Vitrification of biological material

Patent metadata

Field	Value
Publication number	US-11166453-B2
Application number	US-201816167943-A
Country	US
Kind code	B2
Filing date	Oct 23, 2018
Priority date	Oct 15, 2013
Publication date	Nov 9, 2021
Grant date	Nov 9, 2021

Abstract

Provided herein is technology relating to cryopreservation and particularly, but not exclusively, to devices, systems, and methods for cryopreservation of biological materials such as oocytes, zygotes, and embryos. In particular, provided herein are methods of using microfluidic devices to exposing biological material to a vitrification solution having a time dependent concentration of a cryoprotectant agent.

First claim

We claim:

1. A method for cryopreserving a biological material, the method comprising:
loading a biological material into a biological material housing chamber of a microfluidic device that keeps said biological material stationary, wherein said biological material housing chamber comprises a set of height-differential vacuum powered holding channels that maintain said biological material in said housing chamber;
exposing the biological material to a vitrification solution having a time dependent increase in concentration of a cryoprotectant agent comprising at least one permeable cryoprotectant and at least one non-permeable cryoprotectant, wherein said time-dependent increase is a gradient generated by an automated mixing component, and
wherein said time dependent increase in concentration of said cryoprotectant agent controls the rate of cell shrinkage and/or rate of cell swelling of said biological material; and
vitrifying the biological material.

2. The method of claim 1 wherein said automated mixing component comprises two programmable syringe pumps used to pump said cryoprotective agent and a culture medium to provide said time-dependent increase in concentration of said cryoprotective agent in the vitrification solution.

3. The method of claim 1 wherein the cryoprotective agent comprises ethylene glycol, sucrose, and dimethysulfoxide (DMSO).

4. The method of claim 1 further comprising visualizing or monitoring the biological material.

5. The method of claim 4 further comprising selecting at least a portion of the biological material based on the visualizing or monitoring.

6. The method of claim 5 wherein selecting the biological material is based on observed circularity, surface roughness, lack of concave and/or convex features, and/or lipid content.

7. A cryopreserved biological material prepared using a method according to claim 1 .

8. The cryopreserved biological material of claim 7 having improved cell health, post-warming survival, fertility, morphology, lipid retention, and/or developmental competence relative to the biological material prepared by a manual technology.

9. The cryopreserved biological material of claim 7 having experienced less osmotic stress relative to the biological material prepared by a manual technology.

10. The cryopreserved biological material of claim 7 , wherein the cryopreserved biological material is an oocyte, a zygote, a stem cell, an embryo, an ovarian follicle, an embryoid body, an organoid, or a tissue.

11. The cryopreserved biological material of claim 7 , wherein the cryopreserved biological material is from a human.

12. A method for assisted reproduction, fertility preservation, in vitro production of livestock, or animal breeding, wherein the method comprises the method according to claim 1 and further comprises warming the biological material and fertilizing and/or implanting the biological material.

13. A method for stem cell therapy, wherein the method comprises the method according to claim 1 and further comprises warming the biological material and administering the biological material to a subject in need of stem cell therapy.

14. The method of claim 1 , wherein the permeable cryoprotectant agent is glycerol, ethylene glycol, 1,2-propanediol, or DMSO.

15. The method of claim 1 , wherein the cryoprotectant agent is or comprises an impermeable solute.

16. The method of claim 1 , wherein the impermeable cryoprotectant agent is a sugar, dextran, polyvinyl pyrrolidone, hydroxyethyl starch, sucrose, trehalose, raffinose, or stachyose.

17. The method of claim 1 , wherein a rate of cellular shrinkage and/or expansion during cryopreservation of said biological material is reduced relative to that obtained using manual technologies.

18. The method of claim 1 , wherein osmotic stress is reduced during cryopreservation of said biological material relative to manual technologies.

19. The method of claim 1 , wherein crater-like deformations on the cell membrane of said biological material is reduced relative to manual technologies.

20. The method of claim 1 , wherein sphericity of said biological material is increased relative to manual technologies.

21. The method of claim 1 , wherein said gradient is a linear gradient.

22. The method of claim 1 , wherein said biological material housing chamber comprises a suction channel in fluid communication with each of said height-differential vacuum powered holding channels.

Assignees

• Univ Michigan Regents

Inventors

• Lai David
• Takayama Shuichi
• Smith Gary D
• Ding Jun

Classifications

• A01N1/145

  Stationary or portable vessels generating cryogenic temperatures, e.g. liquid nitrogen baths · CPC title

• A01N1/142 Primary

  Apparatus · CPC title

• A01N1/125

  Freeze protecting agents, e.g. cryoprotectants or osmolarity regulators · CPC title

• A01N1/144 Primary

  for temperature control, e.g. refrigerators or freeze-drying apparatus · CPC title

• B01L2200/0647

  Handling flowable solids, e.g. microscopic beads, cells, particles · CPC title