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采用人工模板印迹固相萃取与表面增强拉曼光谱快速分析猪组织中的莱克多巴胺。

Rapid analysis of ractopamine in pig tissues by dummy-template imprinted solid-phase extraction coupling with surface-enhanced Raman spectroscopy.

机构信息

School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275, China.

School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275, China.

出版信息

Talanta. 2015 Jun 1;138:40-45. doi: 10.1016/j.talanta.2015.02.003. Epub 2015 Feb 9.

DOI:10.1016/j.talanta.2015.02.003
PMID:25863369
Abstract

Ritodrine has similar skeleton structure to ractopamine and it was selected as the dummy-template molecule to synthesize the molecular imprinted polymers (MIPs). The MIPs exhibited better selectivity to ractopamine than to the dummy-template molecule: the imprint factor for ractopamine was 8.9, while 7.6 for ritodrine. The MIPs were used as sorbents in solid-phase extraction for selective enrichment of ractopamine, and some key parameters were optimized. After that, a rapid surface-enhanced Raman spectroscopy method was developed for analysis of ractopamine and isoxuprine in pig tissue samples. Under the optimal conditions, good linearity was achieved in the range of 20.0-200.0 μg/L for ractopamine and isoxsuprine at 842 cm(-1) and 993 cm(-1), respectively. The limits of detection were 3.1-4.3 μg/L, which were lower than the maximum allowed by U. S. Food and Drug Administration. The recoveries of ractopamine and isoxsuprine were 72.4-79.7% and 71.0-78.2% for the spiked pork and pig liver, respectively, while the relative standard deviations ranging from 7.4% to 13.0%. The results suggest that the proposed method is sensitive and selective, and it has good potential on the quantitative analysis of trace amounts of β-agonists in complex samples.

摘要

利托君与莱克多巴胺具有相似的骨架结构,因此被选为合成分子印迹聚合物(MIPs)的虚拟模板分子。MIPs 对莱克多巴胺的选择性优于虚拟模板分子:莱克多巴胺的印迹因子为 8.9,而利托君为 7.6。MIPs 被用作固相萃取中的吸附剂,用于选择性富集莱克多巴胺,并对一些关键参数进行了优化。然后,建立了一种快速表面增强拉曼光谱法,用于分析猪组织样品中的莱克多巴胺和异噁唑啉。在最佳条件下,在 20.0-200.0 μg/L 范围内,莱克多巴胺和异噁唑啉在 842 cm(-1) 和 993 cm(-1) 处均具有良好的线性关系。莱克多巴胺和异噁唑啉的检出限分别为 3.1-4.3 μg/L,低于美国食品和药物管理局规定的最大值。莱克多巴胺和异噁唑啉在猪肉和猪肝中的加标回收率分别为 72.4-79.7%和 71.0-78.2%,相对标准偏差在 7.4%-13.0%之间。结果表明,该方法灵敏、选择性好,在复杂样品中痕量 β-激动剂的定量分析中具有良好的应用潜力。

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