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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>1.3.3. Alternative <strong>switchable</strong> <strong>surfaces</strong>Switchability is not only limited to hydrogel systems. There is no lack of other,alternative strategies <strong>for</strong> the development of <strong>switchable</strong> <strong>surfaces</strong> with biodevice<strong>applications</strong>.Lahann et al., [112] developed a surface coating on gold that transducedcon<strong>for</strong>mational changes in a low density SAM initiated by a voltage bias intowettability changes. The SAM was <strong>for</strong>med by attaching a large, cleavable headgrouponto the alkanethiol used (16-mercapto)hexanoic acid (MHA), which limitedthe packing density of the SAM. After cleavage of the head group, a low densitySAM remained. By application of a voltage bias, the ionised carboxylic acid groupwas attracted to the surface, producing a con<strong>for</strong>mational change in the MHAbackbone that exposed a hydrophobic loop at the solid liquid/interface, producing areversible change in hydrophilicity, which was observed as a change in contactangle. Development of these self assembled <strong>surfaces</strong> offers exciting opportunitieswhen applied to the manipulation of biomolecules.Gillies et al., [113] developed a one-off <strong>switchable</strong> system using pH sensitivemicelles. Linear-dendritic block copolymers containing hydrophobic head groups<strong>and</strong> PEG tails were <strong>for</strong>med, which spontaneously <strong>for</strong>med micelles in aqueousconditions. The hydrophobic head group contained a cyclic acetal linker that, uponhydrolysis at lower pH, decomposed, releasing trimethoxy benzene <strong>and</strong> producing adiol end group. This reaction increased the hydrophilicity of the head group <strong>and</strong>essentially removed the driving <strong>for</strong>ce <strong>for</strong> micelle <strong>for</strong>mation, which led to theirbreakdown. The micelles were stable at physiological pH, however, lowering the pHto 5 caused the hydrolysis of the acetal group, initiating the destabilisation of the1-39

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