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DC Field | Value | Language |
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dc.contributor.author | Doddamani D. | |
dc.contributor.author | PonnanEttiyappan J. | |
dc.date.accessioned | 2021-05-05T10:28:06Z | - |
dc.date.available | 2021-05-05T10:28:06Z | - |
dc.date.issued | 2020 | |
dc.identifier.citation | Bulletin of Materials Science Vol. 43 , 1 , p. - | en_US |
dc.identifier.uri | https://doi.org/10.1007/s12034-020-02209-0 | |
dc.identifier.uri | http://idr.nitk.ac.in/jspui/handle/123456789/15812 | - |
dc.description.abstract | Spherical mesoporous hollow core-shell silica nanoparticles (HCSNs) of size 200 ± 50 nm with tunable thickness from 20 to 60 nm are synthesized using a sacrificial sulphonated polystyrene (PS, particle size 160 nm) template. A facile method is adopted for the sulphonation of PS using sulphuric acid, which enhanced the negative charge on the surface of PS as confirmed by zeta potential analysis and Fourier transform infrared radiation analysis. The thickness of the silica shell is tuned by altering the concentration of the silica precursor and is found to increase due to the use of the sulphonated PS template. N2 adsorption/desorption studies reported the variation of specific surface area of HCSNs from 644.1 to 197.8 m2 g−1 and average pore size from 1.55 to 3.4 nm. The drug release behaviour of HCSNs with different shell thicknesses is investigated using doxorubicin as the model drug. A delay in the drug release for ~300 min is successfully achieved by employing HCSNs with enhanced thickness of 60 nm. Application of HCSNs in targeted drug delivery was further supported by the in-vitro cytotoxicity studies carried out on lung adenocarcinoma cells. © 2020, Indian Academy of Sciences. | en_US |
dc.title | Sacrificial sulphonated polystyrene template-assisted synthesis of mesoporous hollow core-shell silica nanoparticles for drug-delivery application | en_US |
dc.type | Article | en_US |
Appears in Collections: | 1. Journal Articles |
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