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体外操纵胶原蛋白基质结构以制备具有更高生理相关性的支架。

Manipulation of in vitro collagen matrix architecture for scaffolds of improved physiological relevance.

作者信息

Hapach Lauren A, VanderBurgh Jacob A, Miller Joseph P, Reinhart-King Cynthia A

出版信息

Phys Biol. 2015 Dec 21;12(6):061002. doi: 10.1088/1478-3975/12/6/061002.

Abstract

Type I collagen is a versatile biomaterial that is widely used in medical applications due to its weak antigenicity, robust biocompatibility, and its ability to be modified for a wide array of applications. As such, collagen has become a major component of many tissue engineering scaffolds, drug delivery platforms, and substrates for in vitro cell culture. In these applications, collagen constructs are fabricated to recapitulate a diverse set of conditions. Collagen fibrils can be aligned during or post-fabrication, cross-linked via numerous techniques, polymerized to create various fibril sizes and densities, and copolymerized into a wide array of composite scaffolds. Here, we review approaches that have been used to tune collagen to better recapitulate physiological environments for use in tissue engineering applications and studies of basic cell behavior. We discuss techniques to control fibril alignment, methods for cross-linking collagen constructs to modulate stiffness, and composite collagen constructs to better mimic physiological extracellular matrix.

摘要

I型胶原蛋白是一种用途广泛的生物材料,因其抗原性弱、生物相容性强以及能够针对广泛的应用进行修饰而被广泛应用于医学领域。因此,胶原蛋白已成为许多组织工程支架、药物递送平台和体外细胞培养底物的主要成分。在这些应用中,胶原蛋白构建体被制造出来以模拟各种不同的条件。胶原蛋白原纤维可以在制造过程中或制造后排列,通过多种技术进行交联,聚合以产生各种原纤维尺寸和密度,并共聚成各种各样的复合支架。在这里,我们综述了用于调整胶原蛋白以更好地模拟用于组织工程应用和基础细胞行为研究的生理环境的方法。我们讨论了控制原纤维排列的技术、交联胶原蛋白构建体以调节硬度的方法以及复合胶原蛋白构建体以更好地模拟生理细胞外基质的方法。

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