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Article: In-situ stable injectable collagen-based hydrogels for cell and growth factor delivery

TitleIn-situ stable injectable collagen-based hydrogels for cell and growth factor delivery
Authors
KeywordsBMP2 protein
Bone defect
Collagen
Human MSC
Injectable hydrogel
Therapeutic delivery
Issue Date2021
Citation
Materialia, 2021, v. 15, article no. 100954 How to Cite?
AbstractHere we report development of in-situ stable injectable hydrogels for delivery of cells and growth factors based on two precursors, alginate, and collagen/calcium sulfate (CaSO4). The alg/col hydrogels were shear-thinning, injectable through commercially available needles and stable right after injection. Rheological measurements revealed that pre-crosslinked alg/col hydrogels fully crosslinked at 37 °C and that the storage modulus of alg/col hydrogels increased with increasing the collagen content or the concentration of CaSO4. The viscoelastic characteristics and injectability of the alg/col hydrogels were not significantly impacted by the storage of precursor solutions for 28 days. An osteoinductive bone morphogenic protein-2 (BMP-2) loaded into alg/col hydrogels was released in 14 days. Human mesenchymal stem cells (hMSCs) encapsulated in alg/col hydrogels had over 90% viability over 7 days after injection. The DNA content of hMSC-laden alg/col hydrogels increased by 6-37 folds for 28 days, depending on the initial cell density. In addition, hMSCs encapsulated in alg/col hydrogels and incubated in osteogenic medium were osteogenically differentiated and formed a mineralized matrix. Finally, a BMP-2 loaded alg/col hydrogel was used to heal a critical size calvarial bone defect in rats after 8 weeks of injection. The alg/col hydrogel holds great promise in tissue engineering and bioprinting applications.
Persistent Identifierhttp://hdl.handle.net/10722/363384

 

DC FieldValueLanguage
dc.contributor.authorMoeinzadeh, Seyedsina-
dc.contributor.authorPark, Youngbum-
dc.contributor.authorLin, Sien-
dc.contributor.authorYang, Yunzhi Peter-
dc.date.accessioned2025-10-10T07:46:25Z-
dc.date.available2025-10-10T07:46:25Z-
dc.date.issued2021-
dc.identifier.citationMaterialia, 2021, v. 15, article no. 100954-
dc.identifier.urihttp://hdl.handle.net/10722/363384-
dc.description.abstractHere we report development of in-situ stable injectable hydrogels for delivery of cells and growth factors based on two precursors, alginate, and collagen/calcium sulfate (CaSO<inf>4</inf>). The alg/col hydrogels were shear-thinning, injectable through commercially available needles and stable right after injection. Rheological measurements revealed that pre-crosslinked alg/col hydrogels fully crosslinked at 37 °C and that the storage modulus of alg/col hydrogels increased with increasing the collagen content or the concentration of CaSO<inf>4</inf>. The viscoelastic characteristics and injectability of the alg/col hydrogels were not significantly impacted by the storage of precursor solutions for 28 days. An osteoinductive bone morphogenic protein-2 (BMP-2) loaded into alg/col hydrogels was released in 14 days. Human mesenchymal stem cells (hMSCs) encapsulated in alg/col hydrogels had over 90% viability over 7 days after injection. The DNA content of hMSC-laden alg/col hydrogels increased by 6-37 folds for 28 days, depending on the initial cell density. In addition, hMSCs encapsulated in alg/col hydrogels and incubated in osteogenic medium were osteogenically differentiated and formed a mineralized matrix. Finally, a BMP-2 loaded alg/col hydrogel was used to heal a critical size calvarial bone defect in rats after 8 weeks of injection. The alg/col hydrogel holds great promise in tissue engineering and bioprinting applications.-
dc.languageeng-
dc.relation.ispartofMaterialia-
dc.subjectBMP2 protein-
dc.subjectBone defect-
dc.subjectCollagen-
dc.subjectHuman MSC-
dc.subjectInjectable hydrogel-
dc.subjectTherapeutic delivery-
dc.titleIn-situ stable injectable collagen-based hydrogels for cell and growth factor delivery-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.mtla.2020.100954-
dc.identifier.scopuseid_2-s2.0-85097350534-
dc.identifier.volume15-
dc.identifier.spagearticle no. 100954-
dc.identifier.epagearticle no. 100954-
dc.identifier.eissn2589-1529-

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