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采用分子印迹整体柱与高效液相色谱在线联用技术,同时定量测定环丙氨嗪和三聚氰胺。

Molecularly imprinted monolith coupled on-line with high performance liquid chromatography for simultaneous quantitative determination of cyromazine and melamine.

机构信息

Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, China.

出版信息

Analyst. 2011 Sep 21;136(18):3672-9. doi: 10.1039/c1an15086c. Epub 2011 Jul 25.

Abstract

We report a novel method for simultaneous determination of cyromazine and melamine based on a molecularly imprinted monolith on-line coupled with high performance liquid chromatography (HPLC). The imprinted monolith was prepared by in situ polymerization using 2,4-diamino-6-undecyl-1,3,5-triazine (DAUTA) as a mimic template. Due to the better solubility of DAUTA in chloroform, hydrogen bonds were effectively developed between the template and the functional monomer and resulted in the formation of highly specific cavities in the obtained imprinted monolith. With methanol as the loading solvent, cyromazine and melamine were both selectively retained by the obtained imprinted monolith, while the nonspecific adsorption on the non-imprinted monolith was negligible. The imprinted monolithic column was on-line coupled with HPLC for purification and concentration of the two analytes from milk samples. To minimize the peak broadening during the on-line transfer of the analytes from the imprinted monolith to the following analytical column, a successive desorption program was developed for the elution step, which enabled on-line stacking of the target compounds before being analyzed by HPLC. Low detection limits of 0.12 μg mL(-1) for melamine and 0.05 μg mL(-1) for cyromazine were achieved with only 0.3 mL of milk sample and a low sensitivity HPLC-UVD instrument. The method may be further extended to detect other analytes of interest in a large variety of samples.

摘要

我们报道了一种基于分子印迹整体柱在线高效液相色谱法同时测定三聚氰胺和环丙氨嗪的新方法。印迹整体柱是通过原位聚合制备的,以 2,4-二氨基-6-十一烷基-1,3,5-三嗪(DAUTA)为模拟模板。由于 DAUTA 在氯仿中的溶解度较好,模板和功能单体之间有效地形成了氢键,导致在所得印迹整体柱中形成了高度特异性的空腔。以甲醇为上样溶剂,环丙氨嗪和三聚氰胺均可被所得印迹整体柱选择性保留,而非印迹整体柱的非特异性吸附可忽略不计。印迹整体柱在线与 HPLC 联用,从牛奶样品中对两种分析物进行纯化和浓缩。为了最大限度地减少分析物从印迹整体柱在线转移到后续分析柱时的峰展宽,开发了一种用于洗脱步骤的连续洗脱程序,该程序可在 HPLC 分析之前对目标化合物进行在线浓缩。仅用 0.3 mL 牛奶样品和低灵敏度 HPLC-UVD 仪器,就可实现三聚氰胺的检测限为 0.12 μg mL(-1),环丙氨嗪的检测限为 0.05 μg mL(-1)。该方法可进一步扩展,用于检测各种样品中其他感兴趣的分析物。

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