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Advanced PLGA hybrid scaffold with a bioactive PDRN/BMP2 nanocomplex for angiogenesis and bone regeneration using human fetal MSCs
Biodegradable polymers have been used with various systems for tissue engineering. Among them, poly(lactic-co-glycolic) acid (PLGA) has been widely used as a biomaterial for bone regeneration because of its great biocompatibility and biodegradability properties. However, there remain substantial cru...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654289/ https://www.ncbi.nlm.nih.gov/pubmed/34878837 http://dx.doi.org/10.1126/sciadv.abj1083 |
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author | Kim, Da-Seul Lee, Jun-Kyu Kim, Jun Hyuk Lee, Jaemin Kim, Dong Seon An, Sanghyun Park, Sung-Bin Kim, Tae-Hyung Rim, Jong Seop Lee, Soonchul Han, Dong Keun |
author_facet | Kim, Da-Seul Lee, Jun-Kyu Kim, Jun Hyuk Lee, Jaemin Kim, Dong Seon An, Sanghyun Park, Sung-Bin Kim, Tae-Hyung Rim, Jong Seop Lee, Soonchul Han, Dong Keun |
author_sort | Kim, Da-Seul |
collection | PubMed |
description | Biodegradable polymers have been used with various systems for tissue engineering. Among them, poly(lactic-co-glycolic) acid (PLGA) has been widely used as a biomaterial for bone regeneration because of its great biocompatibility and biodegradability properties. However, there remain substantial cruxes that the by-products of PLGA result in an acidic environment at the implanting site, and the polymer has a weak mechanical property. In our previous study, magnesium hydroxide (MH) and bone extracellular matrix are combined with a PLGA scaffold (PME) to improve anti-inflammation and mechanical properties and osteoconductivity. In the present study, the development of a bioactive nanocomplex (NC) formed along with polydeoxyribonucleotide and bone morphogenetic protein 2 (BMP2) provides synergistic abilities in angiogenesis and bone regeneration. This PME hybrid scaffold immobilized with NC (PME/NC) achieves outstanding performance in anti-inflammation, angiogenesis, and osteogenesis. Such an advanced PME/NC scaffold suggests an integrated bone graft substitute for bone regeneration. |
format | Online Article Text |
id | pubmed-8654289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-86542892021-12-16 Advanced PLGA hybrid scaffold with a bioactive PDRN/BMP2 nanocomplex for angiogenesis and bone regeneration using human fetal MSCs Kim, Da-Seul Lee, Jun-Kyu Kim, Jun Hyuk Lee, Jaemin Kim, Dong Seon An, Sanghyun Park, Sung-Bin Kim, Tae-Hyung Rim, Jong Seop Lee, Soonchul Han, Dong Keun Sci Adv Biomedicine and Life Sciences Biodegradable polymers have been used with various systems for tissue engineering. Among them, poly(lactic-co-glycolic) acid (PLGA) has been widely used as a biomaterial for bone regeneration because of its great biocompatibility and biodegradability properties. However, there remain substantial cruxes that the by-products of PLGA result in an acidic environment at the implanting site, and the polymer has a weak mechanical property. In our previous study, magnesium hydroxide (MH) and bone extracellular matrix are combined with a PLGA scaffold (PME) to improve anti-inflammation and mechanical properties and osteoconductivity. In the present study, the development of a bioactive nanocomplex (NC) formed along with polydeoxyribonucleotide and bone morphogenetic protein 2 (BMP2) provides synergistic abilities in angiogenesis and bone regeneration. This PME hybrid scaffold immobilized with NC (PME/NC) achieves outstanding performance in anti-inflammation, angiogenesis, and osteogenesis. Such an advanced PME/NC scaffold suggests an integrated bone graft substitute for bone regeneration. American Association for the Advancement of Science 2021-12-08 /pmc/articles/PMC8654289/ /pubmed/34878837 http://dx.doi.org/10.1126/sciadv.abj1083 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Kim, Da-Seul Lee, Jun-Kyu Kim, Jun Hyuk Lee, Jaemin Kim, Dong Seon An, Sanghyun Park, Sung-Bin Kim, Tae-Hyung Rim, Jong Seop Lee, Soonchul Han, Dong Keun Advanced PLGA hybrid scaffold with a bioactive PDRN/BMP2 nanocomplex for angiogenesis and bone regeneration using human fetal MSCs |
title | Advanced PLGA hybrid scaffold with a bioactive PDRN/BMP2 nanocomplex for angiogenesis and bone regeneration using human fetal MSCs |
title_full | Advanced PLGA hybrid scaffold with a bioactive PDRN/BMP2 nanocomplex for angiogenesis and bone regeneration using human fetal MSCs |
title_fullStr | Advanced PLGA hybrid scaffold with a bioactive PDRN/BMP2 nanocomplex for angiogenesis and bone regeneration using human fetal MSCs |
title_full_unstemmed | Advanced PLGA hybrid scaffold with a bioactive PDRN/BMP2 nanocomplex for angiogenesis and bone regeneration using human fetal MSCs |
title_short | Advanced PLGA hybrid scaffold with a bioactive PDRN/BMP2 nanocomplex for angiogenesis and bone regeneration using human fetal MSCs |
title_sort | advanced plga hybrid scaffold with a bioactive pdrn/bmp2 nanocomplex for angiogenesis and bone regeneration using human fetal mscs |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654289/ https://www.ncbi.nlm.nih.gov/pubmed/34878837 http://dx.doi.org/10.1126/sciadv.abj1083 |
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