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Patterned and switchable surfaces for biomaterial applications

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Andrew Hook – <strong>Patterned</strong> <strong>and</strong> <strong>switchable</strong> <strong>surfaces</strong> <strong>for</strong> <strong>biomaterial</strong> <strong>applications</strong>The DNA on PEG was found to be significantly lower than <strong>for</strong> ALAPP over thebulk DNA concentration range studied (Figure 3.4A) confirming that, as expected,PEG resists adsorption of DNA as compared with the ALAPP film. By applying theLangmuir model to the data sets shown in Figure 3.4, the s <strong>and</strong> K <strong>for</strong> DNAadsorption to PEG were found to be 1.75 mg/m 2 <strong>and</strong> 680 ml/mg respectively, whichis significantly lower than the equivalent values of 4.96 mg/m 2 <strong>and</strong> 1600 ml/mgmeasured <strong>for</strong> ALAPP. The small amount of DNA adsorption observed on the PEGfilms is presumably due to weak Van der Waals interactions or hydrogen bonding.At pH 7.4 a more negative -potential was measured <strong>for</strong> ALAPP than <strong>for</strong> PEG. Assuch, electrostatic interactions with the ALAPP film should be less favourable than<strong>for</strong> the PEG film. Significantly, a contact angle difference of 57° was measured <strong>for</strong>the two films, with the PEG film being more hydrophilic, an important disparitybetween these two films at a pH of 7.4. Thus, rather than the stabilisation of a DNAon an ALAPP film being predominantly due to electrostatic interactions,hydrophobic effects between the hydrophobic nucleobases <strong>and</strong> hydrophobicfunctionalities within the ALAPP film were suspected to contribute significantly [18,19]. It is suspected that the brush character of the PEG film, as discussed previously,also contributes to the low DNA seen on the PEG films.To further investigate how DNA interacts with ALAPP <strong>surfaces</strong>, a series ofexperiments monitoring DNA adsorption in various solvents of varying pH, ionconcentration <strong>and</strong> hydrophobicity were conducted. The results are shown in Figure3.5-Figure 3.8. Entropically, the adsorption of DNA is driven by surface dehydration,that is, the removal of water molecules from the surface [20]. However, in order <strong>for</strong>this thermodynamically favourable process to occur, the DNA molecules mustdiffuse close enough to the surface to displace water molecules at the solid/liquid3-117

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