## Abstract Surface initiated living‐radical polymerization (SIP) based on dithiocarbamate iniferters has been used to create molecularly imprinted core‐shell (CS) nanoparticles. Using this approach, propranolol, morphine and naproxen have been successfully imprinted in particle shells (the latter
Surface Molecularly Imprinted Polymer Core–Shell Particles
✍ Scribed by S. R. Carter; S. Rimmer
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 229 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1616-301X
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✦ Synopsis
Abstract
Core–shell molecularly imprinted polymers (CS‐MIPs) have been prepared by aqueous emulsion polymerization using water‐soluble template molecules. An amphiphilic binding monomer, oleyl phenyl hydrogen phosphate and ethylene glycol dimethacrylate were used in the formation of highly crosslinked surfaces around divinyl benzene crosslinked polystyrene core colloids. Evidence was obtained by transmission electron microscopy (TEM) for a change in surface morphology when the polymer shell was formed in the presence of a template. The caffeine‐imprinted polymers were shown to bind caffeine in preference to theophylline from an equimolar mixture of the compounds in aqueous solution at pH 7.0, whilst concentration–binding (Scatchard) curves revealed the presence of two populations of binding sites in aqueous phosphate buffer at pH 8.0 for caffeine and theophylline. Similar studies were also carried out for (S)‐propranolol and (S)‐atenolol at pH 5.5, which also revealed the presence of two populations of binding sites for core–shell particles imprinted with these compounds. (S)‐Propranolol was selectively removed from a solution of (S)‐propranolol and (S)‐atenolol by both of the CS‐MIPs, whereas the non‐imprinted particle showed no selectivity for either component.
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ter, nearly perfectly cylindrical, well-ordered pores with a very low density of defects. It may also be possible to increase pore filling by improving mass transport in the deposition environment with ultrasonication during deposition and careful control over the bath temperature. [25] In summary,
## Abstract **Summary:** The D‐glucose imprinted core‐shell nanosphere with an average size of ≈60 to 80 nm showed a significant preference for the binding of D‐glucose than the non‐imprinted core‐shell nanosphere. Depending on temperature, the binding site in the shell with __N__‐isopropylacrylami
Polymer particles with controlled morphologies and having diameters from about 1-20 can be prepared using a new suspension polymerization-based procedure. In contrast to existing procedures using emulsion polymerization, this process allows efficient preparation of supermicron particles that can be