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      Molecularly imprinted polymers - towards electrochemical sensors and electronic tongues

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          Abstract

          <p id="Par1">Molecularly imprinted polymers (MIPs) are artificially synthesized materials to mimic the molecular recognition process of biological macromolecules such as substrate-enzyme or antigen-antibody. The combination of these biomimetic materials with electrochemical techniques has allowed the development of advanced sensing devices, which significantly improve the performance of bare or catalyst-modified sensors, being able to unleash new applications. However, despite the high selectivity that MIPs exhibit, those can still show some cross-response towards other compounds, especially with chemically analogous (bio)molecules. Thus, the combination of MIPs with chemometric methods opens the room for the development of what could be considered a new type of electronic tongues, i.e. sensor array systems,  based on its usage. In this direction, this review provides an overview of the more common synthetic approaches, as well as the strategies that can be used to achieve the integration of MIPs and electrochemical sensors, followed by some recent examples over different areas in order to illustrate the potential of such combination in very diverse applications. </p><p id="Par2"> <div class="figure-container so-text-align-c"> <img alt="" class="figure" src="/document_file/4b54739a-0ce5-498d-a23c-b0e55cd7246f/PubMedCentral/image/216_2021_3313_Figa_HTML"/> </div> </p>

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          Most cited references108

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          Impedance Spectroscopy

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            Molecularly imprinted polymers and their use in biomimetic sensors.

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              Electrochemical sensor and biosensor platforms based on advanced nanomaterials for biological and biomedical applications.

              Introduction of novel functional nanomaterials and analytical technologies signify a foremost possibility for the advance of electrochemical sensor and biosensor platforms/devices for a broad series of applications including biological, biomedical, biotechnological, clinical and medical diagnostics, environmental and health monitoring, and food industries. The design of sensitive and selective electrochemical biological sensor platforms are accomplished conceivably by offering new surface modifications, microfabrication techniques, and diverse nanomaterials with unique properties for in vivo and in vitro medical analysis via relating a sensibly planned electrode/solution interface. The advantageous attributes such as low-cost, miniaturization, energy efficient, easy fabrication, online monitoring, and the simultaneous sensing capability are the driving force towards continued growth of electrochemical biosensing platforms, which have fascinated the interdisciplinary research arenas spanning chemistry, material science, biological science, and medical industries. The electrochemical biosensor platforms have potential applications in the early-stage detection and diagnosis of disease as stout and tunable diagnostic and therapeutic systems. The key aim of this review is to emphasize the newest development in the design of sensing and biosensing platforms based on functional nanomaterials for biological and biomedical applications. High sensitivity and selectivity, fast response, and excellent durability in biological media are all critical aspects which will also be wisely addressed. Potential applications of electrochemical sensor and biosensor platforms based on advanced functional nanomaterials for neuroscience diagnostics, clinical, point-of-care diagnostics and medical industries are also concisely presented.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Analytical and Bioanalytical Chemistry
                Anal Bioanal Chem
                Springer Science and Business Media LLC
                1618-2642
                1618-2650
                April 30 2021
                Article
                10.1007/s00216-021-03313-8
                70620387-f3a3-4282-b224-f8e9b59a1339
                © 2021

                Free to read

                https://www.springer.com/tdm

                https://www.springer.com/tdm

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