Cranfield Health, Cranfield University, Cranfield, Bedfordshire MK43 0AL, UK.
Nanoscale. 2013 May 7;5(9):3733-41. doi: 10.1039/c3nr00354j. Epub 2013 Mar 15.
The synthesis of core-shell molecularly imprinted polymer nanoparticles (MIP NPs) has been performed using a novel solid-phase approach on immobilised templates. The same solid phase also acts as a protective functionality for high affinity binding sites during subsequent derivatisation/shell formation. This procedure allows for the rapid synthesis, controlled separation and purification of high-affinity materials, with each production cycle taking just 2 hours. The aim of this approach is to synthesise uniformly sized imprinted materials at the nanoscale which can be readily grafted with various polymers without affecting their affinity and specificity. For demonstration purposes we grafted anti-melamine MIP NPs with coatings which introduce the following surface characteristics: high polarity (PEG methacrylate); electro-activity (vinylferrocene); fluorescence (eosin acrylate); thiol groups (pentaerythritol tetrakis(3-mercaptopropionate)). The method has broad applicability and can be used to produce multifunctional imprinted nanoparticles with potential for further application in the biosensors, diagnostics and biomedical fields and as an alternative to natural receptors.
核壳型分子印迹聚合物纳米粒子(MIP NPs)的合成是采用一种新型的固相方法在固定模板上进行的。同样的固相在随后的衍生化/壳形成过程中也起到了高亲和力结合位点的保护功能。这种方法允许快速合成、控制分离和纯化高亲和力的材料,每个生产周期只需 2 小时。这种方法的目的是在纳米尺度上合成均匀尺寸的印迹材料,这些材料可以很容易地与各种聚合物接枝,而不会影响它们的亲和力和特异性。为了演示目的,我们将抗三聚氰胺 MIP NPs 接枝到具有以下表面特性的涂层上:高极性(甲基丙烯酸聚乙二醇酯);电活性(乙烯基二茂铁);荧光(曙红丙烯酰胺);巯基(季戊四醇四(3-巯基丙酸酯))。该方法具有广泛的适用性,可以用于制备多功能印迹纳米粒子,有望在生物传感器、诊断和生物医学领域进一步应用,并作为天然受体的替代品。