Evaluation of the effects of cartilage decellularized ECM in optimizing PHB-chitosan-HNT/chitosan-ECM core-shell electrospun scaffold: Physicochemical and biological properties

IF 6 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS Materials Science & Engineering C-Materials for Biological Applications Pub Date : 2025-07-01 Epub Date: 2025-02-28 DOI:10.1016/j.bioadv.2025.214249
Sepideh Ghadirian, Laleh Shariati, Saeed Karbasi
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Abstract

Cartilage regeneration is still a highly challenging field due to its low self-healing ability. This study used a core-shell electrospinning technique to enhance cartilage tissue engineering by incorporating cartilage extracellular matrix (ECM). The core of fibers included poly(3-hydroxybutyrate)-Chitosan (PHB-Cs) and Halloysite nanotubes. The shell of fibers consisted of Cs and ECM (0, 1, 3, 5 wt%). Subsequently, the scaffolds were named 0E, 1E, 3E, and 5E. The study aimed to assess the impact of ECM on cellular behavior and chondrogenesis. Our findings indicate that ECM reduced fiber diameter from 775 nm for the 0E scaffold to 454 nm for the 1E scaffold. Water contact angle measurements revealed an increasing trend by ECM addition, from 42° for 0E to 67° for 1E. According to mechanical analysis, the 1E scaffold represented the highest strength (5.81 MPa) and strain (3.17%). Based on these analyses, the 1E was considered the optimum scaffold. MTT analysis showed cell viability of over 80% for the 0E and 1E. Also, the gene expression level was assessed for Collagen II, Aggrecan, SOX 9, and Collagen X. The results represented that in the 1E scaffold Collagen II, Aggrecan, and SOX 9 were more upregulated at the end of the 21st day. However, in the 1E scaffold collagen X, as a hypertrophy marker, was downregulated at the end of the experiment. Overall, these results confirmed the potential of the 1E scaffold to be introduced as a promising cartilage tissue engineering scaffold for further studies.

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评价软骨脱细胞ECM在优化phb -壳聚糖- hnt /壳聚糖-ECM核-壳电纺支架中的作用:物理化学和生物学特性
由于软骨的自愈能力较低,因此软骨再生仍然是一个极具挑战性的领域。本研究采用核-壳静电纺丝技术结合软骨细胞外基质(ECM)增强软骨组织工程。纤维芯包括聚3-羟基丁酸-壳聚糖(PHB-Cs)和高岭土纳米管。纤维外壳由Cs和ECM组成(0、1、3、5 wt%)。随后将支架命名为0E、1E、3E、5E。该研究旨在评估ECM对细胞行为和软骨形成的影响。我们的研究结果表明,ECM将纤维直径从0E支架的775 nm减少到1E支架的454nm。水接触角测量结果显示,加入ECM后,水接触角呈增加趋势,从0E的42°增加到1E的67°。力学分析结果表明,1E支架强度最高,为5.81 MPa,应变最高,为3.17%。基于这些分析,1E被认为是最佳的支架。MTT分析显示,0E和1E的细胞存活率均在80%以上。同时,对Collagen II、Aggrecan、SOX 9和Collagen x的基因表达水平进行了评估。结果表明,在第21天结束时,1E支架中Collagen II、Aggrecan和SOX 9的表达水平上调较多。然而,在1E支架中,作为肥大标志物的胶原X在实验结束时被下调。总的来说,这些结果证实了1E支架作为一种有前途的软骨组织工程支架进行进一步研究的潜力。
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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!
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