3D gel-printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivo
Background: /Objective: The treatment of bone defect has always been a difficult problem in orthopedic clinic. The search for alternative biodegradable implants is a hot topic. The development of biodegradable magnesium scaffolds for the treatment of bone defects has long been a goal of the public....
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Format: | Article |
Language: | English |
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Elsevier
2022-03-01
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Series: | Journal of Orthopaedic Translation |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S2214031X21000978 |
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author | Yuxuan Zhang Tao Lin Haoye Meng Xueting Wang Hong Peng Guangbo Liu Shuai Wei Qiang Lu Yu Wang Aiyuan Wang Wenjing Xu Huiping Shao Jiang Peng |
author_facet | Yuxuan Zhang Tao Lin Haoye Meng Xueting Wang Hong Peng Guangbo Liu Shuai Wei Qiang Lu Yu Wang Aiyuan Wang Wenjing Xu Huiping Shao Jiang Peng |
author_sort | Yuxuan Zhang |
collection | DOAJ |
description | Background: /Objective: The treatment of bone defect has always been a difficult problem in orthopedic clinic. The search for alternative biodegradable implants is a hot topic. The development of biodegradable magnesium scaffolds for the treatment of bone defects has long been a goal of the public. Methods: In this study, we proposed a porous magnesium scaffold prepared by 3D gel printing and surface modification with an additional calcium phosphate coating and use of its strength, degradability and slow degradation rate in a bone graft substitute material. The porous magnesium granular scaffold was prepared by 3D gel printing technology and modified by DCPD (Dibasic Calcium Phosphate Dihydrate) coating. The biocompatibility, degradation rate, and osteogenic ability of the scaffold were evaluated in vitro and in vivo. Results: The biocompatibility, in vivo degradation and bone defect healing response of the implants were investigated. Porous magnesium scaffolds were successfully prepared, and the strength of sintered scaffolds reached 5.38 MPa. The degradation rates of scaffolds were significantly reduced after coating with DCPD. The cell compatibility evaluation showed that DCPD-coated Mg scaffold was suitable for cell proliferation. In vivo biosafety monitoring showed that scaffold implantation did not cause an increase in Mg ion concentration in vivo, and no toxic damage was detected in the liver or kidney. Micro-CT and pathological results showed that a large amount of new bone was formed at 6 weeks. At 12 weeks, approximately 52% of the scaffold volume remained. At 24 weeks, osteogenesis, which was stimulated by some residual scaffold, still can be observed. In summary, this study suggests that 3D gel-printed DCPD-coated porous magnesium scaffolds have great potential as bone graft alternatives. Conclusion: In summary, this study suggests that 3D gel-printed DCPD-coated porous magnesium scaffolds have great potential as bone graft alternatives. The Translational potential of this article: The translational potential of this article is to make use of the advantages of 3D gel printing technology with higher efficiency and lower cost compared with SLM and SLS technologies, and use pure magnesium powder as raw material to prepare degradable porous magnesium metal scaffolds, opening up a new technical route for the preparation of degradable porous magnesium scaffolds which are made for bone defect regeneration in the future. |
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institution | Directory Open Access Journal |
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language | English |
last_indexed | 2024-04-13T03:41:32Z |
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spelling | doaj.art-a429b07ef2a4410b918ced08aa65fe662022-12-22T03:04:07ZengElsevierJournal of Orthopaedic Translation2214-031X2022-03-013313233D gel-printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivoYuxuan Zhang0Tao Lin1Haoye Meng2Xueting Wang3Hong Peng4Guangbo Liu5Shuai Wei6Qiang Lu7Yu Wang8Aiyuan Wang9Wenjing Xu10Huiping Shao11Jiang Peng12Medical School of Chinese PLA, Beijing, 100853, China; Institute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory (No BZ0128), Beijing Key Lab of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA, Beijing, 100853, ChinaInstitute for Advanced Materials & Technology, University of Science and Technology Beijing, Beijing, 100083, ChinaInstitute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory (No BZ0128), Beijing Key Lab of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA, Beijing, 100853, ChinaInstitute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory (No BZ0128), Beijing Key Lab of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA, Beijing, 100853, ChinaMedical School of Chinese PLA, Beijing, 100853, ChinaMedical School of Chinese PLA, Beijing, 