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  4. Slow freezing or vitrification of oocytes: Their effects on survival and meiotic spindles, and the time schedule for clinical practice
 
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Slow freezing or vitrification of oocytes: Their effects on survival and meiotic spindles, and the time schedule for clinical practice

Journal
Taiwanese Journal of Obstetrics and Gynecology
Journal Volume
48
Journal Issue
1
Pages
15-22
Date Issued
2009
Author(s)
SHEE-UAN CHEN  
YU-SHIH YANG  
DOI
10.1016/S1028-4559(09)60030-9
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/460295
Abstract
Both the slow-freezing method with increased sucrose concentration and new vitrification techniques significantly improve the results of cryopreservation of human oocytes. The recent perfection for vitrification includes the concepts of increase of cooling and warming rates using minimum volume methods, and decrease of toxicity by reducing the concentration of cryoprotectants. In the recent literature, the survival of cryopreserved oocytes ranged from 74% to 90% using the slow-freezing method and from 84% to 99% by vitrification. Overall, the survival rate of oocytes from vitrification (95%, 899/948) appeared higher than that of the slow-freezing method (75%, 1,275/1,683). The microtubules of meiotic spindles are vulnerable to the thermal changes and will depolymerize. After incubation, the microtubules repolymerize. Spindle recovery is faster after vitrification than slow freezing. Even so, after 3 hours of incubation, spindle recuperation is similar between vitrification and slow freezing. Considering both aspects of spindle recovery and oocyte aging, the time schedule for oocyte cryopreservation program makes fertilization in the optimal time. Intracytoplasmic sperm injection is performed for oocytes at 3 hours of post-thaw incubation from the slow-freezing method and 2 hours from vitrification, with restoration of meiotic spindles. The pregnancy potential of cryopreserved oocytes is comparable to that of fresh oocytes or frozen embryos. Cryopreservation of oocytes would importantly contribute to oocyte donation and preservation of fertility for cancer patients.
SDGs

[SDGs]SDG3

Other Subjects
cell survival; clinical practice; cryopreservation; fertilization in vitro; freezing; human; incubation time; intracytoplasmic sperm injection; microtubule; mitosis spindle; nonhuman; oocyte; oocyte donation; pregnancy; review; temperature acclimatization; vitrification
Type
review

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