Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems

Detalhes bibliográficos
Autor(a) principal: Amorim, Carolina
Data de Publicação: 2021
Outros Autores: Veloso, Sérgio Rafael Silva, Castanheira, Elisabete M. S., Hilliou, L., Pereira, Renato B., Pereira, David M., Martins, J. A., Jervis, Peter John, Ferreira, Paula M. T.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/73443
Resumo: The self-assembly of nanometric structures from molecular building blocks is an effective way to make new functional materials for biological and technological applications. In this work, four symmetrical bolaamphiphiles based on dehydrodipeptides (phenylalanyldehydrophenylalanine and tyrosyldehydrophenylalanine) linked through phenyl or naphthyl linkers (terephthalic acid and 2,6-naphthalenedicarboxylic acid) were prepared, and their self-assembly properties were studied. The results showed that all compounds, with the exception of the bolaamphiphile of tyrosyldehydrophenylalanine and 2,6-naphthalene dicarboxylic acid, gave self-standing hydrogels with critical gelation concentrations of 0.3 wt % and 0.4 wt %, using a pH trigger. The self-assembly of these hydrogelators was investigated using STEM microscopy, which revealed a network of entangled fibers. According to rheology, the dehydrodipeptide bolaamphiphilic hydrogelators are viscoelastic materials with an elastic modulus G' that falls in the range of native tissue (0.37 kPa brain-4.5 kPa cartilage). In viability and proliferation studies, it was found that these compounds were non-toxic toward the human keratinocyte cell line, HaCaT. In sustained release assays, we studied the effects of the charge present on model drug compounds on the rate of cargo release from the hydrogel networks. Methylene blue (MB), methyl orange (MO), and ciprofloxacin were chosen as cationic, anionic, and overall neutral cargo, respectively. These studies have shown that the hydrogels provide a sustained release of methyl orange and ciprofloxacin, while methylene blue is retained by the hydrogel network.
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spelling Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systemsHydrogelsNanoencapsulationDrug deliveryBola-amphiphilesdehydropeptideself-assemblysupramolecular hydrogelsEngenharia e Tecnologia::NanotecnologiaScience & TechnologySaúde de qualidadeThe self-assembly of nanometric structures from molecular building blocks is an effective way to make new functional materials for biological and technological applications. In this work, four symmetrical bolaamphiphiles based on dehydrodipeptides (phenylalanyldehydrophenylalanine and tyrosyldehydrophenylalanine) linked through phenyl or naphthyl linkers (terephthalic acid and 2,6-naphthalenedicarboxylic acid) were prepared, and their self-assembly properties were studied. The results showed that all compounds, with the exception of the bolaamphiphile of tyrosyldehydrophenylalanine and 2,6-naphthalene dicarboxylic acid, gave self-standing hydrogels with critical gelation concentrations of 0.3 wt % and 0.4 wt %, using a pH trigger. The self-assembly of these hydrogelators was investigated using STEM microscopy, which revealed a network of entangled fibers. According to rheology, the dehydrodipeptide bolaamphiphilic hydrogelators are viscoelastic materials with an elastic modulus G' that falls in the range of native tissue (0.37 kPa brain-4.5 kPa cartilage). In viability and proliferation studies, it was found that these compounds were non-toxic toward the human keratinocyte cell line, HaCaT. In sustained release assays, we studied the effects of the charge present on model drug compounds on the rate of cargo release from the hydrogel networks. Methylene blue (MB), methyl orange (MO), and ciprofloxacin were chosen as cationic, anionic, and overall neutral cargo, respectively. These studies have shown that the hydrogels provide a sustained release of methyl orange and ciprofloxacin, while methylene blue is retained by the hydrogel network.Portugal2020, Compete2020, FEDER. PTDC/QUI-QOR/29015/2017. UIDB/04650/2020. UIDB/50006/2020. UID/QUI/00686/2019. UID/CTM/50025/2019. SFRH/BD/144017/2019Multidisciplinary Digital Publishing Institute (MDPI)Universidade do MinhoAmorim, CarolinaVeloso, Sérgio Rafael SilvaCastanheira, Elisabete M. S.Hilliou, L.Pereira, Renato B.Pereira, David M.Martins, J. A.Jervis, Peter JohnFerreira, Paula M. T.2021-04-292021-04-29T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/73443engAmorim, C., Veloso, S. R., Castanheira, E., Hilliou, L., Pereira, R. B., et. al (2021). Bolaamphiphilic bis-dehydropeptide hydrogels as potential drug release systems. Gels, 7(2), 522310-286110.3390/gels7020052https://www.mdpi.com/2310-2861/7/2/52info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:35:52Zoai:repositorium.sdum.uminho.pt:1822/73443Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:31:49.446674Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
title Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
spellingShingle Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
Amorim, Carolina
Hydrogels
Nanoencapsulation
Drug delivery
Bola-amphiphiles
dehydropeptide
self-assembly
supramolecular hydrogels
Engenharia e Tecnologia::Nanotecnologia
Science & Technology
Saúde de qualidade
title_short Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
title_full Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
title_fullStr Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
title_full_unstemmed Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
title_sort Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
author Amorim, Carolina
author_facet Amorim, Carolina
Veloso, Sérgio Rafael Silva
Castanheira, Elisabete M. S.
