Compiègne University of Technology, CNRS UMR 6022, BP20529, Compiègne 60205, France.
Anal Chim Acta. 2012 Mar 2;717:7-20. doi: 10.1016/j.aca.2011.12.026. Epub 2011 Dec 22.
Biosensors are already well established in modern analytical chemistry, and have become important tools for clinical diagnostics, environmental analysis, production monitoring, drug detection or screening. They are based on the specific molecular recognition of a target molecule by a biological receptor such as an antibody or an enzyme. Synthetic biomimetic receptors like molecularly imprinted polymers (MIPs) have been shown to be a potential alternative to biomolecules as recognition element for biosensing. Produced by a templating process at the molecular level, MIPs are capable of recognizing and binding target molecules with similar specificity and selectivity to their natural analogues. One of the main challenges in MIP sensor development is the miniaturization of MIP structures and their interfacing with the transducer or with a microchip. Photostructuring appears thereby as one of the most suitable methods for patterning MIPs at the micro and nano scale, directly on the transducer surface. In the present review, a general overview on MIPs in biosensing applications is given, and the photopolymerization and photopatterning of MIPs are particularly described.
生物传感器在现代分析化学中已经得到了很好的应用,并已成为临床诊断、环境分析、生产监测、药物检测或筛选的重要工具。它们基于生物受体(如抗体或酶)对目标分子的特异性分子识别。已经证明,合成仿生受体如分子印迹聚合物(MIPs)作为生物传感的识别元件,可以替代生物分子。MIPs 通过在分子水平上的模板过程产生,能够以类似于天然类似物的特异性和选择性识别和结合目标分子。在 MIP 传感器的开发中,主要挑战之一是 MIP 结构的小型化及其与换能器或微芯片的接口。因此,光结构化成为在微纳尺度上直接在换能器表面对 MIP 进行图案化的最适合方法之一。在本综述中,概述了生物传感应用中的 MIP,并特别描述了 MIP 的光聚合和光图案化。