The development of collagen-GAG scaffold-membrane composites for tendon tissue engineering
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| Title: | The development of collagen-GAG scaffold-membrane composites for tendon tissue engineering |
|---|---|
| Authors: | Caliari, Steven R.1, Ramirez, Manuel A.2, Harley, Brendan A.C.1,3 bharley@illinois.edu |
| Source: | Biomaterials. Dec2011, Vol. 32 Issue 34, p8990-8998. 9p. |
| Subjects: | Tissue engineering, Tissue scaffolds, Collagen, Glycosaminoglycans, Tendons, Cell proliferation, Biomedical materials, Mechanical behavior of materials |
| Abstract: | Abstract: Current tissue engineering approaches for tendon defects require improved biomaterials to balance microstructural and mechanical design criteria. Collagen-glycosaminoglycan (CG) scaffolds have shown considerable success as in vivo regenerative templates and in vitro constructs to study cell behavior. While these scaffolds possess many advantageous qualities, their mechanical properties are typically orders of magnitude lower than orthopedic tissues such as tendon. Taking inspiration from mechanically efficient core–shell composites in nature such as plant stems and porcupine quills, we have created core–shell CG composites that display high bioactivity and improved mechanical integrity. These composites feature integration of a low density, anisotropic CG scaffold core with a high density, CG membrane shell. CG membranes were fabricated via an evaporative process that allowed separate tuning of membrane thickness and elastic moduli and were found to be isotropic in-plane. The membranes were then integrated with an anisotropic CG scaffold core via freeze-drying and subsequent crosslinking. Increasing the relative thickness of the CG membrane shell was shown to increase composite tensile elastic modulus by as much as a factor of 36 in a manner consistent with predictions from layered composites theory. CG scaffold-membrane composites were found to support tendon cell viability, proliferation, and metabolic activity in vitro, suggesting they maintain sufficient permeability while demonstrating improved mechanical strength. This work suggests an effective, biomimetic approach for balancing strength and bioactivity requirements of porous scaffolds for tissue engineering. [Copyright &y& Elsevier] |
| Copyright of Biomaterials is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: egs DbLabel: Engineering Source An: 65944484 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: The development of collagen-GAG scaffold-membrane composites for tendon tissue engineering – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Caliari%2C+Steven+R%2E%22">Caliari, Steven R.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Ramirez%2C+Manuel+A%2E%22">Ramirez, Manuel A.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Harley%2C+Brendan+A%2EC%2E%22">Harley, Brendan A.C.</searchLink><relatesTo>1,3</relatesTo><i> bharley@illinois.edu</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Biomaterials%22">Biomaterials</searchLink>. Dec2011, Vol. 32 Issue 34, p8990-8998. 9p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Tissue+engineering%22">Tissue engineering</searchLink><br /><searchLink fieldCode="DE" term="%22Tissue+scaffolds%22">Tissue scaffolds</searchLink><br /><searchLink fieldCode="DE" term="%22Collagen%22">Collagen</searchLink><br /><searchLink fieldCode="DE" term="%22Glycosaminoglycans%22">Glycosaminoglycans</searchLink><br /><searchLink fieldCode="DE" term="%22Tendons%22">Tendons</searchLink><br /><searchLink fieldCode="DE" term="%22Cell+proliferation%22">Cell proliferation</searchLink><br /><searchLink fieldCode="DE" term="%22Biomedical+materials%22">Biomedical materials</searchLink><br /><searchLink fieldCode="DE" term="%22Mechanical+behavior+of+materials%22">Mechanical behavior of materials</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Abstract: Current tissue engineering approaches for tendon defects require improved biomaterials to balance microstructural and mechanical design criteria. Collagen-glycosaminoglycan (CG) scaffolds have shown considerable success as in vivo regenerative templates and in vitro constructs to study cell behavior. While these scaffolds possess many advantageous qualities, their mechanical properties are typically orders of magnitude lower than orthopedic tissues such as tendon. Taking inspiration from mechanically efficient core–shell composites in nature such as plant stems and porcupine quills, we have created core–shell CG composites that display high bioactivity and improved mechanical integrity. These composites feature integration of a low density, anisotropic CG scaffold core with a high density, CG membrane shell. CG membranes were fabricated via an evaporative process that allowed separate tuning of membrane thickness and elastic moduli and were found to be isotropic in-plane. The membranes were then integrated with an anisotropic CG scaffold core via freeze-drying and subsequent crosslinking. Increasing the relative thickness of the CG membrane shell was shown to increase composite tensile elastic modulus by as much as a factor of 36 in a manner consistent with predictions from layered composites theory. CG scaffold-membrane composites were found to support tendon cell viability, proliferation, and metabolic activity in vitro, suggesting they maintain sufficient permeability while demonstrating improved mechanical strength. This work suggests an effective, biomimetic approach for balancing strength and bioactivity requirements of porous scaffolds for tissue engineering. [Copyright &y& Elsevier] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Biomaterials is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.biomaterials.2011.08.035 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 9 StartPage: 8990 Subjects: – SubjectFull: Tissue engineering Type: general – SubjectFull: Tissue scaffolds Type: general – SubjectFull: Collagen Type: general – SubjectFull: Glycosaminoglycans Type: general – SubjectFull: Tendons Type: general – SubjectFull: Cell proliferation Type: general – SubjectFull: Biomedical materials Type: general – SubjectFull: Mechanical behavior of materials Type: general Titles: – TitleFull: The development of collagen-GAG scaffold-membrane composites for tendon tissue engineering Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Caliari, Steven R. – PersonEntity: Name: NameFull: Ramirez, Manuel A. – PersonEntity: Name: NameFull: Harley, Brendan A.C. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: Dec2011 Type: published Y: 2011 Identifiers: – Type: issn-print Value: 01429612 Numbering: – Type: volume Value: 32 – Type: issue Value: 34 Titles: – TitleFull: Biomaterials Type: main |
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