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논문 기본 정보

자료유형
학술저널
저자정보
Jung-Ah Do (Ministry of Food and Drug Safety) Eunyoung Noh (Ministry of Food and Drug Safety) Soon-Byung Yoon (Ministry of Food and Drug Safety) Hyoung-Joon Park (Ministry of Food and Drug Safety) Sooyeul Cho (Ministry of Food and Drug Safety) Sung-Kwan Park (Ministry of Food and Drug Safety) Chang-Yong Yoon (Ministry of Food and Drug Safety)
저널정보
한국분석과학회 분석과학 분석과학 제28권 제4호
발행연도
2015.8
수록면
278 - 287 (10page)

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초록· 키워드

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Phosphodiesterase type 5 inhibitors (PDE-5 inhibitors) are used in the treatment of erectile dysfunction. In recent years, a number of reports have been conducted on dietary supplements contaminated with PDE-5 analogues. In this study, 58 analogues of PDE-5 inhibitors were sorted into five groups: tadalafil, sildenafil, hongdenafil, vardenafil, and other analogues. These analogues were then evaluated using a liquid chromatographyquadrupole-time of flight mass spectrometry (LC-QTOF-MS) electrospray ionization mass method. Each compound has a unique fragmentation ion, which can be easily analyzed qualitatively. The fragmentation pathways of the analogues were elucidated based on the QTOF-MS and MS/MS data. Common ions were confirmed for each group by analyzing the structural characteristics and fragmentation pathways. Specifically, common ions were observed at m/z 169.08 and 135.04 (tadalafil analogues), m/z 311.15 and 283.12 (sildenafil analogues and hongdenafil analogues), and m/z 312.16 and 151.09 (vardenafil analogues). The advantage of this method is that the structure of unknown components can be determined by interpreting the product ions. Hence, the developed method can be used for the identification of unknown compounds. Fragmentation pathways may also aid in the detection and identification of PDE-5 inhibitor analogues.

목차

Abstract
1. Introduction
2. Experimental
3. Results and discussion
4. Conclusion
References

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UCI(KEPA) : I410-ECN-0101-2016-433-001790743