Department of Chemistry, Memorial University of Newfoundland, Canada.
Department of Chemistry, Memorial University of Newfoundland, Canada.
Anal Chim Acta. 2021 Dec 1;1187:339135. doi: 10.1016/j.aca.2021.339135. Epub 2021 Oct 1.
Molecularly imprinted polymers (MIPs) have become an important class of materials for selective and efficient adsorption of target analytes. Despite versatility of MIPs for fabrication in numerous formats, these materials have been primarily reported as solid phase extraction packing materials. An effective thin film MIP prepared on stainless steel substrate is reported here for high throughput enrichment of organophosphorus pesticides (OPPs) from water and beverage samples followed by liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis. The key factors controlling performance as well as best practices for optimized fabrication of thin film MIPs are presented. A pseudo-phase diagram is introduced to evaluate and predict the effect of the ratio of porogen (solvent, 1-octanol) volume to relative crosslinker mass on the desired polymer features (i.e., porosity, surface area, capacity, and selectivity). At low porogen ratios, a macroporous polymer with insignificant selectivity is formed, whereas at high porogen ratios a micro-gel polymer with superior selectivity towards targets is obtained. The porosity and morphology determined with nitrogen adsorption and scanning electron microscopy were attributed to specific regions in the pseudo-phase diagram. Other factors influencing selectivity and stability of the polymer, such as type of the template and its ratios with monomer (methacrylic acid) and crosslinker (ethylene glycol dimethacrylate) were optimized. The prepared thin film MIPs were characterized using adsorption isotherms and adsorption kinetics, and evaluated for matrix effects (high humic acid content) and cross-reactivity in presence of other pesticides and pharmaceuticals. The optimized method provided limits of quantitation (LOQs) ranged from 0.002 to 0.02 ng mL in water and from 0.095 to 0.48 ng g in apple juice. Regarding inter-device variability (CV∼10% without normalization), excellent linearity (R > 0.99), satisfactory accuracies (90-110%) and precisions (<15%) were obtained.
分子印迹聚合物(MIPs)已成为一种用于选择性和高效吸附目标分析物的重要材料。尽管 MIPs 具有多种形式的制造通用性,但这些材料主要被报道为固相萃取填充材料。本文报道了一种在不锈钢基底上制备的有效薄膜 MIP,用于高通量从水和饮料样品中富集有机磷农药(OPPs),然后进行液相色谱串联质谱(LC-MS/MS)分析。介绍了关键因素控制性能以及优化薄膜 MIP 制造的最佳实践。引入了伪相图来评估和预测致孔剂(溶剂,1-辛醇)体积与相对交联剂质量比对所需聚合物特性(即孔隙率、表面积、容量和选择性)的影响。在低致孔剂比的情况下,形成具有不重要选择性的大孔聚合物,而在高致孔剂比的情况下,形成具有对目标物具有优异选择性的微凝胶聚合物。氮气吸附和扫描电子显微镜确定的孔隙率和形态归因于伪相图中的特定区域。影响聚合物选择性和稳定性的其他因素,如模板的类型及其与单体(甲基丙烯酸)和交联剂(乙二醇二甲基丙烯酸酯)的比例,也进行了优化。使用吸附等温线和吸附动力学对制备的薄膜 MIP 进行了表征,并评估了其在高腐殖酸含量和存在其他农药和药物时的基质效应和交叉反应性。优化方法提供了在水中的定量限(LOQ)范围为 0.002 至 0.02 ng mL,在苹果汁中为 0.095 至 0.48 ng g。关于设备间变异性(无归一化时 CV∼10%),获得了极好的线性(R>0.99)、令人满意的准确度(90-110%)和精密度(<15%)。