Cork industry waste product valorisation : bioactivity on human keratinocytes
Autor(a) principal: | |
---|---|
Data de Publicação: | 2016 |
Tipo de documento: | Dissertação |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.14/37373 |
Resumo: | Wound healing, a complex process that involves hemostasis, inflammation, proliferation and tissue remodelling, gathers deep scientific interest, since acute and chronic wounds are common as well as pathologic under or overhealing. Cork powder is one of the major waste derived residues in the cork industry, known to possess a strong phenolic content. We herein hypothesized that the products obtained from the cork liquefaction process may have biomedical properties particularly in the wound healing process. In this context, the aim of this work was to investigate the effect of several extracts obtained by manipulation of liquefied cork upon keratinocyte viability, migration and proliferation, key cellular events in the wound healing process. To do this, liquefied (LIQ) cork was produced and it was fractionated in water soluble (WS) and organic (ORG) extracts. Additionally, a glue dispersion (GLUE) was prepared by the addiction of WS extract to distilled water, Desmodur DA-L and cork powder on a ratio of 3:20:1.2:0.2. Several dilutions of each fraction were prepared (1:1, 1:5, 1:10, 1:100 and 1:1000) and used in 24-h treatment of the human keratinocyte HaCat cell line, for viability (MTT and LDH assays), migration capacity (wound-healing assay) and proliferation (BrdU assay) assessment. Additionally, total phenolic content (FolinCiocalteu method), and antioxidant potential (FRAP and DPPH) of each fraction were assessed. The liquefaction cork process achieved a biomass conversion of 94 %. Except for the highest concentration of ORG extract, the fractions were not cytotoxic and GLUE extract increased cell survival. All the cork extracts were able to induce cell proliferation and except for the GLUE fraction, they also induced cell migration capacity. Regarding antioxidant properties, ORG fraction showed the highest reducing power and radical scavenging activity, although LIQ fraction was the richest in phenolic content. On the other hand, GLUE fraction had the lowest phenolic content and accordingly, the lowest reducing power and radical scavenging activity. In conclusion, liquefied cork and its subproducts reveal wound healing-promoting bioactivity. Overall, WS extract produced the most consistent cellular responses, being thus the most promising for a potential biomedical application in wound healing. Nevertheless, further studies are recommended, mainly in vivo tests, to validate these in vitro results. |
id |
RCAP_04c16a38856c248d668f1d969b1823db |
---|---|
oai_identifier_str |
oai:repositorio.ucp.pt:10400.14/37373 |
network_acronym_str |
RCAP |
network_name_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository_id_str |
7160 |
spelling |
Cork industry waste product valorisation : bioactivity on human keratinocytesDomínio/Área Científica::Engenharia e Tecnologia::Engenharia QuímicaWound healing, a complex process that involves hemostasis, inflammation, proliferation and tissue remodelling, gathers deep scientific interest, since acute and chronic wounds are common as well as pathologic under or overhealing. Cork powder is one of the major waste derived residues in the cork industry, known to possess a strong phenolic content. We herein hypothesized that the products obtained from the cork liquefaction process may have biomedical properties particularly in the wound healing process. In this context, the aim of this work was to investigate the effect of several extracts obtained by manipulation of liquefied cork upon keratinocyte viability, migration and proliferation, key cellular events in the wound healing process. To do this, liquefied (LIQ) cork was produced and it was fractionated in water soluble (WS) and organic (ORG) extracts. Additionally, a glue dispersion (GLUE) was prepared by the addiction of WS extract to distilled water, Desmodur DA-L and cork powder on a ratio of 3:20:1.2:0.2. Several dilutions of each fraction were prepared (1:1, 1:5, 1:10, 1:100 and 1:1000) and used in 24-h treatment of the human keratinocyte HaCat cell line, for viability (MTT and LDH assays), migration capacity (wound-healing assay) and proliferation (BrdU assay) assessment. Additionally, total phenolic content (FolinCiocalteu method), and antioxidant potential (FRAP and DPPH) of each fraction were assessed. The liquefaction cork process achieved a biomass conversion of 94 %. Except for the highest concentration of ORG extract, the fractions were not cytotoxic and GLUE extract increased cell survival. All the cork extracts were able to induce cell proliferation and except for the GLUE fraction, they also induced cell migration capacity. Regarding antioxidant properties, ORG fraction showed the highest reducing power and radical scavenging activity, although LIQ fraction was the richest in phenolic content. On the other hand, GLUE fraction had the lowest phenolic content and accordingly, the lowest reducing power and radical scavenging activity. In conclusion, liquefied cork and its subproducts reveal wound healing-promoting bioactivity. Overall, WS extract produced the most consistent cellular responses, being thus the most promising for a potential biomedical application in wound healing. Nevertheless, further studies are recommended, mainly in vivo tests, to validate these in vitro results.A cicatrização de feridas tem reunido um profundo interesse científico, dada a frequência de ocorrência de feridas agudas e crónicas, bem como da cicatrização patológica. O pó de cortiça, rico em compostos fenólicos, é um dos principais resíduos da indústria corticeira. A hipótese motora deste estudo foi que os produtos obtidos a partir do processo de liquefação do pó cortiça possam ter aplicação biomédica, em particular na cicatrização de feridas. Neste contexto, o objetivo deste trabalho foi investigar o efeito de vários extratos da manipulação da cortiça liquefeita sobre a viabilidade, migração e proliferação de queratinócitos, processos celulares essenciais à cicatrização. Foi produzido o extrato liquefeito (LIQ) da cortiça que foi fracionado em extrato hidrossolúvel (WS) e extrato orgânico (ORG). Adicionalmente, foi preparada uma mistura (GLUE) pela adição de água