Method to quickly add cryoprotectants to sperm cells while maintaining viability

• US 5,691,133 A
• Filed: 06/07/1995
• Issued: 11/25/1997
• Est. Priority Date: 05/27/1994
• Status: Expired due to Fees

• Current Assignee: Methodist Hospitals of Dallas
• Original Assignee: Methodist Hospitals of Dallas
• Inventors: Critser, John K., Gao, D. Y.
• Primary Examiner(s): Saucier, Sandra E.
• Application Number:
  US08/475,215
• Time in Patent Office: 902 Days
• Field of Search: 435/1.3, 435/2
• US Class Current: 435/2
• CPC Class Codes: A01N 1/0221 Freeze-process protecting agents, i.e. substances protecting cells from effects of the physical process, e.g. cryoprotectants, osmolarity regulators like oncotic agents
• CPC Class Codes: A01N 1/0263 Non-refrigerated containers specially adapted for transporting or storing living parts whilst preserving, e.g. cool boxes, blood bags or "straws" for cryopreservation
• CPC Class Codes: A61K 35/52 Sperm; Prostate; Seminal fluid; Leydig cells of testes

Abstract

A mathematical model to optimize protocols for the addition or removal of cryoprotectant to or from sperm cells. This disclosure describes the use of four equations to predict optimal protocols to add or remove cryoprotectant to or from sperm cells. The equations particularly require experimentally found date, specific to a species of sperm, regarding the osmotic tolerance of sperm cells, where osmotic tolerance refers to the sperm cells ability to shrink or swell to various changes in osmolality without injury. The equations further require the cryoprotectant permeability coefficient and the water permeability coefficient of the particular sperm cells'"'"' plasma membrane. Also disclosed are two particularly preferred methods to add or remove cryoprotectant to or from sperm. These preferred methods are Fixed-Volume-Step addition/removal of cryoprotectant or Fixed-Molarity-Step addition/removal of cryoprotectant.

Claims

1. A method to add cryoprotectant to the sperm cells of an animal species comprising:

a) predetermining a lower cellular volume limit below which a user-defined fraction of sperm cells lose their viability,

b) selecting a first concentration of cryoprotectant solution,

c) calculating whether said first concentration of cryoprotectant solution will cause the sperm cells to shrink below the lower cellular volume limit by a calculation which uses the water permeability coefficient and the cryoprotectant permeability coefficient of the sperm cells, repeating steps b) and c) as necessary in order to calculate a predetermined concentration of cryoprotectant solution which will permit increasing of the concentration of cryoprotectant in the sperm cells while still maintaining the viability of a user-defined fraction of the sperm cells,

d) contacting said sperm cells with the solution of the predetermined concentration of cryoprotectant.

2. The method of claim 1, wherein steps (b) and, (c) and (d) are repeated for a second concentration of cryoprotectant that is less dilute than said first concentration.

3. The method of claim 1, wherein said lower cellular volume limit is predetermined by shrinking the sperm cells of said animal species in increasingly hypertonic conditions until a predetermined fraction of the sperm cells lose their viability.

4. The method of claim 1, wherein said cryoprotectant comprises glycerol.

5. The method of claim 1, wherein said contacting comprises contacting said sperm cells with the cryoprotectant solution in two or more substantially constant volumes.

6. The method of claim 1, wherein said contacting comprises contacting said sperm cells with the cryoprotectant solution in two or more volumes wherein said volumes increase the level of cryoprotectant in the sperm cells by substantially constant increments in molarity.

7. The method of claim 1, wherein said lower cellular volume limit is about 75% of the isotonic volume of the sperm cells.

8. The method of claim 1, wherein said viability is measured by analysis of sperm motility.

9. The method of claim 1, wherein said concentration of each aliquot shrinks the sperm cells to a volume that is between said lower cellular volume limit and 110% of said lower cellular volume limit.

10. The method of claim 1, wherein said lower cellular volume limit is based upon the sperm cells'"'"' ability to fertilize.

11. A method to add cryoprotectant to sperm cells of an animal species, comprising:

contacting said sperm cells with one or more stepwise additions of aliquots containing said cryoprotectant, wherein each aliquot has a predetermined concentration of said cryoprotectant that is higher than the cryoprotectant concentration within the sperm cells with which it is contacted, said predetermined concentration substantially preventing the volumetric excursion of said sperm cells beyond a predetermined lower cellular volume limit, and said predetermined concentration being predetermined by determining the cellular volume of said sperm cells for a given concentration of said cryoprotectant with differential equations;

##EQU2## wherein J_v =total volume flux, V=cell volume, t=time, N=mole number of the solute, A=cell surface area, L_p =water permeability coefficient, C=concentration of solute, J_CPA =cryoprotectant flux across the cell membrane, superscript e=extracellular, superscript i=intracellular, C_CPA =average cryoprotectant concentration of extracellular and intracellular concentrations, R=gas constant, T=absolute temperature, P_CPA =cryoprotectant permeability coefficient of the sperm cell, σ

=the reflection coefficient of said cryoprotectant, wherein V_b =osmotically-inactive cell volume, V_CPA =partial mole volume of said cryoprotectant, 0=initial condition; and

determining the size of said cellular volume relative to said predetermined lower cellular volume limit.

12. The method of claim 11, wherein said cryoprotectant is selected from the group consisting of dimethyl sulfoxide, glycerol, and ethylene glycol.