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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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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