Combined solid-phase microextraction and high-performance liquid chromatography with ultroviolet detection for simultaneous analysis of clenbuterol, salbutamol and ractopamine in pig samples

被引:39
作者
Du, Wei [1 ]
Zhang, Siruo [2 ]
Fu, Qiang [1 ]
Zhao, Gang [1 ]
Chang, Chun [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Pharmaceut Sci, Xian 710061, Peoples R China
[2] Dalian Med Univ, Dept Microbiol, Dalian 116044, Peoples R China
关键词
solid-phase microextraction; high-performance liquid chromatography-ultraviolet detection; clenbuterol; salbutamol; ractopamine; LINKED-IMMUNOSORBENT-ASSAY; MASS-SPECTROMETRY; BETA-AGONISTS; IMPRINTED POLYMER; WATER SAMPLES; BOVINE URINE; GC-MS; RESIDUES; EXTRACTION; QUANTITATION;
D O I
10.1002/bmc.2993
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple and sensitive method based on the combination of solid-phase microextraction (SPME) and high-performance liquid chromatography with ultroviolet detection was developed for the simultaneous determination of clenbuterol, salbutamol and ractopamine in pig samples. Parameters of the SPME procedure affecting extraction efficiency, such as the type of fiber, extraction time, extraction temperature, ion strength, pH of sample and stirring rate, were optimized. The developed method was validated according to the International Conference on Harmonization guidelines. The calibration curves were linear over a range of 0.5-50 mu g/L for clenbuterol and ractopamine, and 0.2-20 mu g/L for salbutamol. The limits of detection were 0.1 mu g/L for clenbuterol, 0.05 mu g/L for salbutamol and 0.1g/L for ractopamine, respectively. The averages of intra- and inter-day accuracy ranged from 79.8 to 92.4%. The intra-day and inter-day precision were below 9.6% for the three analytes. This method exhibited the advantages of simplicity, rapidity and low solvent consumption, and was suitable for the monitoring of (2)-agonists residue in pig samples. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:1775 / 1781
页数:7
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