Department of Orthopedic Surgery, School of Medicine, AJA University of Medical Science, Tehran, Iran.
Department of Tissue Engineering, School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran; Tissue Engineering and stem cells research center, Shahroud University of Medical Sciences, Shahroud, Iran.
Nanomedicine. 2018 Oct;14(7):2061-2073. doi: 10.1016/j.nano.2018.06.007. Epub 2018 Jun 28.
Large bone defects constitute a major challenge in bone tissue engineering and usually fail to heal due to the incomplete differentiation of recruited mesenchymal stem cells (MSCs) into osteogenic precursor cells. As previously proposed, metformin (MET) induces differentiation of MSCs into osteoblastic lineages in vitro. We fabricated a Poly (lactic acid) and Polycaprolactone (PLA/PCL) scaffold to deliver metformin loaded gelatin nanocarriers (MET/GNs) to critical-sized calvarial bone defects in a rat model. The scaffolds were evaluated regarding their morphology, porosity, contact angle, degradation rate, blood compatibility, biomechanical, cell viability and their osteogenic differentiation. In animal study, the defects were filled with autograft, scaffolds and a group was left empty. qRT-PCR analyses showed the expression level of osteogenic and angiogenic markers considerably increased in MET/GNs-PLA/PCL. The in vivo results showed that MET/GNs-PLA/PCL improved bone ingrowth, angiogenesis and defect reconstruction. Our results represent the applicability of MET/GNs-PLA/PCL for successful bone regeneration.
大骨缺损是骨组织工程的主要挑战,由于募集的间充质干细胞 (MSCs) 向成骨前体细胞的不完全分化,通常无法愈合。如前所述,二甲双胍 (MET) 可诱导 MSCs 体外向成骨谱系分化。我们制备了聚乳酸和聚己内酯 (PLA/PCL) 支架,以将载有二甲双胍的明胶纳米载体 (MET/GNs) 递送至大鼠模型中的临界尺寸颅骨骨缺损。评估了支架的形态、孔隙率、接触角、降解率、血液相容性、生物力学、细胞活力及其成骨分化。在动物研究中,用自体移植物、支架和一组空支架填充缺损。qRT-PCR 分析显示,MET/GNs-PLA/PCL 中骨生成和血管生成标志物的表达水平显著增加。体内结果表明,MET/GNs-PLA/PCL 可改善骨内生长、血管生成和缺损重建。我们的结果代表了 MET/GNs-PLA/PCL 成功用于骨再生的适用性。