Chemical surface modification of parylene C for enhanced protein immobilization and cell proliferation
| Autor: | Frank Markland, Mark E. Thompson, Changhong Zhang, Steve Swenson |
|---|---|
| Rok vydání: | 2011 |
| Předmět: |
Materials science
food.ingredient Polymers Surface Properties Radical polymerization Biomedical Engineering Xylenes Microscopy Atomic Force Polymer brush Biochemistry Gelatin Biomaterials chemistry.chemical_compound food Spectroscopy Fourier Transform Infrared Monolayer Polymer chemistry Cell Adhesion Animals Humans Molecular Biology Cells Cultured Cell Proliferation Carbodiimide chemistry.chemical_classification Acrylate Photoelectron Spectroscopy Serum Albumin Bovine Dermis General Medicine Polymer Fibroblasts Immunohistochemistry Immobilized Proteins chemistry Surface modification Cattle Biotechnology |
| Zdroj: | Acta Biomaterialia. 7:3746-3756 |
| ISSN: | 1742-7061 |
| DOI: | 10.1016/j.actbio.2011.06.003 |
| Popis: | To introduce the adhesion site of proteins and/or cells on parylene C (PC)-coated medical devices that can be used as implantable biosensors or drug delivery capsules, the PC surfaces were initially modified by the Friedel–Crafts acylation reaction to generate active chlorines. These chlorines were then employed to initiate the atom transfer radical polymerization of tert-butyl acrylate (TBA) and form a polymer brush layer of polyTBA on PC; the acrylate groups in the polymer brushes were hydrolyzed to carboxylic acid groups and further activated into succinimidyl ester groups via the 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide coupling reaction. The PC surface grafted with polymer brushes and activated by succinimide showed efficient attachment of proteins, including gelatin, contortrostatin (CN) and bovine serum albumin (BSA), all at high density on the PC surface. The CN density on the surface was evaluated for both monolayer and polymer brush-based coatings. Based on fluorescence measurements, the polymer brush gives a 60-fold higher surface protein density than the monolayer-based system. Gelatin was used as a model protein and covalently coated onto the modified PC surface for cell culture study. Substrates with gelatin coating showed a significantly higher cell attachment and proliferation in 7 days cultures as compared to the uncoated substrates. In addition, a conventional photolithography technique was coupled with the surface chemistry to successfully pattern the BSA labeled with fluorescein isothiocyanate on the modified PC surfaces. |
| Databáze: | OpenAIRE |
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