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Recent years have witnessed significant advancements in the cryopreservation of various tissues and cells, yet several challenges persist. This review evaluates the current state of cryopreservation, focusing on contemporary methods, notable achievements, and ongoing difficulties. Techniques such as slow freezing and vitrification have enabled the successful preservation of diverse biological materials, including embryos and ovarian tissue, marking substantial progress in reproductive medicine and regenerative therapies. These achievements highlight improved post-thaw survival and functionality of cryopreserved samples. However, there are remaining challenges such as ice crystal formation, which can lead to cell damage, and the cryopreservation of larger, more complex tissues and organs. This review also explores the role of cryoprotectants and the importance of optimizing both cooling and warming rates to enhance preservation outcomes. Future research priorities include developing new cryoprotective agents, elucidating the mechanisms of cryoinjury, and refining protocols for preserving complex tissues and organs. This comprehensive overview underscores the transformative potential of cryopreservation in biomedicine, while emphasizing the necessity for ongoing innovation to address existing challenges.
Recent years have witnessed significant advancements in the cryopreservation of various tissues and cells, yet several challenges persist. This review evaluates the current state of cryopreservation, focusing on contemporary methods, notable achievements, and ongoing difficulties. Techniques such as slow freezing and vitrification have enabled the successful preservation of diverse biological materials, including embryos and ovarian tissue, marking substantial progress in reproductive medicine and regenerative therapies. These achievements highlight improved post-thaw survival and functionality of cryopreserved samples. However, there are remaining challenges such as ice crystal formation, which can lead to cell damage, and the cryopreservation of larger, more complex tissues and organs. This review also explores the role of cryoprotectants and the importance of optimizing both cooling and warming rates to enhance preservation outcomes. Future research priorities include developing new cryoprotective agents, elucidating the mechanisms of cryoinjury, and refining protocols for preserving complex tissues and organs. This comprehensive overview underscores the transformative potential of cryopreservation in biomedicine, while emphasizing the necessity for ongoing innovation to address existing challenges.
Introduction. Cryopreservation allows for long-term conservation of biomaterials. The insufficient efficacy of available cryopreservatives and the toxicity of a number of cryocomponents renders the search for low-toxic biocompatible cryoagents highly relevant.Objective. Assessment of morphological and functional features of blood cells in a lactulose-based cryopreservative for storing whole blood at moderately low temperatures (minus 20 °C) using leukocyte, platelet, and erythrocytes parameters.Materials and methods. The study was conducted using peripheral venous blood of 30 female donor volunteers aged 18–23 years. Samples of peripheral venous blood were stabilized by 3-substituted potassium salt of ethylenediaminetetraacetic acid. The cryopreservative was prepared using a 0.9 % sodium chloride solution to maintain the isotonic concentration. Glycerin and dimethyl sulfoxide were used as cell-penetrating cryoprotectors; lactulose disaccharide was used as a non-penetrating cryoprotector. The composition of the obtained cryopreservative was optimized by varying the mass fractions of the components. Clinical blood tests were performed using a Gemalite 1270 automatic hematology analyzer. A computer cytomorphometric study was performed in the MEKOS-C2 hardware and software environment.Results. The conservation of blood samples using the developed cryopreservative for 24 h at a temperature of minus 20 °C increased the percentage of preserved leukocytes, erythrocytes, and platelets to 88.6±0.41 %, 92.1±0.31 %, and 91.4±0.52 %, respectively. The blood cells retained their physiological activity after thawing compared to blood samples stored at room temperature.Conclusions. The morphological and functional safety of blood cells in samples stored with the developed cryopreservative was revealed after 24 h of storage at minus 20°C. The advantages of this cryopreservative include the possibility of its long-term storage without loss of cryoprotective properties, stabilizing blood cells to the effects of sub-moderate low temperatures of minus 20 °C, the use of non-toxic lactulose disaccharide that does not penetrate into the cell. The developed cryopreservative proves effective in freezing conditions at minus 20 °C, being affordable in terms of cost (all components are manufactured in the Russian Federation). Further research in this direction will contribute to the development of safer blood donation approaches and reducing complications during transfusion of blood components.
Article Application of Saccharide Cryoprotectants in the Freezing or Lyophilization Process of Lipid Nanoparticles Encapsulating Gene Drugs for Regenerative Medicine Wanqi Li 1,†, Ting Wang 1,†, Jianyang Chen 1, Minmei Guo 1, Ling Ling 1 and Akon Higuchi 1,2,3,* 1 State Key Laboratory of Ophthalmology, Optometry and Visual Science, Eye Hospital, Wenzhou Medical University, No. 270, Xueyuan Road, Wenzhou 325027, China 2 Department of Chemical and Materials Engineering, National Central University, No. 300, Jhongda RD., Jhongli District, Taoyuan 32001, Taiwan 3 R&D Center for Membrane Technology, Chung Yuan Christian University, Chungli District, Taoyuan 32023, Taiwan * Correspondence: higuchi@ncu.edu.tw or higuchi@wmu.edu.cn † These authors contributed equally to this work. Received: 14 November 2024; Revised: 15 December 2024; Accepted: 16 December 2024; Published: 20 December 2024 Abstract: Lipid nanoparticles (LNPs) have emerged as highly efficient drug delivery systems in gene therapy and regenerative medicine and have demonstrated great potential in recent years. Notably, LNPs encapsulating mRNA vaccines have achieved remarkable success in combating the COVID-19 epidemic. However, LNPs encapsulating mRNA encounter issues of physical and chemical instability and need to be stored and transported under harsh conditions. Lyophilization technology, which is commonly used to increase the stability of nanomedicines, has been increasingly applied to stabilize mRNA-LNPs. Appropriate cryoprotectants, such as saccharides, glycerin, and dimethyl sulfoxide (DMSO), need to be added to mRNA-LNPs during the freezing or lyophilization process to effectively preserve the physical and chemical properties of mRNA-LNPs, ensuring their stability. Saccharides (i.e., sucrose, trehalose, and maltose) are the most widely used cryoprotectants to protect the integrity of mRNA-LNPs. This is because saccharides are relatively safe molecules compared with other chemical molecules for cells and animals. However, different saccharides have varying levels of protective effects on mRNA-LNP formulations, and the optimal saccharide concentration varies depending on the specific mRNA-LNP. This article reviews the application and mechanisms of saccharide-based cryoprotectants in the freezing or lyophilization process of LNP-delivered gene therapies and regenerative medicines, offering guidance for selecting the most appropriate saccharide-based cryoprotectants for mRNA-LNP drugs during freezing or lyophilization processes.
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