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Patterned and switchable surfaces for biomaterial applications

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Chapter 4 – Formation of a chemically patterned substrate <strong>for</strong> cell microarray <strong>applications</strong>to the underlying surface. Another study arrayed monomers of interest with aninitiator that upon UV irradiation instigates the in situ polymerisation of polymermaterial to <strong>for</strong>m rigid polymer spots cross-linked to the substrate surface [145, 146].This polymer microarray has been utilised to study the influence of surface chemistryon transfection [219]. However, this approach is limited to the <strong>for</strong>mation of highlycrosslinked, r<strong>and</strong>omly ordered polymer networks, the structure of which may bedifficult to characterise <strong>and</strong> replicate at a larger scale.Cell microarrays have also been widely utilised <strong>for</strong> the <strong>for</strong>mation of transfectedcell microarrays (TCM), which utilise reverse transfection to <strong>for</strong>m locally transfectedcells within a lawn of cells seeded onto a microarray of DNA vectors of interest [1,8]. Typically, a TCM is <strong>for</strong>med by firstly <strong>for</strong>ming an array of DNA or RNA vectorsof interest. Cells are then seeded onto the array <strong>for</strong> the <strong>for</strong>mation of a lawn of cellssuch that cells attached onto arrayed spots will take up the arrayed vectors <strong>and</strong>express or silence the genes of interest. Recently, use of recombinant adenovirusbased transfection systems allows <strong>for</strong> the use of primary cells with TCMs [169]. Asignificant challenge <strong>for</strong> this type of cell array is the prevention of crosscontaminationbetween the spots <strong>and</strong> the outgrowth of cells from spots of interest.There<strong>for</strong>e, researchers desire cell attachment to be limited to the arrayed spots, whilstthe area in between the spots prevents cell attachment. This can only be achieved bysurface patterning, introducing cell adhesive regions within a background thatprevents protein adsorption <strong>and</strong> concurrently cell attachment, termed ‘low fouling’[67]. A chemical or physical pattern regulating the growth of cells can be generatedusing a range of lithographic techniques including photolithography, softlithography, microfluidics <strong>and</strong> microelectronics (see section 1.2) [66]. However, allof these techniques require microfabrication tools that are not always readily4-130

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