| Literature DB >> 35077645 |
Eleonora Macchia1, Fabrizio Torricelli2, Paolo Bollella3,4, Lucia Sarcina3, Angelo Tricase3, Cinzia Di Franco5, Ronald Österbacka1, Zsolt M Kovács-Vajna2, Gaetano Scamarcio5,6, Luisa Torsi1,3,4.
Abstract
Bioelectronic transducing surfaces that are nanometric in size have been the main route to detect single molecules. Though enabling the study of rarer events, such methodologies are not suited to assay at concentrations below the nanomolar level. Bioelectronic field-effect-transistors with a wide (μm2-mm2) transducing interface are also assumed to be not suited, because the molecule to be detected is orders of magnitude smaller than the transducing surface. Indeed, it is like seeing changes on the surface of a one-kilometer-wide pond when a droplet of water falls on it. However, it is a fact that a number of large-area transistors have been shown to detect at a limit of detection lower than femtomolar; they are also fast and hence innately suitable for point-of-care applications. This review critically discusses key elements, such as sensing materials, FET-structures, and target molecules that can be selectively assayed. The amplification effects enabling extremely sensitive large-area bioelectronic sensing are also addressed.Entities:
Mesh:
Year: 2022 PMID: 35077645 DOI: 10.1021/acs.chemrev.1c00290
Source DB: PubMed Journal: Chem Rev ISSN: 0009-2665 Impact factor: 60.622