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Development of Novel Silk Fibroin/Carboxymethyl Cellulose Based Electrospun Nanofibrous Scaffolds for Bone Tissue Engineering Application

机译:新型丝素蛋白/羧甲基纤维素基静电纺丝纳米纤维支架在骨组织工程中的应用

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摘要

Bone Tissue Engineering (TE) has been evolved as a promising mean to repair and regenerate defect and/or diseased bone tissues through the development of artificial extracellular matrix made from biopolymers. Silk fibroin based biomaterials are considered ideal for developing scaffolds for TE applications. The present research aims to develop novel biomimetic silk fibroin (SF) and carboxymethyl cellulose (CMC) based nanofibrous scaffold by free liquid surface electrospinning method. Randomly oriented electrospun nanofibrous scaffolds were developed from SF/CMC blends. Among the different blend ratios, 98:2 w/w of SF/CMC2 is the optimal achieving a set of superior scaffold properties in comparison to pure SF scaffold. The scaffolds were characterized for morphology (SEM, AFM), structural (XRD, FT-IR), surface property (% water uptake and contact angle measurement) and mechanical strength. The average fiber diameter was obtained as 227.8 ± 87 nm. The scaffold exhibited higher water uptake capacity, hydrophilicity and bioactivity showing uniform nucleation of Ca/P over the surface with controlled particle size of ≤ 100 nm than the pure bombyx mori SF scaffolds. Though the tensile strength of pure SF (12.7 ± 1.5 MPa) was slightly reduced by the addition of CMC (10.54 ± 1.3 MPa), the scaffold still possess sufficient strength to support many types of bone tissue regeneration. In vitro cell culture study has confirmed the cell supportive property of the scaffold as evident from cell attachment, cell proliferation, cell penetration and cellular metabolic activity of hMSCs which was derived from umbilical cord blood over the scaffold. The developed calcified SF/CMC2 blend scaffold possess good osteogenic property as confirmed by ALP activity, biomineralization ability, GAG secretion, osteocalcin, RUN X2 and collagen type1 expression. The osteogenic potential of SF/CMC scaffold was further enhanced by incorporating nano-bioglass thereby SF/CMC/nBG composite scaffold was developed. The surface roughness of SF/CMC/nBG (5 - 20 wt%) scaffolds was linearly increased with nano-bioglass content. Among the various concentration of nBG, SF/CMC loaded with 10%nBG shows optimal tensile strength of 7.591 ± 1.23 MPa and tensile strain at break of 9.62 ± 0.85 %. The ALP activity of hMSCs on SF/CMC/10nBG was significantly (p˂0.05) higher than SF/CMC2 throughout the culture period. The OCN expression on SF/CMC/10%nBG was observed to be 4.1 fold higher than SF/CMC2 and 2.3 fold higher than calcified SF/CMC2 nanofibrous scaffold. Hence, SF/CMC/10%nBG composite scaffold is proven to provide better osteogenic platform for hMSCs. An effort has further been given to improve the angiogenic property of SF/CMC/nBG composite scaffolds by incorporating Cu2+ ion. Among the scaffolds with varied compositions, SF/CMC/Cu1-5%nBG exhibited superior osteogenic and angiogenic property. Though a slightly higher OCN expression was observed over SF/CMC/Cu0.5-5%nBG composite scaffold than SF/CMC/Cu1-5%nBG, the difference in the expression was not statistically significant. However, SF/CMC/Cu1-5%nBG shows higher VEGF expression representing its superior angiogenic property than SF/CMC/Cu0.5-5%nBG scaffold. Thus, copper doped nano bioglass incorporated SF/CMC/Cu1-5%nBG composite nanofibrous matrix was proven to be a potential artificial extracellular matrix with enhanced bioactivity, osteogenic and angiogenic properties which might be a promising scaffold for future bone tissue regeneration.
机译:通过开发由生物聚合物制成的人工细胞外基质,骨组织工程学(TE)已发展成为修复和再生缺损和/或患病的骨组织的有前途的手段。基于丝素蛋白的生物材料被认为是开发TE应用支架的理想选择。本研究旨在通过自由液体表面静电纺丝技术开发新型仿生丝素蛋白(SF)和羧甲基纤维素(CMC)基纳米纤维支架。从SF / CMC共混物开发了随机取向的电纺纳米纤维支架。在不同的混合比例中,与纯SF支架相比,SF / CMC2的98:2 w / w是实现一组优异支架性能的最佳选择。表征支架的形态(SEM,AFM),结构(XRD,FT-IR),表面性质(吸水%和接触角测量)和机械强度。获得的平均纤维直径为227.8±87nm。与纯木棉SF支架相比,该支架表现出更高的吸水能力,亲水性和生物活性,显示出Ca / P在表面上的均匀成核,控制粒径≤100 nm。尽管添加CMC(10.54±1.3 MPa)会使纯SF的抗张强度(12.7±1.5 MPa)有所降低,但支架仍具有足够的强度来支持多种类型的骨组织再生。体外细胞培养研究已经证实了该支架的细胞支持特性,这是从hMSCs的细胞附着,细胞增殖,细胞渗透和细胞代谢活性所证实的,而hMSCs来自于支架上的脐带血。通过ALP活性,生物矿化能力,GAG分泌,骨钙蛋白,RUN X2和1型胶原蛋白的表达证实,所开发的钙化SF / CMC2共混支架具有良好的成骨性。通过加入纳米生物玻璃进一步增强了SF / CMC支架的成骨潜力,从而开发了SF / CMC / nBG复合支架。 SF / CMC / nBG(5-20​​ wt%)支架的表面粗糙度随纳米生物玻璃含量的增加而线性增加。在各种浓度的nBG中,负载10%nBG的SF / CMC的最佳拉伸强度为7.591±1.23 MPa,断裂拉伸应变为9.62±0.85%。在整个培养期间,hMSC对SF / CMC / 10nBG的ALP活性均显着(p˂0.05)高于SF / CMC2。观察到SF / CMC / 10%nBG上的OCN表达比SF / CMC2高4.1倍,比钙化的SF / CMC2纳米纤维支架高2.3倍。因此,事实证明,SF / CMC / 10%nBG复合支架可为hMSCs提供更好的成骨平台。通过掺入Cu 2+离子,进一步努力改善SF / CMC / nBG复合支架的血管生成特性。在具有不同组成的支架中,SF / CMC / Cu1-5%nBG表现出优异的成骨和血管生成特性。尽管在SF / CMC / Cu0.5-5%nBG复合支架上观察到的OCN表达略高于SF / CMC / Cu1-5%nBG,但表达差异无统计学意义。然而,SF / CMC / Cu1-5%nBG显示出比SF / CMC / Cu0.5-5%nBG支架更高的VEGF表达,表示其优越的血管生成特性。因此,掺铜的纳米生物玻璃掺入SF / CMC / Cu1-5%nBG复合纳米纤维基质被证明是潜在的人工细胞外基质,具有增强的生物活性,成骨和血管生成特性,可能是未来骨组织再生的有希望的支架。

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    Singh Bhisham Narayan;

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  • 年度 2017
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