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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>APPENDIX 2.AFM FORCE CURVES OF CROSS-LINKEDPOLYMER ARRAYS9.10.A2.1. IntroductionSurface modification has become of increasing importance <strong>for</strong> a wide range of<strong>applications</strong>. Techniques to modify the outer surface of a material whilst notcompromising the materials bulk properties or integrity are of interest. Of particularinterest are patterned <strong>surfaces</strong> that are able to offer spatial control over the behaviourof biomolecules at a particular surface. Surface patterning may incorporate bothchemical <strong>and</strong> topographical features, <strong>and</strong> can be achieved by a wide range ofapproaches including photolithography, soft lithography, robotic printing,microfluidics <strong>and</strong> microelectronics [66, 74-77, 79, 133, 197, 214]. A significantoutcome of the development of microfabrication is microarrays. DNA <strong>and</strong> proteinmicroarrays have revolutionised genomic studies <strong>and</strong> continue to bring considerableinsight ubiquitously in medical science [98, 127, 135, 309]. Development ofpatterned surface chemistry that precisely match the surface patterns of microarrayscould increase microarray capabilities by allowing higher densities by minimisingthe required separation between adjacent spots, <strong>and</strong> higher signal to noise ratios byincorporating low-fouling <strong>surfaces</strong> that minimise non-specific binding. This is ofparticular interest <strong>for</strong> microarrays containing living cells [1, 45].The <strong>for</strong>mation of a patterned surface, as described in CHAPTER 4, is of particularsuitability <strong>for</strong> DNA microarray <strong>applications</strong>. Initially a polycationic polymer havingbioactive properties is functionalised with a phenylazide cross-linker then arrayedonto a low-fouling surface <strong>and</strong> UV cross-linked to <strong>for</strong>m a covalently linked polymerC

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