Method and apparatus for detection of analyte using an acoustic device
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Abstract
Methods for detecting analytes in a sample are provided. A plurality of particles, each of which is coated with a capture agent having an affinity for the analyte, is combined with the sample to form a plurality of analyte-particle complexes. The system also includes a transport arrangement for transporting the sample to the sensor surface, and a magnetic field inducing structure constructed and arranged to establish a magnetic field at and adjacent to the sensor surface. The resonant sensor produces a signal corresponding to an amount of analyte-particle complexes that are bound to the sensor surface.
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Citations
40 Claims
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1-17. -17. (canceled)
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18. A method for detecting whether one or more analytes is present in a sample comprising:
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a) introducing a plurality of magnetic particles and a competitor molecule into a fluid chamber, said magnetic particles being coated with a first capture agent capable of binding the analyte, wherein at least one surface of the fluid chamber comprises an acoustic device that has been coated with a second capture agent capable of binding to the competitor molecule; b) creating a magnetic flux in proximity to the acoustic device to attract at least one of the plurality of magnetic particles toward said surface, and c) monitoring signal output by said acoustic device, thereby detecting whether one or more analytes is present in the sample.
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19. The method of claim 18, wherein prior to being introduced into the fluid chamber, said plurality of magnetic beads has been exposed to the sample and to the competitor molecule.
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20. The method of claim [[19]]18, wherein the competitor molecule comprises the immunosuppressant bound to a tag and the second capture agent is capable of binding to the tag.
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21. The method of claim 20, wherein the tag is biotin.
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22. The method of claim 18, wherein the competitor molecule comprises two or more analyte molecules bound to a carrier, and the second capture agent is capable of binding the analyte.
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23. The method of claim 22, wherein the carrier is a selected from the group consisting of horseradish peroxidase and albumin.
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24. The method of claim 18, wherein the sample and the competitor molecule have been introduced into the fluid chamber prior to introducing the plurality of particles.
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25. The method of claim 18, wherein the sample is a biological sample.
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26. The method of claim 25, wherein the biological sample is selected from the group consisting of:
- saliva, sputum, cerebrospinal fluid, blood, serum, plasma, urine, and biopsy material.
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27. The method of claim 18, further comprising comparing the signal output of c) to a control signal.
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28. The method of claim 27, wherein the control signal is a standard curve.
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29. The method of claim 27, wherein the control signal is obtained in the absence of sample.
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30. The method of claim 18, wherein the second capture agent is indirectly bound to said surface.
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31. The method of claim 30, wherein said surface is coated with a first member of a binding pair, and the second capture agent is bound to a second member of the binding pair.
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32. The method of claim 31, wherein a first member of the binding pair is biotin.
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33. The method of claim 18, wherein the first or second capture agent is an antibody.
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34-39. -39. (canceled)
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40. The method of claim 32, wherein a second member of the binding pair is a derivative of avidin.
Specification