4.2 Article

Biosynthesis, characterisation and antimicrobial activity of silver nanoparticles using Hibiscus rosa-sinensis petals extracts

期刊

IET NANOBIOTECHNOLOGY
卷 9, 期 5, 页码 288-293

出版社

WILEY
DOI: 10.1049/iet-nbt.2014.0047

关键词

silver; nanoparticles; antibacterial activity; nanofabrication; surface plasmon resonance; particle size; X-ray diffraction; surface morphology; scanning electron microscopy; atomic force microscopy; Fourier transform infrared spectra; surface treatment; nanomedicine; microorganisms; biosynthesis; antimicrobial activity; silver nanoparticles; Hibiscus rosa-sinensis petals extracts; green synthesis; metallic nanoparticles; chemical approach; physical approach; production mechanism; surface plasmon resonance peak; mean particle size; X-ray diffraction patterns; face centred cubic crystalline silver; surface morphology; scanning electron microscopy; atomic force microscopy; Fourier transform infrared spectroscopy; surface modifications; functional groups; pathogenic strains; Vibrio cholerae; Escherichia coli; Klebsiella pneumoniae; Staphylococcus aureus; Ag

资金

  1. National Institute of Technology, Rourkela

向作者/读者索取更多资源

Green synthesis of metallic nanoparticles has lured the world from the chemical and physical approaches owing to its rapid, non-hazardous and economic aspect of production mechanism. In this study, silver nanoparticles (AgNPs) were synthesised using petal extracts of Hibiscus rosa-sinensis. The AgNPs displayed characteristic surface plasmon resonance peak at around 421 nm having a mean particle size of 76.25 +/- 0.17 nm and carried a charge of -41 +/- 0.2 mV. The X-ray diffraction patterns displayed typical peaks of face centred cubic crystalline silver. The surface morphology was characterised by scanning electron microscopy and atomic force microscopy. Fourier transform infrared spectroscopy studies confirmed the surface modifications of the functional groups for the synthesis of AgNPs. Furthermore, the synthesised AgNPs displayed proficient antimicrobial activity against pathogenic strains of Vibrio cholerae, Escherichia coli, Klebsiella pneumoniae and Staphylococcus aureus.

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