Functionalization of an alginate-based material by oxidation and reductive amination

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This research focused on the synthesis of a functional alginate-based material via chemical modification processes with two steps: oxidation and reductive amination. In previous alginate functionalization with a target molecule such as cysteine, the starting material was purified and characterized b...

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Autores: Huamani-Palomino R.G., Córdova B.M., Elvis Renzo Pichilingue L., Venâncio T., Valderrama A.C.
Formato: artículo
Fecha de Publicación:2021
Institución:Consejo Nacional de Ciencia Tecnología e Innovación
Repositorio:CONCYTEC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.concytec.gob.pe:20.500.12390/2409
Enlace del recurso:https://hdl.handle.net/20.500.12390/2409
https://doi.org/10.3390/polym13020255
Nivel de acceso:acceso abierto
Materia:Reductive amination
Alginate
Functionalization
Oxidation
http://purl.org/pe-repo/ocde/ford#1.04.01
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dc.title.none.fl_str_mv Functionalization of an alginate-based material by oxidation and reductive amination
title Functionalization of an alginate-based material by oxidation and reductive amination
spellingShingle Functionalization of an alginate-based material by oxidation and reductive amination
Huamani-Palomino R.G.
Reductive amination
Alginate
Functionalization
Oxidation
http://purl.org/pe-repo/ocde/ford#1.04.01
title_short Functionalization of an alginate-based material by oxidation and reductive amination
title_full Functionalization of an alginate-based material by oxidation and reductive amination
title_fullStr Functionalization of an alginate-based material by oxidation and reductive amination
title_full_unstemmed Functionalization of an alginate-based material by oxidation and reductive amination
title_sort Functionalization of an alginate-based material by oxidation and reductive amination
author Huamani-Palomino R.G.
author_facet Huamani-Palomino R.G.
Córdova B.M.
Elvis Renzo Pichilingue L.
Venâncio T.
Valderrama A.C.
author_role author
author2 Córdova B.M.
Elvis Renzo Pichilingue L.
Venâncio T.
Valderrama A.C.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Huamani-Palomino R.G.
Córdova B.M.
Elvis Renzo Pichilingue L.
Venâncio T.
Valderrama A.C.
dc.subject.none.fl_str_mv Reductive amination
topic Reductive amination
Alginate
Functionalization
Oxidation
http://purl.org/pe-repo/ocde/ford#1.04.01
dc.subject.es_PE.fl_str_mv Alginate
Functionalization
Oxidation
dc.subject.ocde.none.fl_str_mv http://purl.org/pe-repo/ocde/ford#1.04.01
description This research focused on the synthesis of a functional alginate-based material via chemical modification processes with two steps: oxidation and reductive amination. In previous alginate functionalization with a target molecule such as cysteine, the starting material was purified and characterized by UV-Vis,1 H-NMR and HSQC. Additionally, the application of FT-IR techniques during each step of alginate functionalization was very useful, since new bands and spiked signals around the pyranose ring (1200–1000 cm−1) and anomeric region (1000–750 cm−1) region were identified by a second derivative. Additionally, the presence of C1-H1 of β-D-mannuronic acid residue as well as C1-H1 of α-L-guluronic acid residue was observed in the FT-IR spectra, including a band at 858 cm−1 with characteristics of the N-H moiety from cysteine. The possibility of attaching cysteine molecules to an alginate backbone by oxidation and post-reductive amination processes was confirmed through13 C-NMR in solid state; a new peak at 99.2 ppm was observed, owing to a hemiacetal group formed in oxidation alginate. Further, the peak at 31.2 ppm demonstrates the presence of carbon-CH2-SH in functionalized alginate—clear evidence that cysteine was successfully attached to the alginate backbone, with 185 µmol of thiol groups per gram polymer estimated in alginate-based material by UV-Visible. Finally, it was observed that guluronic acid residue of alginate are preferentially more affected than mannuronic acid residue in the functionalization. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
