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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>1.2.5. Robotic contact <strong>and</strong> non-contact microprintingFormation of micron resolution arrays is routinely achieved by robotic contact <strong>and</strong>non-contact microprinting. Robotic contact printing is achieved using a roboticspotter that first dips a pin with microscale diameter into a desired solution then spotsthe sample onto the substrate surface at a specified location. Two types of pins aretypically used. First, a solid pin, which is commonly used <strong>for</strong> transferring proteins<strong>and</strong> other sticky molecules because of their ease of cleaning <strong>and</strong> second, a quilled pinthat has a hollow centre that is able to draw up the solution <strong>and</strong> act as a reservoirallowing repeated spotting without re-dipping. Although, this increases the rate ofmicroarray <strong>for</strong>mation, these pins are much more difficult to keep clean <strong>and</strong> are,there<strong>for</strong>e, only suitable <strong>for</strong> ‘non-sticky’ molecules. Robotic non-contact printing isachieved by ejecting nano-litre volumes of the desired solution from a microcapillaryonto specified positions on a surface. The advantage of this strategy is that commonproblems with pins, such as the risk of contamination if the pins are insufficientlycleaned, inhomogeneous spot geometry <strong>and</strong> variations in the dispensed volume, canbe avoided [94], however, this approach typically suffers from ‘splattering’ ofejected volumes. Such strategies can be used to <strong>for</strong>m DNA <strong>and</strong> protein microarrays<strong>and</strong> more recently also cell microarrays [8, 15, 82, 94-99].This <strong>for</strong>m of patterning is very effective at quickly <strong>and</strong> reproducibly producingmicron resolution patterns that can be used <strong>for</strong> the cost effective, high-throughputanalysis of proteins <strong>and</strong> DNA products using very little reagents on, typically, asingle microscope slide. Microarrays were key to the success of the human genomeproject <strong>and</strong> will underpin further genomic analysis. The development of cellmicroarrays will further advance genomic analysis, <strong>and</strong> as the investigation of more1-29

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