Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1jm14794c
Title: Synthesis of AIZS@SiO 2 core-shell nanoparticles for cellular imaging applications
Authors: Sheng, Y.
Tang, X. 
Xue, J. 
Issue Date: 28-Jan-2012
Citation: Sheng, Y., Tang, X., Xue, J. (2012-01-28). Synthesis of AIZS@SiO 2 core-shell nanoparticles for cellular imaging applications. Journal of Materials Chemistry 22 (4) : 1290-1296. ScholarBank@NUS Repository. https://doi.org/10.1039/c1jm14794c
Abstract: I-III-VI 2 semiconductor nanoparticles such as AgInS 2 have been developed for cell imaging applications in recent years. However, there are few published works reporting the phase transfer (from hydrophobic to hydrophilic) of the AgInS 2 nanoparticles for biomedical application purposes. In this work, we report the successful silica coating for the as-synthesized Zn-doped AgInS 2 (AIZS) nanoparticles via a templated coating route. The silica shell thickness of the obtained AIZS@SiO 2 core-shell nanoparticles could be well controlled within 10-20 nm and their overall size was less than 50 nm. As compared to the AIZS nanoparticles stabilized by cetyltrimethylammonium bromide (CTAB), the obtained AIZS@SiO 2 nanoparticles showed much improved photoluminescence (PL) stability in water. The obtained core-shell nanoparticles were further conjugated with the PEG functional group, and the resultant PEGylated nanoparticles showed excellent colloidal stability in various media such as water, phosphate buffered saline (PBS) and bovine calf serum (BCS). The cellular imaging application of the obtained AIZS@SiO 2 nanoparticles was also demonstrated successfully. © The Royal Society of Chemistry 2012.
Source Title: Journal of Materials Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/86751
ISSN: 09599428
DOI: 10.1039/c1jm14794c
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.