Hilliou, L.
Pereira, Renato B.
Pereira, David M.
Martins, J. A.
Jervis, Peter John
Ferreira, Paula M. T.
author_role author
author2 Veloso, Sérgio Rafael Silva
Castanheira, Elisabete M. S.
Hilliou, L.
Pereira, Renato B.
Pereira, David M.
Martins, J. A.
Jervis, Peter John
Ferreira, Paula M. T.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Amorim, Carolina
Veloso, Sérgio Rafael Silva
Castanheira, Elisabete M. S.
Hilliou, L.
Pereira, Renato B.
Pereira, David M.
Martins, J. A.
Jervis, Peter John
Ferreira, Paula M. T.
dc.subject.por.fl_str_mv Hydrogels
Nanoencapsulation
Drug delivery
Bola-amphiphiles
dehydropeptide
self-assembly
supramolecular hydrogels
Engenharia e Tecnologia::Nanotecnologia
Science & Technology
Saúde de qualidade
topic Hydrogels
Nanoencapsulation
Drug delivery
Bola-amphiphiles
dehydropeptide
self-assembly
supramolecular hydrogels
Engenharia e Tecnologia::Nanotecnologia
Science & Technology
Saúde de qualidade
description The self-assembly of nanometric structures from molecular building blocks is an effective way to make new functional materials for biological and technological applications. In this work, four symmetrical bolaamphiphiles based on dehydrodipeptides (phenylalanyldehydrophenylalanine and tyrosyldehydrophenylalanine) linked through phenyl or naphthyl linkers (terephthalic acid and 2,6-naphthalenedicarboxylic acid) were prepared, and their self-assembly properties were studied. The results showed that all compounds, with the exception of the bolaamphiphile of tyrosyldehydrophenylalanine and 2,6-naphthalene dicarboxylic acid, gave self-standing hydrogels with critical gelation concentrations of 0.3 wt % and 0.4 wt %, using a pH trigger. The self-assembly of these hydrogelators was investigated using STEM microscopy, which revealed a network of entangled fibers. According to rheology, the dehydrodipeptide bolaamphiphilic hydrogelators are viscoelastic materials with an elastic modulus G' that falls in the range of native tissue (0.37 kPa brain-4.5 kPa cartilage). In viability and proliferation studies, it was found that these compounds were non-toxic toward the human keratinocyte cell line, HaCaT. In sustained release assays, we studied the effects of the charge present on model drug compounds on the rate of cargo release from the hydrogel networks. Methylene blue (MB), methyl orange (MO), and ciprofloxacin were chosen as cationic, anionic, and overall neutral cargo, respectively. These studies have shown that the hydrogels provide a sustained release of methyl orange and ciprofloxacin, while methylene blue is retained by the hydrogel network.
publishDate 2021
dc.date.none.fl_str_mv 2021-04-29
2021-04-29T00:00:00Z
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://hdl.handle.net/1822/73443
url http://hdl.handle.net/1822/73443
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Amorim, C., Veloso, S. R., Castanheira, E., Hilliou, L., Pereira, R. B., et. al (2021). Bolaamphiphilic bis-dehydropeptide hydrogels as potential drug release systems. Gels, 7(2), 52
2310-2861
10.3390/gels7020052
https://www.mdpi.com/2310-2861/7/2/52
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute (MDPI)
publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute (MDPI)
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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