Ratiometric test strip and method

• US 20060281188A1
• Filed: 06/12/2006
• Published: 12/14/2006
• Est. Priority Date: 06/13/2005
• Status: Abandoned Application

• Current Assignee: Cornell University
• Original Assignee: Cornell Research Foundation Incorporated (Cornell University)
• Inventors: Mann, Samuel J., Gerber, Linda M.
• Application Number:
  US11/451,285
• Publication Number:
  US 20060281188A1
• Time in Patent Office: Days
• US Class Current: 436/169
• CPC Class Codes: G01N 33/526 the element being adapted for a specific analyte
• CPC Class Codes: G01N 33/70 involving creatine or creatinine
• CPC Class Codes: G01N 33/84 involving inorganic compounds or pH

Abstract

The invention generally relates to devices, systems and methods adapted for use by patients for monitoring their own dietary intake of sodium without any need of laboratory facilities or collection of blood samples. The systems utilize test strips for measuring the concentration of analytes in urine, specifically, chloride and creatinine. Urinary chloride concentrations, normalized by creatinine concentrations to reduce variability contributed mainly by changing states of hydration serve as a conveniently monitored surrogate for salt intake by subjects, especially patients with hypertension or congestive heart failure who must control their salt intake carefully.

Claims

1. A system for monitoring salt intake by a subject without laboratory facilities comprising:

(i) a monitor strip;

(ii) a filtration strip; and

(iii) a sample of said subject'"'"'s urine.

2. The system of claim 1 further comprising a nomogram for converting a read-out of said monitor strip and a read-out of said filtration strip to a value for salt intake by said patient.

3. The system of claim 1 wherein said read-outs are spectrometric.

4. The system of claim 2 wherein said spectrometric read-outs are colorimetric.

5. The system of claim 3 wherein said calorimetric readouts are visually appreciable.

6. The system of claim 1 further comprising a monitor strip that is not reagent-loaded and a filtration strip that is not reagent-loaded.

7. The system of claim 1 further comprising a chloride standard and a creatinine standard.

9. The method of claim 7, wherein said urine is from a patient suspected to have high blood pressure.

10. The method of claim 7, wherein said patient carries out step (b) at home.

13. The method of claim 7, wherein said second test strip comprises a quinoline.

14. The method of claim 7, wherein said first test strip comprises a silver dichromate reagent which gives a measurable calorimetric response in the presence of halide ions.

8. A method of monitoring salt intake performed without laboratory facilities, comprising:

a) providing a first test strip capable of detecting chloride in urine, a second test strip capable of detecting creatinine in urine, and said patient'"'"'s urine;

b) introducing said first and second test strips to said urine so as to obtain first and second values; and

c) calculating a ratio of said first and second values and finding a salt intake value therefrom.

11. The method of claim 8, wherein said salt intake value is between more than about 0 mg/kg body weight/day and less than about 1500 mg/kg body weight/day.

12. The method of claim 8, wherein reduction in salt intake is indicated when said salt intake value exceeds more than about 50 mg/kg body weight/day.

15. A method of monitoring salt intake without laboratory facilities, comprising:

a) providing a device comprising a first test region capable of detecting chloride in urine, a second test region capable of detecting creatinine in urine, said first and second regions on a single test strip, and said patient'"'"'s urine;

b) introducing said first and second regions to said urine so as to obtain first and second values; and

c) calculating a ratio of said first and second values and finding a salt intake value therefrom.

16. A device comprising a first test region capable of detecting chloride in urine, a second test region capable of detecting creatinine in urine.

17. The device of claim 16, wherein said first and second regions are on a single test strip.

18. The device of claim 16, wherein said first and second regions are separated by a hydrophobic barrier.

19. The device of claim 16, wherein said first test region comprises a silver dichromate reagent which gives a measurable colorimetric response in the presence of halide ions.

20. The device of claim 16, wherein said second test region comprises a quinoline.

21. A kit comprising the testing device of claim 16 and instructions for operating the device.