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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>However, at a higher DNA solution concentration of 500 ng/ml, there seems to bea disparity arising between the two methods of analysis. Notably, the initial sharpincrease in DNA adsorption did not plateau until 15000 s, which is at least 5 timeslonger than measurements taken with QCM. The reason <strong>for</strong> this disparity may be dueto diffusion limitations in the fluorescence study, that is, the DNA that adsorbs to thesurface is taken from the solution near the surface, <strong>for</strong>ming a DNA depleted layerclose to the surface that DNA from the bulk must diffuse into. A time delay wouldhence be expected between the change of DNA concentration in a near-surface layer<strong>and</strong> the translation of this change to a concentration change in the bulk, which wasmeasured by the depletion method. Thus, although the measurements of the depletionof solution fluorescence was accurate <strong>for</strong> thermodynamic studies of DNA adsorption,this disparity suggests that at higher DNA concentration (>200 ng/ml) it is notaccurate <strong>for</strong> kinetic analysis.3.3.3. DNA adsorption.Langmuir adsorption is widely used <strong>for</strong> the modelling of biological adsorptionprocesses. In order to minimise the electrostatic repulsion between adsorbed DNA<strong>and</strong> DNA in solution that is approaching the surface, which would cause a deviationfrom the Langmuir model, lower concentrations of DNA (

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