Analytical test devices for competition assay for drugs of non-protein antigens using immunochromatographic techniques

• US 5,238,652 A
• Filed: 06/20/1990
• Issued: 08/24/1993
• Est. Priority Date: 06/20/1990
• Status: Expired due to Fees

• Current Assignee: Casco Standards, Inc.
• Original Assignee: Drug Screening Systems, Inc. (Varsity Brands, Inc.)
• Inventors: Sun, Ming, Pfeiffer, Francis R.
• Primary Examiner(s): Housel, James C.
• Assistant Examiner(s): ALEXANDER, LYLE
• Application Number:
  US07/540,844
• Time in Patent Office: 1,161 Days
• Field of Search: 422/56-58, 422/61, 436/523, 436/528, 436/533, 436/63, 436/531, 436/164, 436/901, 435/7.1, 435/810
• US Class Current: 422/412
• CPC Class Codes: B01L 2300/045 whereby the whole cover is slidable
• CPC Class Codes: B01L 2300/046 Function or devices integrated in the closure
• CPC Class Codes: B01L 2300/0825 Test strips
• CPC Class Codes: B01L 2400/0487 fluid pressure, pneumatics
• CPC Class Codes: B01L 3/5023 with a sample being transported to, and subsequently stored in an absorbent for analysis
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: G01N 33/54388 based on lateral flow
• CPC Class Codes: G01N 33/54389 with bidirectional or multidirectional lateral flow, e.g. wherein the sample flows from a single, common sample application point into multiple strips, lanes or zones
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: G01N 33/585 with a particulate label, e.g. coloured latex
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10S 436/901 Drugs of abuse, e.g. narcotics, amphetamine

Abstract

An analytical test device for competition assay for particular non-protein antigens, such as antigens representing drugs of abuse, is disclosed. The analytical test device is a test kit housing having an opening for introduction of a body fluid sample and a flow path for the body fluid sample. A supply of microscopic colored latex particles is adjacent to the opening along the flow path. A chromatographic membrane support is within the test kit housing for exposing the colored latex particles to the body fluid sample. When non-protein antigens are not present in the body fluid specimen, the colored latex particles accumulate at a predetermined site on the chromatographic membrane by complexing of antibodies on the colored latex particles to a drug conjugate probe on the membrane support to leave a visually perceptible colored mark of the same color as the colored latex particles. When non-protein antigens are present in the body fluid specimen, complexing of the non-protein antigens to the supply of antibodies on the colored latex particles exhausts the antibody supply on the colored latex particles such that the colored latex particles cannot complex to the immobilized drug conjugate probe, leaving no visually perceptible colored mark at the predetermined site. Also disclosed is a process for analytical testing of a body fluid for the presence of non-protein antigens, and an analytical test assembly for simultaneous multiple competition assays.

Claims

1. An analytical test device for producing a visually-perceptible indication of whether particular non-protein antigens are present via competition assay for particular non-protein antigens representing drugs of abuse, consisting essentially of:

a test kit housing having means for introduction of a body fluid sample at a first end of said housing and means defining a flow path for the body fluid sample to a second end of said housing;

a supply of microscopic colored latex particles disposed adjacent to the means for introduction of the body fluid sample along the flow path, the colored latex particles becoming suspended in the body fluid sample and moving with flow of the body fluid sample along the flow path from said first end toward said second end, the latex particles being sensitized with a supply of antibodies for the non-protein antigen at least on a surface thereof, said antibodies being responsive to said non-protein antigens and being operable to complex therewith;

a chromatographic membrane support disposed within the test kit housing and being impregnated at a first predetermined site along the flow path downstream of the colored latex particles towards said second end with an immobilized drug conjugate probe sensitive to said antibodies on the latex particles, and operable to complex therewith; and

,

means for exposing the colored latex particles at said first end to the body fluid sample for substantially complete reaction of the non-protein antigens in the body fluid sample with the antibodies for the non-protein antigen on the latex particles, prior to the body fluid sample reaching the first predetermined site along the flow path;

whereby when said non-protein antigens are not present in the body fluid sample the latex particles accumulate at the first predetermined site by complexing of the antibodies on the latex particles with the drug conjugate probe on the membrane support to leave a visually perceptible colored mark of a same color as the colored latex particles, and when said non-protein antigens are present in the body fluid sample, complexing of the non-protein antigens to the supply of antibodies on the latex particles substantially exhausts the antibody supply on the latex particles such that the latex particles cannot complex to the immobilized drug conjugate probe, leaving no visually perceptible mark at the predetermined site.

