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Patterned and switchable surfaces for biomaterial applications

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Chapter 3 – Comparison of the binding mode of plasmid DNA to allylamine plasma polymer <strong>and</strong> poly(ethyleneglycol) <strong>surfaces</strong>resulting in a film thickness of approximately 30 nm as determined by atomic <strong>for</strong>cemicroscopy (data not shown). After deposition samples were exposed briefly to airbe<strong>for</strong>e storage under a N 2 atmosphere.PEG monoaldehyde (Shearwater Polymers, Huntsville AL, USA) with amolecular weight of 5000 was grafted onto freshly deposited ALAPP films byreductive amination. Grafting was per<strong>for</strong>med under ‘cloud point’ conditions in 20 mlof a 0.1 M sodium phosphate buffer containing K 2 SO 4 (2.2 mg), NaCNBH 3 (60 mg)<strong>and</strong> PEG (50 mg) at pH 6.2. Freshly deposited ALAPP films were incubated in thePEG grafting solution at 60 °C <strong>for</strong> 16 hr.3.2.2. Substrate characterisationContact angle measurements were per<strong>for</strong>med by injecting 100 l of 0.2 mfiltered MilliQ water (18.2 M.cm) onto the surface of interest. Advancing contactangles were measured. Three measurements were taken <strong>for</strong> each sample. Imageswere taken using a Panasonic CCTV camera (WV-BP550) <strong>and</strong> processed usingImageJ software.X-ray photoelectron spectroscopy (XPS) was conducted on an AXIS HSispectrometer (Kratos Analytical Ltd.) equipped with a monochromatised Al K source. The pressure during analysis was typically 5x10 -8mbar. The elementalcomposition of <strong>surfaces</strong> was determined from survey spectra, collected at a passenergy of 320 eV. High-resolution spectra were obtained at a pass energy of 40 eV.Binding energies were referenced to the aliphatic hydrocarbon peak at 285.0 eV.Peak fitting of high-resolution spectra was conducted with Vision 1.5 software,Kratos Analytical Ltd. Two areas of each surface were analysed, <strong>and</strong> each samplepreparation was prepared <strong>and</strong> analysed in duplicate.3-102

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