Post-thaw survival of cryopreserved biological material by hydrostatic pressure challenge
The present invention relates to a method for improving post-thaw survival of cryopreserved biological material comprising applying hydrostatic pressure to said biological material; keeping the said biological material at the hydrostatic pressure for a predetermined time period; releasing the hydrostatic pressure; and freezing the said biological material using any protocol applicable thereto.
1. A method for improving post-thaw survival of cryopreserved viable biological material comprising
(a) applying hydrostatic pressure in the range of 10 to 200 MPa to said viable biological material, optionally according to a predetermined pressure-time profile;
(b) keeping the said viable biological material at the hydrostatic pressure for a predetermined time period;
(c) releasing the hydrostatic pressure;
(d) further cryopreserving the said viable biological material using any protocol applicable thereto,
wherein said biological material is selected from the group consisting of oocytes, sperms, zygotes, morulas, blastocysts, embryos, stem cells and cells of a vertebrate animal.
2. The method according to claim 1 wherein the said hydrostatic pressure is applied for a time period between 1 second and 300 minutes.
3. The method according to claim 2 wherein the said hydrostatic pressure is applied for a time period between 1 second and 150 minutes.
4. The method according to claim 2 wherein the said hydrostatic pressure is applied for a time period between 1 second and 90 minutes.
5. The method according to claim 2 wherein the said hydrostatic pressure is applied for a time period between 1 second and 60 minutes.
6. The method according to claim 1 wherein the pressure is released gradually over a time period between 1 second and 4 hours.
7. The method according to claim 1 wherein the said vertebrate animal is a fish, a bird or a mammal.
8. The method according to claim 7 wherein said vertebrae animal is selected from the group consisting of bovine, equine, caprine, ovine, swine, other livestocks, pets, and primates, including humans.
9. The method according to claim 1 wherein the said hydrostatic pressure is in the range of 10 to 100 MPa.
10. The method according to claim 1 wherein the said hydrostatic pressure is in the range of 30 to 60 MPa.
11. The method according to claim 1 wherein the time period is selected based on the pressure tolerance of the viable biological material.
12. The method according to claim 1 , further comprising before step (a), placing the biological material into a pressurizing device which includes a pressure chamber suitable for receiving the biological material, and means to provide controlled pressure in the range of 10 to 200 MPa.
13. The method according to claim 12 , wherein the pressurizing device comprises means to maintain the pressure for a time period between 1 second and 300 minutes.
14. The method according to claim 12 , wherein a control system is provided for controlling the depressurization of the pressure chamber over a period between 1 second and 4 hours.
15. The method according to claim 1 wherein said biological material is oocytes.
16. The method according to claim 1 wherein said biological material is stem cells.
17. A method for improving post-thaw survival of cryopreserved viable biological material comprising
(a) applying hydrostatic pressure in the range of 10 to 75 MPa 40 MPa to said viable biological material, optionally according to a predetermined pressure-time profile;
(b) keeping the said viable biological material at the hydrostatic pressure for a predetermined time period;
(c) releasing the hydrostatic pressure;
(d) further cryopreserving the said viable biological material using any protocol applicable thereto.
18. The method according to claim 17 wherein said biological material is selected from the group consisting of oocytes, sperms, zygotes, morulas, blastocysts, embryos, stem cells, cells, tissues and organs of a vertebrate animal.