100853, China; Strategic Support Force Medical Center, No.9, Anxiang Beli, Beijing, 100101, ChinaTianjin Hospital, Tianjin University, No. 406 Jiefang South Road, Tianjin, 300211, ChinaInstitute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory (No BZ0128), Beijing Key Lab of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA, Beijing, 100853, ChinaInstitute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory (No BZ0128), Beijing Key Lab of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA, Beijing, 100853, ChinaInstitute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory (No BZ0128), Beijing Key Lab of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA, Beijing, 100853, ChinaInstitute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory (No BZ0128), Beijing Key Lab of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA, Beijing, 100853, ChinaInstitute for Advanced Materials & Technology, University of Science and Technology Beijing, Beijing, 100083, China; Corresponding author.Institute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory (No BZ0128), Beijing Key Lab of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA, Beijing, 100853, China; Corresponding author.Background: /Objective: The treatment of bone defect has always been a difficult problem in orthopedic clinic. The search for alternative biodegradable implants is a hot topic. The development of biodegradable magnesium scaffolds for the treatment of bone defects has long been a goal of the public. Methods: In this study, we proposed a porous magnesium scaffold prepared by 3D gel printing and surface modification with an additional calcium phosphate coating and use of its strength, degradability and slow degradation rate in a bone graft substitute material. The porous magnesium granular scaffold was prepared by 3D gel printing technology and modified by DCPD (Dibasic Calcium Phosphate Dihydrate) coating. The biocompatibility, degradation rate, and osteogenic ability of the scaffold were evaluated in vitro and in vivo. Results: The biocompatibility, in vivo degradation and bone defect healing response of the implants were investigated. Porous magnesium scaffolds were successfully prepared, and the strength of sintered scaffolds reached 5.38 MPa. The degradation rates of scaffolds were significantly reduced after coating with DCPD. The cell compatibility evaluation showed that DCPD-coated Mg scaffold was suitable for cell proliferation. In vivo biosafety monitoring showed that scaffold implantation did not cause an increase in Mg ion concentration in vivo, and no toxic damage was detected in the liver or kidney. Micro-CT and pathological results showed that a large amount of new bone was formed at 6 weeks. At 12 weeks, approximately 52% of the scaffold volume remained. At 24 weeks, osteogenesis, which was stimulated by some residual scaffold, still can be observed. In summary, this study suggests that 3D gel-printed DCPD-coated porous magnesium scaffolds have great potential as bone graft alternatives. Conclusion: In summary, this study suggests that 3D gel-printed DCPD-coated porous magnesium scaffolds have great potential as bone graft alternatives. The Translational potential of this article: The translational potential of this article is to make use of the advantages of 3D gel printing technology with higher efficiency and lower cost compared with SLM and SLS technologies, and use pure magnesium powder as raw material to prepare degradable porous magnesium metal scaffolds, opening up a new technical route for the preparation of degradable porous magnesium scaffolds which are made for bone defect regeneration in the future.http://www.sciencedirect.com/science/article/pii/S2214031X21000978Magnesium scaffoldOsteoanagenesisBone defectDicalcium phosphate dihydrate coatingBiodegradation |
spellingShingle | Yuxuan Zhang Tao Lin Haoye Meng Xueting Wang Hong Peng Guangbo Liu Shuai Wei Qiang Lu Yu Wang Aiyuan Wang Wenjing Xu Huiping Shao Jiang Peng 3D gel-printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivo Journal of Orthopaedic Translation Magnesium scaffold Osteoanagenesis Bone defect Dicalcium phosphate dihydrate coating Biodegradation |
title | 3D gel-printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivo |
title_full | 3D gel-printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivo |
title_fullStr | 3D gel-printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivo |
title_full_unstemmed | 3D gel-printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivo |
title_short | 3D gel-printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivo |
title_sort | 3d gel printed porous magnesium scaffold coated with dibasic calcium phosphate dihydrate for bone repair in vivo |
topic | Magnesium scaffold Osteoanagenesis Bone defect Dicalcium phosphate dihydrate coating Biodegradation |
url | http://www.sciencedirect.com/science/article/pii/S2214031X21000978 |
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