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3D scaffold prepared by electrospun nanofibers for tissue engineering

静电纺丝 脚手架 纳米纤维 明胶 组织工程 戊二醛 材料科学 化学工程 生物医学工程 生物材料 化学 纳米技术 复合材料 聚合物 色谱法 有机化学 工程类 医学
作者
Xiumei Mo,Wei‐Ming Chen
出处
期刊:Frontiers in Bioengineering and Biotechnology [Frontiers Media]
卷期号:4
标识
DOI:10.3389/conf.fbioe.2016.01.02399
摘要

Event Abstract Back to Event 3D scaffold prepared by electrospun nanofibers for tissue engineering Xiumei Mo1 and Weiming Chen1 1 Donghua University, College of Chemistry, Chemical Engineering and Biotechnology, China Introduction: Scaffold plays important role in tissue engineering, which can provide a 3D environment for cells growth and guide tissue regeneration. In recent years, nanofibrous scaffold began to be fabricated which can mimic the structure of the nature extracellular matrix (ECM) 1. There are mainly three processing techniques (electrospinning, self-assembly, and phase separation) for preparing nanofibrous scaffold[1],[2]. In this study, we prepare a 3D nanofibrous scaffold by electrospinning and freeze-drying technique. In contrast to many other scaffolds, this scaffold showed nanofibrous structure and superelastic propertie. Cells culture study showed that the scaffold offered a proper microenvironment for cells growth. Materials: Gelatin was purchased from MP Biomedicals, LLC. PLA was purchased from Jinan Daigang Biomaterial Co., Ltd. All other chemicals were of analytical grade and commercially available. Methods: Gelatin and PLA were dissolved in 1,1,1,3,3,3-Hexafluoro-2-propanol (HFIP), the total concentration of gelation and PLA were 11% (W/V). Then the solution was used for electrospinning. After electrospinning, the electrospun gelatin/PLA nanofibers membranes were cut into small pieces and dispersed in tert-butanol by homogenizer, then the dispersions were frozen and freeze dried. Scaffold was crosslinked by glutaraldehyde or EDC/NHS. At last, the scaffold was washed by water several times for using. The scaffolds were gold sputtered and observed under SEM. Compression tests were carried out by Instron 5969 testing system. The proliferation of cells after cultured on the scaffold 6 days was evaluated by laser scanning confocal microscope. Fig. 1 (a) SEM image of 3D scaffold, (b) Compressive mechanical property of the scaffold in wet state, (c) Confocal image of L-929 cells cultured on 3D scaffold. Results and Discussions: Fig.1 (a) showed the SEM image of scaffold, nanofibers and pores could be found. Fig. 1 (b) showed the compressive stress-strain curves of the scaffold in wet state. The scaffold could bear a compressive strain as high as 80%. Nanofibers with strong bonding were formed after crosslink, so it could recover their original shape after the stress was released. Fig. 1 (c) showed the confocal image of L-929 cultured on scaffold. It could be observed that cells attached and spread to the surface of scaffold. Scaffold might provided enough three dimensional space with porous structure for cell proliferation. Conclusions: The scaffold presented porous morphology. In wet state, the scaffold also showed superelastic property and could bear a compressive strain as high as 80%. This scaffold could enhance cell growth and proliferation. It might be a promising scaffold for tissue engineering. References:[1] J.M. Holzwarth and P.X. Ma, 3D nanofibrous scaffolds for tissue engineering, Journal of Materials Chemistry, 21 (2011) 10243-10251.[2] X. Wang, B. Ding and B. Li, Biomimetic electrospun nanofibrous structures for tissue engineering, Materials Today, 16 (2013) 229-241. Keywords: Tissue Engineering, biomaterial, 3D scaffold Conference: 10th World Biomaterials Congress, Montréal, Canada, 17 May - 22 May, 2016. Presentation Type: Poster Topic: Biomimetic materials Citation: Mo X and Chen W (2016). 3D scaffold prepared by electrospun nanofibers for tissue engineering. Front. Bioeng. Biotechnol. Conference Abstract: 10th World Biomaterials Congress. doi: 10.3389/conf.FBIOE.2016.01.02399 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 27 Mar 2016; Published Online: 30 Mar 2016. Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Xiumei Mo Weiming Chen Google Xiumei Mo Weiming Chen Google Scholar Xiumei Mo Weiming Chen PubMed Xiumei Mo Weiming Chen Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.

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