2010•Guangdong nongye kexueOpen access

Determination of ten β-agonists in feeds by high performance liquid chromatography-tandem mass spectrometry

HU Cui-ping

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Abstract

A high performance liquid chromatography-tandem mass spectrometry method was established for the determination of ten β-agonists in feeds.β-agonists in sample were extracted by perchloric acid solution,purified and concentrated by HLB column.A C18 column was used to separate the β-agonists.Qualitative and quantitative analysis of ten β-agonists which ionized by electrospray ionization interface(ESI) was carried out by multiple reaction monitoring mode(MRM).The calibration curve was linear over the concentration range of 0.5~40.0 μg/L(r0.999).The recoveries ranged from 71.2% to 103% at the spiked level of 0.01,0.02,0.1,0.5 mg/kg.The relative standard deviations were between 3.7% and 9.8%.The limit of quantitation was 0.01 mg/kg.

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A high performance liquid chromatography-tandem mass spectrometry method was established for the determination of ten β-agonists in feeds.β-agonists in sample were extracted by perchloric acid solution,purified and concentrated by HLB column.A C18 column was used to separate the β-agonists.Qualitative and quantitative analysis of ten β-agonists which ionized by electrospray ionization interface(ESI) was carried out by multiple reaction monitoring mode(MRM).The calibration curve was linear over the concentration range of 0.5~40.0 μg/L(r0.999).The recoveries ranged from 71.2% to 103% at the spiked level of 0.01,0.02,0.1,0.5 mg/kg.The relative standard deviations were between 3.7% and 9.8%.The limit of quantitation was 0.01 mg/kg.

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Available abstract

A high performance liquid chromatography-tandem mass spectrometry method was established for the determination of ten β-agonists in feeds.β-agonists in sample were extracted by perchloric acid solution,purified and concentrated by HLB column.A C18 column was used to separate the β-agonists.Qualitative and quantitative analysis of ten β-agonists which ionized by electrospray ionization interface(ESI) was carried out by multiple reaction monitoring mode(MRM).The calibration curve was linear over the concentration range of 0.5~40.0 μg/L(r0.999).The recoveries ranged from 71.2% to 103% at the spiked level of 0.01,0.02,0.1,0.5 mg/kg.The relative standard deviations were between 3.7% and 9.8%.The limit of quantitation was 0.01 mg/kg.

Key concepts: Chromatography, Chemistry, Calibration curve, Electrospray ionization, Selected reaction monitoring, Perchloric acid, Mass spectrometry, Tandem mass spectrometry

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