Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (17)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Chi, H.-J.
Right arrow Articles by Chung, K.-S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chi, H.-J.
Right arrow Articles by Chung, K.-S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 17, No. 8, 2146-2151, August 2002
© 2002 European Society of Human Reproduction and Embryology

Cryopreservation of human embryos using ethylene glycol in controlled slow freezing

Hee-Jun Chi1,3, Jung-Jin Koo1, Moon-Young Kim1, Jin-Young Joo1, Sang-Sik Chang1 and Kil-Saeng Chung2

1 IVF Center, Hanna Women's Clinic and 2 Department of Animal Sciences, Kon-Kuk University, Seoul, Korea

BACKGROUND: Ethylene glycol (EG) has been successfully used as a cryoprotectant for vitrification of mammalian formula embryos (including human embryos) due to its low formula weight and high permeation into cells compared with other cryoprotectants, including propylene glycol (PROH). This study was carried out to evaluate the permeation and toxicity of EG and to investigate the effects of its use in a slow-freezing protocol on post-thaw development of mouse embryos and on pregnancy outcome of frozen human embryos. METHODS: Spare human embryos after embryo transfer were cryopreserved using 1.5 mol/l EG or PROH using a slow-freezing protocol which had been tested previously in mouse experiments. RESULTS: The post-thaw survival rate of human embryos in the EG group (80.6%) was significantly higher than that in the PROH group (65.2%, P < 0.05). The implantation and clinical pregnancy rates of human embryos in the EG group (20.3 and 46.9%) were significantly higher than those in the PROH group (7.5 and 24.6%, P < 0.05). CONCLUSIONS: Ethylene glycol may be a good substitute for PROH to cryopreserve human embryos using a slow-freezing protocol.

Key words: ethylene glycol/permeation/pregnancy outcome/survival rate/toxicity

3 To whom correspondence should be addressed at: Hanna Women's Clinic, 1499-5, Seocho-dong, Seocho-gu, Seoul, 137-070, Korea. E-mail: hanna129{at}hanmail.net


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum ReprodHome page
J. H. Moon, J. R. Lee, B. C. Jee, C. S. Suh, S. H. Kim, H. J. Lim, and H. K. Kim
Successful vitrification of human amnion-derived mesenchymal stem cells
Hum. Reprod., August 1, 2008; 23(8): 1760 - 1770.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
S. Y. Ha, B. C. Jee, C. S. Suh, H. S. Kim, S. K. Oh, S. H. Kim, and S. Y. Moon
Cryopreservation of human embryonic stem cells without the use of a programmable freezer
Hum. Reprod., July 1, 2005; 20(7): 1779 - 1785.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
V. Frederickx, A. Michiels, E. Goossens, G. De Block, A.C. Van Steirteghem, and H. Tournaye
Recovery, survival and functional evaluation by transplantation of frozen-thawed mouse germ cells
Hum. Reprod., April 1, 2004; 19(4): 948 - 953.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
H. Jericho, L. Wilton, D. A. Gook, and D. H. Edgar
A modified cryopreservation method increases the survival of human biopsied cleavage stage embryos
Hum. Reprod., March 1, 2003; 18(3): 568 - 571.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.