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用烯丙胺对皮肤癣菌进行纸片扩散药敏试验。

Disk diffusion susceptibility testing of dermatophytes with allylamines.

作者信息

Venugopal P V, Venugopal T V

机构信息

Institute of Microbiology, Madurai, Medical College, India.

出版信息

Int J Dermatol. 1994 Oct;33(10):730-2. doi: 10.1111/j.1365-4362.1994.tb01522.x.

Abstract

BACKGROUND

Allylamines are a newly developed group of drugs possessing a broad spectrum of activity against a wide range of fungi. With the advent of new antifungal drugs, susceptibility testing of fungi is receiving increased attention as important laboratory procedures for aiding in the selection of appropriate drug therapy.

METHODS

In vitro susceptibility testing of 43 clinical isolates of dermatophytes which included Microsporum sp., (18) Trichophyton sp., (23) and Epidermophyton floccosum (2) were carried out against the two allylamine derivatives, naftifine and terbinafine, by agar dilution and disk diffusion methods.

RESULTS

Terbinafine was found to be more active minimal inhibitory concentration (MIC range < or = 0.0001-0.1 micrograms/mL), inhibiting 50% (MIC 50) and 90% (MIC 90) of the isolates at 0.01 and 0.1 micrograms/mL, respectively. The MIC 50s and MIC 90s of naftifine were 0.1 micrograms/mL (MIC range 0.001-0.5 micrograms/mL). Both the drugs showed good correlation between the MIC and sizes of zones of inhibition around the disks. Regression analysis was used to measure the degree of correlation between the MIC values and matched averaged zones of inhibition; the correlation coefficients for both terbinafine and naftifine were -0.6841 (P < 0.001) and -0.5455 (P < 0.001), respectively.

CONCLUSIONS

The allylamines, naftifine and terbinafine, could be used successfully for susceptibility testing of dermatophytes by the disk diffusion method. With proper standardization of the test conditions, in vitro susceptibility testing of filamentous fungi by disk diffusion would become a useful laboratory procedure in the near future for determining the best drug therapy.

摘要

背景

烯丙胺类是新开发的一类药物,对多种真菌具有广泛的活性。随着新型抗真菌药物的出现,真菌药敏试验作为辅助选择合适药物治疗的重要实验室程序,正受到越来越多的关注。

方法

采用琼脂稀释法和纸片扩散法,对43株皮肤癣菌临床分离株进行体外药敏试验,这些分离株包括小孢子菌属(18株)、毛癣菌属(23株)和絮状表皮癣菌(2株),受试药物为两种烯丙胺衍生物萘替芬和特比萘芬。

结果

发现特比萘芬活性更强(最低抑菌浓度范围≤0.0001 - 0.1微克/毫升),分别在0.01和0.1微克/毫升时抑制50%(MIC50)和90%(MIC90)的分离株。萘替芬的MIC50和MIC90为0.1微克/毫升(MIC范围0.001 - 0.5微克/毫升)。两种药物的MIC与纸片周围抑菌圈大小之间均显示出良好的相关性。采用回归分析来测量MIC值与匹配的平均抑菌圈之间的相关程度;特比萘芬和萘替芬的相关系数分别为-0.6841(P < 0.001)和-0.5455(P < 0.001)。

结论

烯丙胺类药物萘替芬和特比萘芬可通过纸片扩散法成功用于皮肤癣菌的药敏试验。通过对试验条件进行适当标准化,纸片扩散法对丝状真菌进行体外药敏试验在不久的将来将成为确定最佳药物治疗的有用实验室程序。

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