Ellagic acid formulations for use in coagulation assays

• US 9,921,232 B2
• Filed: 09/25/2015
• Issued: 03/20/2018
• Est. Priority Date: 09/26/2014
• Status: Active Grant

• Current Assignee: Abbott Point Of Care Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Point Of Care Incorporated (Abbott Laboratories Incorporated)
• Inventors: Collier, Gordon Bruce, Johns, Jr., Paul Willis, Sutrala, Smitha R K, Wang, Dan, Di Tullio, Katrina Petronilla
• Primary Examiner(s): Mui, Christine T
• Application Number:
  US14/866,518
• Publication Number:
  US 20160091512A1
• Time in Patent Office: 907 Days
• Field of Search: 422 73, 422 681, 422 50, 436 69
• CPC Class Codes: B01L 2200/0605 Metering of fluids
• CPC Class Codes: B01L 2200/0684 Venting, avoiding backpressure, avoid gas bubbles
• CPC Class Codes: B01L 2200/0689 Sealing
• CPC Class Codes: B01L 2200/16 Reagents, handling or storing thereof
• CPC Class Codes: B01L 2300/024 Storing results with means integrated into the container
• CPC Class Codes: B01L 2300/027 Digital display, e.g. LCD, LED
• CPC Class Codes: B01L 2300/0636 Integrated biosensor, microarrays
• CPC Class Codes: B01L 2300/0645 Electrodes
• CPC Class Codes: B01L 2300/069 Absorbents; Gels to retain a fluid
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2300/0867 Multiple inlets and one sample wells, e.g. mixing, dilution
• CPC Class Codes: B01L 2300/161 Control and use of surface tension forces, e.g. hydrophobic, hydrophilic
• CPC Class Codes: B01L 2400/0472 Diffusion
• CPC Class Codes: B01L 2400/0481 squeezing of channels or chambers
• CPC Class Codes: B01L 2400/0487 fluid pressure, pneumatics
• CPC Class Codes: B01L 2400/0688 surface tension valves, capillary stop, capillary break
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: B01L 3/502715 characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
• CPC Class Codes: G01N 2333/974 Thrombin
• CPC Class Codes: G01N 33/86 involving blood coagulating time or factors, or their receptors

Abstract

The present invention relates to ellagic acid formulations for performing coagulation assays that are highly stable for long term storage and reduce assay time. Particularly, aspects of the present invention are directed to a composition and method of preparing ellagic acid in a highly soluble format for use in a coagulation assay. For example, the ellagic acid may be solubilized in one or more of sodium hydroxide, methanol, a polyether compound, particularly polyethylene glycol, polyethylene oxide, or polyoxyethylene, and a cyclodextrin guest-host complex.

Claims

1. A coagulation test system comprising:

a reagent comprising ellagic acid and an agent for stably solubilizing the ellagic acid; and

a substrate comprising a thrombin-cleavable peptide with a detectable moiety,

wherein the agent comprises a cyclodextrin,

wherein the ellagic acid is stably solubilized,

and wherein at least 80% of the ellagic acid is active ellagic acid.

2. The coagulation test system of claim 1, wherein the agent further comprises a polyether compound selected from the group consisting of polyethylene glycol, polyethylene oxide, polyoxyethylene, and mixtures thereof.

3. The coagulation test system of claim 2, wherein the polyether compound is the polyethylene glycol.

4. The coagulation test system of claim 1, wherein the cyclodextrin is selected from the group consisting of (2-hydroxypropyl)-beta-cyclodextrin, (2-hydroxypropyl)-gamma-cyclodextrin, alpha-cyclodextrin, gamma-cyclodextrin, dimethyl-alpha-cyclodextrin, trimethyl-alpha-cyclodextrin, dimethyl-beta-cyclodextrin, trimethyl-beta-cyclodextrin, dimethyl-gamma-cyclodextrin, trimethyl-gamma-cyclodextrin, glycosyl-alpha-cyclodextrin, glycosyl-beta-cyclodextrin, diglycosyl-beta-cyclodextrin, maltosyl-beta-cyclodextrin, dimaltosyl-beta-cyclodextrin, sulfobutylether-beta-cyclodextrin, and mixtures thereof.

