Abstract
Large pore (4.6-7.6 nm) and well-dispersed benzene bridged mesoporous organosilica nanoparticles with uniform particle size of ≈50 nm are prepared via a biphasic approach. They can be directly used as nanocarriers without surface modification for the intracellular delivery of therapeutic proteins.
Keywords:
biphasic synthesis; large pores; mesoporous organosilica nanoparticles; protein delivery.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Benzene / chemistry*
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Cross-Linking Reagents / chemistry
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Delayed-Action Preparations / chemical synthesis
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Diffusion
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Drug Compounding / methods
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Humans
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MCF-7 Cells
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Nanocapsules / administration & dosage
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Nanocapsules / chemistry*
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Nanocapsules / ultrastructure
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Nanoconjugates / chemistry*
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Nanoconjugates / ultrastructure
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Nanopores / ultrastructure*
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Organosilicon Compounds / chemistry*
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Particle Size
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Phase Transition
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Porosity
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Ribonuclease, Pancreatic / administration & dosage
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Ribonuclease, Pancreatic / chemistry*
Substances
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Cross-Linking Reagents
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Delayed-Action Preparations
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Nanocapsules
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Nanoconjugates
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Organosilicon Compounds
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Ribonuclease, Pancreatic
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Benzene