4.6 Article

Deep eutectic solvents as cryoprotective agents for mammalian cells

期刊

JOURNAL OF MATERIALS CHEMISTRY B
卷 10, 期 24, 页码 4546-4560

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2tb00573e

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资金

  1. Australian Research Council [DP190101010, LP160101496, LP190101046]
  2. Jack Brockhoff Foundation [4655-2019-AE]
  3. Australian Government through the National Computational Infrastructure (NCI), under the National Computational Merit Allocation Scheme [kl59]
  4. Australian Research Council [LP190101046, LP160101496] Funding Source: Australian Research Council

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Cryopreservation has been vital in various scientific fields such as assisted reproductive technology, stem cell therapies, and species preservation. However, the toxic nature and limited effectiveness of conventional cryoprotective agents hinder their use in clinical applications. This research explores the potential of deep eutectic solvents as cryoprotectants for mammalian cells, showing that a solvent made from proline and glycerol is effective and less toxic. The study also reveals the importance of multi-component systems and opens the door for the development of new cryoprotective agents tailored to specific cell types.
Cryopreservation has facilitated numerous breakthroughs including assisted reproductive technology, stem cell therapies, and species preservation. Successful cryopreservation requires the addition of cryoprotective agents to protect against freezing damage and dehydration. For decades, cryopreservation has largely relied on the same two primary agents: dimethylsulfoxide and glycerol. However, both of these are toxic which limits their use for cells destined for clinical applications. Furthermore, these two agents are ineffective for hundreds of cell types, and organ and tissue preservation has not been achieved. The research presented here shows that deep eutectic solvents can be used as cryoprotectants. Six deep eutectic solvents were explored for their cryoprotective capacity towards mammalian cells. The solvents were tested for their thermal properties, including glass transitions, toxicity, and permeability into mammalian cells. A deep eutectic solvent made from proline and glycerol was an effective cryoprotective agent for all four cell types tested, even with extended incubation prior to freezing. This deep eutectic solvent was more effective and less toxic than its individual components, highlighting the importance of multi-component systems. Cells were characterised post-thawing using atomic force microscopy and confocal microscopy. Molecular dynamics simulations support the biophysical parameters obtained by experimentation. This is one of the first times that this class of solvents has been systematically tested for cryopreservation of mammalian cells and as such this research opens the way for the development of potentially thousands of new cryoprotective agents that can be tailored to specific cell types. The demonstrated capacity of cells to be incubated with the deep eutectic solvent at 37 degrees C for hours prior to freezing without significant loss of viability is a major step toward the storage of organs and tissues.

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