Literature DB >> 16792858

Are programmable freezers still needed in the embryo laboratory? Review on vitrification.

Gábor Vajta1, Zsolt Péter Nagy.   

Abstract

The predictable answer to the provocative question of whether programmable freezers are still needed in the embryo laboratory is an even more provocative 'no'. However, such a radical statement needs strong support. Based on the extensive literature of the past 5 years, the authors collected arguments either supporting or contradicting their opinion. After an overview of the causes of cryoinjuries and strategies to eliminate them, the evolution of vitrification methods is discussed. Special attention is paid to the biosafety issues. The authors did not find any circumstance in oocyte or embryo cryopreservation where slow freezing offers considerable advantages compared with vitrification. In contrast, the overwhelming majority of published data prove that the latest vitrification methods are more efficient and reliable than any version of slow freezing. Application of the proper vitrification methods increases the efficiency of long-term storage of stem cells and opens new perspectives in cryopreservation of oocytes, both for IVF and somatic cell nuclear transfer. However, lack of support from regulatory authorities, and conservative approachs regarding novel techniques can slow down the implementation of vitrification. The opinion of the authors is that vitrification is the future of cryopreservation. The public have the final say in whether they want and allow this future to arrive.

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Year:  2006        PMID: 16792858     DOI: 10.1016/s1472-6483(10)61091-7

Source DB:  PubMed          Journal:  Reprod Biomed Online        ISSN: 1472-6483            Impact factor:   3.828


  63 in total

1.  Can fresh embryo transfers be replaced by cryopreserved-thawed embryo transfers in assisted reproductive cycles? A randomized controlled trial.

Authors:  Abbas Aflatoonian; Homa Oskouian; Shahnaz Ahmadi; Leila Oskouian
Journal:  J Assist Reprod Genet       Date:  2010-04-06       Impact factor: 3.412

2.  Emerging technologies in medical applications of minimum volume vitrification.

Authors:  Xiaohui Zhang; Paolo N Catalano; Umut Atakan Gurkan; Imran Khimji; Utkan Demirci
Journal:  Nanomedicine (Lond)       Date:  2011-08       Impact factor: 5.307

3.  Human cleavage-stage embryo vitrification is comparable to slow-rate cryopreservation in cycles of assisted reproduction.

Authors:  Martin Graham Wilding; Clemente Capobianco; Nadia Montanaro; Genc Kabili; Loredana Di Matteo; Enrico Fusco; Brian Dale
Journal:  J Assist Reprod Genet       Date:  2010-07-17       Impact factor: 3.412

4.  Damage to fetal bovine ovarian tissue caused by cryoprotectant exposure and vitrification is mitigated during tissue culture.

Authors:  Lara Mouttham; Joanne E Fortune; Pierre Comizzoli
Journal:  J Assist Reprod Genet       Date:  2015-08-07       Impact factor: 3.412

5.  Intracellular ice and cell survival in cryo-exposed embryonic axes of recalcitrant seeds of Acer saccharinum: an ultrastructural study of factors affecting cell and ice structures.

Authors:  James Wesley-Smith; Patricia Berjak; N W Pammenter; Christina Walters
Journal:  Ann Bot       Date:  2013-12-23       Impact factor: 4.357

6.  The outcome of different post-thawed culture period in frozen-thawed embryo transfer cycle.

Authors:  Lei Guo; Chen Luo; Song Quan; Leining Chen; Hong Li; Yangchun Guo; Zhiming Han; Xianghong Ou
Journal:  J Assist Reprod Genet       Date:  2013-10-25       Impact factor: 3.412

Review 7.  The mammalian ovary from genesis to revelation.

Authors:  Mark A Edson; Ankur K Nagaraja; Martin M Matzuk
Journal:  Endocr Rev       Date:  2009-09-23       Impact factor: 19.871

8.  Vitrification of mouse embryos at 2-cell, 4-cell and 8-cell stages by cryotop method.

Authors:  Junqiang Zhang; Ji Cui; Xiufeng Ling; Xiuling Li; Yuzhu Peng; Xirong Guo; Boon Chin Heng; Guo Qing Tong
Journal:  J Assist Reprod Genet       Date:  2009-12-05       Impact factor: 3.412

9.  Vitrification versus slow freezing gives excellent survival, post warming embryo morphology and pregnancy outcomes for human cleaved embryos.

Authors:  Mojtaba Rezazadeh Valojerdi; Poopak Eftekhari-Yazdi; Leila Karimian; Fatemeh Hassani; Bahar Movaghar
Journal:  J Assist Reprod Genet       Date:  2009-06-10       Impact factor: 3.412

10.  The presence of 1 mM glycine in vitrification solutions protects oocyte mitochondrial homeostasis and improves blastocyst development.

Authors:  Deirdre Zander-Fox; Kara S Cashman; Michelle Lane
Journal:  J Assist Reprod Genet       Date:  2012-12-18       Impact factor: 3.412

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