publishDate 2021
dc.date.accessioned.none.fl_str_mv 2024-05-30T23:13:38Z
dc.date.available.none.fl_str_mv 2024-05-30T23:13:38Z
dc.date.issued.fl_str_mv 2021
dc.type.none.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.citation.none.fl_str_mv Huamani-Palomino, R. G., Córdova, B. M., Pichilingue L., E. R., Venâncio, T., & Valderrama, A. C. (2021). Functionalization of an Alginate-Based Material by Oxidation and Reductive Amination. Polymers, 13(2), 255. https://doi.org/10.3390/polym13020255
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12390/2409
dc.identifier.doi.none.fl_str_mv https://doi.org/10.3390/polym13020255
dc.identifier.scopus.none.fl_str_mv 2-s2.0-85099877741
identifier_str_mv Huamani-Palomino, R. G., Córdova, B. M., Pichilingue L., E. R., Venâncio, T., & Valderrama, A. C. (2021). Functionalization of an Alginate-Based Material by Oxidation and Reductive Amination. Polymers, 13(2), 255. https://doi.org/10.3390/polym13020255
2-s2.0-85099877741
url https://hdl.handle.net/20.500.12390/2409
https://doi.org/10.3390/polym13020255
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Polymers
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.uri.none.fl_str_mv https://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0/
dc.publisher.none.fl_str_mv MDPI AG
publisher.none.fl_str_mv MDPI AG
dc.source.none.fl_str_mv reponame:CONCYTEC-Institucional
instname:Consejo Nacional de Ciencia Tecnología e Innovación
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spelling Publicationrp05576600rp05571600rp05948600rp05893600rp05574600Huamani-Palomino R.G.Córdova B.M.Elvis Renzo Pichilingue L.Venâncio T.Valderrama A.C.2024-05-30T23:13:38Z2024-05-30T23:13:38Z2021Huamani-Palomino, R. G., Córdova, B. M., Pichilingue L., E. R., Venâncio, T., & Valderrama, A. C. (2021). Functionalization of an Alginate-Based Material by Oxidation and Reductive Amination. Polymers, 13(2), 255. https://doi.org/10.3390/polym13020255https://hdl.handle.net/20.500.12390/2409https://doi.org/10.3390/polym130202552-s2.0-85099877741This research focused on the synthesis of a functional alginate-based material via chemical modification processes with two steps: oxidation and reductive amination. In previous alginate functionalization with a target molecule such as cysteine, the starting material was purified and characterized by UV-Vis,1 H-NMR and HSQC. Additionally, the application of FT-IR techniques during each step of alginate functionalization was very useful, since new bands and spiked signals around the pyranose ring (1200–1000 cm−1) and anomeric region (1000–750 cm−1) region were identified by a second derivative. Additionally, the presence of C1-H1 of β-D-mannuronic acid residue as well as C1-H1 of α-L-guluronic acid residue was observed in the FT-IR spectra, including a band at 858 cm−1 with characteristics of the N-H moiety from cysteine. The possibility of attaching cysteine molecules to an alginate backbone by oxidation and post-reductive amination processes was confirmed through13 C-NMR in solid state; a new peak at 99.2 ppm was observed, owing to a hemiacetal group formed in oxidation alginate. Further, the peak at 31.2 ppm demonstrates the presence of carbon-CH2-SH in functionalized alginate—clear evidence that cysteine was successfully attached to the alginate backbone, with 185 µmol of thiol groups per gram polymer estimated in alginate-based material by UV-Visible. Finally, it was observed that guluronic acid residue of alginate are preferentially more affected than mannuronic acid residue in the functionalization. