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Fe3O4-silica core-shell nanoporous particles for high-capacity pH-triggered drug delivery
We demonstrate a one-step procedure for the synthesis of Fe 3 O 4 -silica core-shell nanoparticles with hierarchically ultra-large pores independent of any post-treatment such as annealing and template-molecule removal. The nanoporous silica shells with available amine groups were functionalized by...
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Published in: | Journal of materials chemistry 2012-01, Vol.22 (29), p.1445-14457 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We demonstrate a one-step procedure for the synthesis of Fe
3
O
4
-silica core-shell nanoparticles with hierarchically ultra-large pores independent of any post-treatment such as annealing and template-molecule removal. The nanoporous silica shells with available amine groups were functionalized by clickable linkers to produce pH-sensitive amides for regulating the release of an anti-cancer drug, doxorubicin (DOX). The loading amount of DOX reached up to 13.2 mg per 100 mg nanoparticles, 74.2% of which can be effectively released after 63 h at body temperature and pH 5 with decreased side effects. Such excellent features of these nanoparticles appear to arise from the integrated hierarchically ultra-large open-porosities and a homogeneous dispersibility in aqueous solution that has a great potential for their use as drug delivery systems.
We demonstrate a one-step procedure for the synthesis of Fe
3
O
4
-silica core-shell nanoparticles with hierarchically ultra-large pores independent of any post-treatment such as annealing and template-molecule removal. |
---|---|
ISSN: | 0959-9428 1364-5501 |
DOI: | 10.1039/c2jm31749d |