کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
608578 | 880604 | 2011 | 5 صفحه PDF | دانلود رایگان |

This paper describes a performance of precise control of shell thickness in silica-coating of Au nanoparticles based on a sol–gel process, and an investigation into X-ray imaging properties for the silica-coated Au (Au/SiO2) particles. The Au nanoparticles with a size of 16.9 ± 1.2 nm prepared through a conventional citrate reduction method were used as core particles. The Au nanoparticles were silica-coated with a sol–gel reaction using tetraethylorthosilicate (TEOS) as a silica source, sodium hydroxide (NaOH) as a catalyst, and (3-aminopropyl) trimethoxysilane (APMS) as a silane coupling agent. An increase in TEOS concentration resulted in an increase in shell thickness. Under certain concentrations of Au, H2O, NaOH, and APMS, the Au/SiO2 particles with silica shell thickness of 6.0–61.0 nm were produced with varying TEOS concentration. Absorption peak wavelength of surface plasmon resonance of the Au/SiO2 colloid solution depended on silica shell thickness, which agreed approximately with the predictions by Mie theory. The as-prepared colloid solution could be concentrated up to an Au concentration of 0.19 M with salting-out and centrifugation. The concentrated colloid solution showed an X-ray image with high contrast, and a computed tomography value for the colloid solution with an Au concentration of 0.129 M was achieved 1329.7 ± 52.7 HU.
Photograph (a) and X-ray image (b) of the concentrated Au/SiO2 particle colloid solution. TEM image of the Au/SiO2 particles in the colloid solution is also shown in (c).Figure optionsDownload high-quality image (114 K)Download as PowerPoint slideHighlights
► Shell thickness of silica-coated Au nanoparticles was precisely controlled.
► Optical properties of the particles were approximately predicted by Mie theory.
► The particle colloid solution revealed a computed tomography value of 1329.7 ± 52.7 HU.
Journal: Journal of Colloid and Interface Science - Volume 358, Issue 2, 15 June 2011, Pages 329–333