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Exploring the microstructure of hydrated collagen hydrogels under scanning electron microscopy

微尺度化学 自愈水凝胶 微观结构 扫描电子显微镜 环境扫描电子显微镜 材料科学 样品制备 纳米技术 蒸发 生物医学工程 化学工程 复合材料 化学 色谱法 高分子化学 医学 数学教育 数学 物理 工程类 热力学
作者
Daniel J. Merryweather,Nicola Weston,Jordan Roe,Christopher Parmenter,Mark P. Lewis,Paul Roach
出处
期刊:Journal of Microscopy [Wiley]
卷期号:290 (1): 40-52 被引量:7
标识
DOI:10.1111/jmi.13174
摘要

Collagen hydrogels are a rapidly expanding platform in bioengineering and soft materials engineering for novel applications focused on medical therapeutics, medical devices and biosensors. Observations linking microstructure to material properties and function enables rational design strategies to control this space. Visualisation of the microscale organisation of these soft hydrated materials presents unique technical challenges due to the relationship between hydration and the molecular organisation of a collagen gel. Scanning electron microscopy is a robust tool widely employed to visualise and explore materials on the microscale. However, investigation of collagen gel microstructure is difficult without imparting structural changes during preparation and/or observation. Electrons are poorly propagated within liquid-phase materials, limiting the ability of electron microscopy to interrogate hydrated gels. Sample preparation techniques to remove water induce artefactual changes in material microstructure particularly in complex materials such as collagen, highlighting a critical need to develop robust material handling protocols for the imaging of collagen hydrogels. Here a collagen hydrogel is fabricated, and the gel state explored under high-vacuum (10-6 Pa) and low-vacuum (80-120 Pa) conditions, and in an environmental SEM chamber. Visualisation of collagen fibres is found to be dependent on the degree of sample hydration, with higher imaging chamber pressures and humidity resulting in decreased feature fidelity. Reduction of imaging chamber pressure is used to induce evaporation of gel water content, revealing collagen fibres of significantly larger diameter than observed in samples dehydrated prior to imaging. Rapid freezing and cryogenic handling of the gel material is found to retain a porous 3D structure following sublimation of the gel water content. Comparative analysis of collagen hydrogel materials demonstrates the care needed when preparing hydrogel samples for electron microscopy.
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