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논문 기본 정보

자료유형
학술저널
저자정보
Young Bin Yoo (Konyang University) Sung-Soon Kim (Konyang University) Young Kwon Kim (Konyang University) Sunghyun Kim (Catholic University of Pusan)
저널정보
대한의생명과학회 대한의생명과학회지 대한의생명과학회지 제22권 제4호
발행연도
2016.12
수록면
174 - 183 (10page)

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In the present study, a serum-based minimum inhibitory concentration (MIC) testing to caspofungin was optimized and evaluated to solve the limitations of the conventional Clinical and Laboratory Standards Institute (CLSI) guideline-based antifungal agent MIC test and the usefulness of this testing for clinical application was determined. A total of 105 Candida albicans clinical isolates were used for measuring MIC to caspofungin. Results showed that growth characteristics were different according to types of serum and the mouse serum was the most suitable for this assay. In order to measure the optimal concentration of mouse serum, 0 to 100% mouse serum were added to the media during fungal culture. The optimal concentration of serum was 50% when consideration of antifungal agent administration and inoculum size, serum components and ease of hyphae separated, and the consideration of the degree of growth. In comparison of the usefulness between the conventional Alamar-modified broth microdilution MIC assay and 50% mouse serum-based MIC testing, the range of MIC<SUB>80</SUB> of the Alamar-modified broth microdilution MIC assay was 0.13~2.0 μg/mL (SD ±0.42 μg/mL) and that of the 50% mouse serum-based MIC assay was 2.0~32.0 μg/mL (SD ±9.01 μg/mL). The range of MIC<SUB>50</SUB> of the Alamar-modified broth microdilution MIC assay was 0.13~2.0 μg/mL (SD ±0.40 μg/mL) and that of the 50% mouse serum-based MIC assay was 1.0~16.0 μg/mL (SD ±2.36 μg/mL). The MICs of 50% mouse serum-based MIC testing was increased by up to 4 to 64 times than Alamar-modified broth microdilution MIC assay. In conclusion, a 50% mouse serum-based MIC assay was more useful for measuring MIC in Candida albicans clinical isolates than conventional colorimetric broth microdilution MIC testing.

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UCI(KEPA) : I410-ECN-0101-2017-510-002026382