分子印迹聚合物
纳米技术
灵活性(工程)
计算机科学
生物传感器
分析物
生化工程
材料科学
化学
工程类
生物化学
统计
数学
物理化学
选择性
催化作用
作者
Robert D. Crapnell,Nina Dempsey‐Hibbert,Marloes Peeters,Ascanio Tridente,Craig E. Banks
出处
期刊:Talanta open
[Elsevier BV]
日期:2020-10-28
卷期号:2: 100018-100018
被引量:119
标识
DOI:10.1016/j.talo.2020.100018
摘要
Electrochemical biosensors for the detection of vital biomarkers is a well-established technology that utilises a transducer and recognition element in tandem to determine the presence of an analyte. There is growing interest in using Molecularly Imprinted Polymers (MIPs) as recognition elements in a wide range of sensing devices due to their economic viability and scalability. The inherent properties of polymer platforms, alongside the vast array of monomeric options, synthetic routes and incorporation strategies allow for the production of a multitude of sensitive and selective recognition elements that have significant advantages over classically utilised biological entities. MIPs exhibit superior chemical and thermal stability offering a wider variety of immobilization/incorporation strategies, virtually unlimited ambient shelf-life and a longer product lifetime, whilst the vast array of monomers available offer flexibility to their synthesis. Even though some sensor platforms have been reported for the detection of vital biomarkers, the use of MIPs has a number of challenges and drawbacks that need to be overcome in order to produce sensing platforms with the required sensitivity and specificity for clinical use. In this review, we will provide an overview of the reasoning behind using MIPs as recognition elements in electrochemical biosensors for vital biomarkers, discuss the problems synergizing MIPs and electrochemical read-out strategies and offer insights into the future perspectives of this promising and innovative technology.
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