新型恶唑烷酮类抗菌剂DuP 105和DuP 721的体外评价
In vitro evaluation of DuP 105 and DuP 721, two new oxazolidinone antimicrobial agents.
作者信息
Barry A L
机构信息
Clinical Microbiology Institute, Tualatin, Oregon 97062.
出版信息
Antimicrob Agents Chemother. 1988 Jan;32(1):150-2. doi: 10.1128/AAC.32.1.150.
Abstract
DuP 105 and DuP 721 are two members of the oxazolidinones, a new class of synthetic antimicrobial agents with activity against gram-positive bacteria. In vitro tests compared the two new drugs with five other antimicrobial agents against 216 gram-positive isolates representing 4 genera and 10 species. DuP 721 MICs for 50% of the strains tested (MIC50s) ranged from 2.0 to 8.0 micrograms/ml, DuP 105 MIC50S ranged from 4.0 to 16 micrograms/ml, and vancomycin MIC50S ranged from 0.25 to 1.0 microgram/ml. Methicillin-resistant and -susceptible staphylococci were susceptible to ciprofloxacin, vancomycin, and DuP 721.
摘要
DuP 105和DuP 721是恶唑烷酮类药物中的两个成员，恶唑烷酮类是一类新型的合成抗菌剂，对革兰氏阳性菌具有活性。体外试验将这两种新药与其他五种抗菌剂针对代表4个属和10个种的216株革兰氏阳性分离株进行了比较。DuP 721对50%受试菌株的最低抑菌浓度（MIC50）范围为2.0至8.0微克/毫升，DuP 105的MIC50范围为4.0至16微克/毫升，而万古霉素的MIC50范围为0.25至1.0微克/毫升。耐甲氧西林和对甲氧西林敏感的葡萄球菌对环丙沙星、万古霉素和DuP 721敏感。
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