The ICR mice bone marrow nucleated cells(BMNC) were cryopreserved by vitrification. After cryopreservation for 1,5,10,20 and 30 days, the individual samples were separately thawed in 38℃ water bath or by microwave treatment in 300mL 10℃ water under microwave power of 800W, frequency of 2450MHz and thawing duration of 80s, following which the viability of BMNC was assayed.
Methods Rabbit carotids were harvested and cryopreserved in cryoprotective medium containing 1.5 mol/L 1,2-propanediol (PROH) and thawed slowly in ice bag precooled in liquid nitrogen.
Objective To assess the different regenerative capabilities and ultrastructures of the smooth muscle cells(SMCs) of the cryopreserved rabbit carotids with dimethyl sulfoxide (Me_2SO) and 1,2-propanediol (PROH).
Integrating the functions of sample preparation and viability detection, the concept of biochip technology was introduced to the field of cryopreservation, aiming at quickly finding an optimum freezing and thawing program.
The study demonstrated that a biochip with integrated automatic loading and inspection units opens the possibility of a massive optimization of the complex cryopreservation program in a quicker and more economical way.
Objective To evaluate the functional metabolism of cryopreserved homologous heart valve and blood vessels. Method Heart valves and blood vessels were taken from cadavers and frozen with two step method in -196℃ for long term storage. The levels of lactate dehydrogenase(LDH), aspartate transaminase(AST) and the sugar consumption of the cultured frozen thawed samples were measured and compared with that of the fresh tissue. Result All the cryopreserved homografts(23 ̄1297days) had growth ability and meta...
Objective Allosclera has been widely used in ophthalmologic clinic with alcohol as nonviable preservation agent. To explore a viable preservation method for sclera, clinical and experimental studies were carried out on long term cryopreserved viable sclera. Method The enzymic activities of SDH, G 6 PD, LDH, G 6 P and ATP of rabbit sclerae cryopreserved for 53, 362, and 1123 days were determined, and experimental scleral buckling procedures and scleral reinforcement operations with cryopreserved rabb...
To investigate the protective effects and their mechanism of chondroitin sulfate (CS) on corneal endothelial cells in corneal cryopreservation.Thirty six new born bovine corneas were divided into a control group and five experiment groups averasely (six corneas for each group).Cryoprotectant for control group was 7 5%dimethyl sulfoxide (DMSO),while cryoprotectants for experiment groups I to Ⅳwere respectively 0 5%,2 5%,5 0%,7 5%CS with 7 5%DMSO....