Media solutions and methods for cryopreservation and thawing of in vitro fertilization specimens
View Patent ↗A medium solution which will increase the growth, survival and ultimately the live birth rate of oocytes and embryos which have been or will be subjected to cryopreservation. The solution contains varied amounts of glucose, pyruvates, amino acids, vitamins K5 and C, antioxidants, fatty acids to supply the specimens with the chemical ingredients and uptake requirements required to recover and prosper during and after the cryopreservation process. The solution supplies nutrients to the specimens that will replenish depletion and damage to the specimens and their mitochondria, spindles and structural features, such as cell walls. One formulation addresses the additional requirements of frozen specimens as opposed to the current media solutions and methods which treat the un-frozen specimens the same as the frozen specimens when recovering them from cryopreservation.
1. A medium for cryopreservation and post-cryopreservation thawing of oocyte and embryo specimens, said medium comprising effective amounts of glucose, pryuvates, amino acids, vitamins K5 and C, antioxidants, fatty acids sufficient to supply the specimens with the chemical ingredients and uptake requirements to recover and prosper during and after the cryopreservation process; said medium being operative to supply nutrients which will replenish the specimens after thawing from cryopreservation, and protect the specimen from damage associated with cryopreservation.
2. The medium solution of claim 1 , wherein said fatty acids include lipoic acid and linoleic acid.
3. The medium of claim 2 , wherein said lipoic acid is present in a concentration range of about 0.000004 g/L to about 0.000008 g/L.
4. The medium of claim 3 , wherein said linoleic acid is present in a concentration range of about 0.0000025 g/L to about 0.000010 g/L.
5. The medium of claim 1 which includes a HEPES or MOPS buffer.
6. A medium for cryopreservation and post-cryopreservation thawing of oocyte and embryo specimens, said medium comprising effective amounts of glucose, pyruvates, amino acids, vitamins K and C, antioxidants, and fatty acids sufficient to supply the specimens with the chemical ingredients and uptake requirements to recover and prosper during and after the cryopreservation process; said medium being operative to supply nutrients which will replenish the specimens after thawing from cryopreservation and protect the specimens from damage associated with cryopreservation.