Study on survival rate and hatching rate of mouse embryos after cryopreservation-thawing by vitrification and program freezing
Hu Bo
Abstract
Hu Bo
Abstract
Objective: To study the effect of cryopreservation-thawing mouse embryos by two methods-program freezing and vitrification, we will apply vitrification into cryopreservation human embryos. Methods: 2-cells mouse embryos were collected after giving 6~8 weeks old mouse COH (controlled ovarian hyperstimulation) and mated with male mouse; randomly allocated 685 2-cell embryos into two groups: program freezing and vitrification, then cryopreservation-thawing and incubating these embryos. The survival rate and hatching rate were compared. Results: The survival rates of vitrification and program freezing were 63.82%(224/351), 62.57% (209/334) respectively (P0.05); The hatching rates of vitrification and program freezing were 34.2% (120/351), 31.74% (106/334) respectively (P0.05). This result indicate that there are no significantly difference in vitrification and program freezing. Conclusion: Vitrification seems to be an effective, easy and rapid method for the cryopreservation of two-cell mouse embryos. So vitrification is the most of all perfect techniques for cryopreservating mouse embryos that can be used to replace classical program freezing.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective: To study the effect of cryopreservation-thawing mouse embryos by two methods-program freezing and vitrification, we will apply vitrification into cryopreservation human embryos. Methods: 2-cells mouse embryos were collected after giving 6~8 weeks old mouse COH (controlled ovarian hyperstimulation) and mated with male mouse; randomly allocated 685 2-cell embryos into two groups: program freezing and vitrification, then cryopreservation-thawing and incubating these embryos. The survival rate and hatching rate were compared. Results: The survival rates of vitrification and program freezing were 63.82%(224/351), 62.57% (209/334) respectively (P0.05); The hatching rates of vitrification and program freezing were 34.2% (120/351), 31.74% (106/334) respectively (P0.05). This result indicate that there are no significantly difference in vitrification and program freezing. Conclusion: Vitrification seems to be an effective, easy and rapid method for the cryopreservation of two-cell mouse embryos. So vitrification is the most of all perfect techniques for cryopreservating mouse embryos that can be used to replace classical program freezing.
Key concepts: Vitrification, Cryopreservation, Hatching, Embryo, Andrology, Biology, Cell biology, Animal science