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Injectable and porous PLGA microspheres that form highly porous scaffolds at body temperature
Injectable scaffolds are of interest in the field of regenerative medicine because of their minimally invasive mode of delivery. For tissue repair applications, it is essential that such scaffolds have the mechanical properties, porosity and pore diameter to support the formation of new tissue. In t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4226323/ https://www.ncbi.nlm.nih.gov/pubmed/25152354 http://dx.doi.org/10.1016/j.actbio.2014.08.015 |
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author | Qutachi, Omar Vetsch, Jolanda R. Gill, Daniel Cox, Helen Scurr, David J. Hofmann, Sandra Müller, Ralph Quirk, Robin A. Shakesheff, Kevin M. Rahman, Cheryl V. |
author_facet | Qutachi, Omar Vetsch, Jolanda R. Gill, Daniel Cox, Helen Scurr, David J. Hofmann, Sandra Müller, Ralph Quirk, Robin A. Shakesheff, Kevin M. Rahman, Cheryl V. |
author_sort | Qutachi, Omar |
collection | PubMed |
description | Injectable scaffolds are of interest in the field of regenerative medicine because of their minimally invasive mode of delivery. For tissue repair applications, it is essential that such scaffolds have the mechanical properties, porosity and pore diameter to support the formation of new tissue. In the current study, porous poly(dl-lactic acid-co-glycolic acid) (PLGA) microspheres were fabricated with an average size of 84 ± 24 μm for use as injectable cell carriers. Treatment with ethanolic sodium hydroxide for 2 min was observed to increase surface porosity without causing the microsphere structure to disintegrate. This surface treatment also enabled the microspheres to fuse together at 37 °C to form scaffold structures. The average compressive strength of the scaffolds after 24 h at 37 °C was 0.9 ± 0.1 MPa, and the average Young’s modulus was 9.4 ± 1.2 MPa. Scaffold porosity levels were 81.6% on average, with a mean pore diameter of 54 ± 38 μm. This study demonstrates a method for fabricating porous PLGA microspheres that form solid porous scaffolds at body temperature, creating an injectable system capable of supporting NIH-3T3 cell attachment and proliferation in vitro. |
format | Online Article Text |
id | pubmed-4226323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-42263232014-12-01 Injectable and porous PLGA microspheres that form highly porous scaffolds at body temperature Qutachi, Omar Vetsch, Jolanda R. Gill, Daniel Cox, Helen Scurr, David J. Hofmann, Sandra Müller, Ralph Quirk, Robin A. Shakesheff, Kevin M. Rahman, Cheryl V. Acta Biomater Article Injectable scaffolds are of interest in the field of regenerative medicine because of their minimally invasive mode of delivery. For tissue repair applications, it is essential that such scaffolds have the mechanical properties, porosity and pore diameter to support the formation of new tissue. In the current study, porous poly(dl-lactic acid-co-glycolic acid) (PLGA) microspheres were fabricated with an average size of 84 ± 24 μm for use as injectable cell carriers. Treatment with ethanolic sodium hydroxide for 2 min was observed to increase surface porosity without causing the microsphere structure to disintegrate. This surface treatment also enabled the microspheres to fuse together at 37 °C to form scaffold structures. The average compressive strength of the scaffolds after 24 h at 37 °C was 0.9 ± 0.1 MPa, and the average Young’s modulus was 9.4 ± 1.2 MPa. Scaffold porosity levels were 81.6% on average, with a mean pore diameter of 54 ± 38 μm. This study demonstrates a method for fabricating porous PLGA microspheres that form solid porous scaffolds at body temperature, creating an injectable system capable of supporting NIH-3T3 cell attachment and proliferation in vitro. Elsevier 2014-12 /pmc/articles/PMC4226323/ /pubmed/25152354 http://dx.doi.org/10.1016/j.actbio.2014.08.015 Text en © 2014 Elsevier Ltd. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Qutachi, Omar Vetsch, Jolanda R. Gill, Daniel Cox, Helen Scurr, David J. Hofmann, Sandra Müller, Ralph Quirk, Robin A. Shakesheff, Kevin M. Rahman, Cheryl V. Injectable and porous PLGA microspheres that form highly porous scaffolds at body temperature |
title | Injectable and porous PLGA microspheres that form highly porous scaffolds at body temperature |
title_full | Injectable and porous PLGA microspheres that form highly porous scaffolds at body temperature |
title_fullStr | Injectable and porous PLGA microspheres that form highly porous scaffolds at body temperature |
title_full_unstemmed | Injectable and porous PLGA microspheres that form highly porous scaffolds at body temperature |
title_short | Injectable and porous PLGA microspheres that form highly porous scaffolds at body temperature |
title_sort | injectable and porous plga microspheres that form highly porous scaffolds at body temperature |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4226323/ https://www.ncbi.nlm.nih.gov/pubmed/25152354 http://dx.doi.org/10.1016/j.actbio.2014.08.015 |
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