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A compact, high-throughput semi-automated embryo vitrification system based on hydrogel.
Wang, Shanshan; Chen, Lei; Fang, Junshun; Sun, Haixiang.
Afiliação
  • Wang S; Center for Reproductive Medicine and Obstetrics and Gynecology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.; Center for Molecular Reproductive Medicine, Nanjing University, Nanjing, PR China.
  • Chen L; Center for Reproductive Medicine and Obstetrics and Gynecology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.; Center for Molecular Reproductive Medicine, Nanjing University, Nanjing, PR China.
  • Fang J; Center for Reproductive Medicine and Obstetrics and Gynecology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.; Center for Molecular Reproductive Medicine, Nanjing University, Nanjing, PR China.
  • Sun H; Center for Reproductive Medicine and Obstetrics and Gynecology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.; Center for Molecular Reproductive Medicine, Nanjing University, Nanjing, PR China.. Electronic address: stevensunz@163.com.
Reprod Biomed Online ; 48(5): 103769, 2024 May.
Article em En | MEDLINE | ID: mdl-38492415
ABSTRACT
RESEARCH QUESTION What is the efficiency and efficacy of the novel Biorocks semi-automated vitrification system, which is based on a hydrogel?

DESIGN:

This comparative experimental laboratory study used mouse model and human day 6 blastocysts. Mouse oocytes and embryos were quality assessed post-vitrification.

RESULTS:

The Biorocks system successfully automated the solution exchanges during the vitrification process, achieving a significantly improved throughput of up to 36 embryos/oocytes per hour. Using hydrogel for cryoprotective agent delivery, 12 vessels could be processed simultaneously, fitting comfortably within an assisted reproductive technology (ART) workstation. In tests involving the cryopreservation of oocytes and embryos, the system yielded outcomes equivalent to the manual Cryotop method. For example, the survival rate for mouse oocytes was 98% with the Biorocks vitrification system (n = 46) and 95% for the manual Cryotop method (n = 39), of which 46% and 41%, respectively, progressed to blastocysts on day 5 after IVF. CC-grade day 6 human blastocysts processed with the Biorocks system (n = 39) were associated with a 92% 2 h re-expansion rate, equivalent to the 90% with Cryotop (n = 30). The cooling/warming rates achieved by the Biorocks system were 31,900°C/minute and 24,700°C/minute, respectively. Oocyte quality was comparable or better post-vitrification for Biorocks than Cryotop.

CONCLUSIONS:

The Biorocks semi-automated vitrification system offers enhanced throughput without compromising the survival and developmental potential of oocytes and embryos. This innovative system may help to increase the efficiency and standardization of vitrification in ART clinics. Further investigations are needed to confirm its efficacy in a broader clinical context.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Criopreservação / Vitrificação Limite: Animals / Female / Humans Idioma: En Revista: Reprod Biomed Online Assunto da revista: MEDICINA REPRODUTIVA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Criopreservação / Vitrificação Limite: Animals / Female / Humans Idioma: En Revista: Reprod Biomed Online Assunto da revista: MEDICINA REPRODUTIVA Ano de publicação: 2024 Tipo de documento: Article