Rolston K V, LeBlanc B, Gooch G, Ho D H, Bodey G P
Department of Medical Specialities, University of Texas M.D. Anderson Cancer Center, Houston 77030.
J Antimicrob Chemother. 1989 Mar;23(3):363-71. doi: 10.1093/jac/23.3.363.
The in-vitro activity of PD 117558, a new quinolone antimicrobial agent, was compared to that of four other quinolones, imipenem and ceftazidime against a variety of Gram-positive and Gram-negative isolates from cancer patients. PD 117558 was found to have a broad antimicrobial spectrum with excellent activity against all Gram-positive isolates (including methicillin-resistant Staphylococcus aureus, coagulase-negative staphylococci, Streptococcus faecalis and Group JK-corynebacteria). It was also extremely active against Gram-negative bacilli with the exception of Pseudomonas aeruginosa against which ciprofloxacin was more active. Fleroxacin was slightly less active and S-25930 and S-25932 considerably less active than PD 117558. PD 117558 also had lower minimal inhibitory concentrations for most organisms tested than either imipenem or ceftazidime.
将新型喹诺酮抗菌剂PD 117558的体外活性与其他四种喹诺酮类药物、亚胺培南和头孢他啶针对癌症患者分离出的多种革兰氏阳性菌和革兰氏阴性菌的活性进行了比较。结果发现,PD 117558具有广泛的抗菌谱,对所有革兰氏阳性菌(包括耐甲氧西林金黄色葡萄球菌、凝固酶阴性葡萄球菌、粪肠球菌和JK群棒状杆菌)均有出色的活性。它对革兰氏阴性杆菌也极具活性,但对铜绿假单胞菌除外,环丙沙星对其更具活性。氟罗沙星的活性略低于PD 117558,而S - 25930和S - 25932的活性则比PD 117558低得多。对于大多数测试的生物体,PD 117558的最低抑菌浓度也低于亚胺培南或头孢他啶。