ABSTRACT
The intrinsic toxicity of heavy metal ions to human health or other species calls for the need to develop an analytical tool for the easy and rapid detection of these ions based on inexpensive and stable nanomaterials. This article describes the potential utility of stable Cu nanoparticles (CuNPs) in the detection of toxic metal ions by solution and paper strip-based methods. For this, first, a dodecyl sulfate ion-stabilized CuNP (DS-CuNP) colloid was synthesized by a chemical reduction method. This was followed by treating the dispersion with heavy metal ions and monitoring the spectral change by spectrophotometric and colorimetric techniques. Among a host of metal ions, Hg2+, Cd2+, and Pb2+ have been found to significantly affect the surface plasmon resonance band of CuNPs by concomitantly altering the color of its solution. Notably, the brownish color of CuNP solution changed readily to milky white in the presence of Hg2+. Furthermore, the fabricated brownish-yellow test paper strips containing DS-CuNPs transformed to a prominent white color in the presence of a few drops of Hg2+ solution. This change in color of the paper strips could be visually detected by the naked eye. The experiments involving the detection of the various ions were carried out by optimizing the experimental conditions qualitatively as well as quantitatively. The limit of detection of the analytes (metal ions) has been found to be 10 µM. Routine analytical techniques like UV-vis spectroscopy, dynamic light scattering, transmission electron microscopy, and Fourier transform infrared spectroscopy formed part of the experiments.
ABSTRACT
A novel water soluble five coordinate oxovanadium(IV) complex, [VO(C16H15N4O8S)HSO4] incorporating cefuroxime, a cephalosporin group of antibiotic have been prepared from an interaction of vanadyl sulfate and cefuroxime in aqueous solution. The compound was characterized by Fourier transform infrared spectroscopy (FTIR), CHN microanalyses, ultraviolet-visible spectroscopy (UV-Vis), fast atom bombardment (FAB) mass spectrometry and thermogravimetric analysis (TGA). Density Functional Theory (DFT) computation using Gaussian 09 program at B3LYP level revealed a distorted square pyramidal energy optimized geometry for the vanadyl(IV) complex. The molecular docking studies show that the interaction between the vanadium complex and protein receptor, clathrin is dominated by hydrophobic forces. The experimental (1)H nuclear magnetic resonance (NMR) features of the analogous Zn(II) complex matched well with the theoretically computed values further affirming the distorted square pyramidal geometry for the vanadyl(IV) complex. Cyclic voltammetry revealed a metal centered single-electron oxidation-reduction response for VO(IV)/VO(V) couple. The antioxidant activity of the vanadium(IV)-complex vis-à-vis the antibiotic has been assessed by 1,1-diphenyl-2-picrylhydrazyl (DPPH) method. The vanadium complex showed comparatively better radical scavenging ability compared to the antibiotic cefuroxime. The antimicrobial activity of the compound has been assayed for five different microbial strains using minimum inhibitory concentration (MIC) method. Immunomodulatory studies carried out using phagocytosis index, myeloperoxidase release and cytokine assay indicated the vanadium(IV)-complex to be immunosuppressant. The cytotoxicity of the compound was evaluated by MTT (3-(4, 5-dimethyl thiazol-2-yl)-2, 5-diphenyl tetrazolium bromide) reduction assay.
