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Reference type: Journal
Authors: Manesiotis P, Osmani Q, McLoughlin P
Article Title: An enantio-selective chromatographic stationary phase for S-ibuprofen prepared by stoichiometric molecular imprinting.
Publication date: 2012
Journal: Journal of Materials Chemistry
Volume: 22
Issue: (22)
Page numbers: 11201-11207.
DOI: 10.1039/C2JM16659C

Abstract: Molecularly Imprinted Polymers (MIPs) against S-ibuprofen were synthesised using a tailor made functional monomer, 2-acrylamido-4-methylpyridine, following extensive pre-polymerisation studies of template-monomer complexation. An apparent association constant of 340 22 M-1 was calculated that was subsequently corrected to account for dimerisation of ibuprofen (Kdim = 320 95 M-1) resulting in an intrinsic association constant of 715 16 M-1, consistent with previously reported values. Using the synthesised imprinted polymer as a stationary phase, complete resolution of a racemic mixture of ibuprofen was achieved in predominantly aqueous mobile phases. An imprinting factor of 10 was observed, and was found to be in agreement with the difference in the average number of binding sites between MIP and blank polymers, calculated by staircase frontal chromatography. The imprinted polymers exhibited enhanced selectivity for the templated drug over structurally related NSAIDs. When applied as sorbents in solid-phase extraction of ibuprofen from commercial tablets, urine and blood serum samples, recoveries up to 92.2% were achieved
Template and target information: S-ibuprofen


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