» Articles » PMID: 26848960

Development of Cheaper Embryo Vitrification Device Using the Minimum Volume Method

Overview
Journal PLoS One
Date 2016 Feb 6
PMID 26848960
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

This study was designed to compare the efficiency of the Cryotop and Calibrated plastic inoculation loop (CPIL) devices for vitrification of rabbit embryos on in vitro development and implantation rate, offspring rate at birth and embryonic and fetal losses. CPIL is a simple tool used mainly by microbiologists to retrieve an inoculum from a culture of microorganisms. In experiment 1, embryos were vitrified using a Cryotop device and a CPIL device. There were no significant differences in hatched/hatching blastocyst stage rates after 48 h of culture among the vitrified groups (62 ± 4.7% and 62 ± 4.9%, respectively); however, the rates were significantly lower (P<0.05) than those of the fresh group (95 ± 3.4%). In experiment 2, vitrified embryos were transferred using laparoscopic technique. The number of implanted embryos was estimated by laparoscopy as number of implantation sites at day 14 of gestation. At birth, total offspring were recorded. Embryonic and fetal losses were calculated as the difference between implanted embryos and embryos transferred and total born at birth and implanted embryos, respectively. The rate of implantation and development to term was similar between both vitrification devices (56 ± 7.2% and 50 ± 6.8% for implantation rate and 40 ± 7.1% and 35 ± 6.5% for offspring rate at birth); but significantly lower than in the fresh group (78 ± 6.6% for implantation rate and 70 ± 7.2% for offspring rate at birth, P<0.05). Likewise, embryonic losses were similar between both vitrification devices (44 ± 7.2% and 50 ± 6.8%), but significantly higher than in the fresh group (23 ± 6.6%, P < 0.05). However, fetal losses were similar between groups (10 ± 4.4%, 15 ± 4.8% and 8 ± 4.2%, for vitrified, Cryotop or CPIL and fresh, respectively). These results indicate that the CPIL device is as effective as the Cryotop device for vitrification of rabbit embryos, but at a cost of €0.05 per device.

Citing Articles

Three live births after human embryo vitrification with the use of aluminum oxide as an intermediate cooling agent: a case report.

Todorov P, Hristova E, Petrova N, Milachich T F S Rep. 2024; 5(2):145-151.

PMID: 38983741 PMC: 11228792. DOI: 10.1016/j.xfre.2024.01.003.


Zygote cryobanking applied to CRISPR/Cas9 microinjection in mice.

Schlapp G, Meikle M, Porfido J, Menchaca A, Crispo M PLoS One. 2024; 19(7):e0306617.

PMID: 38980864 PMC: 11232997. DOI: 10.1371/journal.pone.0306617.


A 3D-Printed Large Holding Capacity Device for Minimum Volume Cooling Vitrification of Embryos in Prolific Livestock Species.

Marco-Jimenez F, Garcia-Dominguez X, Garcia-Valero L, Vicente J Animals (Basel). 2023; 13(5).

PMID: 36899646 PMC: 10000242. DOI: 10.3390/ani13050791.


Genetically Modified Rabbits for Cardiovascular Research.

Fan J, Wang Y, Chen Y Front Genet. 2021; 12:614379.

PMID: 33603774 PMC: 7885269. DOI: 10.3389/fgene.2021.614379.


Leptin improves the in vitro development of preimplantation rabbit embryos under oxidative stress of cryopreservation.

Alshaheen T, Awaad M, Mehaisen G PLoS One. 2021; 16(2):e0246307.

PMID: 33529203 PMC: 7853501. DOI: 10.1371/journal.pone.0246307.


References
1.
Casillas F, Ducolomb Y, Lemus A, Cuello C, Betancourt M . Porcine embryo production following in vitro fertilization and intracytoplasmic sperm injection from vitrified immature oocytes matured with a granulosa cell co-culture system. Cryobiology. 2015; 71(2):299-305. DOI: 10.1016/j.cryobiol.2015.08.003. View

2.
Moce M, Blasco A, Santacreu M . In vivo development of vitrified rabbit embryos: effects on prenatal survival and placental development. Theriogenology. 2010; 73(5):704-10. DOI: 10.1016/j.theriogenology.2009.11.010. View

3.
Besenfelder U, Brem G . Laparoscopic embryo transfer in rabbits. J Reprod Fertil. 1993; 99(1):53-6. DOI: 10.1530/jrf.0.0990053. View

4.
Kuwayama M, Vajta G, Kato O, Leibo S . Highly efficient vitrification method for cryopreservation of human oocytes. Reprod Biomed Online. 2005; 11(3):300-8. DOI: 10.1016/s1472-6483(10)60837-1. View

5.
Roy T, Brandi S, Tappe N, Bradley C, Vom E, Henderson C . Embryo vitrification using a novel semi-automated closed system yields in vitro outcomes equivalent to the manual Cryotop method. Hum Reprod. 2014; 29(11):2431-8. DOI: 10.1093/humrep/deu214. View