Controlled platelet activation to monitor therapy of ADP antagonists
View Patent ↗A method is provided of determining whether an individual has reduced ability to form platelet thrombi. An ADP platelet activator and one or platelet inhibitors are provided. At least one of the platelet inhibitors is Prostaglandin E1 (PGE1). An alternate signal transduction pathway is produced. A final concentration of ADP is 2 to 35 μM and a final concentration of PGE1 is 2 to 30 nM, preferably 20 to 25 nM.
1. A method for measuring inhibition of platelet aggregation by a P2Y12 antagonist, comprising the steps of:
a) providing a platelet containing blood sample from an individual treated with a P2Y12 antagonist;
b) contacting said platelet containing blood sample with particles comprising an attached GPIIb/IIIa receptor ligand, adenosine diphosphate (ADP) and prostaglandin E1 (PGE1) under conditions suitable for agglutination of said particles mediated by said platelet in said blood sample, wherein said ADP has a final concentration of 2 to 35 μM and said PGE1 has a final concentration of 2 to 30 nM; and
c) assessing said agglutination to determine the level of inhibition of platelet aggregation by said P2Y12 antagonist in said individual, wherein a reduced level of agglutination indicates whether said individual has reduced ability to form platelet aggregation in response to said P2Y12 antagonist treatment.
2. The method of claim 1 , wherein said P2Y12 antagonist is a thienopyridine.
3. The method of claim 2 , wherein said thienopyridine is clopidogrel.
4. The method of claim 2 , wherein said thienopyridine is ticlopidine.
5. The method of claim 1 , wherein said platelet containing blood sample is from an individual treated with a P2Y12 antagonist and aspirin.
6. The method of claim 1 , wherein said particles comprise polystyrene or latex.
7. The method of claim 1 , wherein said particles comprise an infrared dye, the contact between the platelet containing blood sample and the particles forms an assay mixture, the agglutination of said particles mediated by said platelet is assessed by irradiating said assay mixture with a light in the infrared spectrum, and assessing the transmission of infrared light from said assay mixture.
8. The method of claim 1 , wherein said GPIIb/IIIa receptor ligand comprises a substance selected from the group consisting of fibrinogen, monoclonal antibody 10E5, monoclonal antibody c7E3, von Willebrand factor, fibronectin, vitronectin, a ligand that has an arginine glycine-aspartic acid (RGD) sequence, and a peptide or a peptidomimetic that mimics RGD sequence.
9. The method of claim 1 , wherein said GPIIb/IIIa receptor ligand is fibrinogen.
10. The method of claim 1 , wherein said ADP has a final concentration of 15 to 20 μM.
11. The method of claim 1 , wherein said PGE1 has a final concentration of 20 to 25 nM.
12. The method of claim 1 , which is conducted at a temperature ranging from 30° C. to 40° C., and the total time of the readings from the time of the contact among the platelet containing blood sample, the particles comprising an attached GPIIb/IIIa receptor ligand, ADP and PGE1 ranges from about 10 seconds to about 10 minutes.
13. The method of claim 1 , wherein said platelet containing blood sample is a whole blood sample.
14. The method of claim 1 , wherein said platelet containing blood sample is a plasma sample.
15. The method of claim 14 , wherein said plasma sample is a platelet rich plasma (PRP) sample.
16. The method of claim 1 , wherein said particles, ADP and PGE1 are contained in an assay medium.
17. The method of claim 16 , wherein said particles, ADP and PGE1 are contained in an assay medium on a disposable cartridge.
18. The method of claim 16 , wherein said assay medium has an absorption peak at about 800 nm.