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   <subfield code="a">Approaches to preserve human osteochondral allografts</subfield>
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   <subfield code="c">[Eduardo de Sousa, Diego Aguiar, José Barcelos, Maria Duarte, Beni Olej]</subfield>
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   <subfield code="a">Osteochondral defects may progress to osteoarthritis. Many attempts have been developed to overcome this issue, including osteochondral autografts and allografts. The goal of this study was to develop a new protocol for storage of human osteochondral allografts. Osteochondral plugs were randomly allocated in the following groups: control, immediate freezing up to −70°C, cooling at 4°C, and storage at 37°C. Samples from the cooling at 4°C and storage at 37°C groups were stored in tubes containing medium plus human albumin and analyzed after 1, 3, and 14days. The frozen groups' samples were cryopreserved for 1year in cryotubes containing medium only (FM), medium plus human albumin (FA), and medium plus human albumin and glucose (FG) and were then analyzed. Analysis involved histological study with hematoxylin-eosin and Safranin O and a modified Live/Dead assay. In samples stored both at 37 and 4°C, analysis showed statistically significant higher cellular mortality at 14days compared to 1 and 3days, but mortality in the 4°C group was lower. In the freezing protocols, the FA group showed less cellular mortality than the FM and FG groups. Cooling at 4°C offers better preservation capacity than storage at 37°C, but both offer the capacity for preservation for 14days. Adding human albumin to the storage medium is useful in reducing cellular mortality in samples frozen for 1year.</subfield>
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