Bodey G P, Rodriguez V, Weaver S
Antimicrob Agents Chemother. 1976 Apr;9(4):668-74. doi: 10.1128/AAC.9.4.668.
Pirbenicillin is a new semisynthetic penicillin which inhibited 67% of isolates of Proteus aeruginosa tested in our laboratory, 93% of P. mirabilis, 31% of Enterobacter spp., 41% of Serratia spp., and 58% of Escherichia coli at a concentration of 6.25 mug/ml. Its activity appeared to be inoculum dependent and it was virtually inactive against 10(7) inocula of P. aeruginosa. It was more active than carbenicillin or ticarcillin, but less active than BL-P1654 against P. aeruginosa. Carbenicillin and ticarcillin appeared to be more active than pirbenicillin against Proteus spp., but pirbenicillin was active against some isolates of Klebsiella spp.
匹氨西林是一种新型半合成青霉素,在我们实验室中,其在浓度为6.25微克/毫升时,能抑制67%的铜绿假单胞菌分离株、93%的奇异变形杆菌、31%的肠杆菌属、41%的沙雷菌属以及58%的大肠杆菌。其活性似乎与接种量有关,对10⁷接种量的铜绿假单胞菌实际上无活性。它比羧苄西林或替卡西林更具活性,但对铜绿假单胞菌的活性比BL - P1654低。羧苄西林和替卡西林对变形杆菌属的活性似乎比匹氨西林更高,但匹氨西林对某些克雷伯菌属分离株有活性。