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In silico screening of molecular imprinting prepolymerization systems: oseltamivir selective polymers through full-system molecular dynamics-based studies
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. (Linnaeus Ctr Biomat Chem, BMC)
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. (Linnaeus Ctr Biomat Chem, BMC;BBCL)ORCID iD: 0000-0003-4037-1992
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. (PPL;Linnaeus Ctr Biomat Chem, BMC)ORCID iD: 0000-0002-7392-0591
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. (Linnaeus Ctr Biomat Chem, BMC)
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2016 (English)In: Organic and biomolecular chemistry, ISSN 1477-0520, E-ISSN 1477-0539, Vol. 14, no 18, p. 4210-4219Article in journal (Refereed) Published
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Text
Abstract [en]

All-component molecular dynamics studies were used to probe a library of oseltamivir molecularly imprinted polymer prepolymerization mixtures. Polymers included one of five functional monomers (acrylamide, hydroxyethylmethacrylate, methacrylic acid, 2-(triflouromethyl)acrylic acid, 4-vinylpyridine) and one of three porogens (acetonitrile, chloroform, methanol) combined with the crosslinking agent ethylene glycol dimethacrylate and initiator 2,2'-azobis(2-methylpropionitrile). Polymers were characterized by nitrogen gas sorption measurements and SEM, and affinity studies performed using radioligand binding in various media. In agreement with the predictions made from the simulations, polymers prepared in acetonitrile using either methacrylic or trifluoromethacrylic acid demonstrated the highest affinities for oseltamivir. Further, the ensemble of interactions observed in the methanol system provided an explanation for the morphology of polymers prepared in this solvent. The materials developed here offer potential for use in solid-phase extraction or for catalysis. The results illustrate the strength of this in silico strategy as a potential prognostic tool in molecularly imprinted polymer design.

Place, publisher, year, edition, pages
2016. Vol. 14, no 18, p. 4210-4219
National Category
Organic Chemistry
Research subject
Chemistry, Organic Chemistry
Identifiers
URN: urn:nbn:se:lnu:diva-53319DOI: 10.1039/c6ob00305bISI: 000375610600007Scopus ID: 2-s2.0-84967333692OAI: oai:DiVA.org:lnu-53319DiVA, id: diva2:935366
Available from: 2016-06-10 Created: 2016-06-10 Last updated: 2022-03-16Bibliographically approved
In thesis
1. Towards Rational Molecularly Imprinted Polymer Design Using Molecular Dynamics-based Strategies
Open this publication in new window or tab >>Towards Rational Molecularly Imprinted Polymer Design Using Molecular Dynamics-based Strategies
2014 (English)Doctoral thesis, comprehensive summary (Other academic)
Place, publisher, year, edition, pages
Linnaeus University Press, 2014. p. 78
Series
Linnaeus University Dissertations ; 165
National Category
Organic Chemistry
Research subject
Chemistry, Organic Chemistry
Identifiers
urn:nbn:se:lnu:diva-110831 (URN)9789187427794 (ISBN)
Public defence
2014-05-09, N2007, Västergård, 10:00 (English)
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Available from: 2022-03-16 Created: 2022-03-16 Last updated: 2022-06-17Bibliographically approved

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Shoravi, SiamakOlsson, Gustaf D.Karlsson, Björn C. G.Bexborn, FredrikAbghoui, YounesHussain, JavedWiklander, Jesper G.Nicholls, Ian A.

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Shoravi, SiamakOlsson, Gustaf D.Karlsson, Björn C. G.Bexborn, FredrikAbghoui, YounesHussain, JavedWiklander, Jesper G.Nicholls, Ian A.
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Department of Chemistry and Biomedical Sciences
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Organic and biomolecular chemistry
Organic Chemistry

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