Method for the cryopreservation of high-viscosity biological samples
View Patent ↗A protocol for the cryopreservation of high viscosity biological samples, preferably of spermatic samples of crustaceans or insects, that enables maintaining intact the physical properties of the original sample preserving the viability of the sperm packet.
1. A method for cryopreservation of shrimp spermatophores or sperm mass wherein the method comprises the steps of:
a) placing a sample of shrimp spermatophores or sperm mass in a cryovial tube having an inner wall containing an extender aqueous solution for a period of time ranging from 18 to 22 minutes at a temperature of 21° C. to 25° C., said extender aqueous solution comprising 2.125 g/Kg of NaCl, 0.110 g/Kg of KCl, 0.052 g/Kg of H 3 BO 3 , 0.019 g/Kg of NaOH, 0.484 g/Kg of MgSO 4 .7H 2 O and, 20 μl of a solution containing 10000 IU of penicillin, 10 mg of streptomycin and 25 μg of amphotericin B;
b) submerging the sample in Trehalose at 0.25-0.5M for a period of time ranging from 18 to 22 minutes;
c) transferring the sample into a cryoprotectant/vitrification solution comprising 0.25-0.5 M of Trehalose, 10-15% of DMSO, and the extender aqueous solution of step a), submerging only ⅔ of said sample for a period of time ranging from 2 to 4 minutes;
d) removing the sample from the cryoprotectant/vitrification solution and immediately submerge said sample in liquid nitrogen; and
e) placing the sample in a cryovial and storing said cryovial in liquid nitrogen at a temperature ranging from −196° C. to −200° C.
2. The method according to claim 1 , wherein said method additionally comprises the steps of thawing the sample by removing the sample from the liquid nitrogen, and submerging the sample in a water bath at a temperature from 35° C. to 39° C. for a period of time ranging from 4 to 9 minutes, to subsequently remove the sample from the cryovial and place the sample for a period of time of 15-25 minutes in an equilibrated solution containing 0.25 M of Trehalose.