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(Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety) (Ministry of Food and Drug Safety)
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한국분석과학회 한국분석과학회 학술대회 제51회 한국분석과학회 추계학술대회
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    초록·키워드

    The aim of method validation of an analytical procedure is to demonstrate that it is suitable for its intended purpose. Many international guidelines such as Codex, ICH, AOAC suggest the reliable ranges of each parameter and those were referenced to validate method of Fenfluramine Hydrochloride, Didesmethylsibutramine and Desmethylsibutramine in this study. Uncertainty estimation provides quantitative estimates of the level of confidence that a laboratory has in the analytical precision of test results, and is therefore an essential component of a quality system for analytical laboratories. Therefore, both method validation and uncertainty estimation of the three illicit weight-reducing agents were performed in this study. High Performance Liquid Chromatography with PDA detector(Agilient HPLC-PDA) were used to validate a method of three illicit weight-reducing agents in this study. The chromatographic separation of the analytes (Fenfluramine Hydrochloride, Didesmethylsibutramine, Desmethylsibutramine) on a C18 reversed-phase column was achieved using a gradient ... 전체 초록 보기

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      UCI(KEPA) : I410-ECN-0101-2014-430-002631651