Getting an organ from donor to recipient is a race against time, with many going to waste. Now, researchers in Australia have identified new cryoprotectants that could preserve organs and tissues for much longer without damaging them.
Freezing living cells is a good way to preserve them for much longer than at room temperature, but traditional freezing damages those cells as ice crystals form. That’s why your frozen and thawed strawberries or steak are always a bit mushy, but of course the bigger problem is that it can render human donor organs unsuitable for transplant.
Cryoprotective agents can be used to prevent ice crystal formation and the resulting damage, by creating a glassy state instead. They’ve been used to store samples of fluids like blood and animal sperm, but can’t be applied to whole organs because they’re toxic.
For the new study, researchers at RMIT University identified a new type of cryoprotectant that shows promise in preserving types of cells that existing ones can’t. The team systematically tested a class of chemicals called eutectic solvents, and found one that worked to preserve tissues without damaging the cells.
The team tested the chemical on four cell types, including skin and brain cells. First, the cells are incubated with the cryoprotectant at 37 °C (98.6 °F) – human body temperature – for a few hours, before being frozen. Later, the samples were thawed and examined with microscopes for cell damage.
And sure enough, the new cryoprotectant was effective for all four cell types, showing less toxicity and better preservation than existing agents. Intriguingly, that includes its two main ingredients, proline and glycerol.
“This cryoprotectant was more effective and less toxic than its individual components,” said Dr. Saffron Bryant, lead researcher on the study. “This is one of the first times that this class of solvents has been systematically tested for cryopreservation of mammalian cells. This study could lead to the development of potentially thousands of new cryoprotective agents that may be tailored to specific cell types.”
However, the team says that there’s still plenty of work to do before this new technique can be used in whole organs. Next, the researchers plan to investigate other cell types, including some that currently can’t be frozen using other methods.
The research was published in the Journal of Materials Chemistry B.
Source: RMIT University
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