Literature DB >> 19603263

Closed-system solid surface vitrification versus slow programmable freezing of mouse 2-cell embryos.

Teraporn Vutyavanich1, Opas Sreshthaputra, Waraporn Piromlertamorn, Siriporn Nunta.   

Abstract

PURPOSE: To compare closed-system solid surface vitrification with slow freezing.
METHODS: Mouse 2-cell embryos (n = 348) were divided into vitrification, slow freezing and non-frozen groups. For vitrification, embryos were exposed to 10% ethylene glycol (EG), 10% dimethylsulfoxide (DMSO) and 10% fetal bovine serum (FBS) in phosphate-buffered saline (PBS) for 10 min, then transferred into 17.5% EG, 17.5% DMSO, 0.25 M trehalose and 10% FBS in PBS. They were placed on hemi-straws and inserted into 0.5 ml straws inside a previously cooled aluminum cylinder. Slow freezing was done in straws by the conventional method.
RESULTS: Vitrified embryos had significantly higher survival, further cleavage and blastocyst formation rates than those in the slow freezing group (p < 0.001) and were comparable to controls. Blastocysts in the vitrification and control groups had significantly more cells than those in the slow freezing group (p < 0.05).
CONCLUSIONS: Closed-system vitrification was more effective than conventional slow freezing.

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Year:  2009        PMID: 19603263      PMCID: PMC2719071          DOI: 10.1007/s10815-009-9324-8

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  20 in total

1.  Effect of freezing rate and exposure time to cryoprotectant on the development of mouse pronuclear stage embryos.

Authors:  M A Nowshari; G Brem
Journal:  Hum Reprod       Date:  2001-11       Impact factor: 6.918

2.  Blastocyst development after vitrification of multipronuclear zygotes using the Flexipet denuding pipette.

Authors:  Juergen Liebermann; Michael J Tucker; James R Graham; Taylor Han; Alana Davis; Michael J Levy
Journal:  Reprod Biomed Online       Date:  2002 Mar-Apr       Impact factor: 3.828

3.  A strategy for rapid cooling of mouse embryos within a double straw to eliminate the risk of contamination during storage in liquid nitrogen.

Authors:  L L Kuleshova; J M Shaw
Journal:  Hum Reprod       Date:  2000-12       Impact factor: 6.918

4.  Microbial contamination of embryos and semen during long term banking in liquid nitrogen.

Authors:  A Bielanski; H Bergeron; P C K Lau; J Devenish
Journal:  Cryobiology       Date:  2003-04       Impact factor: 2.487

5.  Comparison of the effects of controlled-rate cryopreservation and vitrification on 2-cell mouse embryos and their subsequent development.

Authors:  H Uechi; O Tsutsumi; Y Morita; Y Takai; Y Taketani
Journal:  Hum Reprod       Date:  1999-11       Impact factor: 6.918

6.  Nuclear accumulation of cyclin B1 in mouse two-cell embryos is controlled by the activation of Cdc2.

Authors:  A Ohashi; N Minami; H Imai
Journal:  Biol Reprod       Date:  2001-10       Impact factor: 4.285

7.  Stepwise in-straw dilution and direct transfer using open pulled straws (OPS) in the mouse: a potential model for field manipulation of vitrified embryos.

Authors:  Qi-En Yang; Yun-Peng Hou; Guang-Bin Zhou; Zhong-Qiang Yang; Shi-En Zhu
Journal:  J Reprod Dev       Date:  2006-11-29       Impact factor: 2.214

8.  Improvement of development of vitrified two-cell mouse embryos by vero cell coculture.

Authors:  Mojtaba Rezazadeh Valojerdi; Mansoureh Movahedin; Ahmad Hosseini
Journal:  J Assist Reprod Genet       Date:  2002-01       Impact factor: 3.412

9.  Cryopreservation of goat oocytes and in vivo derived 2- to 4-cell embryos using the cryoloop (CLV) and solid-surface vitrification (SSV) methods.

Authors:  Isabelle Begin; Bhim Bhatia; Hernan Baldassarre; Andras Dinnyes; Carol L Keefer
Journal:  Theriogenology       Date:  2003-04-15       Impact factor: 2.740

Review 10.  Vitrification can be more favorable than slow cooling.

Authors:  Lilia L Kuleshova; Alex Lopata
Journal:  Fertil Steril       Date:  2002-09       Impact factor: 7.329

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  2 in total

1.  Different chromatin and energy/redox responses of mouse morulae and blastocysts to slow freezing and vitrification.

Authors:  Bence Somoskoi; Nicola A Martino; Rosa A Cardone; Giovanni M Lacalandra; Maria E Dell'Aquila; Sandor Cseh
Journal:  Reprod Biol Endocrinol       Date:  2015-03-24       Impact factor: 5.211

2.  Vitrification preserves chromatin integrity, bioenergy potential and oxidative parameters in mouse embryos.

Authors:  Nicola A Martino; Maria E Dell'aquila; Rosa A Cardone; Bence Somoskoi; Giovanni M Lacalandra; Sandor Cseh
Journal:  Reprod Biol Endocrinol       Date:  2013-04-03       Impact factor: 5.211

  2 in total

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