Well-Defined SiO2@P(EtOx-stat-EI) Core-Shell Hybrid Nanoparticles via Sol-Gel Processes
Positively charged nanoparticles (NPs) are very interesting for biomedical and pharmaceutical applications, such as nonviral gene delivery. Here, the synthesis of SiO2 nanoparticles with a covalently grafted poly(2‐ethyl‐2‐oxazoline) (PEtOx) shell (SiO2@PEtOx) is presented. PEtOx with a degree of po...
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Published in | Macromolecular rapid communications. Vol. 37; no. 4; pp. 337 - 342 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Blackwell Publishing Ltd
01.02.2016
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Positively charged nanoparticles (NPs) are very interesting for biomedical and pharmaceutical applications, such as nonviral gene delivery. Here, the synthesis of SiO2 nanoparticles with a covalently grafted poly(2‐ethyl‐2‐oxazoline) (PEtOx) shell (SiO2@PEtOx) is presented. PEtOx with a degree of polymerization of 20 and 38 is synthesized via microwave supported cationic ring‐opening polymerization and subsequently end‐functionalized with a triethoxysilyl linker for subsequent grafting to silica particles with hydrodynamic radii of 7, 31, and 152 nm. The resulting SiO2@PEtOx particles are characterized by using dynamic light scattering (DLS), transmission electron microscopy (TEM, cryoTEM), and scanning electron microscopy (SEM) to determine changes in particle size. Thermal gravimetrical analysis is used to quantify the amount of polymer on the silica surface. Subsequent in situ transformation of SiO2@PEtOx particles into SiO2@P(EtOx‐stat‐EI) (poly(2‐ethyl‐2‐oxazoline‐stat‐ethylene imine) grafted silica particles) under acidic conditions inverts the surface charge from negative to positive according to ζ‐potential measurements. The P(EtOx‐stat‐EI) shell could be used for the deposition of Au NP afterward.
The synthesis of SiO2 nanoparticles (NPs) with a covalently grafted poly(2‐ethyl‐2‐oxazoline) or (poly(2‐ethyl‐2‐oxazoline‐stat‐ethylene imine) shell (SiO2@PEtOx and SiO2@P(EtOx‐stat‐EI)) is presented. Therefore, PEtOx is end‐functionalized with a triethoxysilyl linker and hydrolyzed under acidic conditions after the grafting‐to process. The P(EtOx‐stat‐EI) shell could also be used for the deposition of Au NP afterward. |
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Bibliography: | German Federal Ministry of Education and Research - No. 31P7233 Federal Ministry for Economic Affairs and Energy DFG EFRE ark:/67375/WNG-7RPJVPZX-W Arbeitsgemeinschaft industrieller Forschungsvereinigung istex:513B482CC78115A3E1446C01199DC1279FBCB974 ArticleID:MARC201500467 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1022-1336 1521-3927 |
DOI: | 10.1002/marc.201500467 |