Articular cartilage regeneration with a microgel as a support biomaterial. A rabbit knee model

IF 5.5 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS Materials Science & Engineering C-Materials for Biological Applications Pub Date : 2024-11-26 DOI:10.1016/j.bioadv.2024.214125
Javier Zurriaga Carda , Carmen María Antolinos-Turpin , Joaquín Ródenas-Rochina , Lara Milián , Julia Pla-Salom , Zakaria Oguir , María Sancho-Tello , Manuel Mata , Carmen Carda , Gloria Gallego-Ferrer , José Luis Gómez Ribelles
{"title":"Articular cartilage regeneration with a microgel as a support biomaterial. A rabbit knee model","authors":"Javier Zurriaga Carda ,&nbsp;Carmen María Antolinos-Turpin ,&nbsp;Joaquín Ródenas-Rochina ,&nbsp;Lara Milián ,&nbsp;Julia Pla-Salom ,&nbsp;Zakaria Oguir ,&nbsp;María Sancho-Tello ,&nbsp;Manuel Mata ,&nbsp;Carmen Carda ,&nbsp;Gloria Gallego-Ferrer ,&nbsp;José Luis Gómez Ribelles","doi":"10.1016/j.bioadv.2024.214125","DOIUrl":null,"url":null,"abstract":"<div><div>Articular cartilage has limited regenerative capacity, so focal lesions generate mechanical stress in the joint that induces an aggravation of the damage, which ultimately leads to osteoarthritis. We recently suggested the use of microgels at the site of the cartilage defect, as a support material, to generate a biomechanical environment where pluripotent cells differentiate towards the hyaline cartilage phenotype. Here we propose a chondral regeneration strategy based on subchondral bone injury, and filling the defect site with an agglomerate of two types of microspheres, some rigid made of a biodegradable polyester (40 μm mean diameter), and others with a gel consistency made of platelet-rich plasma obtained from circulating blood (70–110 μm diameter). A 3-mm diameter defect was made in the articular cartilage of the knee joint in rabbits, exposing the subchondral bone, in which incisions were made to produce bleeding. Microgels were implanted filling the defect, which was covered with a synthetic membrane of the same polyester. Three months later, cartilage regeneration was analyzed according to the International Cartilage Repair Society (ICRS) guidelines. The newly formed tissue showed histological characteristics of hyaline cartilage, being significantly closer to native cartilage than when only the membrane was implanted, mainly in parameters such as tissue (70.0 ± 20.9) and cell morphologies (100.0 ± 0.0), and surface architecture (90.0 ± 22.4) and assessment (70.0 ± 11.2), with native tissue having a value of 100. Polyester microspheres and membrane were not bioreabsorbed during the three months, but rather moved towards the subchondral bone, leaving space for the organization of the newly formed tissue.</div></div>","PeriodicalId":51111,"journal":{"name":"Materials Science & Engineering C-Materials for Biological Applications","volume":"168 ","pages":"Article 214125"},"PeriodicalIF":5.5000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Science & Engineering C-Materials for Biological Applications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772950824003686","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

Articular cartilage has limited regenerative capacity, so focal lesions generate mechanical stress in the joint that induces an aggravation of the damage, which ultimately leads to osteoarthritis. We recently suggested the use of microgels at the site of the cartilage defect, as a support material, to generate a biomechanical environment where pluripotent cells differentiate towards the hyaline cartilage phenotype. Here we propose a chondral regeneration strategy based on subchondral bone injury, and filling the defect site with an agglomerate of two types of microspheres, some rigid made of a biodegradable polyester (40 μm mean diameter), and others with a gel consistency made of platelet-rich plasma obtained from circulating blood (70–110 μm diameter). A 3-mm diameter defect was