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Molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs

A novel approach towards recognition of sulfonylureas based on a polymerisable ion pair is presented. A solution association constant >10(5) M(−1) between the model target glibenclamide and 4-vinylbenzyltrimethylammonium methacrylate is measured, and the formation of 1 : 1 complexes verified. Sub...

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Detalles Bibliográficos
Autores principales: Pessagno, Federica, Hasanah, Aliya Nur, Manesiotis, Panagiotis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079912/
https://www.ncbi.nlm.nih.gov/pubmed/35540745
http://dx.doi.org/10.1039/c8ra01135d
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author Pessagno, Federica
Hasanah, Aliya Nur
Manesiotis, Panagiotis
author_facet Pessagno, Federica
Hasanah, Aliya Nur
Manesiotis, Panagiotis
author_sort Pessagno, Federica
collection PubMed
description A novel approach towards recognition of sulfonylureas based on a polymerisable ion pair is presented. A solution association constant >10(5) M(−1) between the model target glibenclamide and 4-vinylbenzyltrimethylammonium methacrylate is measured, and the formation of 1 : 1 complexes verified. Subsequently prepared stoichiometrically imprinted polymers exhibit exceptionally high affinity and binding capacity for glibenclamide, owing to synergistic binding of both the neutral and deprotonated form of the drug by the ion pair monomer. The polymers are applied to the selective extraction of glibenclamide from blood serum samples, achieving recoveries of up to 98% and demonstrating excellent long-term stability, negating the need for regular sorbent regeneration.
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spelling pubmed-90799122022-05-09 Molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs Pessagno, Federica Hasanah, Aliya Nur Manesiotis, Panagiotis RSC Adv Chemistry A novel approach towards recognition of sulfonylureas based on a polymerisable ion pair is presented. A solution association constant >10(5) M(−1) between the model target glibenclamide and 4-vinylbenzyltrimethylammonium methacrylate is measured, and the formation of 1 : 1 complexes verified. Subsequently prepared stoichiometrically imprinted polymers exhibit exceptionally high affinity and binding capacity for glibenclamide, owing to synergistic binding of both the neutral and deprotonated form of the drug by the ion pair monomer. The polymers are applied to the selective extraction of glibenclamide from blood serum samples, achieving recoveries of up to 98% and demonstrating excellent long-term stability, negating the need for regular sorbent regeneration. The Royal Society of Chemistry 2018-04-17 /pmc/articles/PMC9079912/ /pubmed/35540745 http://dx.doi.org/10.1039/c8ra01135d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Pessagno, Federica
Hasanah, Aliya Nur
Manesiotis, Panagiotis
Molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs
title Molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs
title_full Molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs
title_fullStr Molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs
title_full_unstemmed Molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs
title_short Molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs
title_sort molecularly imprinted ‘traps’ for sulfonylureas prepared using polymerisable ion pairs
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079912/
https://www.ncbi.nlm.nih.gov/pubmed/35540745
http://dx.doi.org/10.1039/c8ra01135d
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