destilada, Desmodur DA-L e pó de cortiça ao extrato WS numa proporção de 3:20:1,2:0,2. Foram preparadas várias diluições de cada extrato (1:1, 1:5, 1:10, 1:100 e 1:1000) que foram utilizadas no tratamento de 24 h da linha celular de queratinócitos humanos HaCat, tendo sido posteriormente avaliada a viabilidade (ensaios MTT e LDH), capacidade de migração (ensaio de wound-healing) e proliferação (ensaio BrdU). Além disto, determinou-se o conteúdo em fenóis totais (através do método de Folin-Ciocalteu) e o potencial antioxidante (FRAP e DPPH) de cada extrato. O rendimento do processo de liquefação cortiça foi de 94 %. Exceto para a concentração mais elevada do extrato ORG, as frações não foram citotóxicas e o extrato GLUE promoveu a sobrevivência celular. Todos os extratos de cortiça foram capazes de induzir a proliferação celular e, à exceção da fração GLUE, também foram capazes de induzir capacidade migratória. Relativamente, às propriedades antioxidantes, a fração ORG apresentou o maior poder redutor e atividade antiradicalar, embora a fração LIQ se tenha revelado como a mais rica em compostos fenólicos. A fração GLUE teve o menor poder redutor e atividade antiradicalar e o menor teor em compostos fenólicos. Em suma, a cortiça liquefeita e seus sub-produtos demonstram bioatividade no processo de cicatrização. Globalmente, o extrato WS produziu os resultados mais consistentes nos diferentes ensaios de bioatividade, sendo por isso o mais promissor para uma potencial aplicação biomédica no processo de cicatrização. A execução de ensaios in vivo que permitam a validação destas observações é fortemente recomendada.Ferreira, António César da SilvaKeating, Elisa Oliveira BragaVeritati - Repositório Institucional da Universidade Católica PortuguesaSalvador, Maria Inês Vaz2022-04-27T08:08:13Z2017-03-012016-112017-03-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10400.14/37373TID:201736896enginfo: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:RCAAP2023-07-12T17:42:49Zoai:repositorio.ucp.pt:10400.14/37373Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:30:26.641496Repositório 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 |
Cork industry waste product valorisation : bioactivity on human keratinocytes |
title |
Cork industry waste product valorisation : bioactivity on human keratinocytes |
spellingShingle |
Cork industry waste product valorisation : bioactivity on human keratinocytes Salvador, Maria Inês Vaz Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química |
title_short |
Cork industry waste product valorisation : bioactivity on human keratinocytes |
title_full |
Cork industry waste product valorisation : bioactivity on human keratinocytes |
title_fullStr |
Cork industry waste product valorisation : bioactivity on human keratinocytes |
title_full_unstemmed |
Cork industry waste product valorisation : bioactivity on human keratinocytes |
title_sort |
Cork industry waste product valorisation : bioactivity on human keratinocytes |
author |
Salvador, Maria Inês Vaz |
author_facet |
Salvador, Maria Inês Vaz |
author_role |
author |
dc.contributor.none.fl_str_mv |
Ferreira, António César da Silva Keating, Elisa Oliveira Braga Veritati - Repositório Institucional da Universidade Católica Portuguesa |
dc.contributor.author.fl_str_mv |
Salvador, Maria Inês Vaz |
dc.subject.por.fl_str_mv |
Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química |
topic |
Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química |
description |
Wound healing, a complex process that involves hemostasis, inflammation, proliferation and tissue remodelling, gathers deep scientific interest, since acute and chronic wounds are common as well as pathologic under or overhealing. Cork powder is one of the major waste derived residues in the cork industry, known to possess a strong phenolic content. We herein hypothesized that the products obtained from the cork liquefaction process may have biomedical properties particularly in the wound healing process. In this context, the aim of this work was to investigate the effect of several extracts obtained by manipulation of liquefied cork upon keratinocyte viability, migration and proliferation, key cellular events in the wound healing process. To do this, liquefied (LIQ) cork was produced and it was fractionated in water soluble (WS) and organic (ORG) extracts. Additionally, a glue dispersion (GLUE) was prepared by the addiction of WS extract to distilled water, Desmodur DA-L and cork powder on a ratio of 3:20:1.2:0.2. Several dilutions of each fraction were prepared (1:1, 1:5, 1:10, 1:100 and 1:1000) and used in 24-h treatment of the human keratinocyte HaCat cell line, for viability (MTT and LDH assays), migration capacity (wound-healing assay) and proliferation (BrdU assay) assessment. Additionally, total phenolic content (FolinCiocalteu method), and antioxidant potential (FRAP and DPPH) of each fraction were assessed. The liquefaction cork process achieved a biomass conversion of 94 %. Except for the highest concentration of ORG extract, the fractions were not cytotoxic and GLUE extract increased cell survival. All the cork extracts were able to induce cell proliferation and except for the GLUE fraction, they also induced cell migration capacity. Regarding antioxidant properties, ORG fraction showed the highest reducing power and radical scavenging activity, although LIQ fraction was the richest in phenolic content. On the other hand, GLUE fraction had the lowest phenolic content and accordingly, the lowest reducing power and radical scavenging activity. In conclusion, liquefied cork and its subproducts reveal wound healing-promoting bioactivity. Overall, WS extract produced the most consistent cellular responses, being thus the most promising for a potential biomedical application in wound healing. Nevertheless, further studies are recommended, mainly in vivo tests, to validate these in vitro results. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-11 2017-03-01 2017-03-01T00:00:00Z 2022-04-27T08:08:13Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.14/37373 TID:201736896 |
url |
http://hdl.handle.net/10400.14/37373 |
identifier_str_mv |
TID:201736896 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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.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_ |
1799132025844662272 |