made in the articular cartilage of the knee joint in rabbits, exposing the subchondral bone, in which incisions were made to produce bleeding. Microgels were implanted filling the defect, which was covered with a synthetic membrane of the same polyester. Three months later, cartilage regeneration was analyzed according to the International Cartilage Repair Society (ICRS) guidelines. The newly formed tissue showed histological characteristics of hyaline cartilage, being significantly closer to native cartilage than when only the membrane was implanted, mainly in parameters such as tissue (70.0 ± 20.9) and cell morphologies (100.0 ± 0.0), and surface architecture (90.0 ± 22.4) and assessment (70.0 ± 11.2), with native tissue having a value of 100. Polyester microspheres and membrane were not bioreabsorbed during the three months, but rather moved towards the subchondral bone, leaving space for the organization of the newly formed tissue.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
以微凝胶为支撑材料的关节软骨再生。兔膝模型
关节软骨的再生能力有限,因此局灶性病变在关节内产生机械应力,导致损伤加重,最终导致骨关节炎。我们最近建议在软骨缺损部位使用微凝胶作为支撑材料,以产生一个生物力学环境,使多能细胞向透明软骨表型分化。在这里,我们提出了一种基于软骨下骨损伤的软骨再生策略,并用两种类型的微球团填充缺损部位,一些是由可生物降解聚酯(平均直径40 μm)制成的刚性微球,另一些是由来自循环血液的富含血小板的血浆(直径70-110 μm)制成的凝胶状微球。在兔膝关节关节软骨处做了一个直径3毫米的缺损,暴露了软骨下骨,在软骨下做了切口导致出血。植入微凝胶填充缺陷,并用相同的聚酯合成膜覆盖。3个月后,根据国际软骨修复协会(ICRS)的指南分析软骨再生情况。新形成的组织表现出透明软骨的组织学特征,与仅植入膜时相比,明显更接近天然软骨,主要表现在组织(70.0±20.9)和细胞形态(100.0±0.0)、表面结构(90.0±22.4)和评估(70.0±11.2)等参数上,天然组织的值为100。聚酯微球和膜在三个月内没有被生物重新吸收,而是向软骨下骨移动,为新形成的组织留下空间。
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 去求助
来源期刊
CiteScore
17.80
自引率
0.00%
发文量
501
审稿时长
27 days
期刊介绍: Biomaterials Advances, previously known as Materials Science and Engineering: C-Materials for Biological Applications (P-ISSN: 0928-4931, E-ISSN: 1873-0191). Includes topics at the interface of the biomedical sciences and materials engineering. These topics include: • Bioinspired and biomimetic materials for medical applications • Materials of biological origin for medical applications • Materials for "active" medical applications • Self-assembling and self-healing materials for medical applications • "Smart" (i.e., stimulus-response) materials for medical applications • Ceramic, metallic, polymeric, and composite materials for medical applications • Materials for in vivo sensing • Materials for in vivo imaging • Materials for delivery of pharmacologic agents and vaccines • Novel approaches for characterizing and modeling materials for medical applications Manuscripts on biological topics without a materials science component, or manuscripts on materials science without biological applications, will not be considered for publication in Materials Science and Engineering C. New submissions are first assessed for language, scope and originality (plagiarism check) and can be desk rejected before review if they need English language improvements, are out of scope or present excessive duplication with published sources. Biomaterials Advances sits within Elsevier''s biomaterials science portfolio alongside Biomaterials, Materials Today Bio and Biomaterials and Biosystems. As part of the broader Materials Today family, Biomaterials Advances offers authors rigorous peer review, rapid decisions, and high visibility. We look forward to receiving your submissions!
期刊最新文献
Relation between shape-tailored CeO2 nanoparticles morphology and hemocompatibility and antimicrobial effect Bio-inspired, programmable biomacromolecules based nanostructures driven cancer therapy Erythrocyte membrane vesicles as drug delivery systems: A systematic review of preclinical studies on biodistribution and pharmacokinetics Digital light processing of photo-crosslinkable gelatin to create biomimetic 3D constructs serving small intestinal tissue regeneration Glycosylation-driven interactions of nanoparticles with the extracellular matrix: Implications for inflammation and drug delivery
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1