Green synthesis of zero valent colloidal nanosilver targeting A549 lung cancer cell: In vitro cytotoxicity.

J Genet Eng Biotechnol

Department of Chemistry, University of Mumbai, Santacruz (East), Mumbai 400098, India.

Published: June 2018

An eco-friendly green approach was proposed to synthesise stable, cytotoxic colloidal silver nanoparticles (AgNPs) using () fruit extract. Bioinspired green method adopted for fabrication of AgNPs because of easy, fast, low-cost and benign bioprocess. Phytocomponents played the crucial role in capping, stabilisation and inherent cytotoxic potential of colloidal nanosilver. The physiochemical, crystalline, optical and morphological properties of AgNPs were characterized using UV-vis, FT-IR, XRD, SEM, TEM, EDX and AFM. FT-IR reveals the presence of carbonyl, methyl, polyphenol (flavonoid), primary and secondary amine (protein), carboxyl group, ester as major functional groups over the surface of nanomaterials. Mechanistic pathway for formation and stabilisation of colloidal nanosilver has been discussed. Average crystalline size of AgNPs was found to be 12.55 nm from XRD. TEM shows AgNPs nanosphere with size range 1-13.85 nm. Consistency in spherical morphology was also confirmed through Atomic Force Microscopy (AFM). AFM measurement provided image Rq value 3.62, image Ra 2.47, roughness Rmax 36.4 nm, skewness 1.99 and kurtosis 9.87. The SRB assay revealed substantial noticeable anti-cancer activity of colloidal nanosilver on A549 and HOP-62 human lung cancer cells in a dose dependent manner with IC50 value of 51.93 µg/ml and 76.92 µg/ml. In addition, capped AgNPs were found to be more biocompatible in comparison to FE. Our study demonstrated the integration of green chemistry principle in nanomaterials fabrication and focused on the potential use of fruit extract as an efficient precursor for biocompatible AgNPs anodrug formulation with improved cytotoxic applications.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296562PMC
http://dx.doi.org/10.1016/j.jgeb.2017.12.001DOI Listing

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