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Determination of florfenicol residue in eel muscle by HPLC

YU Kong-jie

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Abstract

A method for detecting florfenicol residue in eel muscle was established. Florfenicol residue was extracted from eel muscle with ethyl acetate, followed by sample cleanup with n-hexane and C_(18) solid-phase extraction cartridge, and quantitation by liquid chromatography with DAD detector. The linear range was 1~200 ng and the results showed a good linear relationship (r=0.9999). For spiked samples, the recoveries were above 90%, the relative standard deviations were 4.24%~7.36%,the limit of detection and limit of quantification were 9.1 μg/kg and 22.3 μg/kg, respectively.

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What this paper is about

A method for detecting florfenicol residue in eel muscle was established. Florfenicol residue was extracted from eel muscle with ethyl acetate, followed by sample cleanup with n-hexane and C_(18) solid-phase extraction cartridge, and quantitation by liquid chromatography with DAD detector. The linear range was 1~200 ng and the results showed a good linear relationship (r=0.9999). For spiked samples, the recoveries were above 90%, the relative standard deviations were 4.24%~7.36%,the limit of detection and limit of quantification were 9.1 μg/kg and 22.3 μg/kg, respectively.

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Available abstract

A method for detecting florfenicol residue in eel muscle was established. Florfenicol residue was extracted from eel muscle with ethyl acetate, followed by sample cleanup with n-hexane and C_(18) solid-phase extraction cartridge, and quantitation by liquid chromatography with DAD detector. The linear range was 1~200 ng and the results showed a good linear relationship (r=0.9999). For spiked samples, the recoveries were above 90%, the relative standard deviations were 4.24%~7.36%,the limit of detection and limit of quantification were 9.1 μg/kg and 22.3 μg/kg, respectively.

Key concepts: Florfenicol, Chemistry, Chromatography, Residue (chemistry), Detection limit, Cartridge, Ethyl acetate, Hexane

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