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This study aimed at developing alternative vitrification solutions, modified either from the original PVS2 vitrification solution by increasing glycerol and sucrose and/or decreasing dimethylsulfoxide and ethylene glycol concentration, or from the original PVS3 vitrification solution by decreasing glycerol and sucrose concentration. The application of these vitrification solutions to two model species, i.e. garlic and chrysanthemum in a droplet-vitrification procedure, revealed that PVS3 and variants were superior to PVS2 and variants and that most PVS2 variants were comparable to the original PVS2. Both species were sensitive to chemical toxicity of permeating cryoprotectants and chrysanthemum was also sensitive to osmotic stress. The lower recovery of cryopreserved garlic shoot apices dehydrated with PVS2 and variants compared with those dehydrated with PVS3 and variants seemed attributed to cytotoxicity of the vitrification solutions tested as well as to insufficient protection against freezing injury. Chrysanthemum shoot tips were very sensitive to both chemical toxicity and osmotic stress and therefore, induction of cytotoxity tolerance during preconditioning was required for successful cryopreservation. The present study revealed that some of the PVS2 variants tested which have increased glycerol and sucrose and/or decreased dimethylsulfoxide and ethylene glycol concentration can be applied when explants are of medium size, tolerant to chemical toxicity and moderately sensitive to osmotic stress. PVS3 and variants can be used widely when samples are heterogeneous, of large size and/or very sensitive to chemical toxicity and tolerant to osmotic stress.
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PLoS One
September 2025
Division of Reproductive Engineering, Center for Animal Resources and Development, Institute of Resource Development and Analysis, Kumamoto University, Kumamoto, Japan.
Zygotes are used to create genetically modified animals by electroporation using the CRISPR-Cas9 system. Such zygotes in rats are obtained from superovulated female rats after mating. Recently, we reported that in vivo-fertilized zygotes had higher cryotolerance and developmental ability than in vitro-fertilized zygotes in Sprague Dawley (SD) and Fischer 344 rats.
View Article and Find Full Text PDFDevice
June 2025
Center for Engineering in Medicine and Surgery, Massachusetts General Hospital, Boston, MA, USA.
Oocyte cryopreservation is a critical step of fertilization (IVF). The handling and loading of cryoprotectant currently rely on manual pipetting methods, which leads to outcome variations, high cost and limited accessibility. Here we developed a low-cost and user-friendly microfluidic device to automate the complex multistep process of oocyte CPA loading, delivering cryopreservation-ready oocytes.
View Article and Find Full Text PDFSci Rep
July 2025
Department of Mechanical Engineering, Texas A&M University, College Station, TX, 77843, USA.
Cryopreservation by vitrification could transform fields ranging from organ transplantation to wildlife conservation, but critical physical challenges remain in scaling this approach from microscopic to macroscopic systems, including the threat of fracture due to accumulated thermal stresses. Here, we provide experimental and computational evidence that these stresses are strongly dependent on the glass transition temperature [Formula: see text] of the vitrification solution, a property which, given the narrow band of chemistries represented within common vitrification solutions, is seldom investigated in thermomechanical analyses. We develop a custom cryomacroscope platform to image glass cracking in four aqueous solution chemistries spanning > 50 °C in [Formula: see text]; we process these images using semantic segmentation deep learning algorithms to analyze the extent of cracking in each; and we perform thermomechanical finite element simulations to disentangle the multiphysics effects driving the observed dependency, providing new insights to inform design of next-generation vitrification solutions that minimize thermal cracking risks.
View Article and Find Full Text PDFMedicina (Kaunas)
June 2025
Discipline of Anatomy & Histology, School of Medical Sciences, University of Sydney, Sydney, NSW 2006, Australia.
Assisted reproduction technology (ART) has advanced significantly over the past four decades, leading to improved pregnancy outcomes and a reduction in complications, particularly those associated with multiple pregnancies. These improvements largely stem from advances in understanding embryonic physiology, which has enabled better culture conditions. As a result, embryologists can now efficiently culture embryos to the blastocyst stage and successfully cryopreserve them for future use.
View Article and Find Full Text PDFReprod Biomed Online
September 2025
Next Fertility GynePro - NextClinics International, Bologna, Italy.
Research Question: Is the universal warming protocol efficient to warm vitrified human blastocysts when combining different brands of vitrification and warming kits, when reducing warming droplet volume, and when using a single rehydration step (universal single-step warming)?
Design: Two retrospective longitudinal cohort studies (CS1 and CS2) were undertaken, including a total of 3071 vitrified/warmed blastocysts. In CS1, embryos were vitrified/warmed with various combinations of different kits, and the universal warming protocol was performed with fixed volumes of warming solutions: 4 ml of 1M non-permeating solute (NPS) at 37°C; and 300 µl of 0.5M NPS and 300 µl of washing solution at room temperature.