Raising public awareness over the emerging health risk due to intake of arsenic-contaminated potable water is a matter of great concern. Exploration of cost-effective, self-testing kits is a substantial way to reach out to the masses and detect the presence of arsenate in water. With this agenda, a photoluminescent Mannich base Zn(II) complex (ZnMC = [Zn(ML)]·(ClO)·(HO); HML = Mannich base ligand) has been synthesized, and its dinuclearity was verified with single-crystal X-ray diffraction structural analysis. Among a range of anions, ZnMC was found to detect arsenate selectively by showing a turn-off emission with a color change from bright green to dark under UV light. The real-life applicability of the ZnMC probe is somewhat restricted to only sensing of arsenate, but not its removal owing to the fact of its homogeneity. Considering the efficacy of ZnMC as well as a need for its easy removal from water, slight modification has been done with chloride ions in the form of ZnMC″ (=[Zn(ML)(Cl)]), and finally, an interface between homogeneous and heterogeneous solid support has been explored with a strategic fabrication of ZnMC″ grafted ZnAlO, named as ZAZ nanomaterial. This not only imparts successful segregation of arsenate from drinking water but also provides naked-eye detection under ambient light as well as UV light. Thermodynamic parameters associated with the binding of arsenate to ZnMC and ZAZ have been evaluated through isothermal calorimetric (ITC) measurements. Steady-state and time-resolved fluorescence titration study, absorption titration study, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and computational calculations have been performed to get deep insights into the sensing properties. Proper justification of the sensing mechanism is the highlight of this work. ZAZ nanomaterial has been exploited to produce a self-test paper kit for arsenate detection with a limit of 9.86 ppb, which potentially enables applications in environmental monitoring.
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http://dx.doi.org/10.1021/acsami.2c04875 | DOI Listing |
Biomedicines
December 2024
Departamento de Ciência Básica, Instituto de Saúde de Nova Fribrugo, Universidade Federal Fluminense, Nova Friburgo 28625-650, RJ, Brazil.
Pyruvate kinase M2, a central regulator of cancer cell metabolism, has garnered significant attention as a promising target for disrupting the metabolic adaptability of tumor cells. This study explores the potential of the Mannich base derived from lawsone () to interfere with PKM2 enzymatic activity both in vitro and in silico. The antiproliferative potential of was tested using MTT assay in various cell lines, including SCC-9, Hep-G2, HT-29, B16-F10, and normal human gingival fibroblast (HGF).
View Article and Find Full Text PDFRSC Adv
December 2024
Petru Poni Institute of Macromolecular Chemistry, Department of Inorganic Polymers Iaşi 700487 Romania
A phenolic Mannich base derived from 1'-hydroxy-2'-acetonaphthone (HAN) as a substrate and morpholine as an amine reagent was synthesized and structurally characterized. The sensing ability toward various metal ions of the s-, p- and d-block of this molecule that has the binding site for metal ions in the starting -hydroxyphenone preserved was examined. Interaction between this phenolic Mannich base and Al, Cr, Cu and Co leads to modifications of the sensing molecule's absorption spectrum.
View Article and Find Full Text PDFInorg Chem
December 2024
MTA-SZTE Lendület Functional Metal Complexes Research Group, University of Szeged, Dóm tér 7-8, Szeged H-6720 , Hungary.
Drug resistance is a major obstacle in cancer treatment. Herein, four novel organometallic complexes, with the general formula [Ru(η--cymene)(HL)Cl]Cl and [Rh(η-CMe)(HL)Cl]Cl, were developed to target multidrug-resistant (MDR) cancer cells, where HL denotes 8-hydroxyquinoline-derived Mannich bases (HQCl-pyr and HQCl-pip). The aim of the complexation was to obtain compounds with improved drug-like properties.
View Article and Find Full Text PDFFree Radic Res
November 2024
Faculty of Chemistry, Belarusian State University, Minsk, Belarus.
Free radicals are ubiquitous in biological systems, being responsible for pathogenesis of degenerative diseases and participating in vitally important biochemical processes, which are mediated by radical regulatory agents. The effects of the aliphatic amine substituents in the catechol-derived Mannich bases on their antioxidant and pro-oxidant activity were investigated. It has been found that the presence of catechol moiety in the structure of Mannich bases allows them to act as Cu(II) reductants, efficient Fe(II) chelators and potent DPPH radical scavengers.
View Article and Find Full Text PDFChemMedChem
November 2024
Department of Chemistry of Bioactive Nitrogen-Containing Heterocyclic Bases, V. P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry of the NAS of Ukraine, Academika Kukharya Str. 1, 02094, Kyiv, Ukraine.
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