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生长培养基对LY 303366抗真菌活性的影响。

Growth medium effect on the antifungal activity of LY 303366.

作者信息

Klepser M E, Ernst E J, Ernst M E, Pfaller M A

机构信息

College of Pharmacy, University of Iowa, Iowa 52242-1112, USA.

出版信息

Diagn Microbiol Infect Dis. 1997 Dec;29(4):227-31. doi: 10.1016/s0732-8893(97)00144-2.

Abstract

The impact of growth medium selection on antifungal susceptibility testing has been well documented. Previously we described the antifungal characteristics of LY 303366 via time-kill curve methods using RPMI 1640 buffered with 0.165 M morpholinepropane-sulfonic acid as growth medium. The purpose of the current study was to compare the previously reported kill curve results with results obtained using antibiotic medium number three (AM #3) as growth medium. Antifungal activity was assessed via susceptibility testing and time-kill studies in both media. Two isolates each of Candida albicans, C. glabrata, and C. tropicalis were studied. MICs for the six isolates were found to be 10 to 100 times lower in AM #3. Time-kill studies were conducted with multiples of the MIC ranging from 0.125 x MIC to 16 x MIC. LY 303366 exhibited fungicidal (> or = 3 log10 reduction in CFU) activity against all isolates in AM #3; however, fungicidal activity was noted only for three of the six isolates when tested in RPMI. Furthermore, the rate of fungicidal activity was more rapid when AM #3 was utilized. Not only were the rate and extent of activity influenced by choice of media, but the relationships between LY 303366 concentrations and activity were also found to be media dependent. The findings from this study serve to highlight further the importance of media selection for in vitro evaluation of antifungal activity. In vivo studies need to be conducted with LY 303366 to determine which media provides the best correlation between in vitro and in vivo findings.

摘要

生长培养基的选择对抗真菌药敏试验的影响已有充分记录。此前我们通过时间-杀菌曲线法,以用0.165M吗啉丙烷磺酸缓冲的RPMI 1640作为生长培养基,描述了LY 303366的抗真菌特性。本研究的目的是将先前报道的杀菌曲线结果与使用三号抗生素培养基(AM #3)作为生长培养基获得的结果进行比较。通过在两种培养基中进行药敏试验和时间-杀菌研究来评估抗真菌活性。对白色念珠菌、光滑念珠菌和热带念珠菌各两个分离株进行了研究。发现这六个分离株在AM #3中的最低抑菌浓度(MIC)低10至100倍。时间-杀菌研究使用了从0.125×MIC到16×MIC的多个MIC倍数进行。LY 303366在AM #3中对所有分离株均表现出杀菌(CFU减少≥3 log10)活性;然而,在RPMI中测试时,六个分离株中只有三个显示出杀菌活性。此外,使用AM #3时杀菌活性的速度更快。不仅活性的速度和程度受培养基选择的影响,而且LY 303366浓度与活性之间的关系也发现依赖于培养基。本研究结果进一步突出了培养基选择在体外抗真菌活性评估中的重要性。需要对LY 303366进行体内研究,以确定哪种培养基能在体外和体内研究结果之间提供最佳相关性。

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