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 inMacromolecular rapid communications. Vol. 37; no. 4; pp. 337 - 342
Main Authors Eckardt, Oliver, Pietsch, Christian, Zumann, Oliver, von der Lühe, Moritz, Brauer, Delia S., Schacher, Felix H.
Format Journal Article
LanguageEnglish
Published Germany Blackwell Publishing Ltd 01.02.2016
Wiley Subscription Services, Inc
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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.
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