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Patterned and switchable surfaces for biomaterial applications

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CHAPTER 3.COMPARISON OF THE BINDING MODE OFPLASMID DNA TO ALLYLAMINE PLASMA POLYMERAND POLY(ETHYLENE GLYCOL) SURFACES3The content of this chapter is based upon reference [188].3.3.1. IntroductionNucleic acid probes have been used extensively in recent years <strong>for</strong> <strong>applications</strong>such as biomimetics, ‘smart’ drug delivery, biosensing <strong>and</strong> tissue engineering [3, 4,6] <strong>and</strong> <strong>for</strong> tasks such as DNA purification <strong>and</strong> gene therapy [1, 8, 14, 127]. Duringthese <strong>applications</strong> the nucleic acid probes are often bound or associated to the surfaceof a <strong>biomaterial</strong>, thus, in order to increase the scope <strong>and</strong> capabilities of these devicesadvanced control over DNA manipulation at <strong>surfaces</strong> is required. Insight into themode of DNA association with a particular surface of interest is, thus, pivotal inorder to maximise DNA-surface interactions <strong>and</strong> allow <strong>for</strong> advanced manipulation ofDNA at a surface such as <strong>switchable</strong> binding.Double-str<strong>and</strong>ed DNA can generally be regarded as a coiled rod with apurine/pyrimidine core <strong>and</strong> a phosphate <strong>and</strong> pentose sugar exterior. The negativecharges of the phosphate groups endow DNA with the characteristic feature of ananionic polyelectrolyte. For this reason, the production of <strong>surfaces</strong> with a positivesurface charge, often achieved by the incorporation of amine functionality, has beeninvestigated <strong>and</strong> achieved by a number of strategies with the basic aim to increaseDNA surface adsorption via electrostatic interactions [27]. As well as commonlyutilised wet chemical silanisation strategies [9, 30] <strong>and</strong> coating <strong>for</strong>mation withpolyamines [29, 78], aminated <strong>surfaces</strong> have been produced by plasma3-97

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