Exploring the microstructure of hydrated collagen hydrogels under scanning electron microscopy

Author:

Merryweather Daniel J.1,Weston Nicola2,Roe Jordan13,Parmenter Christopher2ORCID,Lewis Mark P.4,Roach Paul1ORCID

Affiliation:

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

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

3. Department of Materials Loughborough University Leicestershire UK

4. National Centre for Sport and Exercise Medicine (NCSEM) School of Sport Exercise and Health Sciences Loughborough University Leicestershire UK

Abstract

AbstractCollagen 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.

Publisher

Wiley

Subject

Histology,Pathology and Forensic Medicine

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