Surface-imprinted biosensors for the detection of proteins, cancer markers and viruses

Abstract

Biosensors using artificial recognition elements have generated intensive interest from scientists and medical professionals in recent years. Their high stability and sensitivity make them easier and less costly to use, store, and manufacture than sensors based on biological recognition elements. Surfaceimprinted sensors using the organic self-assembled monolayers (SAMs) of functionalized oligomers on gold surfaces have the advantages of high contact areas, fast response, easy construction, as well as integration of the recognition element with the transducer, all of which can lead to high sensitivity. The possibility of using SAM molecules with different end groups offers the flexibility of changing the affinity of the sensor to the target biomolecules while modification of the gold surface roughness enables imprinting bio-macromolecules much larger than the length of the SAM molecules. Co-dissolution of the bio-macromolecules and the organic molecules in a blend of aqueous/organic solvents ensures the formation of SAMs and at the same time maintains the viability and configuration of the biomacromolecules. Hence the synergy established between the substrate topography, the surface chemistry, the imprinted SAM, and the molecular structure of the analyte is the essential element for the successful construction of the biosensor. This review article focuses on the recent achievements in the development of the surface-imprinted biosensors for proteins, cancer markers and viruses, from multiple groups working in this area.

A chip-based potentiometric sensor for a Zika virus diagnostic using 3D surface molecular imprinting

“…Chip-based biosensing methods are a promising technique for detecting analytes and make wireless transmission of test results possible for remote regions. 51,[53][54][55][56][57][58][59][60] These devices provide results quickly, are relatively inexpensive, portable, and have the capability of being integrated into smart responsive biomedical systems. 59 This MI technique was first introduced in 2003 when octadecyltrichlorosilane (OTS) self-assembled monolayers (SAM) and chiral templates were co-adsorbed on indium-tin oxide (ITO) electrodes to detect amino acids.…”