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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>SUMMARYThe interactions of biomolecules <strong>and</strong> cells at solid-liquid interfaces play a pivotalrole in a range of biomedical <strong>applications</strong> <strong>and</strong> have hence been studied in detail. Animproved underst<strong>and</strong>ing of these interactions results in the ability to manipulatebiomolecules <strong>and</strong> concurrently cells spatially <strong>and</strong> temporally at <strong>surfaces</strong> with highprecision. Spatial control can be achieved using patterned surface chemistries whilsttemporal control is achieved by <strong>switchable</strong> <strong>surfaces</strong>. The combination of these twosurface properties offers unprecedented control over the behaviour of biomolecules<strong>and</strong> cells at the solid-liquid interface. This is particularly relevant <strong>for</strong> cell microarray<strong>applications</strong>, where a range of biological processes must be duly controlled in orderto maximise the efficiency <strong>and</strong> throughput of these devices. Of particular interest aretransfected cell microarrays (TCMs), which significantly widen the scope ofmicroarray genomic analysis by enabling the high-throughput analysis of genefunction within living cellsInitially, this thesis focuses on the spatially controlled, electro-stimulatedadsorption <strong>and</strong> desorption of DNA. Surface modification of a silicon chip with anallylamine plasma polymer (ALAPP) layer resulted in a surface that supported DNAadsorption <strong>and</strong> sustained cell attachment. Subsequent high density grafting ofpoly(ethylene glycol) (PEG) <strong>for</strong>med a layer resistant to biomolecule adsorption <strong>and</strong>cell attachment. PEG grafted <strong>surfaces</strong> also showed significantly reduced attachmentof DNA with an equilibrium binding constant of 23 ml/mg as compared with 1600ml/mg <strong>for</strong> ALAPP modified <strong>surfaces</strong>. Moreover, both hydrophobic <strong>and</strong> electrostaticinteractions were shown to contribute to the binding of DNA to ALAPP. Spatialcontrol over the surface chemistry was achieved using excimer laser ablation of thePEG coating which enabled the production of patterns of re-exposed ALAPP withIV

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