Protein resistance of dextran and dextran-poly(ethylene glycol) copolymer films.
Protein resistance of dextran and dextran-poly(ethylene glycol) copolymer films.
复制标题
葡聚糖和葡聚糖-聚乙二醇共聚物膜的蛋白质抗性。
DOI:
10.1080/08927014.2011.584618
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发表时间:
2011
期刊:
影响因子:
2.7
通讯作者:
Trau,Matt
中科院分区:
文献类型:
--
作者:
Kozak,Darby;Chen,Annie;Bax,Jacinda;Trau,Matt
The protein resistance of dextran and dextran-poly(ethylene glycol) (PEG) copolymer films was examined on an organosilica particle-based assay support. Comb-branched dextran-PEG copolymer films were synthesized in a two step process using the organosilica particle as a solid synthetic support. Particles modified with increasing amounts (0.1–1.2 mg m−2) of three molecular weights (10,000, 66,900, 400,000 g mol−1) of dextran were found to form relatively poor protein-resistant films compared to dextran-PEG copolymers and previously studied PEG films. The efficacy of the antifouling polymer films was found to be dependent on the grafted amount and its composition, with PEG layers being the most efficient, followed by dextran-PEG copolymers, and dextran alone being the least efficient. Immunoglobulin gamma (IgG) adsorption decreased from ∼5 to 0.5 mg m−2with increasing amounts of grafted dextran, but bovine serum albumin (BSA) adsorption increased above monolayer coverage (∼2 mg m−2) indicating ternary adsorption of the smaller protein within the dextran layer.