Author:
Kilbride Peter,Meneghel Julie
Abstract
AbstractFrom early dry-ice-based freezers and passive coolers, cryopreservation devices have come a long way. With increasing interest in the field of cryobiology from new scientific applications, the importance of reliable, traceable, and reproducible cold chain devices is sure to increase, ensuring more precise cryopreservation and enabling better post-thaw outcomes, both for the user and for biological samples. As with any cryopreservation process, it is important to optimize each part of the cold chain for each lab’s biological samples, cryocontainers used, and logistical restraints. In this chapter we describe how freezing technology can be used for cryopreservation of cells.
Reference25 articles.
1. Thurston LM, Holt WV, Watson PF (2003) Post-thaw functional status of boar spermatozoa cryopreserved using three controlled rate freezers: a comparison. Theriogenology 60:101–113
2. Perez-Oteyza J, Bornstein R, Corral M, Hermosa V, Alegre A, Torrabadella M, Ramos P, Garcia J, Odriozola J, Navarro JL (1998) Controlled-rate versus uncontrolled-rate cryopreservation of peripheral blood progenitor cells: a prospective multicenter study. Group for Cryobiology and Biology of Bone Marrow Transplantation (CBTMO), Spain. Haematologica 83:1001–1005
3. Meryman HT (2007) Cryopreservation of living cells: principles and practice. Transfusion 47:935–945
4. Creemers E, Nijs M, Vanheusden E, Ombelet W (2011) Cryopreservation of human sperm: efficacy and use of a new nitrogen-free controlled rate freezer versus liquid nitrogen vapour freezing. Andrologia 43:392–397
5. Baboo J, Kilbride P, Delahaye M, Milne S, Fonseca F, Blanco M, Meneghel J, Nancekievill A, Gaddum N, Morris JG (2019) The impact of varying cooling and thawing rates on the quality of cryopreserved human peripheral blood T cells. Sci Rep 9:3417
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献