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生物活性玻璃-胶原蛋白/聚乙醇酸支架纳米颗粒具有改善的生物学特性,并能增强间充质干细胞的成骨谱系分化。

Bioactive glass-collagen/poly (glycolic acid) scaffold nanoparticles exhibit improved biological properties and enhance osteogenic lineage differentiation of mesenchymal stem cells.

作者信息

Toosi Shirin, Naderi-Meshkin Hojjat, Esmailzadeh Zohreh, Behravan Ghazal, Ramakrishna Seeram, Behravan Javad

机构信息

Tissue Engineering Research Group (TERG), Department of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Stem Cells and Regenerative Medicine Research Group, Iranian Academic Center for Education, Culture and Research (ACECR), Mashhad, Iran.

出版信息

Front Bioeng Biotechnol. 2022 Sep 7;10:963996. doi: 10.3389/fbioe.2022.963996. eCollection 2022.

Abstract

Today's using tissue engineering and suitable scaffolds have got attention to increase healing of non-union bone fractures. In this study, we aimed to prepare and characterize scaffolds with functional and mechanical properties suitable for bone regeneration. Porous scaffolds containing collagen-poly glycolic acid (PGA) blends and various quantities of bioactive glass (BG) 45S5 were fabricated. Scaffolds with different compositions (BG/collagen-PGA ratios (w/w): 0/100; 40/60; 70/30) were characterized for their morphological properties, bioactivity, and mechanical behavior. Then, biocompatibility and osteogenic differentiation potential of the scaffolds were analyzed by seeding mesenchymal stem cells (MSCs). Scaffolds made with collagen-PGA combined with the BG (45S5) were found to have interconnected pores (average pore diameter size 75-115 µm) depending on the percentage of the BG added. Simulated body fluid (SBF) soaking experiments indicated the stability of scaffolds in SBF regardless of their compositions, while the scaffolds retained their highly interconnected structure. The elastic moduli, cell viability, osteogenic differentiation of the BG/collagen-PGA 40/60 and 70/30 scaffolds were superior to the original BG/collagen-PGA (0/100). These results suggest that BG incorporation enhanced the physical stability of our collagen-PGA scaffold previously reported. This new scaffold composition provides a promising platform to be used as a non-toxic scaffold for bone regeneration and tissue engineering.

摘要

如今,利用组织工程和合适的支架来促进骨不连骨折的愈合已受到关注。在本研究中,我们旨在制备并表征具有适合骨再生的功能和力学性能的支架。制备了含有胶原蛋白 - 聚乙醇酸(PGA)共混物和不同量生物活性玻璃(BG)45S5的多孔支架。对具有不同组成(BG/胶原蛋白 - PGA比例(w/w):0/100;40/60;70/30)的支架的形态学特性、生物活性和力学行为进行了表征。然后,通过接种间充质干细胞(MSCs)分析了支架的生物相容性和成骨分化潜力。发现由胶原蛋白 - PGA与BG(45S5)组合制成的支架根据添加的BG百分比具有相互连通的孔隙(平均孔径尺寸75 - 115 µm)。模拟体液(SBF)浸泡实验表明,无论其组成如何,支架在SBF中都具有稳定性,同时支架保留了其高度相互连通的结构。BG/胶原蛋白 - PGA 40/60和70/30支架的弹性模量、细胞活力和成骨分化均优于原始的BG/胶原蛋白 - PGA(0/100)。这些结果表明,BG的掺入增强了我们先前报道的胶原蛋白 - PGA支架的物理稳定性。这种新的支架组成提供了一个有前景的平台,可作为用于骨再生和组织工程的无毒支架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12ec/9490118/d8d9788422d1/fbioe-10-963996-g001.jpg

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