US2006105317A1PendingUtilityA1

Method and solutions for cryopreserving oocytes, especially fresh human oocytes

Assignee: MULTI CULT ASPriority: Mar 20, 2000Filed: Dec 30, 2005Published: May 18, 2006
Est. expiryMar 20, 2020(expired)· nominal 20-yr term from priority
A01N 1/10A01N 1/125
43
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Claims

Abstract

In a method for cryopreserving fresh human oocytes, freezing and thawing solutions are used, which solutions include 1,2 propanediol (PROH) and sucrose at a concentration of at least 0.3M. The oocytes are exposed for 13-15 minutes to a solution including 1.5M PROH and 0.3M sucrose before starting the freezing process.

Claims

exact text as granted — not AI-modified
1 - 11 . (canceled)  
   
   
       12 . A solution for cryopreserving cells, characterized in that it comprises a permeating cryoprotectant and sucrose at a concentration of at least 0.3M.  
   
   
       13 . The solution of  claim 12 , characterized in that the permeating cryoprotectant comprises 1,2-propanediol (PROH) at a concentration of 1.5M and that the solution is adapted for use as a loading solution in cryopreserving processes of oocytes, especially fresh human oocytes.  
   
   
       14 . The solution of  claim 12 , characterized in that the permeating cryoprotectant comprises 1,2 propanediol (PROH) at a concentration of 1.0M and that the solution is adapted for use as a thawing solution in cryopreserving processes of oocytes, especially fresh human oocytes.  
   
   
       15 . The solution of  claim 12 , characterized in that the permeating cryoprotectant comprises 1,2 propanediol (PROH) at a concentration of 0.5M and that the solution is adapted for use as a thawing solution in cryopreserving processes of oocytes, especially fresh human oocytes.  
   
   
       16 . The solution of  claim 12 , characterized in that it is adapted for use as a thawing solution in cryopreserving processes of oocytes, especially fresh human oocytes.

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