Natural melanin: A potential pH-responsive drug release device
Autor(a) principal: | |
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Data de Publicação: | 2014 |
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/10400.6/4648 |
Resumo: | This work proposes melanin as a new nanocarrier for pH-responsive drug release. Melanin is an abundant natural polymer that can be easily extracted from cuttlefish as nanoparticles with a suitable size range for drug delivery. However, despite its high potentiality, the application of this biopolymer in the pharmaceutical and biomedical fields is yet to be explored. Herein, melanin nanoparticles were impregnated with metronidazole, chosen as model antibiotic drug, using supercritical carbon dioxide. The drug release profile was investigated at acidic and physiologic pH, and the dominant mechanism was found to follow a non-Fickian transport. Drug release from melanin shows a strong pH dependency, which allied to its biocompatibility and lack of cytotoxicity envisages its potential application as nanocarrier in formulations for colon and intestine targeted drug delivery. |
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Natural melanin: A potential pH-responsive drug release deviceMelaninPH-responsive drug releaseNanocarrierBiocompatibilitySupercritical carbon dioxideThis work proposes melanin as a new nanocarrier for pH-responsive drug release. Melanin is an abundant natural polymer that can be easily extracted from cuttlefish as nanoparticles with a suitable size range for drug delivery. However, despite its high potentiality, the application of this biopolymer in the pharmaceutical and biomedical fields is yet to be explored. Herein, melanin nanoparticles were impregnated with metronidazole, chosen as model antibiotic drug, using supercritical carbon dioxide. The drug release profile was investigated at acidic and physiologic pH, and the dominant mechanism was found to follow a non-Fickian transport. Drug release from melanin shows a strong pH dependency, which allied to its biocompatibility and lack of cytotoxicity envisages its potential application as nanocarrier in formulations for colon and intestine targeted drug delivery.ElsevieruBibliorumAraújo, MarcoViveiros, RaquelCorreia, Tiago R.Correia, Ilídio Joaquim SobreiraBonifácio, VascoCasimiro, TeresaRicardo, Ana Aguiar2018-03-20T10:32:39Z2014-04-232014-04-23T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.6/4648eng10.1016/j.ijpharm.2014.04.051metadata only accessinfo: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:RCAAP2023-12-15T09:41:50Zoai:ubibliorum.ubi.pt:10400.6/4648Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:45:42.520517Repositório 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 |
Natural melanin: A potential pH-responsive drug release device |
title |
Natural melanin: A potential pH-responsive drug release device |
spellingShingle |
Natural melanin: A potential pH-responsive drug release device Araújo, Marco Melanin PH-responsive drug release Nanocarrier Biocompatibility Supercritical carbon dioxide |
title_short |
Natural melanin: A potential pH-responsive drug release device |
title_full |
Natural melanin: A potential pH-responsive drug release device |
title_fullStr |
Natural melanin: A potential pH-responsive drug release device |
title_full_unstemmed |
Natural melanin: A potential pH-responsive drug release device |
title_sort |
Natural melanin: A potential pH-responsive drug release device |
author |
Araújo, Marco |
author_facet |
Araújo, Marco Viveiros, Raquel Correia, Tiago R. Correia, Ilídio Joaquim Sobreira Bonifácio, Vasco Casimiro, Teresa Ricardo, Ana Aguiar |
author_role |
author |
author2 |
Viveiros, Raquel Correia, Tiago R. Correia, Ilídio Joaquim Sobreira Bonifácio, Vasco Casimiro, Teresa Ricardo, Ana Aguiar |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
uBibliorum |
dc.contributor.author.fl_str_mv |
Araújo, Marco Viveiros, Raquel Correia, Tiago R. Correia, Ilídio Joaquim Sobreira Bonifácio, Vasco Casimiro, Teresa Ricardo, Ana Aguiar |
dc.subject.por.fl_str_mv |
Melanin PH-responsive drug release Nanocarrier Biocompatibility Supercritical carbon dioxide |
topic |
Melanin PH-responsive drug release Nanocarrier Biocompatibility Supercritical carbon dioxide |
description |
This work proposes melanin as a new nanocarrier for pH-responsive drug release. Melanin is an abundant natural polymer that can be easily extracted from cuttlefish as nanoparticles with a suitable size range for drug delivery. However, despite its high potentiality, the application of this biopolymer in the pharmaceutical and biomedical fields is yet to be explored. Herein, melanin nanoparticles were impregnated with metronidazole, chosen as model antibiotic drug, using supercritical carbon dioxide. The drug release profile was investigated at acidic and physiologic pH, and the dominant mechanism was found to follow a non-Fickian transport. Drug release from melanin shows a strong pH dependency, which allied to its biocompatibility and lack of cytotoxicity envisages its potential application as nanocarrier in formulations for colon and intestine targeted drug delivery. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-04-23 2014-04-23T00:00:00Z 2018-03-20T10:32:39Z |
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/10400.6/4648 |
url |
http://hdl.handle.net/10400.6/4648 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.ijpharm.2014.04.051 |
dc.rights.driver.fl_str_mv |
metadata only access info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
metadata only access |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
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) |
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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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1799136354448179200 |