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Article: Silk acid-tyramine hydrogels with rapid gelation properties for 3D cell culture

TitleSilk acid-tyramine hydrogels with rapid gelation properties for 3D cell culture
Authors
Keywords3D cell culture
Chemically-modified silk protein
Degradable biomaterials
Hydrogel
Silk
Issue Date2024
Citation
Acta Biomaterialia, 2024, v. 187, p. 138-148 How to Cite?
AbstractSilk fibroin (SF) can be enzymatically crosslinked through tyrosine residues to fabricate hydrogels with good biocompatibility and tunable mechanical properties. Using tyramine substitution can increase the phenolic group content to facilitate the gelation kinetics and mechanical properties. In this study, a two-step chemical modification method is demonstrated to synthesize silk acid-tyramine (SA-TA) conjugates with a high phenolic group content (>7 mol%). The SA-TA shows rapid enzyme-catalyzed gelation property where the sol–gel transition takes less than 10 s at 37 °C, allowing cell encapsulation with uniform distribution while maintaining high cell viability (>90 %). Furthermore, the enzyme-catalyzed SA-TA hydrogels show enhanced storage modulus than enzyme-catalyzed SF hydrogels, long-term stability, and good cytocompatibility, indicating their great potential in 3D cell culture. The in vivo implantation study demonstrates that the SA-TA hydrogels are biodegradable with a mild immune response. This implies that SA-TA hydrogels can be applied in various medical applications, such as tissue engineering, cell delivery, and 3D bioprinting. Statement of significance: In this study, a two-step chemical modification method is demonstrated to synthesize silk acid-tyramine (SA-TA) conjugates with a high phenolic group content (>7 mol%). Owing to the increased content of the phenolic group, the SA-TA shows rapid enzyme-catalyzed gelation property where the sol–gel transition takes less than 10 s at 37 °C, allowing cell encapsulation with uniform distribution while maintaining high cell viability (>90 %). Furthermore, the enzyme-catalyzed SA-TA hydrogels show enhanced storage modulus than enzyme-catalyzed SF hydrogels, long-term stability, and good cytocompatibility, indicating their great potential in 3D cell culture. The in vivo implantation study demonstrates that the SA-TA hydrogels are biodegradable with a mild immune response. This implies that SA-TA hydrogels can be applied in various medical applications, such as tissue engineering, cell delivery, and 3D bioprinting.
Persistent Identifierhttp://hdl.handle.net/10722/355035
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 1.925

 

DC FieldValueLanguage
dc.contributor.authorWang, Wenzhao-
dc.contributor.authorSun, Ziyang-
dc.contributor.authorXiao, Yixiao-
dc.contributor.authorWang, Min-
dc.contributor.authorWang, Jiaqi-
dc.contributor.authorGuo, Chengchen-
dc.date.accessioned2025-03-21T09:10:46Z-
dc.date.available2025-03-21T09:10:46Z-
dc.date.issued2024-
dc.identifier.citationActa Biomaterialia, 2024, v. 187, p. 138-148-
dc.identifier.issn1742-7061-
dc.identifier.urihttp://hdl.handle.net/10722/355035-
dc.description.abstractSilk fibroin (SF) can be enzymatically crosslinked through tyrosine residues to fabricate hydrogels with good biocompatibility and tunable mechanical properties. Using tyramine substitution can increase the phenolic group content to facilitate the gelation kinetics and mechanical properties. In this study, a two-step chemical modification method is demonstrated to synthesize silk acid-tyramine (SA-TA) conjugates with a high phenolic group content (>7 mol%). The SA-TA shows rapid enzyme-catalyzed gelation property where the sol–gel transition takes less than 10 s at 37 °C, allowing cell encapsulation with uniform distribution while maintaining high cell viability (>90 %). Furthermore, the enzyme-catalyzed SA-TA hydrogels show enhanced storage modulus than enzyme-catalyzed SF hydrogels, long-term stability, and good cytocompatibility, indicating their great potential in 3D cell culture. The in vivo implantation study demonstrates that the SA-TA hydrogels are biodegradable with a mild immune response. This implies that SA-TA hydrogels can be applied in various medical applications, such as tissue engineering, cell delivery, and 3D bioprinting. Statement of significance: In this study, a two-step chemical modification method is demonstrated to synthesize silk acid-tyramine (SA-TA) conjugates with a high phenolic group content (>7 mol%). Owing to the increased content of the phenolic group, the SA-TA shows rapid enzyme-catalyzed gelation property where the sol–gel transition takes less than 10 s at 37 °C, allowing cell encapsulation with uniform distribution while maintaining high cell viability (>90 %). Furthermore, the enzyme-catalyzed SA-TA hydrogels show enhanced storage modulus than enzyme-catalyzed SF hydrogels, long-term stability, and good cytocompatibility, indicating their great potential in 3D cell culture. The in vivo implantation study demonstrates that the SA-TA hydrogels are biodegradable with a mild immune response. This implies that SA-TA hydrogels can be applied in various medical applications, such as tissue engineering, cell delivery, and 3D bioprinting.-
dc.languageeng-
dc.relation.ispartofActa Biomaterialia-
dc.subject3D cell culture-
dc.subjectChemically-modified silk protein-
dc.subjectDegradable biomaterials-
dc.subjectHydrogel-
dc.subjectSilk-
dc.titleSilk acid-tyramine hydrogels with rapid gelation properties for 3D cell culture-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.actbio.2024.08.027-
dc.identifier.pmid39197566-
dc.identifier.scopuseid_2-s2.0-85203294383-
dc.identifier.volume187-
dc.identifier.spage138-
dc.identifier.epage148-
dc.identifier.eissn1878-7568-

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