Artigo Acesso aberto Revisado por pares

Bone marrow processing and cryopreservation.

1982; BMJ; Volume: 35; Issue: 2 Linguagem: Inglês

10.1136/jcp.35.2.186

ISSN

1472-4146

Autores

David C. Linch, L. J. Knott, K.G. Patterson, David Cowan, Peter Harper,

Tópico(s)

Mesenchymal stem cell research

Resumo

Three different closed procedures for concentrating bone marrow progenitor cells prior to cryopreservation have been compared. These were by a manual double centrifugation method, a Hemonetics 30 cell separator and an Aminco Celltrifuge. The best results were achieved using the paediatric pheresis set on the Hemonetics model 30. Marrow was frozen in 120 ml aliquots in a programmed freezer with rapid cooling of the freezing chamber during the phase change from the liquid to the solid state. After freeze-thawing the average nucleated cell recovery was approximately 50% and the progenitor cell recovery 80%.

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