Conduction‐Dominated Cryomesh for Organism Vitrification

Author:

Guo Zongqi1ORCID,Zuchowicz Nikolas1,Bouwmeester Jessica23,Joshi Amey S.1,Neisch Amanda L.4,Smith Kieran1,Daly Jonathan56,Etheridge Michael L.1,Finger Erik B.7,Kodandaramaiah Suhasa B.189,Hays Thomas S.4,Hagedorn Mary23,Bischof John C.1810ORCID

Affiliation:

1. Department of Mechanical Engineering University of Minnesota Minneapolis MN 55455 USA

2. Hawaii Institute of Marine Biology University of Hawaii Kaneohe HI 96744 USA

3. Smithsonian National Zoo and Conservation Biology Institute Front Royal VA 22630 USA

4. Department of Genetics Cell Biology and Development University of Minnesota Minneapolis MN 55455 USA

5. Taronga Conservation Society Australia Mosman New South Wales 2088 Australia

6. School of Biological Earth and Environmental Sciences University of New South Wales Kensington New South Wales 2033 Australia

7. Department of Surgery University of Minnesota Minneapolis MN 55455 USA

8. Department of Biomedical Engineering University of Minnesota Minneapolis MN 55455 USA

9. Graduate Program in Neuroscience University of Minnesota Minneapolis MN 55455 USA

10. Institute for Engineering in Medicine University of Minnesota Minneapolis MN 55455 USA

Abstract

AbstractVitrification‐based cryopreservation is a promising approach to achieving long‐term storage of biological systems for maintaining biodiversity, healthcare, and sustainable food production. Using the “cryomesh” system achieves rapid cooling and rewarming of biomaterials, but further improvement in cooling rates is needed to increase biosystem viability and the ability to cryopreserve new biosystems. Improved cooling rates and viability are possible by enabling conductive cooling through cryomesh. Conduction‐dominated cryomesh improves cooling rates from twofold to tenfold (i.e., 0.24 to 1.2 × 105 °C min−1) in a variety of biosystems. Higher thermal conductivity, smaller mesh wire diameter and pore size, and minimizing the nitrogen vapor barrier (e.g., vertical plunging in liquid nitrogen) are key parameters to achieving improved vitrification. Conduction‐dominated cryomesh successfully vitrifies coral larvae, Drosophila embryos, and zebrafish embryos with improved outcomes. Not only a theoretical foundation for improved vitrification in µm to mm biosystems but also the capability to scale up for biorepositories and/or agricultural, aquaculture, or scientific use are demonstrated.

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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