Single-atom transition metals (Rh, Ir, Co) doped silicon carbide nanotubes (SiCNT) as nonenzymatic nitrotyrosine (NTS) sensor: Insight from theoretical calculations

[Display omitted] •Studies on nitrotyrosine (NTS) as a biomarker for Alzheimer disease.•NTS_Ir@SiCNT has the highest adsorption strength which lead to chemisorption.•Increase in work function and reactivity of the systems after the metal doping enhancement.•Ir@SiCNT metal surface displayed as a prom...

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Veröffentlicht in:Computational and theoretical chemistry 2023-09, Vol.1227, p.114250, Article 114250
Hauptverfasser: Okon, Gideon A., Ogungbemiro, Festus O., Louis, Hitler, Benjamin, Innocent, Agwamba, Ernest C., Adeyinka, Adedapo S.
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Sprache:eng
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Zusammenfassung:[Display omitted] •Studies on nitrotyrosine (NTS) as a biomarker for Alzheimer disease.•NTS_Ir@SiCNT has the highest adsorption strength which lead to chemisorption.•Increase in work function and reactivity of the systems after the metal doping enhancement.•Ir@SiCNT metal surface displayed as a promising drug biomarker surface. Transition metals Namely Rhodium (Rh), Iridium (Ir), and Cobalt (Co) doped silicon carbide nanotube (SiCNT) surfaces were theoretically investigated using first-principles density functional theory (DFT) at the B3LYP-GD3(BJ)/def2SVP computational level of theory to understand the biological adsorption, selectivity, reactivity and trapping efficacy of Nitrotyrosine (NTS) as a biomarker for Alzheimer disease. The different parameters and studies conducted showed that there was an increase in conductivity after doping of the metal impurities on SiCNT nanotubes on adsorption of the drugs there and was increase in adsorption strength which lead to chemisorption of the drug on metal-dope-doped surfaces with adsorption energies of −90.550 kcal/mol, −84.839 kcal/mol, −81.702 kcal/mol, and −34.952 kcal/mol corresponding to NTS_Ir@SiCNT, NTS_Co@SiCNT, NTS_Rh@S,iCNT and NTS_@SiCNT systems, hereby suggesting them as a promising biomarker system for Alzheimer disease control.
ISSN:2210-271X
DOI:10.1016/j.comptc.2023.114250