54 research outputs found
Surface grafting of electrospun fibers using ATRP and RAFT for the control of biointerfacial interactions
BACKGROUND The ability to present signalling molecules within a low fouling 3D environment that mimics the extracellular matrix is an important goal for a range of biomedical applications, both in vitro and in vivo. Cell responses can be triggered by non-specific protein interactions occurring on the surface of a biomaterial, which is an undesirable process when studying specific receptor-ligand interactions. It is therefore useful to present specific ligands of interest to cell surface receptors in a 3D environment that minimizes non-specific interactions with biomolecules, such as proteins. METHOD In this study, surface-initiated atom transfer radical polymerization (SI-ATRP) of poly(ethylene glycol)-based monomers was carried out from the surface of electrospun fibers composed of a styrene/vinylbenzyl chloride copolymer. Surface initiated radical addition-fragmentation chain transfer (SI-RAFT) polymerisation was also carried out to generate bottle brush copolymer coatings consisting of poly(acrylic acid) and poly(acrylamide). These were grown from surface trithiocarbonate groups generated from the chloromethyl styrene moieties existing in the original synthesised polymer. XPS was used to characterise the surface composition of the fibers after grafting and after coupling with fluorine functional XPS labels. RESULTS Bottle brush type coatings were able to be produced by ATRP which consisted of poly(ethylene glycol) methacrylate and a terminal alkyne-functionalised monomer. The ATRP coatings showed reduced non-specific protein adsorption, as a result of effective PEG incorporation and pendant alkynes groups existing as part of the brushes allowed for further conjugation of via azide-alkyne Huisgen 1,3-dipolar cycloaddition. In the case of RAFT, carboxylic acid moieties were effectively coupled to an amine label via amide bond formation. In each case XPS analysis demonstrated that covalent immobilisation had effectively taken place. CONCLUSION Overall, the studies presented an effective platform for the preparation of 3D scaffolds which contain effective conjugation sites for attachment of specific bioactive signals of interest, as well as actively reducing non-specific protein interactions.This research was supported by the Cooperative Research Centre for
Polymers (CRCP)
One step ATRP initiator immobilization on surfaces leading to gradient-grafted polymer brushes
Published: April 30, 2014A method is described that allows potentially any surface to be functionalized covalently with atom transfer radical polymerization (ATRP) initiators derived from ethyl-2-bromoisobutyrl bromide in a single step. In addition, the initiator surface density was variable and tunable such that the thickness of polymer chain grafted from the surface varied greatly on the surfaces providing examples, across the surface of a substrate, of increased chain stretching due to the entropic nature of crowded polymer chains leading toward polymer brushes. An initiator gradient of increasing surface density was deposited by plasma copolymerization of an ATRP initiator (ethyl 2-bromoisobutyrate) and a non-ATRP reactive diluent molecule (ethanol). The deposited plasma polymer retained its chemical ability to surface-initiate polymerization reactions as exemplified by N,N'-dimethyl acrylamide and poly(ethylene glycol) methyl ether methacrylate polymerizations, illustrating linear and bottle-brush-like chains, respectively. A large variation in graft thickness was observed from the low to high chain-density side suggesting that chains were forced to stretch away from the surface interface--a consequence of entropic effects resulting from increased surface crowding. The tert-butyl bromide group of ethyl 2-bromoisobutyrate is a commonly used initiator in ATRP, so a method for covalent linkage to any substrate in a single step desirably simplifies the multistep surface activation procedures currently used.Bryan R. Coad, Katie E. Styan, and Laurence Meaghe
The isoelectric points of sapphire crystals and alpha-alumina powder
Streaming potential measurements and atomic force microscropy (AFM) were used to determine the zeta potentials, diffuse layer potentials and isoelectric points (ieps) of alpha alumina sapphire single crystals for four different crystallographic orientations: c-plane, (0001); a-plane, (1120); m-plane, (1010); and r-plane, (1102). Both types of measurements indicated that the iep of the sapphire crystals was between about pH 5.0 and 6.0 for all crystals investigated. Unfortunately the techniques utilized could not conclusively differentiate any subtle differences in iep between the four orientations studied. The iep of alpha alumina powder was found to be pH 9.4. The difference in the ieps of the two different types of alpha alumina (single crystal and powder) is attributed to the presence of different types of surface hydroxyl groups on the two different types of surfaces. Powder is likely to have a greater fraction of singly coordinated surface hydroxyl groups (that have a high pKa), while sapphire single crystals are more likely to have most surface hydroxyls multiply coordinated (which have a low pKa)
Effect of Dissolved Gas and Salt on the Hydrophobic Force between Polypropylene Surfaces
Controlling the Adsorbed Conformation and Desorption of Polyelectrolyte with Added Surfactant via the Adsorption Mechanism:Â A Direct Force Measurement Study
Interaction Forces between a Bare Silica Surface and an α-Alumina Surface Bearing Adsorbed Polyelectrolyte and Surfactant
Specific control of cell-material interactions: Targeting cell receptors using ligand-functionalized polymer substrates
Cells respond to their environment in complex and sometimes poorly understood ways. Protein, peptide and synthetic peptidomimetic ligands may all be used to stimulate cells via receptor signaling, using interactions that are often highly specific. Polymer substrates that present these ligands provide a promising way to control cell development, both for applications in biotechnology and for fundamental studies of cell biology. Here we review a large range of techniques that have been employed to create and characterize ligand-functionalized substrates, with a particular focus on techniques that allow specific and consistent stimulation
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