5. The coagulation test system of claim 1, wherein the agent is the cyclodextrin, and the cyclodextrin is complexed with the ellagic acid.

6. The coagulation test system of claim 1, wherein the agent is the cyclodextrin, and the cyclodextrin is in a soluble host-guest complex with the ellagic acid at a molar ratio of at least 1:

1 (ellagic acid;

cyclodextrin).

7. The coagulation test system of claim 6, wherein the molar ratio is selected from the group consisting of 1:

2, 1;

3, 1;

4, 1;

5, 1;

6, 1;

7, 1;

8, 1;

9 and 1;

10 (ellagic acid;

cyclodextrin).

8. The coagulation test system of claim 1, wherein the agent is the cyclodextrin, which is a beta-cyclodextrin, and the beta-cyclodextrin is complexed with the ellagic acid.

9. The coagulation test system of claim 2, wherein the agent is the polyether compound and the cyclodextrin, and the cyclodextrin is complexed with the ellagic acid.

10. The coagulation test system of claim 9, wherein the cyclodextrin is selected from the group consisting of (2-hydroxypropyl)-beta-cyclodextrin, (2-hydroxypropyl)-gamma-cyclodextrin, alpha-cyclodextrin, gamma-cyclodextrin, dimethyl-alpha-cyclodextrin, trimethyl-alpha-cyclodextrin, dimethyl-beta-cyclodextrin, trimethyl-beta-cyclodextrin, dimethyl-gamma-cyclodextrin, trimethyl-gamma-cyclodextrin, glycosyl-alpha-cyclodextrin, glycosyl-beta-cyclodextrin, diglycosyl-beta-cyclodextrin, maltosyl-beta-cyclodextrin, dimaltosyl-beta-cyclodextrin, sulfobutylether-beta-cyclodextrin, and mixtures thereof.

11. The coagulation test system of claim 1, wherein the thrombin-cleavable peptide is selected from the group consisting of H-D-Phe-Pip-Arg, H-D-Chg-Abu-Arg, CBZ-Gly-Pro-Arg, Boc-Val-Pro-Arg, H-D-Phe-Pro-Arg, Cyclohexylglycine-Ala-Arg, Tos-Gly-Pro-Arg, Bz-Phe-Val-Arg, Boc-Val-Pro-Arg, Ac-Val-Pro-Arg, Ac-Val-Hyp-Arg, Ac-(8-amino-3,6,dioxaoctanoyl-Val-Pro-Arg, Ac-Gly-Pro-Arg, Ac-(8-amino-3,6,dioxaoctanoyl-Gly-Pro-Arg, Ac-Gly-Hyp-Arg and H-D-Chg-Abu-Arg.

12. The coagulation test system of claim 1, wherein the detectable moiety is selected from the group consisting of p-aminophenol, a quinone, a ferrocene, ferrocyanide, other organometallic species, p-nitroaniline, o-dianisidine, 4,4′

-bensidine, 4-methoxy-2-naphthylamine, N-phenyl-p-phenylenediamine, N-[p-methoxyphenyl-]-p-phenylenediamine, and phenazine derivatives.

13. The coagulation test system of claim 1, further comprising at least one transducer coated with a polymer layer, wherein the polymer layer comprises the thrombin-cleavable peptide with the detectable moiety.

14. The coagulation test system of claim 13, wherein the reagent is an activated partial thromboplastin time (aPTT) reagent formed as (i) a layer over the polymer layer, or (ii) a layer adjacent to the at least one transducer.

15. The coagulation test system of claim 13, wherein the reagent is an activated partial thromboplastin time (aPTT) reagent, and the polymer layer comprises the aPTT reagent.

