Journal
CRYOBIOLOGY
Volume 60, Issue 2, Pages 217-221Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cryobiol.2009.12.003
Keywords
Cartilage; Cryopreservation; Vitrification; Osteochondral grafts
Categories
Funding
- National Institute of Arthritis and Musculoskeletal and Skin Diseases [R44 AR472731]
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The limited availability of fresh osteochondral allograft tissues necessitates the use of banking for longterm storage A vitrification Solution containing a 55% cryoprotectant formulation, VS55, previously studied using rabbit articular cartilage, was evaluated using porcine articular cartilage. Specimens ranging from 2 to 6 mm in thickness were obtained from 6 mill distal femoral cartilage cores and cryopreserved by vitrification or freezing The results of post-rewarming viability assessments employing alamarBlue demonstrated a large decrease (p < 0.001) in viability in all three sizes of cartilage specimen vitrified with V555. This is in marked contrast with prior experience with full thickness, 0 6 mill rabbit cartilage. Microscopic examination following cryosubstitution confirmed ice formation in the chondrocytes of porcine cartilage vitrified using VS55 Experiments using a more concentrated vitrification formulation (83%), VS83, showed a significant treatment benefit for larger segments of articular cartilage Differences between the VS55 and the VS83 treatment groups were significant at p < 0 001 for 2 mm and 4 mm plugs, and at p < 0 01 for full thickness, 6 mill plugs The percentage viability in fresh controls, compared to VS55 and VS83. was 24.7% and 80.7% in the 2 mm size group, 18.2% and 55.5% in the 4 mm size group, and 5.2% and 43.6% in the 6 mm group, respectively The results of this study continue to indicate that vitrification is superior to conventional cryopreservation with low concentrations of dimethyl sulfoxide by freezing for cartilage The vitrification technology presented here may, with further process development, enable the long-term storage and transportation of living cartilage for repair of human articular Surfaces (C) 2009 Elsevier Inc All rights reserved
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