Literature DB >> 21540134

Numerical simulation of cooling rates in vitrification systems used for oocyte cryopreservation.

M Sansinena1, M V Santos, N Zaritzky, J Chirife.   

Abstract

Oocyte cryopreservation is of key importance in the preservation and propagation of germplasm. Interest in oocyte cryopreservation has increased in recent years due to the application of assisted reproductive technologies in farm animals such as in vitro fertilization, nuclear transfer and the need for the establishment of ova/gene banks worldwide. However, the cryopreservation of the female gamete has been met with limited success mainly due to its small surface-area:volume ratio. In the past decade, several vitrification devices such as open pulled straws (OPS), fine and ultra fine pipette tips, nylon loops and polyethylene films have been introduced in order to manipulate minimal volumes and achieve high cooling rates. However, experimental comparison of cooling rates presents difficulties mainly because of the reduced size of these systems. To circumvent this limitation, a numerical simulation of cooling rates of various vitrification systems immersed in liquid nitrogen was conducted solving the non-stationary heat transfer partial differential equation using finite element method. Results indicate the nylon loop (Cryoloop®) is the most efficient heat transfer system analyzed, with a predicted cooling rate of 180,000°C/min for an external heat transfer coefficient h= 1000 W/m(2)K when cooling from 20 to -130°C; in contrast, the open pulled straw method (OPS) showed the lowest performance with a cooling rate of 5521°C/min considering the same value of external heat transfer coefficient. Predicted cooling rates of Miniflex® and Cryotop® (polyethylene film system) were 6164 and 37,500°C/min, respectively, for the same heat transfer coefficient.
Copyright © 2011. Published by Elsevier Inc.

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Year:  2011        PMID: 21540134     DOI: 10.1016/j.cryobiol.2011.04.006

Source DB:  PubMed          Journal:  Cryobiology        ISSN: 0011-2240            Impact factor:   2.487


  6 in total

1.  Large-volume vitrification of human biopsied and non-biopsied blastocysts: a simple, robust technique for cryopreservation.

Authors:  Michael L Reed; Al-Hasen Said; Douglas J Thompson; Charles L Caperton
Journal:  J Assist Reprod Genet       Date:  2014-12-03       Impact factor: 3.412

2.  Cryoprotectant-free cryopreservation of mammalian cells by superflash freezing.

Authors:  Yoshitake Akiyama; Masato Shinose; Hiroki Watanabe; Shigeru Yamada; Yasunari Kanda
Journal:  Proc Natl Acad Sci U S A       Date:  2019-04-01       Impact factor: 11.205

3.  A 3-D printed vitrification device integrated with French straws.

Authors:  Nolan J Tiersch; Jacqueline Paulsen; Yue Liu; Terrence R Tiersch
Journal:  HardwareX       Date:  2022-10-04

4.  Open versus closed vitrification system of human oocytes and embryos: a systematic review and meta-analysis of embryologic and clinical outcomes.

Authors:  Hongcai Cai; Jean Damascene Niringiyumukiza; Yamin Li; Qiaohong Lai; Yinzhao Jia; Ping Su; Wenpei Xiang
Journal:  Reprod Biol Endocrinol       Date:  2018-12-06       Impact factor: 5.211

5.  Comparing the effects of a commercial and a prototype vitrification medium on meiotic spindle morphology and survival rate of mouse oocytes.

Authors:  Iara Gonçalves Roberto Viana; Alessandra Aparecida Vireque; Paula Andrea Navarro
Journal:  JBRA Assist Reprod       Date:  2022-08-04

6.  Comparison of the microdrop and minimum volume cooling methods for vitrification of porcine in vitro-produced zygotes and blastocysts after equilibration in low concentrations of cryoprotectant agents.

Authors:  Van Khanh Nguyen; Huong Thi Thu Vu; Huong Thi Nguyen; Huu Xuan Quan; Lan Doan Pham; Kazuhiro Kikuchi; Son Thanh Nguyen; Tamas Somfai
Journal:  J Reprod Dev       Date:  2018-08-10       Impact factor: 2.214

  6 in total

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