16. The coagulation test system of claim 1, further comprising a buffer and a phospholipid.

17. The coagulation test system of claim 16, wherein the buffer is selected from the group consisting of 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) buffer, N-2-hydroxyethyl piperazine-N-2-ethanesulfonic acid (HEPES), 3-(N-morpholino)-propanesulfonic acid (MOPS), Tris, N,N-bis-(hydroxyethyl)-2-aminoethanesulfoni acid (BES), N-tris-(hydroxymethyl)-methyl-2-aminoethanesulfonic acid (TES), 3-[N-tris (hydroxymethyl) methylamino]-2-hydroxypropanesulfonic acid (TAPSO), and 3-[N-tris-(hydroxymethyl-methylamino]-propanesulfonic acid (TAPS).

18. The coagulation test system of claim 16, wherein the phospholipid is selected from the group consisting of 1,2-dioleoyl-sn-glycero-3 phosphocholine (PC), 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (PE), 1,2-dioleoyl-sn-glycero-3-phosphoinositol (PI), and 1,2-dioleoyl-sn-glycero-3-phospho-L-serine (sodium salt) (PS).

30. The coagulation test system of claim 1, wherein the reagent has a neutral pH.

19. A method of forming a coagulation test system, the method comprising:

preparing an activator solution comprising ellagic acid and an agent comprising a cyclodextrin for stably solubilizing the ellagic acid, wherein the ellagic acid is stably solubilized, and wherein the ellagic acid comprises at least 80% of active ellagic acid;

mixing the activator solution with at least a phospholipid preparation to create a reagent solution; and

adding the reagent solution to a substrate comprising a thrombin-cleavable peptide with a detectable moiety to create an assay cocktail.

20. The method of claim 19, further comprising preparing a polymer matrix comprising a polymer, and adding the polymer matrix to the assay cocktail.

21. The method of claim 20, further comprising dispensing the assay cocktail over at least one transducer of a chip.

22. The method of claim 19, wherein the agent further comprises a polyether compound selected from the group consisting of polyethylene glycol, polyethylene oxide, polyoxyethylene, and mixtures thereof.

23. The method of claim 22, wherein the polyether compound is the polyethylene glycol.

24. The method of claim 19, wherein the cyclodextrin is selected from the group consisting of (2-hydroxypropyl)-beta-cyclodextrin, (2-hydroxypropyl)-gamma-cyclodextrin, alpha-cyclodextrin, gamma-cyclodextrin, dimethyl-alpha-cyclodextrin, trimethyl-alpha-cyclodextrin, dimethyl-beta-cyclodextrin, trimethyl-beta-cyclodextrin, dimethyl-gamma-cyclodextrin, trimethyl-gamma-cyclodextrin, glycosyl-alpha-cyclodextrin, glycosyl-beta-cyclodextrin, diglycosyl-beta-cyclodextrin, maltosyl-beta-cyclodextrin, dimaltosyl-beta-cyclodextrin, sulfobutylether-beta-cyclodextrin, and mixtures thereof.

25. The method of claim 19, wherein the agent is the cyclodextrin, and the cyclodextrin is complexed with the ellagic acid.

26. The method of claim 22, wherein the agent is the polyether compound and the cyclodextrin, and the cyclodextrin is complexed with the ellagic acid.

27. The method of claim 19, wherein the preparing the activator solution comprises:

dissolving the ellagic acid into the activator solution with the agent at neutral pH;

adding an alkali to the activator solution to increase the pH of the activator solution into a pH range of 10-12.5;

mixing the activator solution for a period of about 1 to 10 minutes;

adding an acid to the activator solution to return the pH to the neutral pH; and

mixing the activator solution with a buffer.

28. The method of claim 27, further comprising dispensing the assay cocktail over at least one transducer of a chip.

29. A sample analysis cartridge comprising:

an inlet chamber configured to receive a biological sample;

a conduit fluidically connected to the inlet chamber and configured to receive the biological sample from the inlet chamber; and

a micro-environment activated partial thromboplastin time (aPTT) sensor located within the conduit, the sensor comprising;

a reagent comprising ellagic acid and an agent for stably solubilizing the ellagic acid, wherein the agent comprises a cyclodextrin, wherein the ellagic acid is stably solubilized, and wherein at least 80% of the ellagic acid is active ellagic acid; and

at least one transducer coated with a polymer layer, wherein the polymer layer comprises a thrombin-cleavable peptide with a detectable moiety.