Literature DB >> 11448116

Vitrification of large quantities of immature bovine oocytes using nylon mesh.

H Matsumoto1, J Y Jiang, T Tanaka, H Sasada, E Sato.   

Abstract

Vitrification of oocytes and embryos has recently been improved using new physical supports such as electron microscope (EM) grids, open-pulled straws, and cryoloops. However, the number of samples per container was restricted in each of these methods. In the present study, to develop a novel simple technique for vitrification of large quantities of oocytes or embryos, we examined vitrification of large quantities of immature bovine oocytes using nylon mesh as a novel container. As many as 65 oocyte-cumulus cell complexes could be placed on nylon mesh for vitrification compared with 15 per EM grid. Recovery rates were higher when using nylon mesh than EM grids, while fertilization and development rates were not different. These results indicated that vitrification using nylon mesh is useful and offers a new way to cryopreserve large numbers of oocytes.

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Year:  2001        PMID: 11448116     DOI: 10.1006/cryo.2001.2309

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


  21 in total

1.  Oocyte vitrification: advances, progress and future goals.

Authors:  Ri-Cheng Chian; Yao Wang; Yi-Ran Li
Journal:  J Assist Reprod Genet       Date:  2014-01-30       Impact factor: 3.412

Review 2.  Cryopreservation and in vitro maturation of germinal vesicle stage oocytes of animals for application in assisted reproductive technology.

Authors:  Ken-Ichi Yamanaka; Nobuya Aono; Hiroaki Yoshida; Eimei Sato
Journal:  Reprod Med Biol       Date:  2007-05-14

3.  Advances in the cryopreservation of mammalian oocytes and embryos: Development of ultrarapid vitrification.

Authors:  Magosaburo Kasai
Journal:  Reprod Med Biol       Date:  2002-05-16

4.  The effect of minimal concentration of ethylene glycol (EG) combined with polyvinylpyrrolidone (PVP) on mouse oocyte survival and subsequent embryonic development following vitrification.

Authors:  Yao Wang; Osamu Okitsu; Xiao-Ming Zhao; Yun Sun; Wen Di; Ri-Cheng Chian
Journal:  J Assist Reprod Genet       Date:  2013-11-21       Impact factor: 3.412

Review 5.  Cryopreservation in ART and concerns with contamination during cryobanking.

Authors:  Mark G Larman; Shu Hashimoto; Yoshiharu Morimoto; David K Gardner
Journal:  Reprod Med Biol       Date:  2014-02-05

6.  Development of vitrified-warmed mouse embryos co-cultured with polarized or non-polarized uterine epithelial cells using sequential culture media.

Authors:  Mehri Azadbakht; Mojtaba Rezazadeh Valojerdi
Journal:  J Assist Reprod Genet       Date:  2008-06-18       Impact factor: 3.412

7.  Vitrification of bovine oocytes: implications of follicular size and sire on the rates of embryonic development.

Authors:  Vahida M Anchamparuthy; Arindam Dhali; Whitney M Lott; Ronald E Pearson; Francis C Gwazdauskas
Journal:  J Assist Reprod Genet       Date:  2009-11-11       Impact factor: 3.412

8.  Solid-surface vitrification is an appropriate and convenient method for cryopreservation of isolated rat follicles.

Authors:  Weijie Xing; Canquan Zhou; Jiang Bian; Markus Montag; Yanwen Xu; Yubin Li; Tao Li
Journal:  Reprod Biol Endocrinol       Date:  2010-05-11       Impact factor: 5.211

9.  The dominance of warming rate over cooling rate in the survival of mouse oocytes subjected to a vitrification procedure.

Authors:  Shinsuke Seki; Peter Mazur
Journal:  Cryobiology       Date:  2009-05-07       Impact factor: 2.487

10.  Vitrification: an effective new approach to oocyte banking and preserving fertility in cancer patients.

Authors:  A Cobo; J Domingo; S Pérez; J Crespo; J Remohí; A Pellicer
Journal:  Clin Transl Oncol       Date:  2008-05       Impact factor: 3.405

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