Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1080/09205063.2017.1377024 http://hdl.handle.net/11449/175182 |
Resumo: | Natural rubber latex biomedical (NRLb) obtained from the rubber tree Hevea brasiliensis has shown great potential in biomedicine and biomaterial applications. NRLb has been utilized as a physical barrier against infectious agents and in the controlled release of drugs and extracts. In the present work, NRLb was polymerized in a lyophilizer using different volumes of water to control the resultant membrane porosity and characterized regarding the surface morphology, water vapour permeability (WVP), mechanical properties, haemolytic activity and cytotoxicity. The release of bovine serum albumin protein from the latex membranes was evaluated. Drug release rates increased with porosity and membranes were able to control protein release up to 12 h. In addition, WVP increased with the quantity of pores. The cell viability observed for the porous membrane was higher than that noted for conventional membranes. In summary, the porosity control of natural latex membranes can be used to modulate properties and make them suitable for biomedical applications, such as wound dressings, modulated gas-exchange membranes and controlled drug delivery systems. |
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Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applicationsbiomaterialdrug deliveryLyophilized membranenatural rubber latexthermally Induced Phase Separation (TIPS)Natural rubber latex biomedical (NRLb) obtained from the rubber tree Hevea brasiliensis has shown great potential in biomedicine and biomaterial applications. NRLb has been utilized as a physical barrier against infectious agents and in the controlled release of drugs and extracts. In the present work, NRLb was polymerized in a lyophilizer using different volumes of water to control the resultant membrane porosity and characterized regarding the surface morphology, water vapour permeability (WVP), mechanical properties, haemolytic activity and cytotoxicity. The release of bovine serum albumin protein from the latex membranes was evaluated. Drug release rates increased with porosity and membranes were able to control protein release up to 12 h. In addition, WVP increased with the quantity of pores. The cell viability observed for the porous membrane was higher than that noted for conventional membranes. In summary, the porosity control of natural latex membranes can be used to modulate properties and make them suitable for biomedical applications, such as wound dressings, modulated gas-exchange membranes and controlled drug delivery systems.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Biochemistry and Chemical Technology Institute of Chemistry UNESP–Universidade Estadual PaulistaBioprocess and Biotechnology Department–FCF UNESP–Universidade Estadual PaulistaDrugs and Pharmaceuticals Department–FCF UNESP–Universidade Estadual PaulistaDepartment of Biochemistry and Chemical Technology Institute of Chemistry UNESP–Universidade Estadual PaulistaBioprocess and Biotechnology Department–FCF UNESP–Universidade Estadual PaulistaDrugs and Pharmaceuticals Department–FCF UNESP–Universidade Estadual PaulistaFAPESP: 2011/17411-8FAPESP: 2012/15346-7FAPESP: 2015/02343-8CNPq: 470261/2012-9Universidade Estadual Paulista (Unesp)Miranda, M. C.R. [UNESP]Prezotti, F. G. [UNESP]Borges, F. A. [UNESP]Barros, N. R. [UNESP]Cury, B. S.F. [UNESP]Herculano, R. D. [UNESP]Cilli, E. M. [UNESP]2018-12-11T17:14:43Z2018-12-11T17:14:43Z2017-12-12info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2117-2130application/pdfhttp://dx.doi.org/10.1080/09205063.2017.1377024Journal of Biomaterials Science, Polymer Edition, v. 28, n. 18, p. 2117-2130, 2017.1568-56240920-5063http://hdl.handle.net/11449/17518210.1080/09205063.2017.13770242-s2.0-850295845272-s2.0-85029584527.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Biomaterials Science, Polymer Edition0,5370,537info:eu-repo/semantics/openAccess2024-06-24T13:45:39Zoai:repositorio.unesp.br:11449/175182Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:05:19.772064Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications |
title |
Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications |
spellingShingle |
Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications Miranda, M. C.R. [UNESP] biomaterial drug delivery Lyophilized membrane natural rubber latex thermally Induced Phase Separation (TIPS) |
title_short |
Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications |
title_full |
Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications |
title_fullStr |
Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications |
title_full_unstemmed |
Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications |
title_sort |
Porosity effects of natural latex (Hevea brasiliensis) on release of compounds for biomedical applications |
author |
Miranda, M. C.R. [UNESP] |
author_facet |
Miranda, M. C.R. [UNESP] Prezotti, F. G. [UNESP] Borges, F. A. [UNESP] Barros, N. R. [UNESP] Cury, B. S.F. [UNESP] Herculano, R. D. [UNESP] Cilli, E. M. [UNESP] |
author_role |
author |
author2 |
Prezotti, F. G. [UNESP] Borges, F. A. [UNESP] Barros, N. R. [UNESP] Cury, B. S.F. [UNESP] Herculano, R. D. [UNESP] Cilli, E. M. [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Miranda, M. C.R. [UNESP] Prezotti, F. G. [UNESP] Borges, F. A. [UNESP] Barros, N. R. [UNESP] Cury, B. S.F. [UNESP] Herculano, R. D. [UNESP] Cilli, E. M. [UNESP] |
dc.subject.por.fl_str_mv |
biomaterial drug delivery Lyophilized membrane natural rubber latex thermally Induced Phase Separation (TIPS) |
topic |
biomaterial drug delivery Lyophilized membrane natural rubber latex thermally Induced Phase Separation (TIPS) |
description |
Natural rubber latex biomedical (NRLb) obtained from the rubber tree Hevea brasiliensis has shown great potential in biomedicine and biomaterial applications. NRLb has been utilized as a physical barrier against infectious agents and in the controlled release of drugs and extracts. In the present work, NRLb was polymerized in a lyophilizer using different volumes of water to control the resultant membrane porosity and characterized regarding the surface morphology, water vapour permeability (WVP), mechanical properties, haemolytic activity and cytotoxicity. The release of bovine serum albumin protein from the latex membranes was evaluated. Drug release rates increased with porosity and membranes were able to control protein release up to 12 h. In addition, WVP increased with the quantity of pores. The cell viability observed for the porous membrane was higher than that noted for conventional membranes. In summary, the porosity control of natural latex membranes can be used to modulate properties and make them suitable for biomedical applications, such as wound dressings, modulated gas-exchange membranes and controlled drug delivery systems. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-12-12 2018-12-11T17:14:43Z 2018-12-11T17:14:43Z |
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/10.1080/09205063.2017.1377024 Journal of Biomaterials Science, Polymer Edition, v. 28, n. 18, p. 2117-2130, 2017. 1568-5624 0920-5063 http://hdl.handle.net/11449/175182 10.1080/09205063.2017.1377024 2-s2.0-85029584527 2-s2.0-85029584527.pdf |
url |
http://dx.doi.org/10.1080/09205063.2017.1377024 http://hdl.handle.net/11449/175182 |
identifier_str_mv |
Journal of Biomaterials Science, Polymer Edition, v. 28, n. 18, p. 2117-2130, 2017. 1568-5624 0920-5063 10.1080/09205063.2017.1377024 2-s2.0-85029584527 2-s2.0-85029584527.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Biomaterials Science, Polymer Edition 0,537 0,537 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
2117-2130 application/pdf |
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 |
|
_version_ |
1808128892524822528 |