NanoBios Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Bombay, Mumbai, India.
Biomed Mater. 2017 Sep 25;12(5):055011. doi: 10.1088/1748-605X/aa792b.
The objective of the present investigation was to assess the potential of magnesium oxide nanoparticle (MgO NP)-loaded electrospun polycaprolactone (PCL) polymer composites as a bone-soft tissue engineering scaffold. MgO NPs were synthesized using a hydroxide precipitation sol-gel method and characterized using field emission gun-scanning electron microscopy/energy-dispersive x-ray spectroscopy (FEG-SEM/EDS), field emission gun-transmission electron microscopy (FEG-TEM), and x-ray diffraction (XRD) analysis. PCL and MgO-PCL nanocomposite fibers were fabricated using electrospinning with trifluoroethanol as solvent at 19 kV applied voltage and 1.9 ml h flow rate as optimized process parameters, and were characterized by FEG-TEM, FEG-SEM/EDS, XRD, and differential scanning calorimetry analyses. Characterization studies of as-synthesized nanoparticles revealed diffraction peaks indexed to various crystalline planes peculiar to MgO particles with hexagonal and cubical shape, and 40-60 nm size range. Significant improvement in mechanical properties (tensile strength and elastic modulus) of nanocomposites was observed as compared to neat polymer specimens (fourfold and threefold, respectively), due to uniform dispersion of nanofillers along the polymer fiber length. There was a remarkable bioactivity shown by nanocomposite scaffolds in immersion test, as indicated by formation of surface hydroxyapatite layer by the third day of incubation. MgO-loaded electrospun PCL mats showed enhanced in-vitro biological performance with osteoblast-like MG-63 cells in terms of adhesion, proliferation, and marked differentiation marker activity owing to greater surface roughness, nanotopography, and hydrophilicity facilitating higher protein adsorption. In-vivo subcutaneous implantation study in Sprague Dawley rats revealed initial moderate inflammatory tissue response near implant site at the second week timepoint that subsided later (eighth week) with no adverse effect on vital organ functionalities as seen in histopathological analysis supported by serum biochemical and hematological parameters which did not deviate significantly from normal physiological range, indicating good biocompatibility in-vivo. Thus, MgO-PCL nanocomposite electrospun fibers have potential as an efficient scaffold material for bone-soft tissue engineering applications.
本研究旨在评估氧化镁纳米粒子(MgO NP)负载的静电纺聚己内酯(PCL)聚合物复合材料作为骨-软组织工程支架的潜力。MgO NPs 采用氢氧化物沉淀溶胶-凝胶法合成,并通过场发射枪扫描电子显微镜/能谱分析(FEG-SEM/EDS)、场发射枪透射电子显微镜(FEG-TEM)和 X 射线衍射(XRD)分析进行了表征。PCL 和 MgO-PCL 纳米复合材料纤维采用静电纺丝法制备,以三氟乙醇为溶剂,在优化的工艺参数 19 kV 施加电压和 1.9 ml/h 流速下进行,通过 FEG-TEM、FEG-SEM/EDS、XRD 和差示扫描量热分析进行了表征。对合成的纳米粒子进行的表征研究表明,衍射峰与具有六方和立方形状、40-60nm 尺寸范围的 MgO 颗粒的各种结晶面相对应。与纯聚合物样品相比,纳米复合材料的力学性能(拉伸强度和弹性模量)显著提高(分别提高了四倍和三倍),这是由于纳米填料在聚合物纤维长度上均匀分散所致。在浸入试验中,纳米复合材料支架表现出显著的生物活性,在孵育的第三天就形成了表面羟基磷灰石层。负载 MgO 的静电纺 PCL 垫在体外与成骨样 MG-63 细胞的生物性能得到了增强,这表现在细胞黏附、增殖和显著的分化标志物活性方面,这归因于更大的表面粗糙度、纳米形貌和亲水性,从而促进了更高的蛋白质吸附。在 Sprague Dawley 大鼠的皮下植入研究中,在植入部位附近的第二周时间点观察到初始中度炎症组织反应,随后(第八周)消退,在组织病理学分析支持下,重要器官功能没有受到不利影响,血清生化和血液学参数没有明显偏离正常生理范围,表明体内具有良好的生物相容性。因此,MgO-PCL 纳米复合材料静电纺纤维具有作为骨-软组织工程应用的有效支架材料的潜力。