Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent

Detalhes bibliográficos
Autor(a) principal: Mendes, Juliana Fernandes [UNESP]
Data de Publicação: 2021
Outros Autores: Oshiro Junior, João Augusto [UNESP], Da Silva, Camila Garcia [UNESP], Chiavacci, Leila Aparecida [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.4322/2179-443X.0730
http://hdl.handle.net/11449/233291
Resumo: Organic inorganic hybrids present several advantages as drug release systems, such as: High flexibility, high mechanical and thermal resistance, transparency, and low water solubility. These hybrids are synthesized through a chemical route named sol-gel that usually uses as solvente tetrahydrofuran (THF). Objetives: To develop film formers from hybrid materials replacing THF with ethanol, a less toxic solvent for skin application and for the environment. Methods: Four polymers were used: Two based on polyethylene oxide (PEO) with molecular weight of 500 and 1900 g mol-1 and two based on polypropylene oxide (PPO), with molecular weight of 400 and 2000 g mol-1. The structural analysis was performed by FTIR, 1H-NMR and 29Si-NMR, and the thermal-mechanical analysis by DSC and TG-DTA. Results: The results of the thermo-mechanical analysis revealed that the solvent replacement did not affect the thermal stability and flexibility of the di-ureasil hybrid. Conclusions: Structural characterization confirmed the formation of hybrids both in THF and in ethanol. Therefore, ethanol is an excellent solvent for the synthesis of these hybrid matrices, since it allows obtaining the same material without changing its characteristics, with some advantages, however, over THF. Furthermore, this paper describes the efficiency of ethanol as a solvent, which is environmentally friendly, to replace THF in the physical-chemical characteristics of these filming former materials.
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spelling Synthesis of ureasil-polyether film forming materials by using environmentally friendly solventEthanolFilm formersMechanical analysisOrganic-inorganic hybridsSol-gel processStructural analysisThermal analysisOrganic inorganic hybrids present several advantages as drug release systems, such as: High flexibility, high mechanical and thermal resistance, transparency, and low water solubility. These hybrids are synthesized through a chemical route named sol-gel that usually uses as solvente tetrahydrofuran (THF). Objetives: To develop film formers from hybrid materials replacing THF with ethanol, a less toxic solvent for skin application and for the environment. Methods: Four polymers were used: Two based on polyethylene oxide (PEO) with molecular weight of 500 and 1900 g mol-1 and two based on polypropylene oxide (PPO), with molecular weight of 400 and 2000 g mol-1. The structural analysis was performed by FTIR, 1H-NMR and 29Si-NMR, and the thermal-mechanical analysis by DSC and TG-DTA. Results: The results of the thermo-mechanical analysis revealed that the solvent replacement did not affect the thermal stability and flexibility of the di-ureasil hybrid. Conclusions: Structural characterization confirmed the formation of hybrids both in THF and in ethanol. Therefore, ethanol is an excellent solvent for the synthesis of these hybrid matrices, since it allows obtaining the same material without changing its characteristics, with some advantages, however, over THF. Furthermore, this paper describes the efficiency of ethanol as a solvent, which is environmentally friendly, to replace THF in the physical-chemical characteristics of these filming former materials.Pharmaceutical Sciences School Universidade Estadual Paulista (UNESP)Pharmaceutical Sciences School Universidade Estadual Paulista (UNESP)Universidade Estadual Paulista (UNESP)Mendes, Juliana Fernandes [UNESP]Oshiro Junior, João Augusto [UNESP]Da Silva, Camila Garcia [UNESP]Chiavacci, Leila Aparecida [UNESP]2022-05-01T06:31:25Z2022-05-01T06:31:25Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.4322/2179-443X.0730Revista de Ciencias Farmaceuticas Basica e Aplicada, v. 42.2179-443X1808-4532http://hdl.handle.net/11449/23329110.4322/2179-443X.07302-s2.0-85111002684Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRevista de Ciencias Farmaceuticas Basica e Aplicadainfo:eu-repo/semantics/openAccess2022-05-01T06:31:25Zoai:repositorio.unesp.br:11449/233291Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-05-01T06:31:25Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent
title Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent
spellingShingle Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent
Mendes, Juliana Fernandes [UNESP]
Ethanol
Film formers
Mechanical analysis
Organic-inorganic hybrids
Sol-gel process
Structural analysis
Thermal analysis
title_short Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent
title_full Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent
title_fullStr Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent
title_full_unstemmed Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent
title_sort Synthesis of ureasil-polyether film forming materials by using environmentally friendly solvent
author Mendes, Juliana Fernandes [UNESP]
author_facet Mendes, Juliana Fernandes [UNESP]
Oshiro Junior, João Augusto [UNESP]
Da Silva, Camila Garcia [UNESP]
Chiavacci, Leila Aparecida [UNESP]
author_role author
author2 Oshiro Junior, João Augusto [UNESP]
Da Silva, Camila Garcia [UNESP]
Chiavacci, Leila Aparecida [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Mendes, Juliana Fernandes [UNESP]
Oshiro Junior, João Augusto [UNESP]
Da Silva, Camila Garcia [UNESP]
Chiavacci, Leila Aparecida [UNESP]
dc.subject.por.fl_str_mv Ethanol
Film formers
Mechanical analysis
Organic-inorganic hybrids
Sol-gel process
Structural analysis
Thermal analysis
topic Ethanol
Film formers
Mechanical analysis
Organic-inorganic hybrids
Sol-gel process
Structural analysis
Thermal analysis
description Organic inorganic hybrids present several advantages as drug release systems, such as: High flexibility, high mechanical and thermal resistance, transparency, and low water solubility. These hybrids are synthesized through a chemical route named sol-gel that usually uses as solvente tetrahydrofuran (THF). Objetives: To develop film formers from hybrid materials replacing THF with ethanol, a less toxic solvent for skin application and for the environment. Methods: Four polymers were used: Two based on polyethylene oxide (PEO) with molecular weight of 500 and 1900 g mol-1 and two based on polypropylene oxide (PPO), with molecular weight of 400 and 2000 g mol-1. The structural analysis was performed by FTIR, 1H-NMR and 29Si-NMR, and the thermal-mechanical analysis by DSC and TG-DTA. Results: The results of the thermo-mechanical analysis revealed that the solvent replacement did not affect the thermal stability and flexibility of the di-ureasil hybrid. Conclusions: Structural characterization confirmed the formation of hybrids both in THF and in ethanol. Therefore, ethanol is an excellent solvent for the synthesis of these hybrid matrices, since it allows obtaining the same material without changing its characteristics, with some advantages, however, over THF. Furthermore, this paper describes the efficiency of ethanol as a solvent, which is environmentally friendly, to replace THF in the physical-chemical characteristics of these filming former materials.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-01
2022-05-01T06:31:25Z
2022-05-01T06:31:25Z
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/10.4322/2179-443X.0730
Revista de Ciencias Farmaceuticas Basica e Aplicada, v. 42.
2179-443X
1808-4532
http://hdl.handle.net/11449/233291
10.4322/2179-443X.0730
2-s2.0-85111002684
url http://dx.doi.org/10.4322/2179-443X.0730
http://hdl.handle.net/11449/233291
identifier_str_mv Revista de Ciencias Farmaceuticas Basica e Aplicada, v. 42.
2179-443X
1808-4532
10.4322/2179-443X.0730
2-s2.0-85111002684
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Revista de Ciencias Farmaceuticas Basica e Aplicada
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
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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