Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone

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This study examined the feasibility of removing dexamethasone (DEX) from aqueous solutions using molecularly imprinted polymers (MIPs). The binding energy, used to evaluate the affinity between imprinted molecule and functional monomer, was calculated for DEX using molecular simulation via the densi...

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Detalles Bibliográficos
Autores: Adauto, Anais, Khan, Sabir, Vega Chacón, Jaime, Sotomayor, María D. P. T., Picasso, Gino
Formato: artículo
Fecha de Publicación:2025
Institución:Universidad Nacional de Ingeniería
Repositorio:UNI-Tesis
Lenguaje:inglés
OAI Identifier:oai:cybertesis.uni.edu.pe:20.500.14076/29146
Enlace del recurso:http://hdl.handle.net/20.500.14076/29146
https://doi.org/10.1002/pen.27082
Nivel de acceso:acceso abierto
Materia:Monomers
Molecularly imprinted polymers (MIP)
Dexamethasone
https://purl.org/pe-repo/ocde/ford#1.04.04
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network_name_str UNI-Tesis
repository_id_str 1534
dc.title.en.fl_str_mv Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone
title Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone
spellingShingle Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone
Adauto, Anais
Monomers
Molecularly imprinted polymers (MIP)
Dexamethasone
https://purl.org/pe-repo/ocde/ford#1.04.04
title_short Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone
title_full Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone
title_fullStr Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone
title_full_unstemmed Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone
title_sort Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasone
dc.creator.none.fl_str_mv Picasso, Gino
Sotomayor, María D. P. T.
Adauto, Anais
Khan, Sabir
Vega Chacón, Jaime
Sotomayor, María D. P. T.
Picasso, Gino
Vega Chacón, Jaime
Khan, Sabir
Adauto, Anais
author Adauto, Anais
author_facet Adauto, Anais
Khan, Sabir
Vega Chacón, Jaime
Sotomayor, María D. P. T.
Picasso, Gino
author_role author
author2 Khan, Sabir
Vega Chacón, Jaime
Sotomayor, María D. P. T.
Picasso, Gino
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Adauto, Anais
Khan, Sabir
Vega Chacón, Jaime
Sotomayor, María D. P. T.
Picasso, Gino
dc.subject.en.fl_str_mv Monomers
Molecularly imprinted polymers (MIP)
Dexamethasone
topic Monomers
Molecularly imprinted polymers (MIP)
Dexamethasone
https://purl.org/pe-repo/ocde/ford#1.04.04
dc.subject.ocde.es.fl_str_mv https://purl.org/pe-repo/ocde/ford#1.04.04
description This study examined the feasibility of removing dexamethasone (DEX) from aqueous solutions using molecularly imprinted polymers (MIPs). The binding energy, used to evaluate the affinity between imprinted molecule and functional monomer, was calculated for DEX using molecular simulation via the density functional theory method. From this approach, three different functional monomers were tested: methacrylic acid, N-(Hydroxymethyl) acrylamide, and 2-hydroxyethyl methacrylate designated as MIP-DEX1, MIP-DEX2, MIP-DEX3, respectively. All of them were prepared by the precipitation polymerization method, with trimethylolpropane trimethacrylate used as the crosslinker. Moreover, the kinetics of adsorption and adsorption isotherms were evaluated using different models to assess the adsorption mechanisms of DEX on polymers. The results showed that equilibrium between the polymer and DEX is reached at 180 min, with a maximum adsorption capacity of 117.27 mg g−1 for sample MIP-DEX3. The kinetic studies indicated that the adsorption of DEX on the polymers fits very well with the pseudo-second-order kinetic model. Equilibrium data were best described by the Freundlich model, suggesting that the sorption process occurs on a heterogeneous surface of the polymer cavities. The thermodynamic study confirms the role of selectivity cavities, exhibited in the sample MIP-DEX3. Reusability tests and application on real samples suggest that the synthesized polymers are promising adsorbents.
