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New dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection
BACKGROUND: The treatment of infectious bone defects is a difficult problem to be solved in the clinic. In situ bone defect repair scaffolds with anti-infection and osteogenic abilities can effectively deal with infectious bone defects. In this study, an in situ polycaprolactone (PCL) scaffold conta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503254/ https://www.ncbi.nlm.nih.gov/pubmed/36138479 http://dx.doi.org/10.1186/s13036-022-00302-y |
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author | Yang, Changsheng Zhou, Lei Geng, Xiaodan Zhang, Hui Wang, Baolong Ning, Bin |
author_facet | Yang, Changsheng Zhou, Lei Geng, Xiaodan Zhang, Hui Wang, Baolong Ning, Bin |
author_sort | Yang, Changsheng |
collection | PubMed |
description | BACKGROUND: The treatment of infectious bone defects is a difficult problem to be solved in the clinic. In situ bone defect repair scaffolds with anti-infection and osteogenic abilities can effectively deal with infectious bone defects. In this study, an in situ polycaprolactone (PCL) scaffold containing ampicillin (Amp) and Mg microspheres was prepared by 3D printing technology. RESULTS: Mg and Amp were evenly distributed in PCL scaffolds and could be released slowly to the surrounding defect sites with the degradation of scaffolds. In vitro experiments demonstrated that the PCL scaffold containing Mg and Amp (PCL@Mg/Amp) demonstrated good cell adhesion and proliferation. The osteogenic genes collagen I (COL-I) and Runx2 were upregulated in cells grown on the PCL@Mg/Amp scaffold. The PCL@Mg/Amp scaffold also demonstrated excellent antibacterial ability against E. coli and S. aureus. In vivo experiments showed that the PCL@Mg/Amp scaffold had the strongest ability to promote tibial defect repair in rats compared with the other groups of scaffolds. CONCLUSIONS: This kind of dual-function in situ bone repair scaffold with anti-infection and osteogenic abilities has good application prospects in the field of treating infectious bone defects. |
format | Online Article Text |
id | pubmed-9503254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95032542022-09-24 New dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection Yang, Changsheng Zhou, Lei Geng, Xiaodan Zhang, Hui Wang, Baolong Ning, Bin J Biol Eng Research BACKGROUND: The treatment of infectious bone defects is a difficult problem to be solved in the clinic. In situ bone defect repair scaffolds with anti-infection and osteogenic abilities can effectively deal with infectious bone defects. In this study, an in situ polycaprolactone (PCL) scaffold containing ampicillin (Amp) and Mg microspheres was prepared by 3D printing technology. RESULTS: Mg and Amp were evenly distributed in PCL scaffolds and could be released slowly to the surrounding defect sites with the degradation of scaffolds. In vitro experiments demonstrated that the PCL scaffold containing Mg and Amp (PCL@Mg/Amp) demonstrated good cell adhesion and proliferation. The osteogenic genes collagen I (COL-I) and Runx2 were upregulated in cells grown on the PCL@Mg/Amp scaffold. The PCL@Mg/Amp scaffold also demonstrated excellent antibacterial ability against E. coli and S. aureus. In vivo experiments showed that the PCL@Mg/Amp scaffold had the strongest ability to promote tibial defect repair in rats compared with the other groups of scaffolds. CONCLUSIONS: This kind of dual-function in situ bone repair scaffold with anti-infection and osteogenic abilities has good application prospects in the field of treating infectious bone defects. BioMed Central 2022-09-22 /pmc/articles/PMC9503254/ /pubmed/36138479 http://dx.doi.org/10.1186/s13036-022-00302-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yang, Changsheng Zhou, Lei Geng, Xiaodan Zhang, Hui Wang, Baolong Ning, Bin New dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection |
title | New dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection |
title_full | New dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection |
title_fullStr | New dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection |
title_full_unstemmed | New dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection |
title_short | New dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection |
title_sort | new dual-function in situ bone repair scaffolds promote osteogenesis and reduce infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503254/ https://www.ncbi.nlm.nih.gov/pubmed/36138479 http://dx.doi.org/10.1186/s13036-022-00302-y |
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