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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>1.3.2. Switchable <strong>surfaces</strong> <strong>for</strong> the control of proteins <strong>and</strong> cellsControlling the behaviour of cells firstly requires the ability to manipulate theproteins that cells use to mediate their attachment to <strong>surfaces</strong>. Since a major driving<strong>for</strong>ce <strong>for</strong> protein adsorption is the surface dehydration associated with hydrophobicinteractions, a focus <strong>for</strong> switching protein <strong>and</strong> cell attachment has been theproduction of <strong>surfaces</strong> that are able to alter their wettability when stimulatedappropriately.Okano’s research group has developed a <strong>switchable</strong> polymeric surface <strong>for</strong> cellattachment using poly(N-isopropylacrylamide) (PNIPAAm), which switches from ahydrophilic state to a hydrophobic state by increasing the temperature above itsLCST of 32 °C. Mammalian cells grew on the hydrophobic polymer, but not thehydrophilic polymer enabling cell adhesion to be turned on <strong>and</strong> off [110]. A patternof the PNIPAAm was <strong>for</strong>med on a surface by UV-initiated polymerisation of thepolymer through a metal photomask (Figure 1.7A) in direct contact with the <strong>surfaces</strong>uch that PNIPAAm was only <strong>for</strong>med where the UV was not blocked. Using thistechnique, Yamato et al., [73] were able to produce an array of 1 mm diametercircular domains of PNIPAAm on a background of tissue culture grade PS. Seededrat hepatocytes grew on both the PNIPAAm <strong>and</strong> the PS (Figure 1.7B), however,upon lowering the temperature, the cells detached from the PNIPAAm regions(Figure 1.7C). Upon raising the temperature to 37 °C seeded endothelial cells thenattached to the PNIPAAm, generating a patterned cell co-culture (Figure 1.7D).Alternatively, Yamato et al., [64] seeded rat hepatocytes on the patterned PNIPAAmat 20 °C, below the LCST, such that cells only attached to the unmodified tissueculture grade PS. Subsequently seeded human fetal lung fibroblasts at 37 °C, above1-35

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