Recognition in molecularly imprinted polymer α2-adrenoreceptor mimics
✍ Scribed by Johanna Berglund; Ian A. Nicholls; Christer Lindbladh; Klaus Mosbach
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 325 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0960-894X
No coin nor oath required. For personal study only.
✦ Synopsis
Molecularly imprinted polymers (MIPs) selective for the ct2-adrenoreceptor antagonist yohimbine (1) have been prepared and studied as ot2-adrenoreceptor mimics. Marked ligand stereoselectivity was demonstrated in radioligand binding and HPLC studies upon comparison to blank and corynanthine (2) MIPs. K D values in the nanomolar range have been shown for ant/-1 MIP prepared in chloroform solutions upon rebinding in organic media.
📜 SIMILAR VOLUMES
Molecularly imprinted polymer metal-chelate antibody combining site mimics have been used to examine the roles of metal ion and ligand shape on binding selectivity. Chromatography based recognition studies highlight the utility of metal ion coordination for controlling molecularly imprinted polymer
The use of a novel chiral functional monomer system in molecular imprinting protocols is described. The monomer, dibenzyl (2R,3R)-O-monoacryloyl tartrate, possesses a hydroxyl moiety which can be used to direct template-functional monomer interactions during molecular imprinting polymerization. This
Micro-contact imprinting has been used to form thin-film molecular imprints of ovalbumin (OVA) in polymers supported on glass slides. Thermocalorimetric data was used to optimise the choice of functional monomer and cross-linker to maximise selectivity and minimise non-specific recognition. A polyme
In the present study molecularly imprinted polymers (MIPS) were prepared against a series of structurally related compounds containing various numbers of pyridyl groups. The goal, to increase understanding of the mechanisms of recognition in MIPS, was achieved by comparing the patterns of retention