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Uniform molecularly imprinted microspheres and nanoparticles prepared by precipitation polymerization: The control of particle size suitable for different analytical applications

机译:通过沉淀聚合制备的均一的分子印迹微球和纳米颗粒:粒径控制,适合不同的分析应用

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Molecularly imprinted polymers (MIPs) are being increasingly used as selective adsorbents in different analytical applications. To satisfy the different application purposes, MEN with well controlled physical forms in different size ranges are highly desirable. For examples, MIP nanoparticles are very suitable to be used to develop binding assays and for microfluidic separations, whereas MIP beads with diameter of 1.5-3 mu m can be more appropriate to use in new analytical liquid chromatography systems. Previous studies have demonstrated that imprinted microspheres and nanoparticles can be synthesized using a simple precipitation polymerization method. Despite that the synthetic method is straightforward, the final particle size obtained has been difficult to adjust for a given template. In this work, we initiated to study new synthetic conditions to obtain MIP beads with controllable size in the nano- to micro-meter range, using racemic propranolol as a model template. Varying the composition of the cross-linking monomer allowed the particle size of the MIP beads to be altered in the range of 130 nm to 2.4 mu m, whereas the favorable binding property of the imprinted beads remained intact. The chiral recognition sites were further characterized with equilibrium binding analysis using tritium-labeled (S)-propranolol as a tracer. In general, the imprinted sites displayed a high chiral selectivity: the apparent affinity of the (S)-imprinted sites for (S)-propranolol was 20 times that of for (R)-propranolol. Compared to previously reported irregular particles, the chiral selectivity of competitive radioligand binding assays developed from the present imprinted beads has been increased by six to seven folds in an optimized aqueous solvent. (c) 2006 Elsevier B.V. All rights reserved.
机译:分子印迹聚合物(MIP)在不同的分析应用中越来越多地用作选择性吸附剂。为了满足不同的应用目的,非常需要在不同尺寸范围内具有良好控制的物理形式的MEN。例如,MIP纳米粒子非常适合用于开发结合测定和微流体分离,而直径为1.5-3μm的MIP珠子更适合用于新型分析型液相色谱系统。先前的研究表明,可以使用简单的沉淀聚合方法合成印迹的微球和纳米颗粒。尽管合成方法很简单,但是对于给定的模板,很难调节最终的粒径。在这项工作中,我们开始研究新的合成条件,以消旋普萘洛尔为模型模板,获得纳米级至微米级尺寸可控制的MIP珠。交联单体的组成的变化允许MIP珠粒的粒径在130nm至2.4μm的范围内变化,而压印珠粒的有利的粘合性质保持不变。使用equilibrium标记的(S)-心得安作为示踪剂,通过平衡结合分析进一步表征手性识别位点。通常,印迹位点显示出高的手性选择性:(S)印迹位点对(S)-普萘洛尔的表观亲和力是(R)-普萘洛尔的表观亲和力。与以前报道的不规则颗粒相比,由本发明印迹珠子开发的竞争性放射性配体结合测定的手性选择性在优化的水性溶剂中提高了六到七倍。 (c)2006 Elsevier B.V.保留所有权利。

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