Assay Devices with Integrated Sample Dilution and Dilution Verification and Methods of Using Same
US-2015233862-A1 · Aug 20, 2015 · US
US9846152B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9846152-B2 |
| Application number | US-201514702590-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 1, 2015 |
| Priority date | Dec 3, 2010 |
| Publication date | Dec 19, 2017 |
| Grant date | Dec 19, 2017 |
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The invention is to devices and method for rapid determination of analytes in liquid samples by various assays including immunoassays incorporating a sample dilution feature for forming a diluted sample for analysis. The devices and methods also include a dilution verification feature for verifying the degree of dilution of the diluted sample. The devices preferably are capable of being used in the point-of-care diagnostic field is provided.
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What is claimed is: 1. A method of performing an assay for an analyte in a sample, said method comprising the steps of: introducing the sample into a sample chamber of a cartridge, wherein the sample chamber terminates in a sample extraction unit; loading said extraction unit with said sample; washing a portion of said sample from the extraction unit by pumping a volume of diluent from a diluent conduit through the extraction unit to form a diluted sample; analyzing said diluted sample for an analyte; and determining a dilution ratio of the diluted sample. 2. The method of claim 1 , wherein said extraction unit comprises a dilution determinant marker, which is used in characterizing the dilution ratio. 3. The method of claim 2 , wherein said dilution determinant marker is selected from the group consisting of an electrochemical species, ferricyanide, ruthenium hexamine, a ferrocene, ferrocene monocarboxylic acid, an optical dye, fluorescein, an acridinium salt, and methylene blue. 4. The method of claim 2 , wherein the dilution determinant marker concentration is measured using an electrochemical analysis system for amperometric measurements. 5. The method of claim 2 , wherein the dilution determinant marker concentration is measured using a potentiometric sensor. 6. The method of claim 2 , wherein the dilution determinant marker concentration is measured using a spectrophotometer. 7. The method of claim 1 , wherein the volume of diluent is a metered volume of diluent. 8. The method of claim 1 , further comprising: transporting said diluted sample to a sensor; and performing an analyte assay at said sensor. 9. The method of claim 1 , wherein the sample is diluted in the range of about 50:1 to about 50,000:1 parts by volume diluent:sample. 10. The method of claim 1 , wherein a volume of a portion of the sample extraction unit defines a metered volume of the sample loaded into the extraction unit. 11. The method of claim 10 , wherein the volume of the diluent is a metered volume of the diluent defined by a volume within a portion of the diluent conduit. 12. The method of claim 11 , wherein the metered volume of the diluent and the metered volume of the sample are used to provide the dilution ratio. 13. The method of claim 12 , wherein the extraction unit comprises a dilution determinant marker, which is used in characterizing the dilution ratio. 14. The method of claim 1 , wherein the volume of the diluent is pumped from a diluent chamber of the cartridge, said diluent chamber comprising the diluent. 15. The method of claim 1 , wherein said extraction unit comprises a porous material. 16. The method of claim 15 , wherein said porous material has a porosity of from 20 μm to 0.1 μm. 17. The method of claim 15 , wherein said porous material is a hydrophilic porous material. 18. The method of claim 15 , wherein said porous material is a transverse filter material. 19. The method of claim 1 , wherein said extraction unit is configured to become saturated with a volume of the sample loaded from the sample chamber. 20. The method of claim 1 , wherein in the loading step the sample passively flows from the sample chamber until it reaches the extraction unit, which is configured to inhibit or prevent further passive flow of the sample.
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