2005
DOI: 10.1016/j.cis.2004.07.009
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Surface modification and functionalization through the self-assembled monolayer and graft polymerization

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Cited by 256 publications
(163 citation statements)
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“…Most of the surface modification work in the literature has been focusing on the modification of device surfaces or thin films [117][118][119][120]. Our group recently developed a few techniques to effectively modify the internal pore surfaces of 3D porous polymer scaffolds.…”
Section: Surface Modificationmentioning
confidence: 99%
“…Most of the surface modification work in the literature has been focusing on the modification of device surfaces or thin films [117][118][119][120]. Our group recently developed a few techniques to effectively modify the internal pore surfaces of 3D porous polymer scaffolds.…”
Section: Surface Modificationmentioning
confidence: 99%
“…by preventing the aggregation of nanoparticles which can occur due to their high interfacial reactivity and high surface tension energy, and by improving the compatibility between nanoparticles and polymer, which is usually accomplished after the adequate surface modification of nanoparticles. The most common way to modify the surface of nanoparticles, control nanoparticles aggregation and stabilize the colloidal nanoparticles is to attach suitable organic groups to the surface atoms of nanoparticles [15][16][17]. After the appropriate surface modification, nanoparticles become hydrophobic, which can decrease their surface tension and lead to better miscibility and compatibility of nanoparticles with the polymer matrix [18].…”
Section: Introductionmentioning
confidence: 99%
“…An aperture could then be created through the centre of the channel by SACE. To 2 Lipid bilayers are typically formed by self-assembly of an initially thick lipid-solvent film, which will have a monolayer of amphipathic lipid molecules at each of its aqueous interfaces [23]. As previously noted, thinning of the lipid-solvent film arises primarily from the wetting of the hydrophobic support by the organic solvent.…”
Section: Incorporation Into a Microfluidic Devicementioning
confidence: 99%
“…This is due to the bilayer formation process relying upon surface-tensioninduced drainage of the non-polar solvent (decane in this case) to thin the initially thick lipid-solvent layer down to that of a lipid bilayer. Silane coupling agents are widely used for modifying the surface chemistry of glass substrates [23], as the silane anchor group (which couples to surface hydroxyl groups via siloxy linkages) can be attached to a wide variety of functional groups. In PF-TCS, the silane group is linked to a hydrophobic, fluorinated carbon chain.…”
Section: Silanization Of Glass Aperturesmentioning
confidence: 99%