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.Fondo Nacional de Desarrollo Científico y Tecnológico - FondecytengMDPI AGPolymersinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/4.0/Reductive aminationAlginate-1Functionalization-1Oxidation-1http://purl.org/pe-repo/ocde/ford#1.04.01-1Functionalization of an alginate-based material by oxidation and reductive aminationinfo:eu-repo/semantics/articlereponame:CONCYTEC-Institucionalinstname:Consejo Nacional de Ciencia Tecnología e Innovacióninstacron:CONCYTEC#PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE#ORIGINALFunctionalization - polymers-13-00255-v2.pdfFunctionalization - polymers-13-00255-v2.pdfapplication/pdf5103941https://repositorio.concytec.gob.pe/bitstreams/a025a8b7-24a3-42be-9729-e94532793790/downloadf16a335bf6ead0ae534922a214d916a7MD51TEXTFunctionalization - polymers-13-00255-v2.pdf.txtFunctionalization - polymers-13-00255-v2.pdf.txtExtracted texttext/plain45891https://repositorio.concytec.gob.pe/bitstreams/7b3bb85d-0ac6-4663-87f7-f15f8e732b12/downloade4fe7eaebce1a37167eecfda3532b6bfMD52THUMBNAILFunctionalization - polymers-13-00255-v2.pdf.jpgFunctionalization - polymers-13-00255-v2.pdf.jpgGenerated Thumbnailimage/jpeg5660https://repositorio.concytec.gob.pe/bitstreams/51b1495a-3951-42c9-ada0-efd1aa59346f/downloada9ba42445bdc42ce033585a54ea661f5MD5320.500.12390/2409oai:repositorio.concytec.gob.pe:20.500.12390/24092025-01-19 22:01:05.103https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessopen accesshttps://repositorio.concytec.gob.peRepositorio Institucional CONCYTECrepositorio@concytec.gob.pe#PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE#<Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="e1c1d398-ca19-4609-a625-5dd69510111d"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>Functionalization of an alginate-based material by oxidation and reductive amination</Title> <PublishedIn> <Publication> <Title>Polymers</Title> </Publication> </PublishedIn> <PublicationDate>2021</PublicationDate> <DOI>https://doi.org/10.3390/polym13020255</DOI> <SCP-Number>2-s2.0-85099877741</SCP-Number> <Authors> <Author> <DisplayName>Huamani-Palomino R.G.</DisplayName> <Person id="rp05576" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Córdova B.M.</DisplayName> <Person id="rp05571" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Elvis Renzo Pichilingue L.</DisplayName> <Person id="rp05948" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Venâncio T.</DisplayName> <Person id="rp05893" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Valderrama A.C.</DisplayName> <Person id="rp05574" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>MDPI AG</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>https://creativecommons.org/licenses/by/4.0/</License> <Keyword>Reductive amination</Keyword> <Keyword>Alginate</Keyword> <Keyword>Functionalization</Keyword> <Keyword>Oxidation</Keyword> <Abstract>This research focused on the synthesis of a functional alginate-based material via chemical modification processes with two steps: oxidation and reductive amination. In previous alginate functionalization with a target molecule such as cysteine, the starting material was purified and characterized by UV-Vis,1 H-NMR and HSQC. Additionally, the application of FT-IR techniques during each step of alginate functionalization was very useful, since new bands and spiked signals around the pyranose ring (1200–1000 cm−1) and anomeric region (1000–750 cm−1) region were identified by a second derivative. Additionally, the presence of C1-H1 of β-D-mannuronic acid residue as well as C1-H1 of α-L-guluronic acid residue was observed in the FT-IR spectra, including a band at 858 cm−1 with characteristics of the N-H moiety from cysteine. The possibility of attaching cysteine molecules to an alginate backbone by oxidation and post-reductive amination processes was confirmed through13 C-NMR in solid state; a new peak at 99.2 ppm was observed, owing to a hemiacetal group formed in oxidation alginate. Further, the peak at 31.2 ppm demonstrates the presence of carbon-CH2-SH in functionalized alginate—clear evidence that cysteine was successfully attached to the alginate backbone, with 185 µmol of thiol groups per gram polymer estimated in alginate-based material by UV-Visible. Finally, it was observed that guluronic acid residue of alginate are preferentially more affected than mannuronic acid residue in the functionalization. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication> -1
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