DEVELOPMENT OF MECHANICAL CHARACTERIZATION METHOD OF HYDROGEL SCAFFOLDS USING SYNCHROTRON PROPAGATION-BASED IMAGING
| dc.contributor.advisor | Chen, Daniel | |
| dc.contributor.advisor | Zhu, Ning | |
| dc.contributor.committeeMember | McWalter, Emily | |
| dc.contributor.committeeMember | Cao, Tate | |
| dc.creator | Li, Naitao | |
| dc.creator.orcid | 0000-0002-3679-0505 | |
| dc.date.accessioned | 2023-10-26T15:50:58Z | |
| dc.date.available | 2023-10-26T15:50:58Z | |
| dc.date.copyright | 2023 | |
| dc.date.created | 2023-10 | |
| dc.date.issued | 2023-10-26 | |
| dc.date.submitted | October 2023 | |
| dc.date.updated | 2023-10-26T15:50:58Z | |
| dc.description.abstract | Hydrogel-based scaffolds have been widely used in soft tissue regeneration due to their biocompatible and tissue-like environment for maintaining cellular functions and tissue regeneration. Understanding the mechanical properties and internal microstructure of hydrogel-based scaffold, once implanted, is imperative in many tissue engineering applications and longitude studies. Notably, this has been challenging to date as various conventional characterization methods by, for example, mechanical testing (for mechanical properties) and microscope (for internal microstructure) are destructive as they require removing scaffolds from the implantation site and processing samples for characterization. Synchrotron propagation-based imaging – computed tomography (PBI-CT) is feasible and promising for non-destructive monitoring of hydrogel scaffolds. As inspired, this study aimed to perform a study on the characterization of mechanical properties and microstructure of hydrogel scaffolds based on the PBI-CT. The hydrogel solutions were prepared from 3% w/v alginate + 1% w/v gelatin and then printed by using the needle with a diameter of 200 μm, to form scaffolds with a dimension of 10×10×5 mm3. After successfully crosslinking of scaffolds, some of the scaffolds were degraded in a 37 °C media of phosphate buffered saline over 3 days, for the subsequent examination, along with those without degradation. The scaffolds both with and without degradation were subject to compressive testing, where the compression speed was set at 0.1 mm/s to reach the strain of 10%, 20%, 30%, 40%, and 50%, respectively. Once reached, the strain was held for 5 minutes for measuring the force and thus the stress within scaffolds, yielding the stress–strain curves. After that, the scaffolds were imaged and examined by SR-PBI-CT at the BMIT-ID beamline at Canadian Light Source (CLS). During the imaging process, the scaffolds were mechanically loaded, respectively, with the strains same as the ones in the aforementioned compressive testing, and at each strain, the scaffold was imaged and scanned with a pixel size of 13 µm for analysis. From the stress-strain curves obtained in the compression testing, the Young’s modulus was evaluated to characterize the elastic behavior of scaffolds: with the range between around 5-25 kPa; from the images captured by SR-PBI-CT, the scaffolds microstructures were examined in terms of the strand cross-section area, pore size, and hydrogel volume. Further, from the SR-PBI-CT images, the stress within hydrogel of scaffolds were evaluated, showing the agreement with those obtained from compression testing. These results have illustrated that the mechanical properties and microstructures of scaffolds, ether being degraded or not, can be examined and characterized by the SR-PBI-CT imaging, in a non-destructive manner. This would represent a significant advance for facilitating longitude studies on the scaffolds once implanted in-vivo. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.uri | https://hdl.handle.net/10388/15178 | |
| dc.language.iso | en | |
| dc.subject | Tissue Engineering, Bioprinting, Hydrogel Scaffolds, Mechanical Characterization, Micro-CT. | |
| dc.title | DEVELOPMENT OF MECHANICAL CHARACTERIZATION METHOD OF HYDROGEL SCAFFOLDS USING SYNCHROTRON PROPAGATION-BASED IMAGING | |
| dc.type | Thesis | |
| dc.type.material | text | |
| thesis.degree.department | Biomedical Engineering | |
| thesis.degree.discipline | Biomedical Engineering | |
| thesis.degree.grantor | University of Saskatchewan | |
| thesis.degree.level | Masters | |
| thesis.degree.name | Master of Science (M.Sc.) |