Abstract
A straightforward methodology for the synthesis of isothiocyanate-functionalized mesoporous silica nanoparticles (MSNs) by exposure of aminated MSNs to 1,1′-thiocarbonyldi-2(1H)-pyridone is reported. These nanoparticles are chemically stable, water tolerant, and readily react with primary amines without the formation of any by-product. This feature allows the easy modification of the surface of the nanoparticles for tuning their physical properties and the introduction of gatekeepers on the pore outlets. As a proof-of-concept, amino-isothiocyanate-functionalized MSNs have been used for the design of a nanocontainer able to release the drug Ataluren. The release profile of the drug can be easily fine-tuned with the careful choice of the capping amine.
| Original language | English |
|---|---|
| Article number | 1219 |
| Number of pages | 16 |
| Journal | Nanomaterials |
| Volume | 9 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Sept 2019 |
Keywords
- Drug delivery
- Isothiocyanate
- Mesoporous silica nanoparticles
- Regioselective functionalization
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