This is the authors' abstract. We don't add key points for this paper.
Long-term cryopreservation of blood vessels is crucial for cardiovascular disease treatments. To avoid ice crystal-induced injuries and achieve higher recovery, viability, function, and scalability of blood vessels, ice-free vitrification technology is required. However, traditional ice-free vitrification often necessitates high concentrations of toxic cryopreservation agents (CPAs), such as VS55 at concentrations up to 8.4 M. In this study, we successfully achieved low-concentration vitrification using a novel CPA formulation (BTP solution) containing zwitterionic betaine and polyglutamic acid at only 3.6 M. The incorporation of polyglutamic acid significantly enhanced hydration properties, enabling a substantial reduction in the betaine concentration, while enhancing effective vitrification. To achieve uniform rewarming in a large system, gum-acid-coated magnetic nanoparticles were synthesized to facilitate rapid and even rewarming, thereby reducing tissue damage. With this low-concentration BTP, we successfully preserved porcine blood vessels for at least 2 months. After cryopreservation, the vessels retained 92.1% structural integrity, 92.6% biomechanical properties, and normal fiber content and maintained contraction-relaxation capabilities. This low-concentration vitrification technique holds considerable promise for further development and broader application in the cryopreservation of biological tissues and organs.
No takes yet. Share an insight, caveat, or question.
Liu et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: