A facile one pot synthesis of collagen protected gold nanoparticles using Na–malanodialdehyde
Uniform and stable collagen protected spherical gold nanoparticles were synthesized using sodium salt of malanodialdehyde as a reducing agent. Further it was observed that the morphology of the particles was found out to be spherical. Formation of spherical gold nanoparticles was well characterized...
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Veröffentlicht in: | Materials letters 2012-07, Vol.79, p.199-201 |
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Sprache: | eng |
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Zusammenfassung: | Uniform and stable collagen protected spherical gold nanoparticles were synthesized using sodium salt of malanodialdehyde as a reducing agent. Further it was observed that the morphology of the particles was found out to be spherical. Formation of spherical gold nanoparticles was well characterized using UV–Visible spectroscopy and transmission electron microscopy (TEM) analysis. The TEM measurements show evidence of particle shapes such as spheres of nearly. The variation in particle shape is probably due to the effect of the reduced gold to collagen ratio as the reaction proceeds.
In the present work, uniform and stable collagen protected spherical gold nanoparticles were synthesized using sodium salt of malanodialdehyde as a reducing agent. Further it was observed that the morphology of the particles was found out to be spherical. Formation of spherical gold nanoparticles were well characterized using UV–Visible spectroscopy and transmission electron microscopy (TEM) analysis. The TEM measurements show evidence of particle shapes such as spheres of nearly. Here, the particle shape caries probably due to the effect of the reduced gold to collagen ratio as the reaction proceeds. The particles size of the gold nanoparticles was found out to be 20nm. [Display omitted]
► Uniform and stable collagen protected spherical gold nanoparticles were synthesized. ► And characterized by UV–Visible spect., TEM analysis and FTIR techniques. ► Found difference in peak intensity of collagen and Au NPs coated in FTIR spectra. |
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ISSN: | 0167-577X 1873-4979 |
DOI: | 10.1016/j.matlet.2012.04.001 |