Chondroitin Sulfate-Based Biomineralizing Surface Hydrogels for Bone Tissue Engineering
Chondroitin sulfate (CS) is the major component of glycosaminoglycan in connective tissue. In this study, we fabricated methacrylated PEGDA/CS-based hydrogels with varying CS concentration (0, 1, 5, and 10%) and investigated them as biomineralizing three-dimensional scaffolds for charged ion binding...
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Published in | ACS applied materials & interfaces Vol. 9; no. 26; pp. 21639 - 21650 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
05.07.2017
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Abstract | Chondroitin sulfate (CS) is the major component of glycosaminoglycan in connective tissue. In this study, we fabricated methacrylated PEGDA/CS-based hydrogels with varying CS concentration (0, 1, 5, and 10%) and investigated them as biomineralizing three-dimensional scaffolds for charged ion binding and depositions. Due to its negative charge from the sulfate group, CS exhibited an osteogenically favorable microenvironment by binding charged ions such as calcium and phosphate. Particularly, ion binding and distribution within negatively charged hydrogel was dependent on CS concentration. Furthermore, CS dependent biomineralizing microenvironment induced osteogenic differentiation of human tonsil-derived mesenchymal stem cells in vitro. Finally, when we transplanted PEGDA/CS-based hydrogel into a critical sized cranial defect model for 8 weeks, 10% CS hydrogel induced effective bone formation with highest bone mineral density. This PEGDA/CS-based biomineralizing hydrogel platform can be utilized for in situ bone formation in addition to being an investigational tool for in vivo bone mineralization and resorption mechanisms. |
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AbstractList | Chondroitin sulfate (CS) is the major component of glycosaminoglycan in connective tissue. In this study, we fabricated methacrylated PEGDA/CS-based hydrogels with varying CS concentration (0, 1, 5, and 10%) and investigated them as biomineralizing three-dimensional scaffolds for charged ion binding and depositions. Due to its negative charge from the sulfate group, CS exhibited an osteogenically favorable microenvironment by binding charged ions such as calcium and phosphate. Particularly, ion binding and distribution within negatively charged hydrogel was dependent on CS concentration. Furthermore, CS dependent biomineralizing microenvironment induced osteogenic differentiation of human tonsil-derived mesenchymal stem cells in vitro. Finally, when we transplanted PEGDA/CS-based hydrogel into a critical sized cranial defect model for 8 weeks, 10% CS hydrogel induced effective bone formation with highest bone mineral density. This PEGDA/CS-based biomineralizing hydrogel platform can be utilized for in situ bone formation in addition to being an investigational tool for in vivo bone mineralization and resorption mechanisms. |
Author | Yu, Seung Jung An, Young-Hyeon Lee, Eunjee A Kim, Hwan D Lee, Seunghun S Jang, Hae Lin Nam, Ki Tae Hwang, Nathaniel S Im, Sung Gap Kim, Seunghyun L |
AuthorAffiliation | Department of Chemical and Bimolecular Engineering Interdisciplinary Program in Bioengineering Department of Materials Science and Engineering Korea Advanced Institute of Technology Seoul National University School of Chemical and Biological Engineering, N-Bio Institute, Institute of Chemical Process |
AuthorAffiliation_xml | – name: School of Chemical and Biological Engineering, N-Bio Institute, Institute of Chemical Process – name: Department of Chemical and Bimolecular Engineering – name: Korea Advanced Institute of Technology – name: Seoul National University – name: Interdisciplinary Program in Bioengineering – name: Department of Materials Science and Engineering |
Author_xml | – sequence: 1 givenname: Hwan D orcidid: 0000-0001-7656-9920 surname: Kim fullname: Kim, Hwan D organization: Seoul National University – sequence: 2 givenname: Eunjee A surname: Lee fullname: Lee, Eunjee A organization: Seoul National University – sequence: 3 givenname: Young-Hyeon surname: An fullname: An, Young-Hyeon organization: Seoul National University – sequence: 4 givenname: Seunghyun L surname: Kim fullname: Kim, Seunghyun L organization: Seoul National University – sequence: 5 givenname: Seunghun S surname: Lee fullname: Lee, Seunghun S organization: Seoul National University – sequence: 6 givenname: Seung Jung surname: Yu fullname: Yu, Seung Jung organization: Korea Advanced Institute of Technology – sequence: 7 givenname: Hae Lin surname: Jang fullname: Jang, Hae Lin organization: Seoul National University – sequence: 8 givenname: Ki Tae orcidid: 0000-0001-6353-8877 surname: Nam fullname: Nam, Ki Tae organization: Seoul National University – sequence: 9 givenname: Sung Gap orcidid: 0000-0001-7562-2929 surname: Im fullname: Im, Sung Gap organization: Korea Advanced Institute of Technology – sequence: 10 givenname: Nathaniel S orcidid: 0000-0003-3735-7727 surname: Hwang fullname: Hwang, Nathaniel S email: nshwang@snu.ac.kr organization: Seoul National University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28605908$$D View this record in MEDLINE/PubMed |
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Snippet | Chondroitin sulfate (CS) is the major component of glycosaminoglycan in connective tissue. In this study, we fabricated methacrylated PEGDA/CS-based hydrogels... |
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SubjectTerms | Bone and Bones Cell Differentiation Cells, Cultured Chondroitin Sulfates - chemistry Humans Hydrogels Mesenchymal Stem Cells Osteogenesis Tissue Engineering Tissue Scaffolds |
Title | Chondroitin Sulfate-Based Biomineralizing Surface Hydrogels for Bone Tissue Engineering |
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