Healing of Osteochondral Defects Implanted with Biomimetic Scaffolds of Poly(ε-Caprolactone)/Hydroxyapatite and Glycidyl-Methacrylate-Modified Hyaluronic Acid in a Minipig

Articular cartilage is a structure lack of vascular distribution. Once the cartilage is injured or diseased, it is unable to regenerate by itself. Surgical treatments do not effectively heal defects in articular cartilage. Tissue engineering is the most potential solution to this problem. In this st...

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Main Authors: Yi-Ho Hsieh, Bo-Yuan Shen, Yao-Horng Wang, Bojain Lin, Hung-Maan Lee, Ming-Fa Hsieh
Format: Article
Language:English
Published: MDPI AG 2018-04-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/19/4/1125
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spelling doaj-3b55e0ddc0474aaf8af5c53e3b17ccf02020-11-25T00:38:34ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-04-01194112510.3390/ijms19041125ijms19041125Healing of Osteochondral Defects Implanted with Biomimetic Scaffolds of Poly(ε-Caprolactone)/Hydroxyapatite and Glycidyl-Methacrylate-Modified Hyaluronic Acid in a MinipigYi-Ho Hsieh0Bo-Yuan Shen1Yao-Horng Wang2Bojain Lin3Hung-Maan Lee4Ming-Fa Hsieh5Department of Biomedical Engineering, Chung Yuan Christian University, 200 Chung Pei Road, Chung-Li District, Taoyuan City 320, TaiwanMater Program for Nanotechnology, Chung Yuan Christian University, 200 Chung Pei Road, Chung-Li District, Taoyuan City 320, TaiwanDepartment of Nursing, Yuanpei University of Medical Technology, 306, Yuanpei Street, Hsinchu 300, TaiwanDepartment of Biomedical Engineering, Chung Yuan Christian University, 200 Chung Pei Road, Chung-Li District, Taoyuan City 320, TaiwanDepartment of Biomedical Engineering, Chung Yuan Christian University, 200 Chung Pei Road, Chung-Li District, Taoyuan City 320, TaiwanDepartment of Biomedical Engineering, Chung Yuan Christian University, 200 Chung Pei Road, Chung-Li District, Taoyuan City 320, TaiwanArticular cartilage is a structure lack of vascular distribution. Once the cartilage is injured or diseased, it is unable to regenerate by itself. Surgical treatments do not effectively heal defects in articular cartilage. Tissue engineering is the most potential solution to this problem. In this study, methoxy poly(ethylene glycol)-block-poly(ε-caprolactone) (mPEG-PCL) and hydroxyapatite at a weight ratio of 2:1 were mixed via fused deposition modeling (FDM) layer by layer to form a solid scaffold. The scaffolds were further infiltrated with glycidyl methacrylate hyaluronic acid loading with 10 ng/mL of Transforming Growth Factor-β1 and photo cross-linked on top of the scaffolds. An in vivo test was performed on the knees of Lanyu miniature pigs for a period of 12 months. The healing process of the osteochondral defects was followed by computer tomography (CT). The defect was fully covered with regenerated tissues in the control pig, while different tissues were grown in the defect of knee of the experimental pig. In the gross anatomy of the cross section, the scaffold remained in the subchondral location, while surface cartilage was regenerated. The cross section of the knees of both the control and experimental pigs were subjected to hematoxylin and eosin staining. The cartilage of the knee in the experimental pig was partially matured, e.g., few chondrocyte cells were enclosed in the lacunae. In the knee of the control pig, the defect was fully grown with fibrocartilage. In another in vivo experiment in a rabbit and a pig, the composite of the TGF-β1-loaded hydrogel and scaffolds was found to regenerate hyaline cartilage. However, scaffolds that remain in the subchondral lesion potentially delay the healing process. Therefore, the structural design of the scaffold should be reconsidered to match the regeneration process of both cartilage and subchondral bone.http://www.mdpi.com/1422-0067/19/4/1125cartilagebiomimeticfused deposition modelingpoly(ε-caprolactone)hyaluronic acidlarge animal models
