Methods and devices for measuring the levels of analytes in body fluids
A method of testing for an analyte in an individual comprises providing colour information obtained from a digital image of a coloured reagent on an analyte test strip, the coloured reagent having been generated in accordance with analyte in a test sample, converting the colour information from the image into an analyte level, recording the analyte level in association with user-specific information (e.g. a QR code), repeating the above steps to obtain two or more records of analyte levels for the same user at different times and using the records to monitor personal health or to predict the likely development of a disease or condition or to diagnose a disease or condition or to monitor a treatment regime associated with variation in analyte levels in saliva.
1. A method of testing for an analyte in an individual, comprising:
providing color information obtained from a digital image of a colored reagent on an analyte test strip, the colored reagent having been generated in accordance with analyte in a test sample;
converting the color information from the digital image into an analyte level;
recording the analyte level in association with user-specific information, wherein the digital image comprises user specific information;
repeating the above steps to obtain two or more records of analyte levels for the same user at different times; and
using the records to monitor personal health or to predict the likely development of a disease or condition or to diagnose a disease or condition or to monitor a treatment regime associated with variation in analyte levels in saliva; and
further comprising a preliminary step of capturing the digital image of the colored reagent on the analyte test strip at a first site; and
transmitting the digital image to a monitoring station at a second, remote site, where the color information from the image is converted into the analyte level.
2. The method according to claim 1 , wherein the digital image comprises a color reference.
3. The method according to claim 1 , wherein converting the color information from the digital image into an analyte level comprises:
comparing color information from the digital image with color information obtained from images generated during a clinical trial, wherein the color information obtained from images generated during the clinical trial has been linked to levels of a given analyte.
4. The method according to claim 1 , further comprising processing the digital image to obtain the color information from the digital image.
5. The method according to claim 1 , further comprising determining the analyte level based upon luminance, saturation, or both luminance and saturation of the color.
6. The method according to claim 3 , comprising using the comparison to identify incidence of high urate levels.
7. The method according to claim 1 is used for diagnosis of fetal stress.
8. The method according to claim 1 is used for diagnosis of risk of pre-eclampsia.
9. A method of testing for an analyte in an individual, comprising:
(a) providing (i) a saliva sample from an individual in a pad of absorbent material, spaced from (ii) a test strip containing an indicator which is capable of generating a color change in accordance with the presence of an analyte;
(b) bringing the pad into contact with the test strip and holding the pad in contact with the test strip for sufficient time for saliva in the pad to be combined with the indicator and generate a color in accordance with a level of an analyte if present; and
(c) determining the level of analyte based upon the color change;
wherein step (c) comprises transmitting information concerning the level of an analyte to a monitoring station at a remote site; and
wherein the information transmitted comprises color information contained in or obtained from an image of the color on the test strip, and
further comprising
storing at least 5 test results for the same user taken at different times; and
comparing these test results to monitor personal health or predict the likely development of a disease or condition or diagnose a disease or condition or to monitor a treatment regime associated with variation in analyte levels in saliva.
10. The method according to claim 9 , wherein the indicator is capable of generating a color change in accordance with the concentration of an analyte.
11. The method according to claim 9 , wherein the method comprises determining the analyte level based upon luminance, saturation, or both luminance and saturation of the color.
12. The method according to claim 9 , comprising comparing test results to identify incidence of high urate levels.
13. The method according to claim 9 , comprising carrying out the test using a device comprising:
(a) a first arm, on which is mounted a pad of absorbent material; and
(b) a second arm, comprising a test strip, wherein the test strip comprises a reagent portion comprising the indicator capable of generating a color change in accordance with the presence of an analyte;
wherein the arms are connected by a hinge and can be pivoted on the hinge to bring the pad into contact with the reagent portion; and
wherein the second arm additionally comprises a color calibration icon.
14. The method according to claim 13 , wherein the second arm comprises a user identifier.
15. The method according to claim 9 is used for diagnosis of fetal stress.
16. The method according to claim 9 is used for diagnosis of pre-eclampsia.