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Removal of Trace Elements by Cupric Oxide Nanoparticles from Uranium In Situ Recovery Bleed Water and Its Effect on Cell Viability
Published on: June 21, 2015
Eco-synthesis, process optimisation, and therapeutic assessment of cow urine distillate derived copper nanoparticles
Gauri Pai Angle1, Sameer Nadaf2, Srinivasan Prabhu3
1Department of Pharmacognosy, PES's Rajaram and Tarabai Bandekar College of Pharmacy, Goa University, Ponda, 403401, Goa, India.
Abstract:
The present research successfully validates a sustainable, straightforward, cost-effective, and non-toxic biosynthesis of biologically active copper nanoparticles (CuNPs) using cow urine distillate (CUD), a traditional component of Vedic medicine. The study also investigates the effect of different process variables: reductant concentration, pH, reaction temperature, and reaction time, employing a factorial design approach (Box-Behnken design) on the synthesis of CUD-CuNPs. UV-Vis spectroscopy confirmed nanoparticle formation, showing surface plasmon resonance peaks between 269 and 275 nm. Morphological analysis using Transmission Electron Microscopy and Scanning Electron Microscopy-Energy Dispersive X-ray demonstrated the formation of spherical nanoparticles. XRD analysis showed a crystalline structure with prominent reflections at 43.4°, 50.5°, and 74.2°. The synthesized CUD-CuNPs had an average size of 232.76 nm, a polydispersity index of 0.421, and a zeta potential of -16.45 mV. Antimicrobial assessment of CUD-CuNPs using the agar well diffusion assay demonstrated their bactericidal potential against Staphylococcus epidermidis and Pseudomonas aeruginosa, with remarkable inhibitory zones of 25.66 ± 0.57 mm. Significant inhibition was also observed against E. coli (25.66 ± 0.57 mm) and B. subtilis (25.25 ± 1.00 mm). Furthermore, CUD-CuNPs significantly suppressed the activity of α-amylase and α-glucosidase enzymes, with IC50 values of 30.88 ± 1.07 µg/mL and 24.94 ± 1.02 µg/mL, respectively. In DPPH, nitric oxide, and H2O2 scavenging assays, CUD-CuNPs exhibited considerably stronger radical scavenging activity than CUD. This enhanced potency indicates a promising avenue for utilizing biosynthesized CUD-CuNPs in developing therapeutic drugs.

