Abstrac~ Sorption isotherms of water vapour were determined for crosslinked poly-2-hydroxyethyl methacrylate (PHEMA), poly-2-(2'-hydroxyethoxy)ethyl methacrylate (PHEOEMA) and statistical copolymers at 35'. In the case of PHEMA the amount sorbed does not depend on the porosity of structure: sorption
Hydrophilic molecularly imprinted poly(hydroxyethyl-methacrylate) polymers
✍ Scribed by Ebru Oral; Nicholas A. Peppas
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 189 KB
- Volume
- 78A
- Category
- Article
- ISSN
- 1549-3296
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Highly cross‐linked 2‐hydroxyethyl methacrylate (HEMA) and poly(ethylene glycol) dimethacrylate with poly(ethylene glycol) of molecular weight 600 (PEG600DMA) were molecularly imprinted with hydrophilic templates glucose and proxyphylline using water as a solvent. Glucose‐imprinted polymers showed increased recognitive capacity compared to nonimprinted polymers as well as increased glucose uptake compared to structurally similar galactose and methylglucopyranoside. Increasing glucose concentration in the imprinting mixture resulted in higher capacity and selective binding. Similar results were obtained for proxyphylline‐imprinted P(HEMA‐co‐PEG600DMA) polymers, where the proxyphylline uptake was higher than structurally similar theophylline. Glucose‐imprinted networks also showed diffusion coefficients on the order of 10^−6^ cm^2^/s, conducive to applications in drug delivery and tissue engineering. This work showed that using pairs of hydrogen‐bonding monomers and templates, selective, high‐affinity sites could be created despite nonspecific binding. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006
📜 SIMILAR VOLUMES
The technique of molecular imprinting has been used for inducing affinity sites towards speciÐc molecules in synthetic polymers. We have used the method for creating recognition sites for cholesterol in poly(2-hydroxyethyl methacrylate) which was polymerised by c-irradiation. Our preliminary studies
Because of its chemical versatility and demonstrated biocom-sion between the cells and the polymer surface. Cell adhesion patibility, poly(2-hydroxyethyl methacrylate) (pHEMA) has was weaker on pHEMA, as a significant fraction of the fibrobeen widely used as a polymer for biomedical applications. b