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Remote Eradication of Bacteria on Orthopedic Implants via Delayed Delivery of Polycaprolactone Stabilized Polyvinylpyrrolidone Iodine
Bacteria-associated late infection of the orthopedic devices would further lead to the failure of the implantation. However, present ordinary antimicrobial strategies usually deal with early infection but fail to combat the late infection of the implants due to the burst release of the antibiotics....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9589933/ https://www.ncbi.nlm.nih.gov/pubmed/36278664 http://dx.doi.org/10.3390/jfb13040195 |
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author | Wang, Yikai Teng, Wangsiyuan Zhang, Zengjie Ma, Siyuan Jin, Zhihui Zhou, Xingzhi Ye, Yuxiao Zhang, Chongda Gou, Zhongru Yu, Xiaohua Ye, Zhaoming Ren, Yijun |
author_facet | Wang, Yikai Teng, Wangsiyuan Zhang, Zengjie Ma, Siyuan Jin, Zhihui Zhou, Xingzhi Ye, Yuxiao Zhang, Chongda Gou, Zhongru Yu, Xiaohua Ye, Zhaoming Ren, Yijun |
author_sort | Wang, Yikai |
collection | PubMed |
description | Bacteria-associated late infection of the orthopedic devices would further lead to the failure of the implantation. However, present ordinary antimicrobial strategies usually deal with early infection but fail to combat the late infection of the implants due to the burst release of the antibiotics. Thus, to fabricate long-term antimicrobial (early antibacterial, late antibacterial) orthopedic implants is essential to address this issue. Herein, we developed a sophisticated MAO-I(2)-PCLx coating system incorporating an underlying iodine layer and an upper layer of polycaprolactone (PCL)-controlled coating, which could effectively eradicate the late bacterial infection throughout the implantation. Firstly, micro-arc oxidation was used to form a microarray tubular structure on the surface of the implants, laying the foundation for iodine loading and PCL bonding. Secondly, electrophoresis was applied to load iodine in the tubular structure as an efficient bactericidal agent. Finally, the surface-bonded PCL coating acts as a controller to regulate the release of iodine. The hybrid coatings displayed great stability and control release capacity. Excellent antibacterial ability was validated at 30 days post-implantation via in vitro experiments and in vivo rat osteomyelitis model. Expectedly, it can become a promising bench-to-bedside strategy for current infection challenges in the orthopedic field. |
format | Online Article Text |
id | pubmed-9589933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95899332022-10-25 Remote Eradication of Bacteria on Orthopedic Implants via Delayed Delivery of Polycaprolactone Stabilized Polyvinylpyrrolidone Iodine Wang, Yikai Teng, Wangsiyuan Zhang, Zengjie Ma, Siyuan Jin, Zhihui Zhou, Xingzhi Ye, Yuxiao Zhang, Chongda Gou, Zhongru Yu, Xiaohua Ye, Zhaoming Ren, Yijun J Funct Biomater Article Bacteria-associated late infection of the orthopedic devices would further lead to the failure of the implantation. However, present ordinary antimicrobial strategies usually deal with early infection but fail to combat the late infection of the implants due to the burst release of the antibiotics. Thus, to fabricate long-term antimicrobial (early antibacterial, late antibacterial) orthopedic implants is essential to address this issue. Herein, we developed a sophisticated MAO-I(2)-PCLx coating system incorporating an underlying iodine layer and an upper layer of polycaprolactone (PCL)-controlled coating, which could effectively eradicate the late bacterial infection throughout the implantation. Firstly, micro-arc oxidation was used to form a microarray tubular structure on the surface of the implants, laying the foundation for iodine loading and PCL bonding. Secondly, electrophoresis was applied to load iodine in the tubular structure as an efficient bactericidal agent. Finally, the surface-bonded PCL coating acts as a controller to regulate the release of iodine. The hybrid coatings displayed great stability and control release capacity. Excellent antibacterial ability was validated at 30 days post-implantation via in vitro experiments and in vivo rat osteomyelitis model. Expectedly, it can become a promising bench-to-bedside strategy for current infection challenges in the orthopedic field. MDPI 2022-10-19 /pmc/articles/PMC9589933/ /pubmed/36278664 http://dx.doi.org/10.3390/jfb13040195 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Yikai Teng, Wangsiyuan Zhang, Zengjie Ma, Siyuan Jin, Zhihui Zhou, Xingzhi Ye, Yuxiao Zhang, Chongda Gou, Zhongru Yu, Xiaohua Ye, Zhaoming Ren, Yijun Remote Eradication of Bacteria on Orthopedic Implants via Delayed Delivery of Polycaprolactone Stabilized Polyvinylpyrrolidone Iodine |
title | Remote Eradication of Bacteria on Orthopedic Implants via Delayed Delivery of Polycaprolactone Stabilized Polyvinylpyrrolidone Iodine |
title_full | Remote Eradication of Bacteria on Orthopedic Implants via Delayed Delivery of Polycaprolactone Stabilized Polyvinylpyrrolidone Iodine |
title_fullStr | Remote Eradication of Bacteria on Orthopedic Implants via Delayed Delivery of Polycaprolactone Stabilized Polyvinylpyrrolidone Iodine |
title_full_unstemmed | Remote Eradication of Bacteria on Orthopedic Implants via Delayed Delivery of Polycaprolactone Stabilized Polyvinylpyrrolidone Iodine |
title_short | Remote Eradication of Bacteria on Orthopedic Implants via Delayed Delivery of Polycaprolactone Stabilized Polyvinylpyrrolidone Iodine |
title_sort | remote eradication of bacteria on orthopedic implants via delayed delivery of polycaprolactone stabilized polyvinylpyrrolidone iodine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9589933/ https://www.ncbi.nlm.nih.gov/pubmed/36278664 http://dx.doi.org/10.3390/jfb13040195 |
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