The novel surface imprinted polymer composites (MIP/K 2 Ti 4 O 9 ) were prepared using dibenzothiophene (DBT) as the template, 4-vinylpyridine as the functional monomer and potassium tetratitanate whisker (K 2 Ti 4 O 9 ) as the carrier. The synthetic product was characterized by Fourier transform in
Preparation and recognition performance of cytisine alkaloid-imprinted material prepared using novel surface molecular imprinting technique
โ Scribed by Baojiao Gao; Qinyuan Niu; Ruikui Du
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 444 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
โฆ Synopsis
Preparation and recognition performance of cytisine alkaloid-imprinted material prepared using novel surface molecular imprinting technique
Methacrylic acid was first graft-polymerized on the surfaces of micron-sized silica gel particles in the manner of ''grafting from'' using 3-methacryloxypropyl trimethoxysilane as an intermedia, obtaining the grafted particle polymethacrylic acid PMAA/SiO 2 . By adopting the novel surface-molecular imprinting technique put forward by us, cytisine molecule-imprinted material MIP-PMAA/SiO 2 was prepared with ethylene glycol diglycidyl ether as crosslinking agent. The binding characteristics of MIP-PMAA/SiO 2 towards cytisine was investigated in depth with both batch and column methods and using matrine and oxymatrine as two contrast alkaloids, which with cytisine coexist in sophora alopecuroides and their chemical structure is similar to cytisine to a certain extent. The experimental results show that the surface-imprinted material MIP-PMAA/SiO 2 has excellent binding affinity for cytisine (20.1 g/100 g of binding capacity), and it is more important that MIP-PMAA/SiO 2 has very high recognition selectivity for cytisine in relation to the two contrast alkaloids. The selectivity coefficients of the grafted particles PMAA/SiO 2 (non-imprinted material) for cytosine in relation to matrine and oxymatrine are only 1.03 and 1.06, respectively, displaying no recognition selectivity for cytisine. However, after imprinting, the selectivity coefficient of MIP-PMAA/SiO 2 for cytisine in respect to matrine and oxymatrine are remarkably enhanced to 12.08 and 15.05, respectively.
๐ SIMILAR VOLUMES
Molecular imprinting and phage display library technologies are rapidly being accepted as useful techniques for the generation of ligand-selective recognition motifs. The use of molecular imprinting to produce a novel type 11 aldolase mimic selective for the cobalt(I1)-mediated aldol condensation of