2014Journal of Instrumental AnalysisRequires access

Preparation and Application of Immunoaffinity Column for Ractopamine,Salbutamol and Clenbuterol

Li‐Qing Yu

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Abstract

The anti-ractopamine monoclonal antibody and anti-clenbuterol monoclonal antibody were both coupled with CNBr activated Sepharose 4B to make the immunoaffinity column. The column performance was tested and the use conditions were optimized by HPLC-MS /MS. The results showed that the column capacity to ractopamine,salbutamol and clenbuterol were 49,27,24 ng /mL glue,respectively,the storage time was five months,and the best eluent was methanol. The average recoveries of three lean meat essences ranged from 78. 9% to 96. 5% with relative standard deviations( RSD) lower than 1. 5%. The limits of detection( LOD) ranged from 0. 1 ng/g to 1 ng/g. The method could be applied in the simultaneous determination of the lean meat essence contents in feed samples.

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What this paper is about

The anti-ractopamine monoclonal antibody and anti-clenbuterol monoclonal antibody were both coupled with CNBr activated Sepharose 4B to make the immunoaffinity column. The column performance was tested and the use conditions were optimized by HPLC-MS /MS. The results showed that the column capacity to ractopamine,salbutamol and clenbuterol were 49,27,24 ng /mL glue,respectively,the storage time was five months,and the best eluent was methanol. The average recoveries of three lean meat essences ranged from 78. 9% to 96. 5% with relative standard deviations( RSD) lower than 1. 5%. The limits of detection( LOD) ranged from 0. 1 ng/g to 1 ng/g. The method could be applied in the simultaneous determination of the lean meat essence contents in feed samples.

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Available abstract

The anti-ractopamine monoclonal antibody and anti-clenbuterol monoclonal antibody were both coupled with CNBr activated Sepharose 4B to make the immunoaffinity column. The column performance was tested and the use conditions were optimized by HPLC-MS /MS. The results showed that the column capacity to ractopamine,salbutamol and clenbuterol were 49,27,24 ng /mL glue,respectively,the storage time was five months,and the best eluent was methanol. The average recoveries of three lean meat essences ranged from 78. 9% to 96. 5% with relative standard deviations( RSD) lower than 1. 5%. The limits of detection( LOD) ranged from 0. 1 ng/g to 1 ng/g. The method could be applied in the simultaneous determination of the lean meat essence contents in feed samples.

Key concepts: Ractopamine, Clenbuterol, Chemistry, Chromatography, Salbutamol, Affinity chromatography, Monoclonal antibody, Column chromatography

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Preparation and Application of Immunoaffinity Column for Ractopamine,Salbutamol and Clenbuterol — Research Paper | ScholarLens