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Preparation and characterization of biomimetic silk fibroin/chitosan composite nanofibers by electrospinning for osteoblasts culture

机译:静电纺丝法制备仿生丝素蛋白/壳聚糖复合纳米纤维及其表征

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摘要

In this study, we have successfully fabricated electrospun bead-free silk fibroin [SF]/chitosan [CS] composite nanofibers [NFs] covering the whole range of CS content (0%, 25%, 50%, 75%, and 100%). SF/CS spinning solutions were prepared in a mixed solvent system of trifluoroacetic acid [TFA] and dichloromethane. The morphology of the NFs was observed by scanning electron microscope, and the average fiber diameter ranges from 215 to 478 nm. Confocal laser scanning microscopy confirms the uniform distribution of SF and CS within the composite NFs. To increase biocompatibility and preserve nanostructure when seeded with cells in culture medium, NFs were treated with an ethanol/ammonia aqueous solution to remove residual TFA and to change SF protein conformation. After the chemical treatment, SF/CS NFs could maintain the original structure for up to 54 days in culture medium. Properties of pristine and chemically treated SF/CS NFs were investigated by Fourier transform infrared spectroscopy [FT-IR], X-ray diffraction [XRD], and thermogravimetry/differential scanning calorimetry [TG/DSC]. Shift of absorption peaks in FT-IR spectra confirms the conformation change of SF from random coil to β-sheet by the action of ethanol, which is also consistent with the SF crystalline diffraction patterns measured by XRD. From TG/DSC analysis, the decomposition temperature peaks due to salt formation from TFA and protonated amines disappeared after chemical treatment, indicating complete removal of TFA by binding with ammonium ions during the treatment. This was also confirmed with the disappearance of F1s peak in X-ray photoelectron spectroscopy spectra and disappearance of TFA salt peaks in FT-IR spectra. The composite NFs could support the growth and osteogenic differentiation of human fetal osteoblastic [hFOB] cells, but each component in the composite NF shows distinct effect on cell behavior. SF promotes hFOB proliferation while CS enhances hFOB differentiation. The composite SF/CS NFs will be suitable for bone tissue engineering applications by choosing a suitable blend composition.>PACS: 87.85.jf; 87.85.Rs; 68.37.Hk.
机译:在这项研究中,我们成功地制造出涵盖了CS含量整个范围(0%,25%,50%,75%和100%)的电纺无珠丝素蛋白[SF] /壳聚糖[CS]复合纳米纤维[NFs]。 )。 SF / CS纺丝溶液是在三氟乙酸[TFA]和二氯甲烷的混合溶剂体系中制备的。用扫描电子显微镜观察NFs的形态,平均纤维直径为215-478nm。共聚焦激光扫描显微镜证实了SF和CS在复合NF中的均匀分布。为了在细胞中接种细胞后增加生物相容性并保留纳米结构,用乙醇/氨水溶液处理NF,以去除残留的TFA并改变SF蛋白的构象。化学处理后,SF / CS NFs可以在培养基中维持长达54天的原始结构。通过傅立叶变换红外光谱[FT-IR],X射线衍射[XRD]和热重分析/差示扫描量热法[TG / DSC]研究了原始和化学处理过的SF / CS NF的性质。 FT-IR光谱中吸收峰的移动证实了在乙醇作用下SF从无规卷曲到β折叠的构象变化,这也与XRD测量的SF晶体衍射图一致。根据TG / DSC分析,化学处理后因TFA和质子化胺形成盐而导致的分解温度峰消失,表明在处理过程中通过与铵离子结合而完全去除了TFA。 X射线光电子能谱中F1s峰的消失和FT-IR光谱中TFA盐峰的消失也证实了这一点。复合核因子可以支持人类胎儿成骨细胞[hFOB]细胞的生长和成骨分化,但是复合核因子中的每个成分均对细胞行为表现出明显的影响。 SF促进hFOB增殖,而CS增强hFOB分化。通过选择合适的混合成分,SF / CS复合NFs将适用于骨组织工程应用。> PACS: 87.85.jf; 87.85卢比; 68.37。

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