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PC-904,一种新型的具有显著抗假单胞菌活性的广谱半合成青霉素:微生物学评价

PC-904, a novel broad-spectrum semisynthetic penicillin with marked antipseudomonal activity: microbiological evaluation.

作者信息

Noguchi H, Eda Y, Tobiki H, Nakagome T, Komatsu T

出版信息

Antimicrob Agents Chemother. 1976 Feb;9(2):262-73. doi: 10.1128/AAC.9.2.262.

Abstract

PC-904, sodium 6-{d(-)-alpha-(4-hydroxy-1,5-naphthyridine-3-carboxamido) phenylacetamido}-penicillanate, is a novel semisynthetic penicillin derivative that possesses a broad spectrum of in vitro and in vivo antibacterial activities. In low concentrations, PC-904 inhibits growth against large proportions of the gram-positive and gram-negative organisms susceptible to carbenicillin and gentamicin. In addition, PC-904 is several times more potent than carbenicillin against organisms such as Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, Proteus vulgaris, Shigella, Salmonella, Neisseria gonorrhoeae, and Bacteroides fragilis. Most striking are the inhibitory effects of PC-904 against P. aeruginosa and K. pneumoniae. Against these two clinical isolates, PC-904 is, respectively, 35 and 100 times more active than carbenicillin. The minimum inhibitory concentrations of PC-904 against P. aeruginosa are comparable to those of gentamicin. PC-904 acts bactericidally. The effect of inoculum size on the antibacterial activity is often small and generally comparable to carbenicillin. The rate of binding to serum protein is high (88 to 98%), but the effect of the addition of serum on the drug's activity is not marked, because such binding is reversible. It is confirmed that PC-904 has a very potent in vivo antibacterial activity against gram-negative and gram-positive organisms. Against systemic infections with P. aeruginosa, K. pneumoniae, and E. coli in mice, PC-904 is 7 to 10 times, over 8 times, and 2 to 15 times more active than carbenicillin, respectively.

摘要

PC - 904,即6 - {d(-)-α-(4 - 羟基 - 1,5 - 萘啶 - 3 - 甲酰胺基)苯乙酰氨基}青霉烷酸钠,是一种新型半合成青霉素衍生物,具有广泛的体外和体内抗菌活性。在低浓度下,PC - 904能抑制对羧苄西林和庆大霉素敏感的大部分革兰氏阳性和革兰氏阴性菌的生长。此外,PC - 904对铜绿假单胞菌、肺炎克雷伯菌、大肠杆菌、普通变形杆菌、志贺菌、沙门菌、淋病奈瑟菌和脆弱拟杆菌等细菌的活性比羧苄西林强几倍。PC - 904对铜绿假单胞菌和肺炎克雷伯菌的抑制作用最为显著。针对这两种临床分离株,PC - 904的活性分别比羧苄西林高35倍和100倍。PC - 904对铜绿假单胞菌的最低抑菌浓度与庆大霉素相当。PC - 904具有杀菌作用。接种量对抗菌活性的影响通常较小,一般与羧苄西林相当。与血清蛋白的结合率很高(88%至98%),但加入血清对药物活性的影响不明显,因为这种结合是可逆性的。已证实PC - 904对革兰氏阴性和革兰氏阳性菌具有非常强的体内抗菌活性。在小鼠体内,针对铜绿假单胞菌、肺炎克雷伯菌和大肠杆菌引起的全身感染,PC - 904的活性分别比羧苄西林高7至10倍、超过8倍和2至15倍。

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