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Updated: May 3, 2026

Bulk Droplet Vitrification for Primary Hepatocyte Preservation
Published on: October 25, 2019
Synthetic polymers enable non-vitreous cellular cryopreservation by reducing ice crystal growth during thawing
Robert C Deller1, Manu Vatish2, Daniel A Mitchell3
11] Department of Chemistry, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, UK [2] Clinical Sciences Research Laboratories, University of Warwick, Clifford Bridge Road, Coventry CV2 2DX, UK [3] Molecular Organisation and Assembly in Cells (MOAC), Doctoral Training Centre, University of Warwick, Coventry CV4 7AL, UK.
Abstract:
The cryopreservation of cells, tissue and organs is fundamental to modern biotechnology, transplantation medicine and chemical biology. The current state-of-the-art method of cryopreservation is the addition of large amounts of organic solvents such as glycerol or dimethyl sulfoxide, to promote vitrification and prevent ice formation. Here we employ a synthetic, biomimetic, polymer, which is capable of slowing the growth of ice crystals in a manner similar to antifreeze (glyco)proteins to enhance the cryopreservation of sheep and human red blood cells. We find that only 0.1 wt% of the polymer is required to attain significant cell recovery post freezing, compared with over 20 wt% required for solvent-based strategies. These results demonstrate that synthetic antifreeze (glyco)protein mimics could have a crucial role in modern regenerative medicine to improve the storage and distribution of biological material for transplantation.
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