A fluidics-based assay device for detecting the presence or quantity of an analyte residing in a test sample is provided. The device utilizes a self-calibrated magnetic binding assay format (e.g., sandwich, competitive, etc.) that includes detection probes capable of generating a detection signal (
A fluidics-based assay device for detecting the presence or quantity of an analyte residing in a test sample is provided. The device utilizes a self-calibrated magnetic binding assay format (e.g., sandwich, competitive, etc.) that includes detection probes capable of generating a detection signal (e.g., fluorescent non-magnetic particles) and calibration probes capable of generating a calibration signal (e.g., fluorescent magnetic particles). The amount of the analyte within the test sample is proportional (e.g., directly or inversely) to the intensity of the detection signal calibrated by the intensity of the calibration signal. It has been discovered that the fluidics-based device of the present invention provides an accurate, inexpensive, and readily controllable method of determining the presence of an analyte in a test sample.
대표청구항▼
What is claimed is: 1. A fluidics-based assay device for detecting the presence or quantity of an analyte residing in a test sample, the device comprising: a reaction chamber for containing the test sample; detection probes that comprise particles that are conjugated with a first specific binding m
What is claimed is: 1. A fluidics-based assay device for detecting the presence or quantity of an analyte residing in a test sample, the device comprising: a reaction chamber for containing the test sample; detection probes that comprise particles that are conjugated with a first specific binding member for the analyte and labeled with a first detectable substance, the first detectable substance being capable of producing a detection signal; calibration probes that comprise magnetic particles labeled with a detectable substance second, the detectable substance second being capable of producing a calibration signal; wherein the first and second detectable substances are different non-fluorescent magnetic particles that are conjugated with a second specific binding member for the analyte; a channel in fluid communication with the reaction chamber, the channel defining a detection zone; and a magnetic device positioned adjacent to the detection zone; wherein the amount of the analyte within the test sample is directly or inversely proportional to the intensity of the detection signal produced at the detection zone calibrated by the intensity of the calibration signal produced at the detection zone. 2. The assay device of claim 1, wherein the detectable substance of both the detection probes and the calibration probes is selected from the group consisting of fluorescent compounds, chemiluminescent compounds, phosphorescent compounds, and combinations thereof. 3. The assay device of claim 1, wherein the amount of the analyte within the test sample is directly or inversely proportional to the intensity of the detection signal produced at the detection zone divided by the intensity of the calibration signal produced at the detection zone. 4. The assay device of claim 1, wherein the amount of the analyte within the test sample is directly proportional to the intensity of the detection signal produced at the detection zone calibrated by the intensity of the calibration signal produced at the detection zone. 5. The assay device of claim 1, wherein the amount of the analyte within the test sample is inversely proportional to the intensity of the detection signal produced at the detection zone calibrated by the intensity of the calibration signal produced at the detection zone. 6. The assay device of claim 1, wherein the channel facilitates capillary flow of the test sample. 7. The assay device of claim 1, further comprising a barrier disposed between the reaction chamber and the channel, the barrier being configured to hold the test sample within the reaction chamber for a certain period of time. 8. The assay device of claim 7, wherein the barrier is configured to substantially dissolve. 9. The assay device of claim 8, wherein the barrier contains a material selected from the group consisting of carbohydrates, salts, and combinations thereof. 10. The assay device of claim 7, wherein the barrier is configured to physically rupture. 11. The assay device of claim 1, wherein the detectable substance of both the detection probes and the calibration probes is a fluorescent compound. 12. The assay device of claim 1, wherein the detection probes comprise non-magnetic particles labeled with a fluorescent compound. 13. The assay device of claim 1, wherein the calibration probes comprise magnetic particles labeled with a fluorescent compound. 14. The assay device of claim 13, wherein the fluorescent magnetic particles are blocked. 15. The assay device of claim 13, wherein the fluorescent magnetic particles are conjugated with a specific binding member. 16. The assay device of claim 1, wherein the detection probes, the calibration probes, or combinations thereof comprise a specific binding member. 17. The assay device of claim 1, wherein the specific binding member is selected from the group consisting of antigens, haptens, aptamers, antibodies, and complexes thereof.
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