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Divinyl Sulfone Cross-Linked Cyclodextrin-Based Polymeric Materials: Synthesis and Applications as Sorbents and Encapsulating Agents

The aim of this study was to evaluate the crosslinking abilities of divinyl sulfone (DVS) for the preparation of novel water-insoluble cyclodextrin-based polymers (CDPs) capable of forming inclusion complexes with different guest molecules. Reaction of DVS with native α-cyclodextrin (α-CD), β-cyclod...

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Autores principales: Morales-Sanfrutos, Julia, Lopez-Jaramillo, Francisco Javier, Elremaily, Mahmoud A. A., Hernández-Mateo, Fernando, Santoyo-Gonzalez, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272569/
https://www.ncbi.nlm.nih.gov/pubmed/25706758
http://dx.doi.org/10.3390/molecules20033565
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author Morales-Sanfrutos, Julia
Lopez-Jaramillo, Francisco Javier
Elremaily, Mahmoud A. A.
Hernández-Mateo, Fernando
Santoyo-Gonzalez, Francisco
author_facet Morales-Sanfrutos, Julia
Lopez-Jaramillo, Francisco Javier
Elremaily, Mahmoud A. A.
Hernández-Mateo, Fernando
Santoyo-Gonzalez, Francisco
author_sort Morales-Sanfrutos, Julia
collection PubMed
description The aim of this study was to evaluate the crosslinking abilities of divinyl sulfone (DVS) for the preparation of novel water-insoluble cyclodextrin-based polymers (CDPs) capable of forming inclusion complexes with different guest molecules. Reaction of DVS with native α-cyclodextrin (α-CD), β-cyclodextrin (β-CD) and/or starch generates a variety of homo- and hetero-CDPs with different degrees of crosslinking as a function of the reactants’ stoichiometric ratio. The novel materials were characterized by powder X-ray diffraction, electron microscopy and for their sorption of phenol and 4-nitrophenol. They were further evaluated as sorbents with phenolic pollutants (bisphenol A and β-naphthol) and bioactive compounds (the hormone progesterone and curcumin). Data obtained from the inclusion experiments show that the degree of cross-linking has a minor influence on the yield of inclusion complex formation and highlight the important role of the CDs, supporting a sorption process based on the formation of inclusion complexes. In general, the inclusion processes are better described by a Freundlich isotherm although an important number of them can also be fitted to the Langmuir isotherm with R(2) ≥ 0.9, suggesting a sorption onto a monolayer of homogeneous sites.
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spelling pubmed-62725692018-12-31 Divinyl Sulfone Cross-Linked Cyclodextrin-Based Polymeric Materials: Synthesis and Applications as Sorbents and Encapsulating Agents Morales-Sanfrutos, Julia Lopez-Jaramillo, Francisco Javier Elremaily, Mahmoud A. A. Hernández-Mateo, Fernando Santoyo-Gonzalez, Francisco Molecules Article The aim of this study was to evaluate the crosslinking abilities of divinyl sulfone (DVS) for the preparation of novel water-insoluble cyclodextrin-based polymers (CDPs) capable of forming inclusion complexes with different guest molecules. Reaction of DVS with native α-cyclodextrin (α-CD), β-cyclodextrin (β-CD) and/or starch generates a variety of homo- and hetero-CDPs with different degrees of crosslinking as a function of the reactants’ stoichiometric ratio. The novel materials were characterized by powder X-ray diffraction, electron microscopy and for their sorption of phenol and 4-nitrophenol. They were further evaluated as sorbents with phenolic pollutants (bisphenol A and β-naphthol) and bioactive compounds (the hormone progesterone and curcumin). Data obtained from the inclusion experiments show that the degree of cross-linking has a minor influence on the yield of inclusion complex formation and highlight the important role of the CDs, supporting a sorption process based on the formation of inclusion complexes. In general, the inclusion processes are better described by a Freundlich isotherm although an important number of them can also be fitted to the Langmuir isotherm with R(2) ≥ 0.9, suggesting a sorption onto a monolayer of homogeneous sites. MDPI 2015-02-19 /pmc/articles/PMC6272569/ /pubmed/25706758 http://dx.doi.org/10.3390/molecules20033565 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Morales-Sanfrutos, Julia
Lopez-Jaramillo, Francisco Javier
Elremaily, Mahmoud A. A.
Hernández-Mateo, Fernando
Santoyo-Gonzalez, Francisco
Divinyl Sulfone Cross-Linked Cyclodextrin-Based Polymeric Materials: Synthesis and Applications as Sorbents and Encapsulating Agents
title Divinyl Sulfone Cross-Linked Cyclodextrin-Based Polymeric Materials: Synthesis and Applications as Sorbents and Encapsulating Agents
title_full Divinyl Sulfone Cross-Linked Cyclodextrin-Based Polymeric Materials: Synthesis and Applications as Sorbents and Encapsulating Agents
title_fullStr Divinyl Sulfone Cross-Linked Cyclodextrin-Based Polymeric Materials: Synthesis and Applications as Sorbents and Encapsulating Agents
title_full_unstemmed Divinyl Sulfone Cross-Linked Cyclodextrin-Based Polymeric Materials: Synthesis and Applications as Sorbents and Encapsulating Agents
title_short Divinyl Sulfone Cross-Linked Cyclodextrin-Based Polymeric Materials: Synthesis and Applications as Sorbents and Encapsulating Agents
title_sort divinyl sulfone cross-linked cyclodextrin-based polymeric materials: synthesis and applications as sorbents and encapsulating agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272569/
https://www.ncbi.nlm.nih.gov/pubmed/25706758
http://dx.doi.org/10.3390/molecules20033565
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