海藻酸盐微球包封MG-63细胞并将其递送至聚己内酯支架:组织工程构建的一种新的生物制造方法

L. Narayanan, Arun Kumar, Zhuo Tan, S. Bernacki, B. Starly, Rohan A. Shirwaiker
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引用次数: 6

摘要

支架在组织工程中发挥着重要的作用,它为细胞的附着、增殖和分泌细胞外基质提供了结构框架和表面。为了实现有效的组织形成,使用传统的静态和动态播种方法将足够的细胞输送到支架三维(3D)基质中仍然是一个关键的挑战。在这项研究中,我们研究了一种新的细胞递送方法,利用水凝胶-细胞包膜微球沉积到聚己内酯(PCL)支架中,以提高播种效率。将MG-63模型骨细胞接种于静电生成的海藻酸钙微球(O 405±13 μm)内,在静态培养7天后对三维生物绘制的PCL构建体(0度/90度放置,284±6 μm链宽,555±8 μm链间距)进行评估。观察到微球均匀分布在PCL支架的横截面上。在整个测试期间,包被细胞在构建物内保持活力,第4天的增殖率最高。这项研究证明了新方法的可行性,并强调了成功利用3d生物打印进行微囊化细胞递送的作用和需要解决的关键挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alginate Microspheroid Encapsulation and Delivery of MG-63 Cells Into Polycaprolactone Scaffolds: A New Biofabrication Approach for Tissue Engineering Constructs
Scaffolds play an important role in tissue engineering by providing structural framework and a surface for cells to attach, proliferate, and secrete extracellular matrix (ECM). In order to enable efficient tissue formation, delivering sufficient cells into the scaffold three-dimensional (3D) matrix using traditional static and dynamic seeding methods continues to be a critical challenge. In this study, we investigate a new cell delivery approach utilizing deposition of hydrogel-cell encapsulated microspheroids into polycaprolactone (PCL) scaffolds to improve the seeding efficiency. Three-dimensional-bioplotted PCL constructs (0 deg/90 deg lay down, 284 ± 6 μm strand width, and 555 ± 8 μm strand separation) inoculated with MG-63 model bone cells encapsulated within electrostatically generated calcium-alginate microspheroids (O 405 ± 13 μm) were evaluated over seven days in static culture. The microspheroids were observed to be uniformly distributed throughout the PCL scaffold cross section. Encapsulated cells remained viable within the constructs over the test interval with the highest proliferation noted at day 4. This study demonstrates the feasibility of the new approach and highlights the role and critical challenges to be addressed to successfully utilize 3D-bioprinting for microencapsulated cell delivery.
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