Novel antifouling oligo(ethylene glycol) methacrylate particles via surfactant-free emulsion polymerization
Cross-linked PEGEEM colloids that display novel antifouling surface properties are introduced. A simple surfactant-free emulsion polymerization is used to prepare monodisperse cross-linked particles which were characterized by DLS and TEM. [Display omitted] ► PEGEEM colloids with novel antifouling s...
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Veröffentlicht in: | Journal of colloid and interface science 2011-03, Vol.355 (1), p.76-80 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Cross-linked PEGEEM colloids that display novel antifouling surface properties are introduced. A simple surfactant-free emulsion polymerization is used to prepare monodisperse cross-linked particles which were characterized by DLS and TEM.
[Display omitted]
► PEGEEM colloids with novel antifouling surface properties is reported for the first time. ► Surfactant-free emulsion polymerization was used to prepare monodisperse crosslinked particles. ► A prominent blockage of BSA adsorption was obtained for the PEG-based sub-micron colloids.
The use of particle formulations with antifouling surface properties attracts increasing interest in several biotechnological applications. Majority of these studies utilize a poly(ethylene glycol) coating to render the corresponding surface nonrecognizable to biological macromolecules. Herein, we report a simple way to prepare novel antifouling colloids composed of oligo(ethylene glycol) backbones via surfactant-free emulsion polymerization. Monodisperse cross-linked poly(ethylene glycol) ethyl ether methacrylate particles were characterized by dynamic light scattering and transmission electron microscopy. The effects of monomer, cross-linker and initiator on particle characteristics were investigated. More importantly, a prominent blockage of bovine serum albumin adsorption was obtained for the poly(ethylene glycol)-based sub-micron (∼200
nm) particles when compared with similar-sized poly(methyl methacrylate) counterparts. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2010.11.081 |