publishDate 2025
dc.date.accessioned.none.fl_str_mv 2026-04-06T20:49:05Z
dc.date.available.none.fl_str_mv 2026-04-06T20:49:05Z
dc.date.issued.fl_str_mv 2025-02
dc.type.es.fl_str_mv info:eu-repo/semantics/article
dc.type.version.es.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
format article
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.14076/29146
dc.identifier.doi.es.fl_str_mv https://doi.org/10.1002/pen.27082
url http://hdl.handle.net/20.500.14076/29146
https://doi.org/10.1002/pen.27082
dc.language.iso.en.fl_str_mv eng
language eng
dc.relation.isPartOf.es.fl_str_mv urn:issn:1548-2634
dc.rights.es.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.uri.es.fl_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.format.es.fl_str_mv application/pdf
dc.publisher.es.fl_str_mv Inspiring Plastics Professionals
dc.source.es.fl_str_mv Universidad Nacional de Ingeniería
Repositorio Institucional - UNI
dc.source.none.fl_str_mv reponame:UNI-Tesis
instname:Universidad Nacional de Ingeniería
instacron:UNI
instname_str Universidad Nacional de Ingeniería
instacron_str UNI
institution UNI
reponame_str UNI-Tesis
collection UNI-Tesis
bitstream.url.fl_str_mv http://cybertesis.uni.edu.pe/bitstream/20.500.14076/29146/2/license.txt
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repository.name.fl_str_mv Repositorio Institucional Universidad Nacional de Ingeniería
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spelling Adauto, AnaisKhan, SabirVega Chacón, JaimeSotomayor, María D. P. T.Picasso, GinoPicasso, GinoSotomayor, María D. P. T.Adauto, AnaisKhan, SabirVega Chacón, JaimeSotomayor, María D. P. T.Picasso, GinoVega Chacón, JaimeKhan, SabirAdauto, Anais2026-04-06T20:49:05Z2026-04-06T20:49:05Z2025-02http://hdl.handle.net/20.500.14076/29146https://doi.org/10.1002/pen.27082This study examined the feasibility of removing dexamethasone (DEX) from aqueous solutions using molecularly imprinted polymers (MIPs). The binding energy, used to evaluate the affinity between imprinted molecule and functional monomer, was calculated for DEX using molecular simulation via the density functional theory method. From this approach, three different functional monomers were tested: methacrylic acid, N-(Hydroxymethyl) acrylamide, and 2-hydroxyethyl methacrylate designated as MIP-DEX1, MIP-DEX2, MIP-DEX3, respectively. All of them were prepared by the precipitation polymerization method, with trimethylolpropane trimethacrylate used as the crosslinker. Moreover, the kinetics of adsorption and adsorption isotherms were evaluated using different models to assess the adsorption mechanisms of DEX on polymers. The results showed that equilibrium between the polymer and DEX is reached at 180 min, with a maximum adsorption capacity of 117.27 mg g−1 for sample MIP-DEX3. The kinetic studies indicated that the adsorption of DEX on the polymers fits very well with the pseudo-second-order kinetic model. Equilibrium data were best described by the Freundlich model, suggesting that the sorption process occurs on a heterogeneous surface of the polymer cavities. The thermodynamic study confirms the role of selectivity cavities, exhibited in the sample MIP-DEX3. Reusability tests and application on real samples suggest that the synthesized polymers are promising adsorbents.Submitted by Quispe Rabanal Flavio (flaviofime@hotmail.com) on 2026-04-06T20:49:05Z No. of bitstreams: 1 adauto_a.pdf: 9819430 bytes, checksum: 423f9de618fb53eea167923bd8c20b3d (MD5)Made available in DSpace on 2026-04-06T20:49:05Z (GMT). No. of bitstreams: 1 adauto_a.pdf: 9819430 bytes, checksum: 423f9de618fb53eea167923bd8c20b3d (MD5) Previous issue date: 2025-02Este trabajo fue financiado por el Programa Nacional de Investigación Científica y Estudios Avanzados (Prociencia - Perú) en el marco del "Desarrollo de dispositivos analíticos empleando polímeros de impresión molecular para la cuantificación de medicamentos usados en el tratamiento de COVID-19 presentes en los ríos del Perú" [número de contrato 057-2021]application/pdfengInspiring Plastics Professionalsinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/4.0/Universidad Nacional de IngenieríaRepositorio Institucional - UNIreponame:UNI-Tesisinstname:Universidad Nacional de Ingenieríainstacron:UNIMonomersMolecularly imprinted polymers (MIP)Dexamethasonehttps://purl.org/pe-repo/ocde/ford#1.04.04Effect of functional monomers on the binding properties of molecularly imprinted polymers (MIPs) for selective recognition of dexamethasoneinfo:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85urn:issn:1548-2634LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://cybertesis.uni.edu.pe/bitstream/20.500.14076/29146/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD5220.500.14076/29146oai:cybertesis.uni.edu.pe:20.500.14076/291462026-04-06 15:54:32.095Repositorio Institucional Universidad Nacional de Ingenieríarepositorio@uni.edu.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