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司帕沙星(CI-978;AT-4140)对癌症患者临床分离株的体外活性。

In vitro activity of sparfloxacin (CI-978; AT-4140) against clinical isolates from cancer patients.

作者信息

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

机构信息

Department of Medical Specialities, University of Texas, M. D. Anderson Cancer Center, Houston 77030.

出版信息

Antimicrob Agents Chemother. 1990 Nov;34(11):2263-6. doi: 10.1128/AAC.34.11.2263.

Abstract

The in vitro activity of sparfloxacin, a new quinolone, was compared with those of ciprofloxacin and fleroxacin against gram-positive and gram-negative bacteria, greater than 90% of which were isolated from blood culture specimens of cancer patients. Sparfloxacin was extremely active against Acinetobacter species, Aeromonas hydrophila, Citrobacter diversus, Enterobacter species, Escherichia coli, Klebsiella species, Proteus vulgaris, and Serratia marcescens (inhibiting greater than 90% of these isolates at a concentration of 0.5 microgram/ml) and moderately active against Pseudomonas species, other Proteus species, and Citrobacter freundii. Sparfloxacin inhibited greater than 90% of staphylococci (including methicillin-resistant and coagulase-negative strains) at a concentration of 0.12 microgram/ml and greater than 90% of streptococci (including Streptococcus pneumoniae) at a concentration of 1.0 microgram/ml. It was also active against Bacillus cereus, Enterococcus species, and Corynebacterium jeikeium, organisms that have become fairly common in cancer patients.

摘要

将新喹诺酮类药物司帕沙星的体外活性与环丙沙星和氟罗沙星针对革兰氏阳性菌和革兰氏阴性菌的活性进行了比较,其中超过90%的菌株分离自癌症患者的血培养标本。司帕沙星对不动杆菌属、嗜水气单胞菌、多变枸橼酸杆菌、肠杆菌属、大肠杆菌、克雷伯菌属、普通变形杆菌和粘质沙雷氏菌具有极强的活性(在浓度为0.5微克/毫升时可抑制超过90%的这些分离菌株),对假单胞菌属、其他变形杆菌属和弗氏枸橼酸杆菌具有中等活性。司帕沙星在浓度为0.12微克/毫升时可抑制超过90%的葡萄球菌(包括耐甲氧西林菌株和凝固酶阴性菌株),在浓度为1.0微克/毫升时可抑制超过90%的链球菌(包括肺炎链球菌)。它对蜡样芽孢杆菌、肠球菌属和杰氏棒状杆菌也有活性,这些菌在癌症患者中已相当常见。

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Am J Med. 1987 Jun 26;82(6B):40-6. doi: 10.1016/0002-9343(87)90617-6.
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