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      3,4-Methylenedioxypyrovalerone (MDPV) Sensing Based on Electropolymerized Molecularly Imprinted Polymers on Silver Nanoparticles and Carboxylated Multi-Walled Carbon Nanotubes

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          Abstract

          3,4-methylenedioxypyrovalerone (MDPV) is a harmful and controlled synthetic cathinone used as a psychostimulant drug and as sport-enhancing substance. A sensor was developed for the direct analysis of MDPV by transducing its oxidation signal by means of an electropolymerized molecularly imprinted polymer (e-MIP) built in-situ on the screen-printed carbon electrode’s (SPCE) surface previously covered with multi-walled carbon nanotubes (MWCNTs) and silver nanoparticles (AgNPs). Benzene-1,2-diamine was used as the functional monomer while the analyte was used as the template monomer. Each step of the sensor’s development was studied by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) in a solution containing ferricyanide, however no redox probe was required for the actual MDPV measurements. The interaction between the poly( o-phenylenediamine) imprinted polymer and MDPV was studied by density-functional theory (DFT) methods. The SPCE-MWCNT-AgNP-MIP sensor responded adequately to the variation of MDPV concentration. It was shown that AgNPs enhanced the electrochemical signal by around a 3-fold factor. Making use of square-wave voltammetry (SWV) the developed sensor provided a limit of detection (LOD) of 1.8 μmol L –1. The analytical performance of the proposed sensor paves the way to the development of a portable device for MDPV on-site sensing to be applied in forensic and doping analysis.

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          A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu.

          The method of dispersion correction as an add-on to standard Kohn-Sham density functional theory (DFT-D) has been refined regarding higher accuracy, broader range of applicability, and less empiricism. The main new ingredients are atom-pairwise specific dispersion coefficients and cutoff radii that are both computed from first principles. The coefficients for new eighth-order dispersion terms are computed using established recursion relations. System (geometry) dependent information is used for the first time in a DFT-D type approach by employing the new concept of fractional coordination numbers (CN). They are used to interpolate between dispersion coefficients of atoms in different chemical environments. The method only requires adjustment of two global parameters for each density functional, is asymptotically exact for a gas of weakly interacting neutral atoms, and easily allows the computation of atomic forces. Three-body nonadditivity terms are considered. The method has been assessed on standard benchmark sets for inter- and intramolecular noncovalent interactions with a particular emphasis on a consistent description of light and heavy element systems. The mean absolute deviations for the S22 benchmark set of noncovalent interactions for 11 standard density functionals decrease by 15%-40% compared to the previous (already accurate) DFT-D version. Spectacular improvements are found for a tripeptide-folding model and all tested metallic systems. The rectification of the long-range behavior and the use of more accurate C(6) coefficients also lead to a much better description of large (infinite) systems as shown for graphene sheets and the adsorption of benzene on an Ag(111) surface. For graphene it is found that the inclusion of three-body terms substantially (by about 10%) weakens the interlayer binding. We propose the revised DFT-D method as a general tool for the computation of the dispersion energy in molecules and solids of any kind with DFT and related (low-cost) electronic structure methods for large systems.
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            • Record: found
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            VMD: Visual molecular dynamics

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              • Record: found
              • Abstract: not found
              • Article: not found

              Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

                Bookmark

                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Nanomaterials (Basel)
                Nanomaterials (Basel)
                nanomaterials
                Nanomaterials
                MDPI
                2079-4991
                01 February 2021
                February 2021
                : 11
                : 2
                : 353
                Affiliations
                [1 ]REQUIMTE, LAQV, Laboratory of Applied Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-213 Porto, Portugal; rcouto@ 123456ff.up.pt (R.A.S.C.); tino44coelho@ 123456gmail.com (C.C.)
                [2 ]Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo (USP), São Paulo, SP 05508-000, Brazil; bassim.mounssef@ 123456usp.br (B.M.J.); sara.famorais@ 123456usp.br (S.F.d.A.M.); ataualpa@ 123456iq.usp.br (A.A.C.B.)
                [3 ]Departamento de Química, Universidade Federal dos Vales do Jequitinhonha e Mucuri, Diamantina, MG 39100-000, Brazil; camila.lima@ 123456ufvjm.edu.br
                [4 ]Departamento de Farmácia, Universidade Federal dos Vales do Jequitinhonha e Mucuri, Diamantina, MG 39100-000, Brazil; wallanst@ 123456ufvjm.edu.br
                [5 ]REQUIMTE, UCIBIO, Laboratory of Toxicology, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, 4050-213 Porto, Portugal; felixdc@ 123456ff.up.pt
                [6 ]Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, 1649-003 Lisbon, Portugal; cmprodrigues@ 123456ff.ulisboa.pt
                Author notes
                [* ]Correspondence: lmgoncalves@ 123456iq.usp.br (L.M.G.); bquinaz@ 123456ff.up.pt (M.B.Q.)
                Author information
                https://orcid.org/0000-0001-5209-5986
                https://orcid.org/0000-0001-6585-9930
                https://orcid.org/0000-0003-3858-3494
                https://orcid.org/0000-0002-4829-754X
                https://orcid.org/0000-0001-7392-3701
                https://orcid.org/0000-0002-4290-656X
                Article
                nanomaterials-11-00353
                10.3390/nano11020353
                7912732
                33535439
                f5a88dcd-291c-49db-a678-5818b629df18
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 22 December 2020
                : 25 January 2021
                Categories
                Article

                analytical chemistry,‘bath salts’,biomimetics,drug analysis,electropolymerization,electroanalysis,forensic chemistry,modified electrodes,new psychoactive substances (nps),o-phenylenediamine

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