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冷冻干燥胶原支架中水合作用、力学和流体流动的结构决定因素。

Structural determinants of hydration, mechanics and fluid flow in freeze-dried collagen scaffolds.

机构信息

Nanoscience Centre, Department of Engineering, University of Cambridge, Cambridge CB3 0FF, UK; Cambridge Centre for Medical Materials, Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB3 0FF, UK.

Cambridge Centre for Medical Materials, Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB3 0FF, UK.

出版信息

Acta Biomater. 2016 Sep 1;41:193-203. doi: 10.1016/j.actbio.2016.05.024. Epub 2016 May 30.

Abstract

UNLABELLED

Freeze-dried scaffolds provide regeneration templates for a wide range of tissues, due to their flexibility in physical and biological properties. Control of structure is crucial for tuning such properties, and therefore scaffold functionality. However, the common approach of modeling these scaffolds as open-cell foams does not fully account for their structural complexity. Here, the validity of the open-cell model is examined across a range of physical characteristics, rigorously linking morphology to hydration and mechanical properties. Collagen scaffolds with systematic changes in relative density were characterized using Scanning Electron Microscopy, X-ray Micro-Computed Tomography and spherical indentation analyzed in a time-dependent poroelastic framework. Morphologically, all scaffolds were mid-way between the open- and closed-cell models, approaching the closed-cell model as relative density increased. Although pore size remained constant, transport pathway diameter decreased. Larger collagen fractions also produced greater volume swelling on hydration, although the change in pore diameter was constant, and relatively small at ∼6%. Mechanically, the dry and hydrated scaffold moduli varied quadratically with relative density, as expected of open-cell materials. However, the increasing pore wall closure was found to determine the time-dependent nature of the hydrated scaffold response, with a decrease in permeability producing increasingly elastic rather than viscoelastic behavior. These results demonstrate that characterizing the deviation from the open-cell model is vital to gain a full understanding of scaffold biophysical properties, and provide a template for structural studies of other freeze-dried biomaterials.

STATEMENT OF SIGNIFICANCE

Freeze-dried collagen sponges are three-dimensional microporous scaffolds that have been used for a number of exploratory tissue engineering applications. The characterization of the structure-properties relationships of these scaffolds is necessary to understand their biophysical behavior in vivo. In this work, the relationship between morphology and physical properties in the dry and hydrated states was investigated across a range of solid concentrations in the scaffolds. The quantitative results provided can aid the design of scaffolds with a target trade-off between mechanical properties and structural features important for their biological activity.

摘要

未标记

冻干支架为广泛的组织提供了再生模板,这要归功于其在物理和生物特性方面的灵活性。结构的控制对于调整这些特性以及支架的功能至关重要。然而,将这些支架建模为开孔泡沫的常见方法不能完全说明其结构的复杂性。在这里,通过一系列物理特性来检查开孔模型的有效性,严格将形态与水合和机械性能联系起来。使用扫描电子显微镜、X 射线微计算机断层扫描和球形压痕对具有系统相对密度变化的胶原支架进行了特征描述,并在时变多孔弹性框架中进行了分析。形态上,所有支架都处于开孔和闭孔模型之间,随着相对密度的增加,逐渐接近闭孔模型。尽管孔径保持不变,但传输路径直径减小。较大的胶原分数在水合时也会产生更大的体积膨胀,尽管孔径的变化是恒定的,相对较小,约为 6%。在机械方面,干燥和水合支架的模量与相对密度呈二次关系,这是开孔材料的预期结果。然而,发现增加的孔壁闭合决定了水合支架响应的时变性质,渗透率的降低会产生越来越弹性而不是粘弹性的行为。这些结果表明,表征偏离开孔模型对于充分了解支架的生物物理特性至关重要,并为其他冻干生物材料的结构研究提供了模板。

意义声明

冻干胶原海绵是一种三维微孔支架,已被用于许多探索性组织工程应用。这些支架的结构-性能关系的特征化对于理解它们在体内的生物物理行为是必要的。在这项工作中,研究了一系列支架中固体浓度范围内干燥和水合状态下形态和物理性质之间的关系。提供的定量结果可以帮助设计具有机械性能和对其生物活性重要的结构特征之间目标折衷的支架。

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