明胶
自愈水凝胶
共焦显微镜
共焦
显微镜
材料科学
共焦激光扫描显微镜
化学工程
生物医学工程
化学
光学
高分子化学
病理
医学
物理
生物化学
工程类
作者
Alexis Franco,Bo Van Durme,Sandra Van Vlierberghe,C. Gillain
出处
期刊:Tissue Engineering Part C-methods
[Mary Ann Liebert, Inc.]
日期:2024-07-01
卷期号:30 (7): 307-313
被引量:14
标识
DOI:10.1089/ten.tec.2024.0117
摘要
It is a well-documented phenomenon that the porous structure of hydrogels observed with vacuum-based imaging techniques is generated during the freezing and drying process employed prior to observation. Nevertheless, vacuum-based techniques, such as scanning electron microscopy (SEM), are still being commonly used to measure pore sizes in hydrogels, which is often not representative of the actual pore size in hydrated conditions. The frequent underestimation of the impact of freezing and drying on hydrogel structures could stem from a lack of cross-fertilization between materials science and biomedical or food science communities, or from the simplicity and visually appealing nature of SEM imaging, which may lead to an overemphasis on its use. Our study provides a straightforward and impactful way of pinpointing this phenomenon exploiting two hydrogels ubiquitously applied in tissue engineering, including gelatin methacryloyl and alginate as proof-of-concept hydrogels. By comparing images of the samples in the native hydrated state, followed by freezing, freeze-drying, and rehydration using SEM and confocal microscopy, we highlight discrepancies between hydrogel pore sizes in the hydrated versus the dry state. To conclude, our study offers recommendations for researchers seeking insight in hydrogel properties and emphasizes key factors that require careful control when using SEM as a characterization tool.
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