collection DOAJ
language English
format Article
sources DOAJ
author Yi-Ho Hsieh
Bo-Yuan Shen
Yao-Horng Wang
Bojain Lin
Hung-Maan Lee
Ming-Fa Hsieh
spellingShingle Yi-Ho Hsieh
Bo-Yuan Shen
Yao-Horng Wang
Bojain Lin
Hung-Maan Lee
Ming-Fa Hsieh
Healing of Osteochondral Defects Implanted with Biomimetic Scaffolds of Poly(ε-Caprolactone)/Hydroxyapatite and Glycidyl-Methacrylate-Modified Hyaluronic Acid in a Minipig
International Journal of Molecular Sciences
cartilage
biomimetic
fused deposition modeling
poly(ε-caprolactone)
hyaluronic acid
large animal models
author_facet Yi-Ho Hsieh
Bo-Yuan Shen
Yao-Horng Wang
Bojain Lin
Hung-Maan Lee
Ming-Fa Hsieh
author_sort Yi-Ho Hsieh
title Healing of Osteochondral Defects Implanted with Biomimetic Scaffolds of Poly(ε-Caprolactone)/Hydroxyapatite and Glycidyl-Methacrylate-Modified Hyaluronic Acid in a Minipig
title_short Healing of Osteochondral Defects Implanted with Biomimetic Scaffolds of Poly(ε-Caprolactone)/Hydroxyapatite and Glycidyl-Methacrylate-Modified Hyaluronic Acid in a Minipig
title_full Healing of Osteochondral Defects Implanted with Biomimetic Scaffolds of Poly(ε-Caprolactone)/Hydroxyapatite and Glycidyl-Methacrylate-Modified Hyaluronic Acid in a Minipig
title_fullStr Healing of Osteochondral Defects Implanted with Biomimetic Scaffolds of Poly(ε-Caprolactone)/Hydroxyapatite and Glycidyl-Methacrylate-Modified Hyaluronic Acid in a Minipig
title_full_unstemmed Healing of Osteochondral Defects Implanted with Biomimetic Scaffolds of Poly(ε-Caprolactone)/Hydroxyapatite and Glycidyl-Methacrylate-Modified Hyaluronic Acid in a Minipig
title_sort healing of osteochondral defects implanted with biomimetic scaffolds of poly(ε-caprolactone)/hydroxyapatite and glycidyl-methacrylate-modified hyaluronic acid in a minipig
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2018-04-01
description Articular cartilage is a structure lack of vascular distribution. Once the cartilage is injured or diseased, it is unable to regenerate by itself. Surgical treatments do not effectively heal defects in articular cartilage. Tissue engineering is the most potential solution to this problem. In this study, methoxy poly(ethylene glycol)-block-poly(ε-caprolactone) (mPEG-PCL) and hydroxyapatite at a weight ratio of 2:1 were mixed via fused deposition modeling (FDM) layer by layer to form a solid scaffold. The scaffolds were further infiltrated with glycidyl methacrylate hyaluronic acid loading with 10 ng/mL of Transforming Growth Factor-β1 and photo cross-linked on top of the scaffolds. An in vivo test was performed on the knees of Lanyu miniature pigs for a period of 12 months. The healing process of the osteochondral defects was followed by computer tomography (CT). The defect was fully covered with regenerated tissues in the control pig, while different tissues were grown in the defect of knee of the experimental pig. In the gross anatomy of the cross section, the scaffold remained in the subchondral location, while surface cartilage was regenerated. The cross section of the knees of both the control and experimental pigs were subjected to hematoxylin and eosin staining. The cartilage of the knee in the experimental pig was partially matured, e.g., few chondrocyte cells were enclosed in the lacunae. In the knee of the control pig, the defect was fully grown with fibrocartilage. In another in vivo experiment in a rabbit and a pig, the composite of the TGF-β1-loaded hydrogel and scaffolds was found to regenerate hyaline cartilage. However, scaffolds that remain in the subchondral lesion potentially delay the healing process. Therefore, the structural design of the scaffold should be reconsidered to match the regeneration process of both cartilage and subchondral bone.
topic cartilage
biomimetic
fused deposition modeling
poly(ε-caprolactone)
hyaluronic acid
large animal models
url http://www.mdpi.com/1422-0067/19/4/1125
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