Citation: WANG Lijun, CAO Xumin, SUN Xiaoliang, WANG Shuting, LIU Jing, HAO Zhihui, QU Baohan, ZHAO Sijun. Rapid determination of 15 β ₂-agonists residues in swine urine by ultra performance liquid chromatography-tandem mass spectrometry coupled with molecularly imprinted solid phase extraction[J]. Chinese Journal of Chromatography, ;2016, 34(3): 240-248. doi: 10.3724/SP.J.1123.2015.11003 shu

Rapid determination of 15 β ₂-agonists residues in swine urine by ultra performance liquid chromatography-tandem mass spectrometry coupled with molecularly imprinted solid phase extraction

WANG Lijun ^1,2,3 ,
CAO Xumin ^2,3 ,
SUN Xiaoliang ^2,3 ,
WANG Shuting ^2,3 ,
LIU Jing ² ,
HAO Zhihui ¹ ,
QU Baohan ^1,, ,
ZHAO Sijun ^2,3,,

1.
1. School of Chemistry and Pharmaceutical Sciences, Qingdao Agricultural University, Qingdao 266109, China;
2.
2. Department for Safety Supervision of Animal Products, China Animal Health and Epidemiology Center, Qingdao 266032, China;
3.
3. Livestock and Poultry Products Quality and Safety Risk Assessment Laboratory, Ministry of Agriculture (Qingdao), Qingdao 266032, China

Corresponding author: QU Baohan, ZHAO Sijun,
Received Date: 2 November 2015

Fund Project: 国家畜禽质量安全风险评估项目(GJFP2015007) (GJFP2015007)中国动物卫生与流行病学中心创新基金项目(2014IF-0003FF). (2014IF-0003FF)

An ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method coupled with molecularly imprinted solid phase extraction (MISPE) for rapid determination of 15 β ₂-agonists residues in swine urine has been established. In order to obtain the optimized purification conditions, different pH values of loading, washing and elution solvents for the MISPE procedure were optimized. Finally, the swine urine samples (pH 7.0) were performed directly by MISPE column, then the column was washed with water, acetonitrile and 0.5%(v/v) acetic acid in acetonitrile, and eluted with 10%(v/v) acetic acid in methanol. Meanwhile, the parameters of UPLC-MS/MS have been optimized.The UPLC separation was performed on a BEH C₁₈ column, and eluted with the mobile phase consisting of 0.1%(v/v) formic acid aqueous solution and acetonitrile with linear gradient program. The analysis was in ESI positive ion scan mode and multiple reaction monitoring (MRM) mode. Under the optimum conditions, the blank swine urine was spiked with different concentrations analytes and taken for analysis to evaluate the established method. To highlight the advantage of MISPE, specificity adsorption for the 15 β ₂-agonists in swine urine was investigate. The linear ranges were 0.1-20 μ g/L for the 15 β ₂-agonists ( r ²≥0.992). The limits of detection (LODs) and the limits of quantification (LOQs) were 0.03 and 0.1 μ g/L, respectively. At the spiked levels of 0.1, 0.5 and 2.5 μ g/L in blank samples, the mean recoveries were 65.6%-115.0% with the relative standard deviations (RSDs, n=6) of 0.57%-16.1%. Overall, the proposed method is simple, quick, reliable,sensitive, and can be applied in large scale supervision of illegal usage of the 15 β ₂-agonists.
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Rapid determination of 15 β 2-agonists residues in swine urine by ultra performance liquid chromatography-tandem mass spectrometry coupled with molecularly imprinted solid phase extraction

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Rapid determination of 15 β ₂-agonists residues in swine urine by ultra performance liquid chromatography-tandem mass spectrometry coupled with molecularly imprinted solid phase extraction