期刊
PROGRESS IN ORGANIC COATINGS
卷 151, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.porgcoat.2020.106098
关键词
Palladium nanoparticles; Orthosiphonstamineus; Neem gum; NG@Pd NPs; Antibiofilm efficiency; Antimicrobial potential; Anticancer activity
资金
- RUSA phase 2.0 [F. 24-51/2014-U]
- DST through the Department of Science and Technology - Promotion of University Research and Scientific Excellence (DST-PURSE)
- Department of Science and Technology, New Delhi [SR/PURSE Phase 2/38 (G)]
This study fabricated biocompatible neem gum coated palladium nanoparticles and evaluated their pharmacological applications, demonstrating enhanced antimicrobial and anticancer properties of NG@Pd NPs compared to Pd NPs alone, making them promising candidates for antimicrobial and lung cancer therapy.
The present study highlights a quick and cost effective, fabrication of biocompatible and water dispersible neem gum coated palladium nanoparticles (NG@Pd NPs) and assessment of their pharmacological applications. Palladium nanoparticles were synthesized through a biogenic route using the aqueous leaf extract of Orthosiphon stamineus. The fabricated nanocomposite was characterized by spectroscopic and microscopic analyses. The results of antimicrobial studies revealed that the NG@Pd NPs exhibited enhanced antibacterial activity against E. coli, S. aureus and Extended spectrum beta lactamase (ESBL) strain when compared to the Pd NPs alone. Antibiofilm studies illustrated a concentration dependent inhibition of biofilm formation in MSSA strain with the IC50 value of 15.25 +/- 0.012 mu g/mL, while the Pd NPs showed lower inhibitory effect. Anticancer potential illustrated that the NG@Pd NPs showed potent antiproliferative effect against A549 cells in proportion to the concentration with 50 % inhibition at 45.6 +/- 0.25 mu g/mL. NG@Pd NPs exhibited enhanced reactive oxygen species leading to DNA fragmentation, disruption of mitochondrial membrane potential inducing apoptosis through the activation of caspase 3/9. Safety evaluation studies revealed that the NG@Pd NPs exhibited neither cytotoxicity nor hemolysis illustrating the biocompatible nature of NG@Pd NPs. Overall, the present work manifests the possibility of developing NG@Pd NPs as a suitable candidate for antimicrobial and lung cancer therapy.
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