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扫描电子显微镜下观察水合胶原水凝胶的微观结构。

Exploring the microstructure of hydrated collagen hydrogels under scanning electron microscopy.

机构信息

Department of Chemistry, School of Science, Loughborough University, Leicestershire, UK.

Nanoscale and Microscale Research Centre, University of Nottingham, Nottingham, UK.

出版信息

J Microsc. 2023 Apr;290(1):40-52. doi: 10.1111/jmi.13174. Epub 2023 Feb 13.

Abstract

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  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.

摘要

胶原水凝胶是生物工程和软物质工程中一个快速发展的平台,用于关注医学治疗、医疗设备和生物传感器的新型应用。将微观结构与材料特性和功能联系起来的观察结果,使控制这一空间的合理设计策略成为可能。由于胶原凝胶的水合作用和分子组织之间的关系,这些软湿材料的微观组织的可视化呈现出独特的技术挑战。扫描电子显微镜是一种广泛用于可视化和探索微观材料的强大工具。然而,如果在制备和/或观察过程中不引入结构变化,胶原凝胶的微观结构的研究就会很困难。电子在液相材料中传播不良,限制了电子显微镜对水合凝胶的探测能力。为了去除水而采用的样品制备技术会在材料微观结构中引起人为变化,特别是在胶原等复杂材料中,这突出表明需要开发稳健的材料处理协议来对胶原水凝胶进行成像。在这里,制备了胶原水凝胶,并在高真空(10 Pa)和低真空(80-120 Pa)条件下以及环境扫描电子显微镜腔室中探索了凝胶状态。发现胶原纤维的可视化依赖于样品的水合程度,较高的成像腔室压力和湿度会导致特征保真度降低。降低成像腔室压力可用于诱导凝胶含水量蒸发,从而揭示出比在成像前脱水的样品中观察到的胶原纤维直径大得多的胶原纤维。发现凝胶材料的快速冷冻和低温处理可在凝胶含水量升华后保留多孔 3D 结构。对胶原水凝胶材料的比较分析表明,在准备电子显微镜用的水凝胶样品时需要小心谨慎。

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