alexa Evaluation of a New Vitrification Protocol for Oocyte C
ISSN: 2161-0436

Human Genetics & Embryology
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Evaluation of a New Vitrification Protocol for Oocyte Cryopreservation

Maria Panagopoulou1, Konstantinos Charalabopoulos1, Demetrios N. Papachristou2, Elias Tsakos3 and Byron Asimakopoulos1*

1Laboratory of Physiology, School of Medicine, Democritus University of Thrace, Greece

2Division of Endocrinology, Metropolitan Hospital, Faliron, Athens, Greece

3Gynaecology and Fertility Centre, Thessaloniki, Greece

*Corresponding Author:
Byron Asimakopoulos, PhD
Assistant Professor
Laboratory of Physiology
School of Medicine
Democritus University of Thrace
68100 Alexandroupolis, Greece
Tel: +30 2551030538
Fax: +30 2551030504
E-mail: [email protected]

Received Date: February 20, 2013; Accepted Date: March 20, 2013; Published Date: March 22, 2013

Citation: Panagopoulou M, Charalabopoulos K, Papachristou DN, Tsakos E, Asimakopoulos B (2013) Evaluation of a New Vitrification Protocol for Oocyte Cryopreservation. Human Genet Embryol 3:103. doi: 10.4172/2161-0436.1000103

Copyright: © 2013 Panagopoulou M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



During the last years, vitrification was introduced into clinical practice. Although vitrification counts several years of experimental studies, this method is still under development. In this study, a new vitrification protocol was evaluated. Materials and methods: An experimental study conducted in a University laboratory evaluated a new, short vitrification protocol including two vitrification and two thawing solutions, made in-house. The vitrification solutions contained dimethyl sulfoxide, ethylenoglycol and human serum albumin. The thawing solutions contained sucrose and human serum albumin. Rat oocytes, allocated in two groups, were used. In the control group, the oocytes were vitrified using a standard protocol. In the experimental group, the oocytes were vitrified using the new protocol. The endpoint was the survival rate of the oocytes just after thawing and 48 hours later. Results: The survival rate just after thawing was similar in the two groups (62.5% for the control group and 60% for the experimental group, p=0.18). However after 48 hour incubation, there was a significant difference between the two groups: 55% survival for the control group and 45% for the experimental group (p=0.008). Conclusion: The two vitrification protocols achieved similar survival rates just after thawing. However, after 48 hours incubation of thawed oocytes, the standard method had higher survival rates, than the in-house one.

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