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Electrodeposition of Silver Amalgam on Thin Gold Film Electrodes for Voltammetric Detection of 4-Nitrophenol and DNA Labeled with Osmium Tetroxide-Bipyridine Complex

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    0518368 - BFÚ 2020 RIV DE eng J - Journal Article
    Havranová-Vidláková, Pavlína - Ligmajer, Filip - Daňhel, Aleš
    Electrodeposition of Silver Amalgam on Thin Gold Film Electrodes for Voltammetric Detection of 4-Nitrophenol and DNA Labeled with Osmium Tetroxide-Bipyridine Complex.
    Electroanalysis. Roč. 31, č. 10 (2019), s. 1952-1960. ISSN 1040-0397. E-ISSN 1521-4109
    R&D Projects: GA ČR(CZ) GJ17-23634Y
    Institutional support: RVO:68081707
    Keywords : nucleic-acid * carbon * nanoparticles * electrochemistry
    OECD category: Analytical chemistry
    Impact factor: 2.544, year: 2019
    Method of publishing: Open access
    http://dspace.lib.vutbr.cz/xmlui/bitstream/11012/184643/1/2019%20Electroanalsis%20Havranova%20Preprint.pdf

    Alternative electrode materials suitable to prepare novel working electrode applicable in detecting biopolymers such as nucleic acids, proteins or glycoproteins, represent a significant contribution to bio-electroanalysis. Herein, electrodes made of vapor-deposited thin gold films (vAuE) were used as an alternative substrate for the electrodeposition of silver amalgam particles (AgAPs), next to indium tin oxide and pyrolytic graphite, which are already used. The conditions and parameters of double pulse chronoamperometry were optimized for the most-sensitive voltammetric detection of 4-nitrophenol (4-NP). The resulting electrodes were characterized by scanning electron microscope with energy dispersive X-ray spectroscopy. While 4-NP could not be detected by bare nonactivated vAuEs at all, their electrochemical activation offered a limit of detection (LoD) of 25 and 5 mu mol.l(-1) by means of CV and DPV, respectively. AgAP electrodeposited on vAuE, offered 2.5-times lower LoDs 10 mu mol.l(-1) by CV and comparable LoD 5 mu mol.l(-1) by DPV. Advantageously, AgAPs could be repeatedly deposited on and anodically dissolved from the vAuE with a relative standard deviation 13 % of the ten-times repeated DPV signal of 4-NP (100 mu mol.l(-1)). In comparison to vAuE, the vAuE-AgAP offered about 400 mV broader potential window, which allowed detection of single strand DNA fragment labeled by osmium tetroxide-bipyridine complex down to 2 ng.mu l(-1) by means of DPV.
    Permanent Link: http://hdl.handle.net/11104/0303524

     
     
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