Enhancing cartilage regeneration and repair through bioactive and biomechanical modification of 3D acellular dermal matrix

IF 5.6 1区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Wei Gao, Tan Cheng, Zhengya Tang, Wenqiang Zhang, Yong Xu, Min Han, Guangdong Zhou, Chunsheng Tao, Xu Ning, Huitang Xia, Weijie Sun
{"title":"Enhancing cartilage regeneration and repair through bioactive and biomechanical modification of 3D acellular dermal matrix","authors":"Wei Gao, Tan Cheng, Zhengya Tang, Wenqiang Zhang, Yong Xu, Min Han, Guangdong Zhou, Chunsheng Tao, Xu Ning, Huitang Xia, Weijie Sun","doi":"10.1093/rb/rbae010","DOIUrl":null,"url":null,"abstract":"\n Acellular dermal matrix (ADM) shows promise for cartilage regeneration and repair. However, an effective decellularization technique that removes cellular components while preserving the extracellular matrix, the transformation of 2D-ADM into a suitable 3D scaffold with porosity, and the enhancement of bioactive and biomechanical properties in the 3D-ADM scaffold are yet to be fully addressed. In this study, we present an innovative decellularization method involving 0.125% trypsin and 0.5% SDS and a 1% Triton X-100 solution for preparing ADM and converting 2D-ADM into 3D-ADM scaffolds. These scaffolds exhibit favorable physicochemical properties, exceptional biocompatibility, and significant potential for driving cartilage regeneration in vitro and in vivo. To further enhance the cartilage regeneration potential of 3D-ADM scaffolds, we incorporated porcine-derived small intestinal submucosa (SIS) for bioactivity and calcium sulfate hemihydrate (CSH) for biomechanical reinforcement. The resulting 3D-ADM+SIS scaffolds displayed heightened biological activity, while the 3D-ADM+CSH scaffolds notably bolstered biomechanical strength. Both scaffold types showed promise for cartilage regeneration and repair in vitro and in vivo, with considerable improvements observed in repairing cartilage defects within a rabbit articular cartilage model. In summary, this research introduces a versatile 3D-ADM scaffold with customizable bioactive and biomechanical properties, poised to revolutionize the field of cartilage regeneration.","PeriodicalId":20929,"journal":{"name":"Regenerative Biomaterials","volume":null,"pages":null},"PeriodicalIF":5.6000,"publicationDate":"2024-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Regenerative Biomaterials","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1093/rb/rbae010","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

Acellular dermal matrix (ADM) shows promise for cartilage regeneration and repair. However, an effective decellularization technique that removes cellular components while preserving the extracellular matrix, the transformation of 2D-ADM into a suitable 3D scaffold with porosity, and the enhancement of bioactive and biomechanical properties in the 3D-ADM scaffold are yet to be fully addressed. In this study, we present an innovative decellularization method involving 0.125% trypsin and 0.5% SDS and a 1% Triton X-100 solution for preparing ADM and converting 2D-ADM into 3D-ADM scaffolds. These scaffolds exhibit favorable physicochemical properties, exceptional biocompatibility, and significant potential for driving cartilage regeneration in vitro and in vivo. To further enhance the cartilage regeneration potential of 3D-ADM scaffolds, we incorporated porcine-derived small intestinal submucosa (SIS) for bioactivity and calcium sulfate hemihydrate (CSH) for biomechanical reinforcement. The resulting 3D-ADM+SIS scaffolds displayed heightened biological activity, while the 3D-ADM+CSH scaffolds notably bolstered biomechanical strength. Both scaffold types showed promise for cartilage regeneration and repair in vitro and in vivo, with considerable improvements observed in repairing cartilage defects within a rabbit articular cartilage model. In summary, this research introduces a versatile 3D-ADM scaffold with customizable bioactive and biomechanical properties, poised to revolutionize the field of cartilage regeneration.
通过对三维非细胞真皮基质进行生物活性和生物力学改性,促进软骨再生和修复
细胞外基质(ADM)有望用于软骨再生和修复。然而,一种既能去除细胞成分又能保留细胞外基质的有效脱细胞技术、将二维-ADM 转化为具有多孔性的合适三维支架以及增强三维-ADM 支架的生物活性和生物力学性能等问题仍有待全面解决。在本研究中,我们提出了一种创新的脱细胞方法,该方法采用 0.125% 胰蛋白酶、0.5% SDS 和 1% Triton X-100 溶液制备 ADM,并将 2D-ADM 转化为 3D-ADM 支架。这些支架表现出良好的物理化学特性、优异的生物相容性以及在体外和体内促进软骨再生的巨大潜力。为了进一步提高三维-ADM 支架的软骨再生潜力,我们加入了取自小肠粘膜(SIS)的孔雀石以增强生物活性,并加入半水硫酸钙(CSH)以增强生物力学性能。由此产生的 3D-ADM+SIS 支架显示出更强的生物活性,而 3D-ADM+CSH 支架则显著增强了生物力学强度。这两种类型的支架在体外和体内都显示出软骨再生和修复的前景,在兔子关节软骨模型中观察到其在修复软骨缺损方面有显著改善。总之,这项研究引入了一种具有可定制生物活性和生物力学特性的多功能 3D-ADM 支架,有望在软骨再生领域掀起一场革命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Regenerative Biomaterials
Regenerative Biomaterials Materials Science-Biomaterials
CiteScore
7.90
自引率
16.40%
发文量
92
审稿时长
10 weeks
期刊介绍: Regenerative Biomaterials is an international, interdisciplinary, peer-reviewed journal publishing the latest advances in biomaterials and regenerative medicine. The journal provides a forum for the publication of original research papers, reviews, clinical case reports, and commentaries on the topics relevant to the development of advanced regenerative biomaterials concerning novel regenerative technologies and therapeutic approaches for the regeneration and repair of damaged tissues and organs. The interactions of biomaterials with cells and tissue, especially with stem cells, will be of particular focus.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信