Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale

Detalhes bibliográficos
Autor(a) principal: Rodriguez-Chanfrau, Jorge Enrique [UNESP]
Data de Publicação: 2019
Outros Autores: Rodriguez-Riera, Zalua, Gamiotea-Turro, Daylin [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.33263/BRIAC95.279283
http://hdl.handle.net/11449/194896
Resumo: Starting from the chitin obtained from the lobster carapace, chitosan was obtained. This polymer, due to its high biodegradability, biocompatibility and mucoadhesivity, has a wide use in the pharmaceutical and food industry. Currently, it has great importance in the development of biomaterials for the regeneration of bone and cartilaginous tissues. However, its applications are limited by the insolubility at pH greater than 6. To increase its solubility, different methodologies have been reported. The intensive methylation of the chitosan has been one of the methodologies that have been studied in the last years, generating the N,N,N-trimethylchitosan. This molecule has the characteristic of having permanent positive charges in the chain as a consequence of the quaternization of the amino groups present in the structure of chitosan. Previous studies showed the influence of the agitation rate and the reaction time on the methylation process of the chitosan, using as an alkylating agent the dimethyl sulfate. This allowed to establish a technological process to transform the chitosan. The aim of this work was to obtain N,N,N-trimethylchitosan chloride from chitosan obtained chitin from lobster carapace bench scale. Infrared spectroscopy, Energy dispersive X-ray spectrometry, Nuclear Magnetic Resonance and Intrinsic viscosity were used to characterize the product obtained. The results of the analysis by Infrared spectroscopy, Energy dispersive X-ray spectrometry and Nuclear Magnetic Resonance showed that the methylation process of the chitosan proposed in this work was effective to obtain the desired product. The degree of quaternization, degree of dimethylation and degree of acetylation were 49.2%, 57.5% and 13.3%, respectively. While the value of the intrinsic viscosity [eta] of the sample was 78.5 cm(3)/g. The results corroborate the possibility of modifying chitosan by applying the methodology proposed in this work.
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spelling Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scaleChitosanN,N,N-trimethylchitosan hydrochlorideChitosan trimethylation processDegree of quaternizationStarting from the chitin obtained from the lobster carapace, chitosan was obtained. This polymer, due to its high biodegradability, biocompatibility and mucoadhesivity, has a wide use in the pharmaceutical and food industry. Currently, it has great importance in the development of biomaterials for the regeneration of bone and cartilaginous tissues. However, its applications are limited by the insolubility at pH greater than 6. To increase its solubility, different methodologies have been reported. The intensive methylation of the chitosan has been one of the methodologies that have been studied in the last years, generating the N,N,N-trimethylchitosan. This molecule has the characteristic of having permanent positive charges in the chain as a consequence of the quaternization of the amino groups present in the structure of chitosan. Previous studies showed the influence of the agitation rate and the reaction time on the methylation process of the chitosan, using as an alkylating agent the dimethyl sulfate. This allowed to establish a technological process to transform the chitosan. The aim of this work was to obtain N,N,N-trimethylchitosan chloride from chitosan obtained chitin from lobster carapace bench scale. Infrared spectroscopy, Energy dispersive X-ray spectrometry, Nuclear Magnetic Resonance and Intrinsic viscosity were used to characterize the product obtained. The results of the analysis by Infrared spectroscopy, Energy dispersive X-ray spectrometry and Nuclear Magnetic Resonance showed that the methylation process of the chitosan proposed in this work was effective to obtain the desired product. The degree of quaternization, degree of dimethylation and degree of acetylation were 49.2%, 57.5% and 13.3%, respectively. While the value of the intrinsic viscosity [eta] of the sample was 78.5 cm(3)/g. The results corroborate the possibility of modifying chitosan by applying the methodology proposed in this work.Univ Estadual Paulista, Inst Chem, Araraquara, BrazilHigher Inst Technol & Appl Sci InsTEC, Havana, CubaUniv Estadual Paulista, Inst Chem, Araraquara, BrazilBiointerface Research Applied ChemistryUniversidade Estadual Paulista (Unesp)Higher Inst Technol & Appl Sci InsTECRodriguez-Chanfrau, Jorge Enrique [UNESP]Rodriguez-Riera, ZaluaGamiotea-Turro, Daylin [UNESP]2020-12-10T16:58:00Z2020-12-10T16:58:00Z2019-10-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article4279-4283http://dx.doi.org/10.33263/BRIAC95.279283Biointerface Research In Applied Chemistry. Bucuresti: Biointerface Research Applied Chemistry, v. 9, n. 5, p. 4279-4283, 2019.2069-5837http://hdl.handle.net/11449/19489610.33263/BRIAC95.279283WOS:000489980300011Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiointerface Research In Applied Chemistryinfo:eu-repo/semantics/openAccess2021-10-23T00:00:24Zoai:repositorio.unesp.br:11449/194896Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:10:57.276430Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale
title Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale
spellingShingle Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale
Rodriguez-Chanfrau, Jorge Enrique [UNESP]
Chitosan
N,N,N-trimethylchitosan hydrochloride
Chitosan trimethylation process
Degree of quaternization
title_short Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale
title_full Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale
title_fullStr Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale
title_full_unstemmed Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale
title_sort Trimethylchitosan hydrochloride obtained from lobster carapace chitin on a bench scale
author Rodriguez-Chanfrau, Jorge Enrique [UNESP]
author_facet Rodriguez-Chanfrau, Jorge Enrique [UNESP]
Rodriguez-Riera, Zalua
Gamiotea-Turro, Daylin [UNESP]
author_role author
author2 Rodriguez-Riera, Zalua
Gamiotea-Turro, Daylin [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Higher Inst Technol & Appl Sci InsTEC
dc.contributor.author.fl_str_mv Rodriguez-Chanfrau, Jorge Enrique [UNESP]
Rodriguez-Riera, Zalua
Gamiotea-Turro, Daylin [UNESP]
dc.subject.por.fl_str_mv Chitosan
N,N,N-trimethylchitosan hydrochloride
Chitosan trimethylation process
Degree of quaternization
topic Chitosan
N,N,N-trimethylchitosan hydrochloride
Chitosan trimethylation process
Degree of quaternization
description Starting from the chitin obtained from the lobster carapace, chitosan was obtained. This polymer, due to its high biodegradability, biocompatibility and mucoadhesivity, has a wide use in the pharmaceutical and food industry. Currently, it has great importance in the development of biomaterials for the regeneration of bone and cartilaginous tissues. However, its applications are limited by the insolubility at pH greater than 6. To increase its solubility, different methodologies have been reported. The intensive methylation of the chitosan has been one of the methodologies that have been studied in the last years, generating the N,N,N-trimethylchitosan. This molecule has the characteristic of having permanent positive charges in the chain as a consequence of the quaternization of the amino groups present in the structure of chitosan. Previous studies showed the influence of the agitation rate and the reaction time on the methylation process of the chitosan, using as an alkylating agent the dimethyl sulfate. This allowed to establish a technological process to transform the chitosan. The aim of this work was to obtain N,N,N-trimethylchitosan chloride from chitosan obtained chitin from lobster carapace bench scale. Infrared spectroscopy, Energy dispersive X-ray spectrometry, Nuclear Magnetic Resonance and Intrinsic viscosity were used to characterize the product obtained. The results of the analysis by Infrared spectroscopy, Energy dispersive X-ray spectrometry and Nuclear Magnetic Resonance showed that the methylation process of the chitosan proposed in this work was effective to obtain the desired product. The degree of quaternization, degree of dimethylation and degree of acetylation were 49.2%, 57.5% and 13.3%, respectively. While the value of the intrinsic viscosity [eta] of the sample was 78.5 cm(3)/g. The results corroborate the possibility of modifying chitosan by applying the methodology proposed in this work.
publishDate 2019
dc.date.none.fl_str_mv 2019-10-15
2020-12-10T16:58:00Z
2020-12-10T16:58:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.33263/BRIAC95.279283
Biointerface Research In Applied Chemistry. Bucuresti: Biointerface Research Applied Chemistry, v. 9, n. 5, p. 4279-4283, 2019.
2069-5837
http://hdl.handle.net/11449/194896
10.33263/BRIAC95.279283
WOS:000489980300011
url http://dx.doi.org/10.33263/BRIAC95.279283
http://hdl.handle.net/11449/194896
identifier_str_mv Biointerface Research In Applied Chemistry. Bucuresti: Biointerface Research Applied Chemistry, v. 9, n. 5, p. 4279-4283, 2019.
2069-5837
10.33263/BRIAC95.279283
WOS:000489980300011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biointerface Research In Applied Chemistry
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 4279-4283
dc.publisher.none.fl_str_mv Biointerface Research Applied Chemistry
publisher.none.fl_str_mv Biointerface Research Applied Chemistry
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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