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Cited by 81Tissue Engineering and Regenerative MedicineOsteoarthritis Treatment and MechanismsHydrogels: synthesis, properties, applications

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Comparison of natural crosslinking agents for the stabilization of xenogenic articular cartilage

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Pinheiro, Amanda, Cooley, Avery, Liao, Jun, Prabhu, Rajkumar, Elder, Steven·2016·Journal of Orthopaedic Research

Abstract

Osteochondral xenografts are potentially inexpensive, widely available alternatives to fresh allografts. However, antigen removal from xenogenic cartilage may damage the extracellular matrix and reduce compressive stiffness. Non‐crosslinked xenogenic cartilage may also undergo rapid enzymatic degradation in vivo. We hypothesized that natural crosslinking agents could be used in place of glutaraldehyde to improve the mechanical properties and enzymatic resistance of decellularized cartilage. This study compared the effects of genipin (GNP), proanthocyanidin (PA), and epigallocatechin gallate (EGCG), on the physical and mechanical properties of decellularized porcine cartilage. Glutaraldehyde (GA) served as a positive control. Porcine articular cartilage discs were decellularized in 2% sodium dodecyl sulfate and DNase I followed by fixation in 0.25% GNP, 0.25% PA, 0.25% EGCG, or 2.5% GA. Decellularization decreased DNA by 15% and GAG by 35%. For natural crosslinkers, the average degree of crosslinking ranged from approximately 50% (EGCG) to 78% (GNP), as compared to 83% for the GA control. Among the natural crosslinkers, only GNP significantly affected the disc diameter, and shrinkage was under 2%. GA fixation had no significant effect on disc diameter. Decellularization decreased aggregate modulus; GA and GNP, but not EGCG and PA, were able to restore it to its original level. GNP, PA, and GA conferred a similar, almost complete resistance to collagenase degradation. EGCG also conferred substantial resistance but to a lesser degree. Overall, the data support our hypothesis and suggest that natural crosslinkers may be suitable alternatives to glutaraldehyde for stabilization of decellularized cartilage. © 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:1037–1046, 2016.

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Metadata

Authors
Pinheiro, A., Cooley, A., Liao, J., Prabhu, R., & Elder, S.
Affiliations
  • University of Akron (US)
  • Mississippi State University (US)
  • Department of Agricultural and Biological Engineering Mississippi State University Starkville Mississippi 39762
Corresponding author
Elder, Steven
Venue
Journal of Orthopaedic Research
Publisher
Wiley
Published
2015-12-18
Volume
34
Issue
6
Pages
1037-1046
ISSN
  • 0736-0266 (ISSN-L)
  • 1554-527X
OpenAlex
W2187784371
Cited by
81
References
1
Citations by year
2026: 2 · 2025: 8 · 2024: 10 · 2023: 8 · 2022: 8 · 2021: 9 · 2020: 16 · 2019: 8 · 2018: 4 · 2017: 5 · 2016: 3
FWCI
4.03
Type
journal article
Language
en
Open access
Locations
  • Journal of Orthopaedic Research® (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institutes of Health (R15AR066926)
  • National Science Foundation (1359437)
Topics
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
  • Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
  • Physical Sciences › Materials Science › Biomaterials › Hydrogels: synthesis, properties, applications
Keywords
decellularization, genipin, proanthocyanidins, epigallocatechin gallate, glutaraldehyde, cartilage biomechanics, collagenase resistance, extracellular matrix, porcine cartilage, antigen removal
MeSH terms
Animals, Cartilage, Cartilage, Articular, Catechin, Cross-Linking Reagents, Drug Evaluation, Preclinical, Swine, Collagenases, Iridoids, Proanthocyanidins, Grape Seed Extract, Heterografts

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