Abstract
Large-pore mesoporous silica nanoparticles (LP-MSNs) with defined particle size (<200 nm) are promising carrier systems for the cellular delivery of macromolecules. Ideal nanocarriers should be adaptable in their surface properties to optimize host-guest interactions;thus, surface functionalization of the nanovehicles is highly desirable. In this study, we synthesized various monofunctional LP-MSNs by incorporating different organic groups into the silica framework via a co-condensation approach. Further, we applied a delayed co-condensation strategy to create spatially segregated core-shell bifunctional LP-MSNs. Diverse particle morphologies were obtained by adding different organosilanes to the silica precursor solution. The effect of organosilanes in the co-condensation process on particle size and pore structure formation is also discussed. Surface functional groups were then used for binding stimuli-responsive linkers. These were finally exploited for copper-free click chemistry for cargo conjugation to create a delivery system with controlled cargo release. Model cargo release experiments in buffer using these new multifunctional LP-MSNs demonstrate their ability in controlled cargo uptake and release and their potential for biomolecule delivery.
Item Type: | Journal article |
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Faculties: | Chemistry and Pharmacy > Department of Chemistry |
Research Centers: | Center for NanoScience (CENS) |
Subjects: | 500 Science > 500 Science 500 Science > 540 Chemistry |
ISSN: | 0897-4756 |
Language: | English |
Item ID: | 68004 |
Date Deposited: | 19. Jul 2019, 12:23 |
Last Modified: | 04. Nov 2020, 13:50 |