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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.
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http://dx.doi.org/10.1021/acsami.5c06356 | DOI Listing |
Cryobiology
September 2025
Shinbashi Yume Clinic, Advanced medical research institute of fertility, 2-5-1 Shinbashi Minato-ku, Tokyo, 105-0004, Japan.
This study evaluated the effects of different warming protocols on the recovery rate and blebbing frequency of vitrified hatched blastocysts, aiming to optimize embryo warming methods for improved clinical outcomes. A total of 650 patients (857 cycles) were included, with blastocysts warmed using either the conventional multi-step dilution method or a rapid warming method involving direct immersion in a low-concentration sucrose solution. Recovery rate, blebbing frequency, implantation rate, and clinical pregnancy rate were compared, along with the relationship to embryo morphology at the time of freezing.
View Article and Find Full Text PDFLangmuir
July 2025
Department of Electronic Engineering and Information Science, University of Science and Technology of China, Hefei 230027, China.
Vitrification is the direct conversion of free water from a liquid phase to a glassy solid phase without ice formation and is a widely used method for cryopreservation. However, high concentrations of penetrating cryoprotectants are usually required to achieve vitrification, which causes osmotic stress and toxic effects on cell organelles and membranes. Therefore, low-concentration penetrating cryoprotectants are crucial for vitrification and are urgently required.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2025
Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, China.
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.
View Article and Find Full Text PDFAnimals (Basel)
August 2024
Animal Breeding and Genomics, Wageningen University & Research, 6700 AH Wageningen, The Netherlands.
Biopreserv Biobank
August 2024
Institute of Biothermal Science & Technology, University of Shanghai for Science and Technology, Shanghai, China.
Oocyte vitrification has become a widely adopted method in clinical practice. However, the solidification behavior and its impact on oocytes during the ultrarapid cooling process remain poorly understood. In this study, we established a system and methodology to observe crystallization behavior in oocytes during quench cooling and warming.
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