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Electrospun Hydroxyapatite-Containing Chitosan Nanofibers Crosslinked with Genipin for Bone Tissue Engineering

机译:Electrom淘硝基磷灰石的壳聚糖纳米纤维与Genipin交联用于骨组织工程

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摘要

Reconstruction of large bone defects remains problematic in orthopedic and craniofacial clinical practice. Autografts are limited in supply and are associated with donor site morbidity while other materials show poor integration with the host’s own bone. This lack of integration is often due to the absence of periosteum, the outer layer of bone that contains osteoprogenitor cells and is critical for the growth and remodeling of bone tissue. In this study we developed a one-step platform to electrospin nanofibrous scaffolds from chitosan, which also contain hydroxyapatite nanoparticles and are crosslinked with genipin. We hypothesized that the resulting composite scaffolds represent a microenvironment that emulates the physical, mineralized structure and mechanical properties of non-weight bearing bone extracellular matrix while promoting osteoblast differentiation and maturation similar to the periosteum. The ultrastructure and physicochemical properties of the scaffolds were studied using scanning electron microscopy and spectroscopic techniques. The average fiber diameters of the electrospun scaffolds were 227±154 nm as spun, and increased to 335±119 nm after crosslinking with genipin. Analysis by X-ray diffraction, Fourier transformed infrared spectroscopy and energy dispersive spectroscopy confirmed the presence of characteristic features of hydroxyapatite in the composite chitosan fibers. The Young’s modulus of the composite fibrous scaffolds was 142±13 MPa, which is similar to that of the natural periosteum. Both pure chitosan scaffolds and composite hydroxyapatite-containing chitosan scaffolds supported adhesion, proliferation and osteogenic differentiation of mouse 7F2 osteoblast-like cells. Expression and enzymatic activity of alkaline phosphatase, an early osteogenic marker, were higher in cells cultured on the composite scaffolds as compared to pure chitosan scaffolds, reaching a significant, 2.4 fold, difference by day 14 (p<0.05). Similarly, cells cultured on hydroxyapatite-containing scaffolds had the highest rate of osteonectin mRNA expression over 2 weeks, indicating enhanced osteoinductivity of the composite scaffolds. Our results suggest that crosslinking electrospun hydroxyapatite-containing chitosan with genipin yields bio-composite scaffolds, which combine non-weight-bearing bone mechanical properties with a periosteum-like environment and facilitate the proliferation, differentiation and maturation of osteoblast-like cells. We propose that these scaffolds might be useful for the repair and regeneration of maxillofacial defects and injuries.
机译:在骨科和颅面临床实践中,大骨缺损的重建仍然存在问题。自体移植物的供应有限,并且与供体部位的发病率有关,而其他材料显示出与宿主自身骨骼的整合性较差。这种缺乏整合通常是由于缺乏骨膜,骨膜是骨外层,含有骨祖细胞,对骨组织的生长和重塑至关重要。在这项研究中,我们开发了一个一步平台来静电纺丝壳聚糖的纳米纤维支架,该支架还包含羟基磷灰石纳米颗粒,并与Genipin交联。我们假设所得的复合支架代表了一个微环境,该环境模拟了非负重骨细胞外基质的物理,矿化结构和机械性能,同时促进了成骨细胞的分化和成熟(类似于骨膜)。使用扫描电子显微镜和光谱技术研究了支架的超微结构和理化性质。静电纺丝支架的平均纤维直径为227±154 nm,在与Genipin交联后增加到335±119 nm。通过X射线衍射,傅立叶变换红外光谱和能量色散光谱分析证实复合壳聚糖纤维中存在羟基磷灰石的特征。复合纤维支架的杨氏模量为142±13 MPa,与天然骨膜相似。纯壳聚糖支架和复合含羟基磷灰石的壳聚糖支架均支持小鼠7F2成骨细胞样细胞的粘附,增殖和成骨分化。与纯壳聚糖支架相比,复合支架上培养的细胞中碱性磷酸酶(一种早期成骨标记)的表达和酶活性更高,在第14天时达到了2.4倍的显着差异(p <0.05)。类似地,在含羟基磷灰石的支架上培养的细胞在2周内有最高的骨连接蛋白mRNA表达率,表明复合支架的骨诱导性增强。我们的研究结果表明,将含静电纺丝羟基磷灰石的壳聚糖与Genipin交联可产生生物复合支架,该支架将不承重骨骼的机械性能与骨膜样环境相结合,并促进成骨细胞样细胞的增殖,分化和成熟。我们建议这些脚手架可能对修复和再生颌面缺损和损伤有用。

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