Physical vitrification and nanowarming at liter-scale CPA volumes: toward organ cryopreservation

Organ banking via vitrification could transform transplantation, but has never been achieved at human organ scales. This study tested vitrification and rewarming in 0.5-3 L volumes using cryoprotective agents (CPAs): M22, VS55, and 40%EG + 0.6 M Sucrose. Ice formation and cracking was avoided through optimized convective cooling, and successful vitrification was confirmed via visual inspection, thermometry, and X-ray µCT. M22 and EG+sucrose vitrified at 0.5 L, but only M22 succeeded at 3 L; VS55 failed at all volumes. Porcine livers (~0.6-1 L total volume; ~0.23-0.75 L organ volume) were also vitrified using EG+sucrose, though not rewarmed. Future experiments are needed to optimize the protocol and achieve liver rewarming. Using nanowarming with iron-oxide nanoparticles and a newly developed 120 kW RF coil, uniform rewarming was achieved in up to 2 L volumes of M22 at ~88 °C/min. This work serves as a proof-of-concept that human organ scale vitrification and rewarming is physically possible, thereby enabling human organ banking in the future.

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Publication Details

Journal
Nature Communications
Published
2025-09-26
DOI
https://doi.org/10.1038/s41467-025-63483-2
Citations
4
Primary Topic
Organ Transplantation Techniques and Outcomes
Type
article
Field-Weighted Citation Impact
8.03

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article

Physical vitrification and nanowarming at liter-scale CPA volumes: toward organ cryopreservation

Bat‐Erdene Namsrai, John C. Bischof, Michael L. Etheridge, Lakshya Gangwar et al.
4 citations
Nature Communications
Organ Transplantation Techniques and Outcomes
8.03
article

Physical vitrification and nanowarming at liter-scale CPA volumes: toward organ cryopreservation

Bat‐Erdene Namsrai, John C. Bischof, Michael L. Etheridge, Lakshya Gangwar, Zonghu Han, Erik B. Finger, Saurin Kantesaria, Cameron Scheithauer, R. M. Goldstein
article en
4 citations

Abstract

Organ banking via vitrification could transform transplantation, but has never been achieved at human organ scales. This study tested vitrification and rewarming in 0.5-3 L volumes using cryoprotective agents (CPAs): M22, VS55, and 40%EG + 0.6 M Sucrose. Ice formation and cracking was avoided through optimized convective cooling, and successful vitrification was confirmed via visual inspection, thermometry, and X-ray µCT. M22 and EG+sucrose vitrified at 0.5 L, but only M22 succeeded at 3 L; VS55 failed at all volumes. Porcine livers (~0.6-1 L total volume; ~0.23-0.75 L organ volume) were also vitrified using EG+sucrose, though not rewarmed. Future experiments are needed to optimize the protocol and achieve liver rewarming. Using nanowarming with iron-oxide nanoparticles and a newly developed 120 kW RF coil, uniform rewarming was achieved in up to 2 L volumes of M22 at ~88 °C/min. This work serves as a proof-of-concept that human organ scale vitrification and rewarming is physically possible, thereby enabling human organ banking in the future.

Nature CommunicationsVol. 16(1)
University of Minnesota (US), Life Systems (United States) (US)
National Science Foundation, University of Minnesota, National Institutes of Health
Openalex Percentile: Top 2%
Organ Transplantation Techniques and Outcomes
8.03
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