Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives
Autor(a) principal: | |
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Data de Publicação: | 2015 |
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/10400.6/4677 |
Resumo: | The synthesis, functionalization and characterization of low molecular weight L-lactic acid based oligomers to be used as new UV-curable bioadhesives are presented herein. Prepolymers hydroxyl terminated were produced by L-lactic acid dehydration with 1,4-butanediol. The prepolymer was further modified with photoreactive sites by adding an isocyanate-functional unsaturated acrylic ester, which was used for the first time in the biomedical field (LAROMER® LR 9000). Films were afterwards produced upon UV irradiation for 120 s, using a biocompatible photoinitiator (Irgacure® 2959), and finally characterized. The synthesized films exhibited a moderate swelling ratio, suitable for the envisioned application. DSC analysis confirmed an increase in Tg values after each synthesis step. Nevertheless, the film Tg remains lower than the physiological and room temperature. TGA confirmed an improved stability of films at high temperatures. The in vitro degradation tests showed their susceptibility to hydrolysis at 37 °C, suitable for short-term uses. Preliminary evaluation of the adhesion capacity suggested that the synthesized material may be effective in sustaining wound closure and repair. The surface energy was also measured and its value was lower than the ones from blood or skin which supports the previous statement. Blood compatibility studies, cell viability assays (using human dermal fibroblasts) and bacterial inhibition tests (using two bacteria models) were performed. The results indicated that cured adhesive is bio/haemocompatible and possesses antimicrobial activity. Altogether, characterization results showed that the produced material presented a set of properties suitable for biomedical applications, particularly as a surgical adhesive. |
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Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesivesBiocompatibilityBioadhesivesBlood compatibilityL-Lactic acidPhotocrosslinkingThe synthesis, functionalization and characterization of low molecular weight L-lactic acid based oligomers to be used as new UV-curable bioadhesives are presented herein. Prepolymers hydroxyl terminated were produced by L-lactic acid dehydration with 1,4-butanediol. The prepolymer was further modified with photoreactive sites by adding an isocyanate-functional unsaturated acrylic ester, which was used for the first time in the biomedical field (LAROMER® LR 9000). Films were afterwards produced upon UV irradiation for 120 s, using a biocompatible photoinitiator (Irgacure® 2959), and finally characterized. The synthesized films exhibited a moderate swelling ratio, suitable for the envisioned application. DSC analysis confirmed an increase in Tg values after each synthesis step. Nevertheless, the film Tg remains lower than the physiological and room temperature. TGA confirmed an improved stability of films at high temperatures. The in vitro degradation tests showed their susceptibility to hydrolysis at 37 °C, suitable for short-term uses. Preliminary evaluation of the adhesion capacity suggested that the synthesized material may be effective in sustaining wound closure and repair. The surface energy was also measured and its value was lower than the ones from blood or skin which supports the previous statement. Blood compatibility studies, cell viability assays (using human dermal fibroblasts) and bacterial inhibition tests (using two bacteria models) were performed. The results indicated that cured adhesive is bio/haemocompatible and possesses antimicrobial activity. Altogether, characterization results showed that the produced material presented a set of properties suitable for biomedical applications, particularly as a surgical adhesive.ElsevieruBibliorumSantos, JoãoMarques, DinaAlves, PatríciaCorreia, Tiago R.Correia, Ilídio Joaquim SobreiraBaptista, Cristina Maria dos Santos GaudêncioFerreira, Paula2018-03-21T09:59:54Z2015-07-212015-07-21T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.6/4677engSantos, J.M.C., Marques, D.S., Alves, P., Correia, T.R., Correia, I.J., Baptista, C.M.S.G. e Ferreira, P. (2015) “Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives”, Reactive and Functional Polymers, Vol. 94, pp. 43-5410.1016/j.reactfunctpolym.2015.07.003metadata 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:RCAAP2024-02-07T02:30:50Zoai:ubibliorum.ubi.pt:10400.6/4677Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:45:43.974700Repositório 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 |
Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives |
title |
Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives |
spellingShingle |
Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives Santos, João Biocompatibility Bioadhesives Blood compatibility L-Lactic acid Photocrosslinking |
title_short |
Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives |
title_full |
Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives |
title_fullStr |
Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives |
title_full_unstemmed |
Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives |
title_sort |
Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives |
author |
Santos, João |
author_facet |
Santos, João Marques, Dina Alves, Patrícia Correia, Tiago R. Correia, Ilídio Joaquim Sobreira Baptista, Cristina Maria dos Santos Gaudêncio Ferreira, Paula |
author_role |
author |
author2 |
Marques, Dina Alves, Patrícia Correia, Tiago R. Correia, Ilídio Joaquim Sobreira Baptista, Cristina Maria dos Santos Gaudêncio Ferreira, Paula |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
uBibliorum |
dc.contributor.author.fl_str_mv |
Santos, João Marques, Dina Alves, Patrícia Correia, Tiago R. Correia, Ilídio Joaquim Sobreira Baptista, Cristina Maria dos Santos Gaudêncio Ferreira, Paula |
dc.subject.por.fl_str_mv |
Biocompatibility Bioadhesives Blood compatibility L-Lactic acid Photocrosslinking |
topic |
Biocompatibility Bioadhesives Blood compatibility L-Lactic acid Photocrosslinking |
description |
The synthesis, functionalization and characterization of low molecular weight L-lactic acid based oligomers to be used as new UV-curable bioadhesives are presented herein. Prepolymers hydroxyl terminated were produced by L-lactic acid dehydration with 1,4-butanediol. The prepolymer was further modified with photoreactive sites by adding an isocyanate-functional unsaturated acrylic ester, which was used for the first time in the biomedical field (LAROMER® LR 9000). Films were afterwards produced upon UV irradiation for 120 s, using a biocompatible photoinitiator (Irgacure® 2959), and finally characterized. The synthesized films exhibited a moderate swelling ratio, suitable for the envisioned application. DSC analysis confirmed an increase in Tg values after each synthesis step. Nevertheless, the film Tg remains lower than the physiological and room temperature. TGA confirmed an improved stability of films at high temperatures. The in vitro degradation tests showed their susceptibility to hydrolysis at 37 °C, suitable for short-term uses. Preliminary evaluation of the adhesion capacity suggested that the synthesized material may be effective in sustaining wound closure and repair. The surface energy was also measured and its value was lower than the ones from blood or skin which supports the previous statement. Blood compatibility studies, cell viability assays (using human dermal fibroblasts) and bacterial inhibition tests (using two bacteria models) were performed. The results indicated that cured adhesive is bio/haemocompatible and possesses antimicrobial activity. Altogether, characterization results showed that the produced material presented a set of properties suitable for biomedical applications, particularly as a surgical adhesive. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-07-21 2015-07-21T00:00:00Z 2018-03-21T09:59:54Z |
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/10400.6/4677 |
url |
http://hdl.handle.net/10400.6/4677 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Santos, J.M.C., Marques, D.S., Alves, P., Correia, T.R., Correia, I.J., Baptista, C.M.S.G. e Ferreira, P. (2015) “Synthesis, functionalization and characterization of UV-curable lactic acid based oligomers to be used as surgical adhesives”, Reactive and Functional Polymers, Vol. 94, pp. 43-54 10.1016/j.reactfunctpolym.2015.07.003 |
dc.rights.driver.fl_str_mv |
metadata only access info:eu-repo/semantics/openAccess |
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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 |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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