Self-calibration system for a magnetic binding assay

• US 7,432,105 B2
• Filed: 08/27/2002
• Issued: 10/07/2008
• Est. Priority Date: 08/27/2002
• Status: Expired due to Fees

• Current Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Original Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Inventors: Song, Xuedong, Kaylor, Rosann
• Primary Examiner(s): Le; Long V.
• Assistant Examiner(s): Do; Pensee T.
• Application Number:
  US10/228,837
• Publication Number:
  US 20040043512A1
• Time in Patent Office: 2,233 Days
• Field of Search: 436/8, 436/172, 436/905, 436/518, 436/523, 436/546, 436/15, 436/164, 436/165, 436/166, 436/169, 436/800, 436/10, 435/4, 435/7.1, 435/7.92, 435 793- 795, 435/967, 356/42, 356/243
• US Class Current: 436/8
• CPC Class Codes: G01N 33/54326 Magnetic particles
• CPC Class Codes: G01N 33/582 with fluorescent label
• CPC Class Codes: Y10S 435/967 Standards, controls, materials, e.g. validation studies, buffer systems
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine
• CPC Class Codes: Y10S 436/905 Photochemical activation of reactions
• CPC Class Codes: Y10T 436/10 Composition for standardization, calibration, simulation, stabilization, preparation or preservation; processes of use in preparation for chemical testing
• CPC Class Codes: Y10T 436/101666 Particle count or volume standard or control [e.g., platelet count standards, etc.]
• CPC Class Codes: Y10T 436/105831 Protein or peptide standard or control [e.g., hemoglobin, etc.]

Abstract

A self-calibrated, magnetic binding assay (e.g., sandwich, competitive, etc.) for detecting the presence or quantity of an analyte residing in a test sample is provided. The magnetic binding assay includes detection probes capable of generating a detection signal (e.g., fluorescent non-magnetic particles) and calibration probes capable of generating calibration signal (e.g., fluorescent magnetic particles). The amount of the analyte within the test sample is proportional to the intensity of the detection signal calibrated by the intensity of the calibration signal.

Claims

1. A method for detecting the presence or quantity of an analyte residing in a test sample, the method comprising:

i) contacting a test sample containing the analyte with detection probes having fluorescent non-magnetic particles conjugated with a first specific binding member, non-fluorescent magnetic particles that are conjugated with a second specific binding member for the analyte, and a predetermined amount of calibration probes wherein the analyte forms a sandwhich complex with the detection probe and the conjugated non-fluorescent magnetic particle;

ii) separating the complex and the calibration probes from the test sample using a magnetic device;

iii) exciting the separated complex and the separated calibration probes, wherein the excitation causes the separated complex to produce a detection signal and the separated calibration probes to produce a calibration signal;

iv) measuring the intensity of the detection signal and the intensity of the calibration signal; and

v) comparing the intensity of the detection signal to the calibration signal, wherein the amount of the analyte within the test sample is directly or inversely proportional to the intensity of the detection signal calibrated by the intensity of the calibration signal.

2. The method of claim 1, wherein the detection signal is measured at a first emission wavelength.

3. The method of claim 2, wherein the calibration signal is measured at a second emission wavelength.

4. The method of claim 3, wherein the first emission wavelength is different than the second emission wavelength.

5. The method of claim 1, further comprising producing a calibration curve by plotting the intensity of the detection signal calibrated by the intensity of the calibration signal for a plurality of predetermined analyte concentrations.

6. The method of claim 1, wherein the separated complex and the separated calibration probes are excited simultaneously.

7. The method of claim 1, wherein the intensity of the detection signal and the calibration signal are measured simultaneously.

8. The method 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 divided by the intensity of the calibration signal.

9. The method of claim 1, wherein the amount of the analyte within the test sample is directly proportional to the intensity of the detection signal calibrated by the intensity of the calibration signal.

10. The method of claim 1, wherein the amount of the analyte within the test sample is inversely proportional to the intensity of the detection signal calibrated by the intensity of the calibration signal.

11. The method of claim 1, wherein the detection probes comprise particles labeled with a detectable substance capable of producing the detection signal.

12. The method of claim 11, wherein the calibration probes comprise particles that are labeled with a detectable substance capable of producing the calibration signal.

13. The method of claim 12, 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.

14. The method of claim 12, wherein the detectable substance of both the detection probes and the calibration probes is a fluorescent compound.

15. The method of claim 12, wherein the particles of the calibration probes are magnetic.

16. The method of claim 15, wherein the magnetic particles include a metal, metal alloy, metal oxide, or a combination thereof.

17. The method of claim 1, wherein the calibration probes comprise magnetic particles labeled with a fluorescent compound.

18. The method of claim 17, wherein the magnetic particles are conjugated with a specific binding member.

19. The method of claim 17, wherein the fluorescent magnetic particles are blocked.

20. The method of claim 1, wherein the detection probes, the calibration probes, or combinations thereof comprise a specific binding member.

21. The method of claim 20, wherein the specific binding member is selected from the group consisting of antigens, haptens, aptamers, antibodies, and complexes thereof.

22. The method of claim 20, wherein the specific binding member of the detection probes is capable of specifically binding to the analyte.