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The cell-assembled extracellular matrix: A focus on the storage stability and terminal sterilization of this human “bio” material
The Cell-Assembled extracellular Matrix (CAM) is an attractive biomaterial because it provided the back-bone of vascular grafts that were successfully implanted in patients, and because it can now be assembled in “human textiles”. For future clinical development, it is important to consider key manu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614989/ https://www.ncbi.nlm.nih.gov/pubmed/37149079 http://dx.doi.org/10.1016/j.actbio.2023.05.002 |
Sumario: | The Cell-Assembled extracellular Matrix (CAM) is an attractive biomaterial because it provided the back-bone of vascular grafts that were successfully implanted in patients, and because it can now be assembled in “human textiles”. For future clinical development, it is important to consider key manufacturing questions. In this study, the impact of various storage conditions and sterilization methods were evaluated. After 1 year of dry frozen storage, no change in mechanical nor physicochemical properties were detected. However, storage at 4 °C and room temperature resulted in some mechanical changes, especially for dry CAM, but physicochemical changes were minor. Sterilization modified CAM mechanical and physicochemical properties marginally except for hydrated gamma treatment. All sterilized CAM supported cell proliferation. CAM ribbons were implanted subcutaneously in immunodeficient rats to assess the impact of sterilization on the innate immune response. Sterilization accelerated strength loss but no significant difference could be shown at 10 months. Very mild and transient inflammatory responses were observed. Supercritical CO(2) sterilization had the least effect. In conclusion, the CAM is a promising biomaterial since it is unaffected by long-term storage in conditions available in hospitals (hydrated at 4 °C), and can be sterilized terminally (scCO(2)) without compromising in vitro nor in vivo performance. |
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