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      Electrospun fibrillary scaffold for electrochemical cell biomarkers detection

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          Abstract

          A novel scaffold for in situ electrochemical detection of cell biomarkers was developed using electrospun nanofibers and commercial adhesive polymeric membranes. The electrochemical sensing of cell biomarkers requires the cultivation of the cells on/near the (bio)sensor surface in a manner to preserve an appropriate electroactive available surface and to avoid the surface passivation and sensor damage. This can be achieved by employing biocompatible nanofiber meshes that allow the cells to have a normal behavior and do not alter the electrochemical detection. For a better mechanical stability and ease of handling, nylon 6/6 nanofibers were collected on commercial polymeric membranes, at an optimal fiber density, obtaining a double-layered platform. To demonstrate the functionality of the fabricated scaffold, the screening of cellular stress has been achieved integrating melanoma B16-F10 cells and the (bio)sensor components on the transducer whereas the melanin exocytosis was successfully quantified using a commercial electrode. Either directly on the surface of the (bio)sensor or spatially detached from it, the integration of cell cultures in biosensing platforms based on electrospun nanofibers represents a powerful bioanalytical tool able to provide real-time information about the biomarker release, enzyme activity or inhibition, and monitoring of various cellular events.

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          Supplementary Information

          The online version contains supplementary material available at 10.1007/s00604-024-06523-w.

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          Electrospinning of Nanofibers from Polymer Solutions and Melts

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            The role of fibroblast activation protein in health and malignancy

            Fibroblast activation protein-α (FAP) is a type-II transmembrane serine protease expressed almost exclusively to pathological conditions including fibrosis, arthritis, and cancer. Across most cancer types, elevated FAP is associated with worse clinical outcomes. Despite the clear association between FAP and disease severity, the biological reasons underlying these clinical observations remain unclear. Here we review basic FAP biology and FAP's role in non-oncologic and oncologic disease. We further explore how FAP may worsen clinical outcomes via its effects on extracellular matrix remodeling, intracellular signaling regulation, angiogenesis, epithelial-to-mesenchymal transition, and immunosuppression. Lastly, we discuss the potential to exploit FAP biology to improve clinical outcomes.
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              Recent Advances in Applications of Droplet Microfluidics

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                Author and article information

                Contributors
                adrian.enache@infim.ro
                Journal
                Mikrochim Acta
                Mikrochim Acta
                Mikrochimica Acta
                Springer Vienna (Vienna )
                0026-3672
                1436-5073
                29 June 2024
                29 June 2024
                2024
                : 191
                : 7
                : 435
                Affiliations
                [1 ]Functional Nanostructures Laboratory, National Institute of Materials Physics, ( https://ror.org/002ghjd91) Atomistilor Str. 405A, 077125 Magurele, Romania
                [2 ]Faculty of Physics, University of Bucharest, ( https://ror.org/02x2v6p15) Atomistilor Str. 405, 077125 Magurele, Romania
                Author information
                http://orcid.org/0000-0002-1848-6753
                Article
                6523
                10.1007/s00604-024-06523-w
                11217050
                38949689
                03ee96fc-5d10-4eaa-8cf4-e37d5f2b699e
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 March 2024
                : 21 June 2024
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100006595, Unitatea Executiva pentru Finantarea Invatamantului Superior, a Cercetarii, Dezvoltarii si Inovarii;
                Award ID: PN-III-P4-ID-PCE-2020-1403
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004616, Consiliul National al Cercetarii Stiintifice;
                Award ID: PC1- PN23080101
                Categories
                Original Paper
                Custom metadata
                © Springer-Verlag GmbH Austria, part of Springer Nature 2024

                Analytical chemistry
                electrospinning,nanofibers,scaffold,melanin,b16 cell line,electrochemical detection

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