聚己内酯-胶原纳米纤维负载地塞米松和辛伐他汀作为骨诱导和免疫相容性支架的骨再生应用

Q3 Biochemistry, Genetics and Molecular Biology
Hilal Ahmad Rather , Johnna Francis Varghese , Bindiya Dhimmar , Umesh C.S. Yadav , Rajesh Vasita
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引用次数: 2

摘要

生理性炎症已被证明能促进骨再生;然而,长期的炎症会阻碍成骨和骨修复过程。为了克服后者,我们旨在开发一种双重药物递送纳米纤维支架来促进间充质基质细胞(MSCs)的成骨分化和调节巨噬细胞的促炎反应。采用静电纺丝法制备了含有地塞米松和辛伐他汀的聚己内酯-胶原纳米纤维递送体系。人单核细胞(U937细胞)的形态学分析和促炎和抗炎细胞因子mRNA及蛋白表达均证实了双释药纳米纤维支架的免疫相容性作用。一氧化氮估计也证实了双重药物释放支架的抗炎作用。经过17天的细胞培养,通过增强碱性磷酸酶(ALP)活性和矿物质沉积,支架显示了脂肪来源的MSCs的成骨分化。runt相关转录因子-2 (RUNX-2)和骨钙素在mRNA和蛋白水平上的表达增加,支持了双重药物负载纤维支架的成骨潜力。因此,研究结果表明,我们制备的纳米纤维支架具有免疫调节特性,并可在进一步的体内验证后用于骨再生应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polycaprolactone-collagen nanofibers loaded with dexamethasone and simvastatin as an osteoinductive and immunocompatible scaffold for bone regeneration applications

Polycaprolactone-collagen nanofibers loaded with dexamethasone and simvastatin as an osteoinductive and immunocompatible scaffold for bone regeneration applications

Polycaprolactone-collagen nanofibers loaded with dexamethasone and simvastatin as an osteoinductive and immunocompatible scaffold for bone regeneration applications

Polycaprolactone-collagen nanofibers loaded with dexamethasone and simvastatin as an osteoinductive and immunocompatible scaffold for bone regeneration applications

Physiological inflammation has been shown to promote bone regeneration; however, prolonged inflammation impedes the osteogenesis and bone repair process. To overcome the latter we aimed to develop a dual drug delivering nanofibrous scaffold to promote osteogenic differentiation of mesenchymal stromal cells (MSCs) and modulate the pro-inflammatory response of macrophages. The polycaprolactone (PCL)-collagen nanofibrous delivery system incorporating dexamethasone and simvastatin was fabricated by electrospinning process. The morphological analysis and mRNA, as well as protein expression of proinflammatory and anti-inflammatory cytokines in human monocytes (U937 cells), demonstrated the immunocompatibility effect of dual drug-releasing nanofibrous scaffolds. Nitric oxide estimation also demonstrated the anti-inflammatory effect of dual drug releasing scaffolds. The scaffolds demonstrated the osteogenic differentiation of adipose-derived MSCs by enhancing the alkaline phosphatase (ALP) activity and mineral deposition after 17 days of cell culture. The increased expression of Runt-related transcription factor-2 (RUNX-2) and osteocalcin at mRNA and protein levels supported the osteogenic potential of dual drug-loaded fibrous scaffolds. Hence, the results indicate that our fabricated nanofibrous scaffolds exhibit immunomodulatory properties and could be employed for bone regeneration applications after further in-vivo validation.

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