Surface functionalization and biomolecule immobilization using plasma-generated free radicals on polypropylene

被引:7
作者
de Jesus Martinez-Gomez, Alvaro [2 ]
Manolache, Sorin O. [1 ]
Young, Raymond A.
Denes, Ferencz S.
机构
[1] Univ Wisconsin, Ctr Plasma Aided Mfg, Madison, WI 53706 USA
[2] Univ Guadalajara, Dept Chem Engn, Guadalajara 44430, Jalisco, Mexico
关键词
alpha-chymotrypsin; Argon plasma; Biomolecule immobilization; Free radicals; Oxygen plasma; Plasma functionalization; Polypropylene; Spacer; LASER-INDUCED FLUORESCENCE; NITRIC-OXIDE; GLOW-DISCHARGE; ACRYLIC-ACID; POLYMERIZATION; SPECTROSCOPY; STRATEGIES; NITROGEN; FILMS;
D O I
10.1007/s00289-010-0258-1
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study are presented evidences for the functionalization of polypropylene surfaces accomplished in a sequential process: argon- or oxygen-plasma enhanced generation of free radical sites on polypropylene surfaces was followed by "in situ" gas phase derivatization in the absence of plasma using ethylene diamine, or propylene diamine; and an "in situ", gas phase derivatization using oxallyl chloride or "ex situ" derivatization in the presence of glutaraldehyde. The free radicals' presence on the plasma-exposed polypropylene surfaces was confirmed using "in situ" sulfur dioxide or nitric oxide labeling techniques. It was shown that the free radical sites readily react under "in situ" conditions with the stable chain-precursor components and generate the desired spacer-chain molecules revealed by ESCA analysis. Functionalized polypropylene substrates were used for immobilization of alpha-chymotrypsin in the presence of spacer-chain molecules. The activity of the immobilized alpha-chymotrypsin was found to be comparable to the activity of the free enzyme when the spacer molecules have been used.
引用
收藏
页码:293 / 308
页数:16
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