2012Zhongguo jiaqinRequires access

Residues Detection of Dehydroacetic Acid in Chicken Tissues by High Performance Liquid Chromatography

Yumei Zhang

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Abstract

A high performance liquid chromatography(HPLC)method was established to determine the residues of dehydroacetic acid(DHA)in chicken tissues.The tissue samples(muscle,liver and kidney)were extracted with acetonitrile,liquid-liquid extraction by hexane,purified by PAX solid phase extraction column.A C18 column with ultraviolet absorption detection at 290 nm,using methanol-water which includes 0.02% ammonium acetate(20/80,v/v)as eluent was used in HPLC.A linear calibration curve with coefficient relation(R2≥0.9996)in the range of 0.2 to 5.0 mg/L of DHA concentration was made.When DHA was added to tissues at dose of 0.5,1.0 and 5.0 mg/kg,the average recoveries in different tissues were ranged from 68.28% to 93.49%,with CV% ranged from 3.38% to 7.94% within-day and 4.31% to 7.80% between-day.The limit of detection and limit of quantitation of DHA were observed at 0.1 mg/kg and 0.2 mg/kg respectively.The established method was suitable for the determination of DHA residues in animal foods,be also useful to the investigation of DHA depletion,the maximum residue limit and its withdraw time.

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What this paper is about

A high performance liquid chromatography(HPLC)method was established to determine the residues of dehydroacetic acid(DHA)in chicken tissues.The tissue samples(muscle,liver and kidney)were extracted with acetonitrile,liquid-liquid extraction by hexane,purified by PAX solid phase extraction column.A C18 column with ultraviolet absorption detection at 290 nm,using methanol-water which includes 0.02% ammonium acetate(20/80,v/v)as eluent was used in HPLC.A linear calibration curve with coefficient relation(R2≥0.9996)in the range of 0.2 to 5.0 mg/L of DHA concentration was made.When DHA was added to tissues at dose of 0.5,1.0 and 5.0 mg/kg,the average recoveries in different tissues were ranged from 68.28% to 93.49%,with CV% ranged from 3.38% to 7.94% within-day and 4.31% to 7.80% between-day.The limit of detection and limit of quantitation of DHA were observed at 0.1 mg/kg and 0.2 mg/kg respectively.The established method was suitable for the determination of DHA residues in animal foods,be also useful to the investigation of DHA depletion,the maximum residue limit and its withdraw time.

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Available abstract

A high performance liquid chromatography(HPLC)method was established to determine the residues of dehydroacetic acid(DHA)in chicken tissues.The tissue samples(muscle,liver and kidney)were extracted with acetonitrile,liquid-liquid extraction by hexane,purified by PAX solid phase extraction column.A C18 column with ultraviolet absorption detection at 290 nm,using methanol-water which includes 0.02% ammonium acetate(20/80,v/v)as eluent was used in HPLC.A linear calibration curve with coefficient relation(R2≥0.9996)in the range of 0.2 to 5.0 mg/L of DHA concentration was made.When DHA was added to tissues at dose of 0.5,1.0 and 5.0 mg/kg,the average recoveries in different tissues were ranged from 68.28% to 93.49%,with CV% ranged from 3.38% to 7.94% within-day and 4.31% to 7.80% between-day.The limit of detection and limit of quantitation of DHA were observed at 0.1 mg/kg and 0.2 mg/kg respectively.The established method was suitable for the determination of DHA residues in animal foods,be also useful to the investigation of DHA depletion,the maximum residue limit and its withdraw time.

Key concepts: Chromatography, Detection limit, High-performance liquid chromatography, Chemistry, Residue (chemistry), Extraction (chemistry), Dehydroacetic acid, Ammonium acetate

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