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Bioconjug Chem ; 22(9): 1804-10, 2011 Sep 21.
Article in English | MEDLINE | ID: mdl-21815632

ABSTRACT

Significant cell damage occurs during cryopreservation resulting in a decreased number of viable and functional cells post-thawing. Recent studies have correlated the unsuccessful outcome of regenerative therapies with poor cell viability after cryopreservation. Cell damage from ice recrystallization during freeze-thawing is one cause of decreased viability after cryopreservation. We have assessed the ability of two C-AFGPs that are potent inhibitors of ice recrystallization to increase cell viability after cryopreservation. Our results indicate that a 1-1.5 mg/mL (0.5-0.8 mM) solution of C-AFGP 1 is an excellent alternative to a 2.5% DMSO solution for the cryopreservation of human embryonic liver cells.


Subject(s)
Antifreeze Proteins/chemistry , Antifreeze Proteins/pharmacology , Cryoprotective Agents/chemistry , Cryoprotective Agents/pharmacology , Antifreeze Proteins/chemical synthesis , Cell Survival/drug effects , Cells, Cultured , Cryopreservation/methods , Dose-Response Relationship, Drug , Humans , Ice , Liver/cytology , Liver/embryology
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