Key Laboratory of Food Nutrition and Safety, Ministry of Education of China, Tianjin University of Science and Technology, Tianjin Economy and Technology Development Area, Tianjin, China.
Anal Bioanal Chem. 2013 Jul;405(19):6353-63. doi: 10.1007/s00216-013-7036-5. Epub 2013 Jun 18.
In this work, molecularly imprinted polymer (MIP) particles were synthesized using a semicovalent method based on a specific thermally reversible bond, and these particles were used for the rapid detection of the azo dye acid orange II. The imprinted polymers-which were prepared via the covalent reaction of 3-(triethoxysilyl)propyl isocyanate with the template molecules-were attached to the surface of silica-coated magnetic nanoparticles, and a simple thermal reaction was then performed to remove the templates, leaving spaces with specific noncovalent bonds for target re-recognition. The conditions for the synthesis of the MIP were optimized during the polymerization experiments to improve the adsorption capacity and selectivity. The resulting polymers were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, and transmission electron microscopy to confirm their structure. The MIPs were subjected to an online solid-phase extraction and a magnetic molecularly imprinted solid-phase extraction procedure. For both methods, all samples were prepared with spiking levels of 5.0, 10.0, and 15.0 μg kg(-1) using high-performance liquid chromatography with UV/vis detection; after the preconcentration of 50-mL sample solutions, the enhancement factors reached 710 and 629. The limits of detection (signal-to-noise ratio of 3) were 9.83 and 17.41 ng L(-1), with relative standard deviations (n = 9) of 6.72% and 8.25%, respectively, for a 4.0 μg L(-1) standard template solution. These two methods were developed to quantify trace acid orange II contents in food and environmental samples; the recoveries ranged from 72 to 105% and from 70 to 94%, respectively.
在这项工作中,采用基于特定热可逆键的半共价方法合成了分子印迹聚合物(MIP)颗粒,并用这些颗粒快速检测偶氮染料酸性橙 II。印迹聚合物是通过 3-(三乙氧基硅基)丙基异氰酸酯与模板分子的共价反应制备的,然后将其附着在涂覆有二氧化硅的磁性纳米颗粒的表面上,然后进行简单的热反应以除去模板,留下具有特定非共价键的空间用于目标重新识别。在聚合实验中优化了 MIP 的合成条件,以提高吸附能力和选择性。使用傅里叶变换红外光谱、扫描电子显微镜和透射电子显微镜对所得聚合物进行了表征,以确认其结构。将 MIP 进行在线固相萃取和磁性分子印迹固相萃取程序。对于这两种方法,所有样品均使用高效液相色谱法进行检测,用紫外/可见检测法进行预处理,添加浓度分别为 5.0、10.0 和 15.0μgkg(-1);在浓缩 50-mL 样品溶液后,增强因子分别达到 710 和 629。检出限(信噪比为 3)分别为 9.83 和 17.41ngL(-1),对于 4.0μg L(-1)标准模板溶液,相对标准偏差(n=9)分别为 6.72%和 8.25%。这两种方法用于定量食品和环境样品中的痕量酸性橙 II 含量;回收率范围分别为 72%至 105%和 70%至 94%。