Freeze-dried platelets, method of making and method of use as a diagnostic agent

• US 8,097,403 B2
• Filed: 12/14/2007
• Issued: 01/17/2012
• Est. Priority Date: 12/14/2006
• Status: Active Grant

• Current Assignee: Cellphire, Inc.
• Original Assignee: Cellphire, Inc.
• Inventors: Ho, David, Jones, Heather
• Primary Examiner(s): SAUCIER, SANDRA E
• Application Number:
  US11/956,830
• Publication Number:
  US 20080145834A1
• Time in Patent Office: 1,495 Days
• Field of Search: None
• US Class Current: 435/2
• CPC Class Codes: A01N 1/02 Preservation of living parts
• 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: C12N 2503/00 Use of cells in diagnostics
• CPC Class Codes: C12N 5/0644 Platelets; Megakaryocytes

Abstract

The present invention provides freeze-dried platelets and compositions comprising freeze-dried platelets for use as a diagnostic and calibration reagent for blood coagulation function. The invention also provides methods of diagnosing or monitoring blood coagulation function, including diagnosing or monitoring blood coagulation diseases and disorders. Kits for performing the methods of the invention are also included.

Claims

1. A freeze-dried platelet composition comprising platelets, cryoprecipitate or a fraction thereof, polysucrose and trehalose made by the process of:

obtaining fresh platelets;

incubating the platelets in DMSO;

isolating the platelets by centrifugation;

resuspending the platelets in a loading buffer which comprises trehalose and ethanol thereby forming a first mixture;

incubating the first mixture;

mixing cryoprecipitate or a fraction thereof and polysucrose with the first mixture, thereby forming a second mixture; and

lyophilizing the second mixture to form a freeze dried composition comprising platelets, cryoprecipitate or a fraction thereof, polysucrose and trehalose.

2. The freeze-dried platelet composition of claim 1, wherein the cryoprecipitate or fraction thereof comprises fibrinogen.

3. The freeze-dried platelets of claim 1, wherein the freeze-dried platelets are used as a control reagent.

4. A composition comprising the freeze-dried platelets of claim 1, further comprising one or more biologically tolerable substances.

5. A kit comprising the freeze-dried platelets of claim 1 and further comprising at least one substance that affects the blood clotting system.

6. The kit of claim 5, wherein the substance is a drug.

7. The kit of claim 6, wherein the drug has anti-platelet activity.

8. The kit of claim 6, wherein the drug reduces the ability of a patient'"'"'s blood to clot.

9. The kit of claim 6, comprising multiple containers containing the freeze-dried platelets.

10. The kit of claim 6, comprising multiple containers containing two or more different substances.

11. A method of determining the blood clotting capability of a sample comprising blood or a blood component, said method comprising:

combining fresh blood or a blood component with the platelets of claim 1; and

assaying the mixture of fresh blood or a blood component and the platelets of claim 1 for one or more biological or biochemical functions indicative of one or more blood clotting functions.

12. The method of claim 11, wherein the method is a method of diagnosing a disease or disorder of the blood clotting system.

13. The method of claim 11, wherein the freeze-dried platelets are obtained from a patient having, or suspected of having, a defect in his blood clotting system.

14. The method of claim 11, wherein the fresh blood or blood component is obtained from a patient having, or suspected of having, a defect in his blood clotting system.

15. The method of claim 11, wherein the method is a method of monitoring the progression of a disease or disorder of the blood clotting system.

16. The method of claim 11, which is a method of monitoring the effects of a treatment regimen for a patient on the blood clotting system of that patient.

17. A method of making a freeze-dried platelet composition comprising platelets, cryoprecipitate or a fraction thereof, polysucrose and trehalose comprising:

obtaining fresh platelets;

incubating the platelets in DMSO;

isolating the platelets by centrifugation;

resuspending the platelets in a loading buffer which comprises trehalose and ethanol thereby forming a first mixture;

incubating the first mixture;

mixing cryoprecipitate or a fraction thereof and polysucrose with the first mixture, thereby forming a second mixture; and

lyophilizing the second mixture to form a freeze-dried composition comprising platelets, cryoprecipitate or a fraction thereof, polysucrose and trehalose.

18. The method of claim 17, wherein the cryoprecipitate or fraction thereof comprises fibrinogen.

19. A rehydrated platelet composition comprising platelets, cryoprecipitate or a fraction thereof, polysucrose and trehalose made by the process of:

obtaining fresh platelets;

incubating the platelets in DMSO;

isolating the platelets by centrifugation;

resuspending the platelets in a loading buffer which comprises trehalose and ethanol thereby forming a first mixture;

incubating the first mixture;

mixing cryoprecipitate or a fraction thereof and polysucrose with the first mixture, thereby forming a second mixture;

lyophilizing the second mixture to form a freeze-dried composition comprising platelets, cryoprecipitate or a fraction thereof, polysucrose and trehalose; and

rehydrating the freeze-dried composition.