Ovarian large cortex piece vitrified cryopreservation protection liquid and cryopreservation method thereof
A vitrification and protection solution technology, which is applied in the preservation, application, and animal husbandry of human or animal bodies, and can solve problems such as the method of vitrification and protection solution freezing for large ovarian cortex slices, and achieve good cryopreservation effect , shorten transplantation, improve the effect of follicle survival
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Embodiment 1
[0044] Example 1: Method for vitrification of large ovarian cortex slices
[0045] (1) Vitrification
[0046] The large cortex samples of sheep ovaries aged 2 to 6 months were fixed to a thickness of 2 mm, and were divided into:
[0047] Sample (40mm 3 =5mm×4mm×2mm),
[0048] Medium sample (80mm 3 =10mm×4mm×2mm),
[0049] Large sample (160mm 3 =10mm×8mm×2mm),
[0050] Two-step osmotic equilibrium method was used for vitrification, and the whole process was carried out at room temperature (22-24°C):
[0051] The first step is pre-osmosis balance: 1.5mol / L ethylene glycol (EG) + 20% calf serum (ICS), small sample: 15min, medium sample: 20min, large sample: 25min;
[0052] The second step is vitrification osmotic balance: EG 5.5 / 30 solution (the specific formula of EG 5.5 / 30 solution is: EG+30% polysucrose+0.5mol / L sucrose), small sample: 5min~8min, medium sample: 10min~13min , Large sample: 17min~20min (the vitrification penetration equilibrium time of each cortical slic...
Embodiment 2
[0065] Example 2: Vitrification of sheep ovary large cortex slices
[0066] In the present invention, suitable gonadotropins are added to vitrification solution of 5.5mol / L EG+30% polysucrose+0.5mol / L sucrose. Among them, sheep were supplemented with 10 μg / mL FSH. Compared with the group without gonadotropin, no matter in vitro culture or in vivo transplantation after freezing, the follicle development, endothelial growth factor increased, and the number of surviving follicles in the group with gonadotropin were significantly different.
[0067] 1.1 Materials
[0068] 1.1.1 Sheep ovary
[0069] Sheep ovaries came from discarded ovaries of 2-6 month-old sheep slaughtered in Najiahu Halal Beef and Mutton Slaughterhouse, Yongning County, Yinchuan City, Ningxia, and were sent back to the laboratory in sterile culture medium at 4°C within 2 hours after slaughter.
[0070] 1.1.2 Experimental animals
[0071] BALB / CA male nude mice aged 8-12 weeks were provided by Beijing Weitong...
Embodiment 3
[0102] Example 3: Relevant research on the reduction of follicle apoptosis by FSH intervention at different periods of vitrified cryopreservation of mouse ovaries
[0103] In the present invention, suitable gonadotropin is added to the vitrification solution of 5.5 mol / L EG+30% polysucrose+0.5 mol / L sucrose. The mice were supplemented with 0.3IU / mL FSH. As a survival factor of follicles, FSH not only has an anti-apoptotic effect, but also participates in the development and maturation of follicles. The development of follicles is inseparable from the cell communication between gap junctions, and Cx43 can enhance this intercellular signal exchange. Therefore, this study intervened with FSH in different stages of vitrification, and observed the protective effect of FSH on ovarian vitrification by detecting the expression of Cx43 and activated caspase-3 (active caspase-3).
[0104] 1.1 Materials
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