae tested, the frequency of strains resistant to BRL 17421 was found to be low, and there was a slow rate of emergence of resistance during in vitro studies. BRL 17421 was highly active against Haemophilus influenzae and Neisseria gonorrhoeae, including beta-lactamase-producing strains. The compound was markedly less active against Pseudomonas aeruginosa and Bacteroides fragilis than against the Enterobacteriaceae. Against the gram-positive bacteria, BRL 17421 showed a very low level of activity. BRL 17421 was found to be 85% bound to human serum, and the antibacterial activity was diminished two- to fourfold in the presence of human serum. Against experimental infections in mice, the activity of BRL 17421 reflected the properties observed in vitro. Studies in human volunteers showed unusually high and prolonged serum concentrations of the compound after parenteral dosage, with a serum half-life of about 5 h, and approximately 85% of the dose was recovered unchanged in the urine. BRL 17421 was poorly absorbed after oral administration. The compound was well tolerated after intramuscular and intravenous administration in volunteers, with no adverse side effects.
BRL 17421是一种新型半合成β-内酰胺抗生素,具有不同寻常的抗菌活性谱。该化合物对多种细菌β-内酰胺酶表现出非凡的稳定性,对大多数肠杆菌科细菌具有活性,包括对目前可用的许多青霉素和头孢菌素高度耐药的菌株。在所测试的肠杆菌科临床分离株中,发现对BRL 17421耐药的菌株频率较低,并且在体外研究期间耐药性出现的速率较慢。BRL 17421对流感嗜血杆菌和淋病奈瑟菌具有高度活性,包括产β-内酰胺酶的菌株。该化合物对铜绿假单胞菌和脆弱拟杆菌的活性明显低于对肠杆菌科细菌的活性。对于革兰氏阳性菌,BRL 17421显示出非常低的活性水平。发现BRL 17421与人类血清的结合率为85%,并且在存在人类血清的情况下抗菌活性降低了两到四倍。对于小鼠的实验性感染,BRL 17421的活性反映了体外观察到的特性。在人类志愿者中的研究表明,肠胃外给药后该化合物的血清浓度异常高且持续时间长,血清半衰期约为5小时,并且约85%的剂量在尿液中未发生变化地被回收。口服给药后BRL 17421吸收不良。该化合物在志愿者中进行肌肉注射和静脉注射后耐受性良好,没有不良副作用。