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新型喹诺酮类药物PD127,391对癌症患者细菌分离株的体外活性

In vitro activity of PD127,391, a new quinolone against bacterial isolates from cancer patients.

作者信息

Rolston K V, Ho D H, LeBlanc B, Bodey G P

机构信息

Department of Medical Specialties, University of Texas M.D. Anderson Cancer Center, Houston.

出版信息

Chemotherapy. 1990;36(5):365-72. doi: 10.1159/000238789.

Abstract

The in vitro activity of PD127,391, a new 4-quinolone, was compared to that of ciprofloxacin against common clinical bacterial isolates from patients with cancer. PD127,391 was found to have a broad antimicrobial spectrum with excellent activity against gram-positive isolates (including multidrug-resistant organism such as Corynebacterium jeikeium, Enterococcus faecalis, Enterococcus faecium, methicillin-resistant Staphylococcus aureus and coagulase-negative Staphylococcus spp.). It was also extremely active against gram-negative bacilli including Pseudomonas aeruginosa. Against organisms such as Achromobacter xylosoxidans, Acinetobacter spp. and Xanthomonas maltophilia, which are frequently resistant to a variety of antimicrobial agents, PD127,391 exhibited good activity, inhibiting all such isolates at a concentration of 0.5 micrograms/ml. Overall, PD127,391 was far more potent than ciprofloxacin against gram-positive isolates and slightly more active against gram-negative isolates. No bacterium that we examined needed more than 2 micrograms/ml of PD127,391 for inhibition.

摘要

将新型4-喹诺酮类药物PD127,391的体外活性与环丙沙星针对癌症患者常见临床分离菌株的活性进行了比较。发现PD127,391具有广泛的抗菌谱,对革兰氏阳性分离菌(包括多重耐药菌,如杰氏棒状杆菌、粪肠球菌、屎肠球菌、耐甲氧西林金黄色葡萄球菌和凝固酶阴性葡萄球菌属)具有优异的活性。它对包括铜绿假单胞菌在内的革兰氏阴性杆菌也极具活性。对于经常对多种抗菌剂耐药的木糖氧化无色杆菌、不动杆菌属和嗜麦芽窄食单胞菌等菌株,PD127,391表现出良好的活性,在浓度为0.5微克/毫升时可抑制所有此类分离菌株。总体而言,PD127,391对革兰氏阳性分离菌的效力远高于环丙沙星,对革兰氏阴性分离菌的活性略高。我们检测的细菌中,没有一种需要超过2微克/毫升的PD127,391来抑制。

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