Bolaamphiphilic Bis-Dehydropeptide hydrogels as potential drug release systems
Autor(a) principal: | |
---|---|
Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , |
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. |
id |
RCAP_9a12c6197d74d47d4dff7cf143741b86 |
---|---|
oai_identifier_str |
oai:repositorium.sdum.uminho.pt:1822/73443 |
network_acronym_str |
RCAP |
network_name_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository_id_str |
7160 |
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 instacron:RCAAP |
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 |
repository.mail.fl_str_mv |
|
_version_ |
1799132827695972352 |