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A novel vehicle-like drug delivery 3D printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo

The high surface area ratio and special structure of mesoporous bioactive glass (MBG) endow it with excellent physical adsorption of various drugs without destroying the chemical activity. Silicate 1393 bioactive glass (1393) is famous for its fantastic biodegradability and osteogenesis. Herein, we...

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Autores principales: Wang, Hui, Deng, Zhengwei, Chen, Jing, Qi, Xin, Pang, Libing, Lin, Bocai, Adib, Yan Teik Yuin, Miao, Na, Wang, Deping, Zhang, Yadong, Li, Jiusheng, Zeng, Xiangqiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211168/
https://www.ncbi.nlm.nih.gov/pubmed/32398952
http://dx.doi.org/10.7150/ijbs.37552
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author Wang, Hui
Deng, Zhengwei
Chen, Jing
Qi, Xin
Pang, Libing
Lin, Bocai
Adib, Yan Teik Yuin
Miao, Na
Wang, Deping
Zhang, Yadong
Li, Jiusheng
Zeng, Xiangqiong
author_facet Wang, Hui
Deng, Zhengwei
Chen, Jing
Qi, Xin
Pang, Libing
Lin, Bocai
Adib, Yan Teik Yuin
Miao, Na
Wang, Deping
Zhang, Yadong
Li, Jiusheng
Zeng, Xiangqiong
author_sort Wang, Hui
collection PubMed
description The high surface area ratio and special structure of mesoporous bioactive glass (MBG) endow it with excellent physical adsorption of various drugs without destroying the chemical activity. Silicate 1393 bioactive glass (1393) is famous for its fantastic biodegradability and osteogenesis. Herein, we have built a novel vehicle-like drug delivery 3D printing scaffold with multiplexed drug delivery capacity by coating MBG on the surface of 1393 (1393@MBG). Furthermore, we have applied DEX and BMP-2 on the 1393@MBG scaffold to endow it with antibacterial and osteogenic properties. Results indicated that this 1393@MBG scaffold could effectively load and controlled release BMP-2, DNA and DEX, which can be applied for orthopedic treatment. The in vitro study showed that the DEX loaded 1393@MBG exhibited excellent antibacterial ability, which was evaluated by Staphylococcus aureus (S. aureus), and the BMP-2 loaded 1393@MBG can improve the alkaline phosphatase (ALP) activity and upregulate the expression of osteogenesis-related genes (OCN and RUNX2) of human bone mesenchymal stem cells (hBMSCs). Moreover, the in vivo study further confirmed that the BMP-2 loaded 1393@MBG group showed better osteogenic capacity as compared to that of the 1393 group in a rat femoral defect. Together, these results suggested that the vehicle-like drug delivery 3D printing scaffold 1393@MBG could be a promising candidate for bone repair and relative bone disease treatment.
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spelling pubmed-72111682020-05-12 A novel vehicle-like drug delivery 3D printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo Wang, Hui Deng, Zhengwei Chen, Jing Qi, Xin Pang, Libing Lin, Bocai Adib, Yan Teik Yuin Miao, Na Wang, Deping Zhang, Yadong Li, Jiusheng Zeng, Xiangqiong Int J Biol Sci Research Paper The high surface area ratio and special structure of mesoporous bioactive glass (MBG) endow it with excellent physical adsorption of various drugs without destroying the chemical activity. Silicate 1393 bioactive glass (1393) is famous for its fantastic biodegradability and osteogenesis. Herein, we have built a novel vehicle-like drug delivery 3D printing scaffold with multiplexed drug delivery capacity by coating MBG on the surface of 1393 (1393@MBG). Furthermore, we have applied DEX and BMP-2 on the 1393@MBG scaffold to endow it with antibacterial and osteogenic properties. Results indicated that this 1393@MBG scaffold could effectively load and controlled release BMP-2, DNA and DEX, which can be applied for orthopedic treatment. The in vitro study showed that the DEX loaded 1393@MBG exhibited excellent antibacterial ability, which was evaluated by Staphylococcus aureus (S. aureus), and the BMP-2 loaded 1393@MBG can improve the alkaline phosphatase (ALP) activity and upregulate the expression of osteogenesis-related genes (OCN and RUNX2) of human bone mesenchymal stem cells (hBMSCs). Moreover, the in vivo study further confirmed that the BMP-2 loaded 1393@MBG group showed better osteogenic capacity as compared to that of the 1393 group in a rat femoral defect. Together, these results suggested that the vehicle-like drug delivery 3D printing scaffold 1393@MBG could be a promising candidate for bone repair and relative bone disease treatment. Ivyspring International Publisher 2020-04-01 /pmc/articles/PMC7211168/ /pubmed/32398952 http://dx.doi.org/10.7150/ijbs.37552 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wang, Hui
Deng, Zhengwei
Chen, Jing
Qi, Xin
Pang, Libing
Lin, Bocai
Adib, Yan Teik Yuin
Miao, Na
Wang, Deping
Zhang, Yadong
Li, Jiusheng
Zeng, Xiangqiong
A novel vehicle-like drug delivery 3D printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo
title A novel vehicle-like drug delivery 3D printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo
title_full A novel vehicle-like drug delivery 3D printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo
title_fullStr A novel vehicle-like drug delivery 3D printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo
title_full_unstemmed A novel vehicle-like drug delivery 3D printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo
title_short A novel vehicle-like drug delivery 3D printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo
title_sort novel vehicle-like drug delivery 3d printing scaffold and its applications for a rat femoral bone repairing in vitro and in vivo
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211168/
https://www.ncbi.nlm.nih.gov/pubmed/32398952
http://dx.doi.org/10.7150/ijbs.37552
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