Stable Protein-Repellent Zwitterionic Polymer Brushes Grafted from Silicon Nitride

density Molecular Structure Protein Stability Surface Properties poly(ethylene oxide) brushes transfer radical polymerization Silicon Compounds self-assembled monolayers Acrylic Resins Proteins 02 engineering and technology organic monolayers IR-99606 molecular simulation Betaine adhesion adsorption biosensor applications Adsorption 0210 nano-technology surface modification
DOI: 10.1021/la104657c Publication Date: 2011-02-03T17:31:49Z
ABSTRACT
Zwitterionic poly(sulfobetaine acrylamide) (SBMAA) brushes were grafted from silicon-rich silicon nitride (SixN4, x > 3) surfaces by atom transfer radical polymerization (ATRP) and studied in protein adsorption experiments. To this aim ATRP initiators immobilized onto SixN4 through stable Si−C linkages via three consecutive reactions. A UV-induced reaction of 1,2-epoxy-9-decene with hydrogen-terminated was followed conversion the epoxide 1,2-ethylenediamine resulting primary secondary amine-terminated surfaces. 2-bromoisobutyryl bromide led to initiator-covered polymer SBMAA grown these initiator-coated (thickness ∼30 nm), polymer-coated characterized detail static water contact angle measurements, X-ray photoelectron spectroscopy (XPS), an atomic force microscope (AFM). The proteins zwitterionic coated evaluated situ reflectometry, using a fibrinogen (FIB) solution 0.1 g·L−1, compared hexadecyl-coated (C16−SixN4), uncoated air-based plasma oxidized (SiOy−SixN4), hexa(ethylene oxide)-coated (EO6−SixN4). Excellent repellence (>99%) observed for during exposure FIB as C16−SixN4 Furthermore, stability surveyed exposing 1 week phosphate buffered saline (PBS) at room temperature. before after PBS XPS, AFM, their protein-repelling properties reflectometry. After solution, coating remained intact, its thickness unchanged within experimental error. No hydrolysis still repelled 98% surfaces, demonstrating long-term efficiency easily prepared surface coatings.
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