Abstract
Sperm cryopreservation has immense potential and serves as a powerful tool in the field of assisted reproductive technology. Slow-freezing protocol has been routinely used for cryopreservation of human spermatozoa. This method exerts detrimental effect on spermatozoa that leads to a significant decrease in sperm viability and motility and ultimately in decreased fertilization potential. Whether sperm is cryopreserved as a fertility preservation measure or as a backup for assisted reproduction, the recovery rate of functionally competent spermatozoa is critical. The exact nature of cryodamage stills remains to be elucidated; however, major causes include osmotic imbalance, hypothermic injury, loss of membrane integrity, and extracellular ice crystal formation. Vitrification, an ultrarapid method of cryopreservation, is now considered as a potential alternative to slow freezing. Vitrification involves direct immersion of the cells into liquid nitrogen. It makes use of high concentration of the cryoprotectant thus creating a vitrified glass-like state, thus preventing the formation of ice crystals. The present chapter includes the fundamentals of cryobiology, benefits and limitations of sperm vitrification, and finally its clinical applications and outcome.
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Kagalwala, S. (2015). Sperm Vitrification. In: Allahbadia, G., Kuwayama, M., Gandhi, G. (eds) Vitrification in Assisted Reproduction. Springer, New Delhi. https://doi.org/10.1007/978-81-322-1527-1_4
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DOI: https://doi.org/10.1007/978-81-322-1527-1_4
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