TY - JOUR
T1 - Synthesis of imprinted beads by aqueous suspension polymerisation for chiral recognition of antihistamines
AU - Walsh, Rachel
AU - Osmani, Qendresa
AU - Hughes, Helen
AU - Duggan, Patrick
AU - McLoughlin, Peter
PY - 2011/11/15
Y1 - 2011/11/15
N2 - A novel non-stabilised aqueous suspension polymerisation methodology for the preparation of spherical molecularly imprinted polymers is described with chlorpheniramine (CP), d-chlorpheniramine (d-CP), brompheniramine (BP) and d-brompheniramine (d-BP) as the templates, respectively. Using this rapid and simple technique, controlled polymer beads in the low micron range with narrow size distributions were generated by photo-polymerisation. The use of agitation speed as a method of controlling bead size distribution was demonstrated. Enantioselective properties of the imprinted beads were examined and the polymers prepared using d-chlorpheniramine and d-brompheniramine were capable of discriminating between the enantiomers of the template. Cross-selectivity studies were performed by batch rebinding with the influence of template size and functional group orientation of analytes on the recognition properties of the imprinted polymers investigated. Physical characteristics of all polymers were studied by nitrogen sorption porosimetry, particle size analysis and scanning electron microscopy (SEM) in order to gain an insight into the role of such properties on retention behaviour.
AB - A novel non-stabilised aqueous suspension polymerisation methodology for the preparation of spherical molecularly imprinted polymers is described with chlorpheniramine (CP), d-chlorpheniramine (d-CP), brompheniramine (BP) and d-brompheniramine (d-BP) as the templates, respectively. Using this rapid and simple technique, controlled polymer beads in the low micron range with narrow size distributions were generated by photo-polymerisation. The use of agitation speed as a method of controlling bead size distribution was demonstrated. Enantioselective properties of the imprinted beads were examined and the polymers prepared using d-chlorpheniramine and d-brompheniramine were capable of discriminating between the enantiomers of the template. Cross-selectivity studies were performed by batch rebinding with the influence of template size and functional group orientation of analytes on the recognition properties of the imprinted polymers investigated. Physical characteristics of all polymers were studied by nitrogen sorption porosimetry, particle size analysis and scanning electron microscopy (SEM) in order to gain an insight into the role of such properties on retention behaviour.
KW - Aqueous suspension polymerisation
KW - Brompheniramine
KW - Chiral separation
KW - Chlorpheniramine
KW - Microspheres
KW - Molecularly imprinted polymers
UR - http://www.scopus.com/inward/record.url?scp=80555149378&partnerID=8YFLogxK
U2 - 10.1016/j.jchromb.2011.09.036
DO - 10.1016/j.jchromb.2011.09.036
M3 - Article
C2 - 21982909
AN - SCOPUS:80555149378
SN - 1570-0232
VL - 879
SP - 3523
EP - 3530
JO - Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences
JF - Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences
IS - 30
ER -