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Novel Conducting and Biodegradable Copolymers with Noncytotoxic Properties toward Embryonic Stem Cells
[Image: see text] Electroactive biomaterials that are easily processed as scaffolds with good biocompatibility for tissue regeneration are difficult to design. Herein, the synthesis and characterization of a variety of novel electroactive, biodegradable biomaterials based on poly(3,4-ethylenedioxyth...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045332/ https://www.ncbi.nlm.nih.gov/pubmed/30023923 http://dx.doi.org/10.1021/acsomega.8b00510 |
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author | da Silva, Aruã C. Semeano, Ana Teresa S. Dourado, André H. B. Ulrich, Henning Cordoba de Torresi, Susana I. |
author_facet | da Silva, Aruã C. Semeano, Ana Teresa S. Dourado, André H. B. Ulrich, Henning Cordoba de Torresi, Susana I. |
author_sort | da Silva, Aruã C. |
collection | PubMed |
description | [Image: see text] Electroactive biomaterials that are easily processed as scaffolds with good biocompatibility for tissue regeneration are difficult to design. Herein, the synthesis and characterization of a variety of novel electroactive, biodegradable biomaterials based on poly(3,4-ethylenedioxythiphene) copolymerized with poly(d,l lactic acid) (PEDOT-co-PDLLA) are presented. These copolymers were obtained using (2,3-dihydrothieno[3,4-b][1,4]dioxin-2-yl)methanol (EDOT-OH) as an initiator in a lactide ring-opening polymerization reaction, resulting in EDOT–PDLLA macromonomer. Conducting PEDOT-co-PDLLA copolymers (in three different proportions) were achieved by chemical copolymerization with 3,4-ethylenedioxythiophene (EDOT) monomers and persulfate oxidant. The PEDOT-co-PDLLA copolymers were structurally characterized by (1)H NMR and Fourier transform infrared spectroscopy. Cyclic voltammetry confirmed the electroactive character of the materials, and conductivity measurements were performed via electrochemical impedance spectroscopy. In vitro biodegradability was evaluated using proteinase K over 35 days, showing 29–46% (w/w) biodegradation. Noncytotoxicity was assessed by adhesion, migration, and proliferation assays using embryonic stem cells (E14.tg2a); excellent neuronal differentiation was observed. These novel electroactive and biodegradable PEDOT-co-PDLLA copolymers present surface chemistry and charge density properties that make them potentially useful as scaffold materials in different fields of applications, especially for neuronal tissue engineering. |
format | Online Article Text |
id | pubmed-6045332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60453322018-07-16 Novel Conducting and Biodegradable Copolymers with Noncytotoxic Properties toward Embryonic Stem Cells da Silva, Aruã C. Semeano, Ana Teresa S. Dourado, André H. B. Ulrich, Henning Cordoba de Torresi, Susana I. ACS Omega [Image: see text] Electroactive biomaterials that are easily processed as scaffolds with good biocompatibility for tissue regeneration are difficult to design. Herein, the synthesis and characterization of a variety of novel electroactive, biodegradable biomaterials based on poly(3,4-ethylenedioxythiphene) copolymerized with poly(d,l lactic acid) (PEDOT-co-PDLLA) are presented. These copolymers were obtained using (2,3-dihydrothieno[3,4-b][1,4]dioxin-2-yl)methanol (EDOT-OH) as an initiator in a lactide ring-opening polymerization reaction, resulting in EDOT–PDLLA macromonomer. Conducting PEDOT-co-PDLLA copolymers (in three different proportions) were achieved by chemical copolymerization with 3,4-ethylenedioxythiophene (EDOT) monomers and persulfate oxidant. The PEDOT-co-PDLLA copolymers were structurally characterized by (1)H NMR and Fourier transform infrared spectroscopy. Cyclic voltammetry confirmed the electroactive character of the materials, and conductivity measurements were performed via electrochemical impedance spectroscopy. In vitro biodegradability was evaluated using proteinase K over 35 days, showing 29–46% (w/w) biodegradation. Noncytotoxicity was assessed by adhesion, migration, and proliferation assays using embryonic stem cells (E14.tg2a); excellent neuronal differentiation was observed. These novel electroactive and biodegradable PEDOT-co-PDLLA copolymers present surface chemistry and charge density properties that make them potentially useful as scaffold materials in different fields of applications, especially for neuronal tissue engineering. American Chemical Society 2018-05-24 /pmc/articles/PMC6045332/ /pubmed/30023923 http://dx.doi.org/10.1021/acsomega.8b00510 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | da Silva, Aruã C. Semeano, Ana Teresa S. Dourado, André H. B. Ulrich, Henning Cordoba de Torresi, Susana I. Novel Conducting and Biodegradable Copolymers with Noncytotoxic Properties toward Embryonic Stem Cells |
title | Novel Conducting and Biodegradable Copolymers with
Noncytotoxic Properties toward Embryonic Stem Cells |
title_full | Novel Conducting and Biodegradable Copolymers with
Noncytotoxic Properties toward Embryonic Stem Cells |
title_fullStr | Novel Conducting and Biodegradable Copolymers with
Noncytotoxic Properties toward Embryonic Stem Cells |
title_full_unstemmed | Novel Conducting and Biodegradable Copolymers with
Noncytotoxic Properties toward Embryonic Stem Cells |
title_short | Novel Conducting and Biodegradable Copolymers with
Noncytotoxic Properties toward Embryonic Stem Cells |
title_sort | novel conducting and biodegradable copolymers with
noncytotoxic properties toward embryonic stem cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6045332/ https://www.ncbi.nlm.nih.gov/pubmed/30023923 http://dx.doi.org/10.1021/acsomega.8b00510 |
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