Calibration of fluidic devices
The present invention provides methods of calibrating a fluidic device useful for detecting an analyte of interest in a bodily fluid. The invention also provides methods for assessing the reliability of an assay for an analyte in a bodily fluid with the use of a fluidic device. Another aspect of the invention is a method for performing a trend analysis on the concentration of an analyte in a subject using a fluidic device.
1. A method for use with a bodily sample, comprising:
providing a system, said system comprising a fluidic device, said fluidic device comprising a sample collection unit and an assay assembly, wherein said sample collection unit allows the bodily sample to react with reactants contained within said assay assembly, and a reader assembly for detecting the presence of said analyte;
using at least one reader assembly shipping condition sensor and at least one assay assembly shipping condition sensor to determine a change during shipping of the reader assembly or the assay assembly that impact operation parameters under which the system normally operates, wherein the assay assembly shipping condition sensor is operable to detect change even when not operably coupled to the reader assembly;
coupling said fluidic device with the reader assembly to perform the assay;
using a detector on the reader assembly to obtain shipping condition data from said shipping condition sensor located on the fluidic device when the fluidic device is coupled to the reader assembly;
using a communication assembly on the reader assembly to send said shipping condition data and raw assay data to a computer server external to the reader assembly;
evaluating both the reader assembly and the assay assembly to provide an analyte measurement based on shipping condition data and raw assay data sent to the server.
2. The method of claim 1 further comprising improving the reliability of said assay by adjusting the operating parameters to effect normal functioning of the system.
3. The method of claim 1 wherein said change comprises a change in temperature.
4. The method of claim 1 wherein said change comprises a change in pressure.
5. The method of claim 1 , further comprising adjusting a calibration step of said system based on information from at least one sensor.
6. The method of claim 1 , further comprising wirelessly communicating said change via a handheld device.
7. The method of claim 1 wherein said sensor is associated with said device.
8. The method of claim 7 where said sensor is capable of communicating said change to said reader assembly.
9. The method of claim 1 where said sensor is associated with said reader assembly.
10. The method of claim 9 where said sensor is capable of communicating said change to an external device.
11. The method of claim 9 wherein said change comprises a change in temperature.
12. The method of claim 9 wherein said change comprises a change in pressure.
13. The method of claim 1 wherein a dye is formed when thiosyanate and iron salt are mixed, whereby the dye is a visual indication of the presence of moisture.
14. The method of claim 13 wherein said bodily sample comprises a bodily fluid.
15. A method of assessing the reliability of an assay for an analyte in a bodily sample with the use of a device, comprising:
providing a system, said system comprising a device, said device comprising a sample collection unit and an assay assembly, wherein said sample collection unit allows the bodily sample to react with reactants contained within said assay assembly, for detecting the presence of an analyte in the bodily sample from a subject, and a reader assembly for detecting the presence of said analyte;
using at least one reader assembly shipping condition sensor and at least one assay assembly sensor to sense a change in operation parameters under which the system normally operates;
transmitting, said change to an external device;
assessing the reliability of the assay for the analyte based on said change associated with the assay assembly and at least one sensor in the reader assembly during shipping, wherein the sensor in the shipping package is operable to detect change during transport when it is not operably coupled to the reader assembly;
using a communication assembly on the reader assembly to send said shipping condition data of both the reader assembly and the device to a computer server external to the reader assembly; and
evaluating both the reader assembly and the assay assembly based on shipping data sent to the server.
16. The method of claim 15 further comprising improving the reliability of said assay by adjusting the operating parameters to effect normal functioning of the system.
17. The method of claim 15 , further comprising adjusting a calibration step of said system.
18. The method of claim 15 , further comprising wirelessly communicating said change via a handheld device.
19. The method of claim 15 , wherein said bodily sample comprises a bodily fluid.
20. The method of claim 15 wherein said sensor is associated with said device.
21. The method of claim 20 where said sensor is capable of communicating said change to said reader assembly.
22. The method of claim 20 wherein said change comprises a change in temperature.
23. The method of claim 20 wherein said change comprises a change in pressure.
24. The method of claim 15 where said sensor is associated with said reader assembly.
25. The method of claim 24 wherein said change comprises a change in temperature.
26. The method of claim 24 wherein said change comprises a change in pressure.