2. The analytical test device according to claim 1, wherein the latex particles further comprise a supply of second immunoreaction protein antibodies bonded to the latex particles, the second immunoreaction antibodies being non-responsive to the non-protein antibodies and being responsive to protein antigens, the chromatographic membrane support being impregnated at a second predetermined site along the flow path downstream of the first predetermined site further towards the second and with a further immobilized immunoreaction antibody probe sensitive to said second immunoreaction protein and operable to complex therewith, the second and further immunologic probe complexing the latex particles to the membrane support at said second predetermined site leaving a visually perceptible colored mark of a same color as the colored latex particles at said second predetermined site, thereby indicating at least one of completion of the test and operability of the test device.

3. The analytical test device according to claim 1, wherein the test kit housing defines a reception cavity adjacent said means for introduction of the body fluid sample at the first end and said latex particles are immobilized at the reception cavity prior to introduction of the body fluid sample.

4. The analytical test device according to claim 3, wherein the test kit housing includes means for initiating flow along the flow path from the reception cavity to the membrane support.

5. The analytical test device according to claim 4, wherein said means for initiating flow includes two sections of said housing, said sections disposed for relative movement with respect to each other, the flow path being closed when the two sections are abutted and opened when the two sections are relatively displaced.

6. The analytical test device according to claim 3, further comprising a first absorptive pad in communicating relationship with the means for introduction of the body fluid sample at said first end.

7. The analytical test device according to claim 6, further comprising at least one additional absorptive pad toward said second end and downstream of the first absorptive pad and the membrane support, the additional absorptive pad receiving flow of the body fluid sample following passage thereof through and along the membrane support.

8. The analytical test device according to claim 1, wherein said immobilized drug probe contains an antigen conjugate for one of a drug of abuse or a metabolite of a drug of abuse.

9. The analytical test device according to claim 8, wherein the membrane support is a porous material and the body fluid sample proceeds along the flow path of the membrane support by capillary action.

10. The analytical test device according to claim 8, wherein the drugs of abuse are at least one of cocaine, cannabinoids, amphetamine/methamphetamine, phencyclidene, and opiates.

11. The analytical test device according to claim 8, wherein the colored latex particles are finally blocked with protein to substantially completely coat the colored latex particles.

12. The analytical test device according to claim 8, wherein the housing defines at least one capillary passage along the flow path dimensioned to draw the body fluid by surface tension.

13. The analytical test device according to claim 12, wherein the membrane support is a porous material and the flow path proceeds along the membrane support by capillary action of the porous material.

14. The analytical test device according to claim 8, wherein the colored latex particles are substantially formed as latex spheres.

15. The analytical test device according to claim 14, wherein the latex spheres have a diameter of about 0.1 micron to 1.0 micron.

16. An analytical test assembly for producing a visually-perceptible indication of whether particular non-protein antigens are present via simultaneous multiple competition assays for said particular non-protein antigens representing drugs of abuse, consisting essentially of:

a plurality of test kit housings each having means for introduction of a body fluid sample at a first end of said housings and means defining a flow path for the body fluid sample to a second end within said housings;

a supply of microscopic colored latex particles disposed adjacent to each of the means for introduction of the body fluid sample along the flow path, the colored latex particles becoming suspended in the body fluid sample and moving with flow of the body fluid sample along the flow path from said first end toward said second end, the colored latex particles being sensitized with a supply of antibodies for the non-protein antigen at least on a surface thereof, said antibodies being responsive to said non-protein antigens and being operable to complex therewith;

a chromatographic membrane support disposed within each of the test kit housings and being impregnated at a first predetermined site along the flow path downstream of the colored latex particles towards said second end with an immobilized drug conjugate probe sensitive to said antibodies on the latex particles, and operable to complex therewith;

means for exposing the colored latex particles at said first end to the body fluid sample for substantially complete reaction of the non-protein antigens in the body fluid sample with the antibodies for the non-protein antigen on the colored latex particles, prior to the body fluid sample reaching the predetermined site along the flow path whereby when said non-protein antigens are not present in the body fluid sample the colored latex particles accumulate at the predetermined site downstream of said first end by complexing of the antibodies on the colored latex particles with the drug conjugate probe on the membrane support to leave a visually perceptible colored mark of a same color as the colored latex particles, and when said non-protein antigens are present in the body fluid sample, complexing of the non-protein antigens to the supply of antibodies on the colored latex particles substantially exhausts the antibody supply on the colored latex particles such that the colored latex particles cannot complex to the immobilized drug conjugate probe, leaving no visually perceptible mark at the predetermined site; and

,

a holder for maintaining a plurality of analytical test devices, each said analytical test device including one of said test kit housings, said supply of microscopic colored latex particles and chromatographic membranes in fixed relationship, comprising;

a holder body adapted to removably receive the plurality of analytical test devices, and means for securing the plurality of analytical test devices in the holder.

17. The analytical test assembly according to claim 16, wherein the securing means is a press fit.

18. The analytical test assembly according to claim 16, wherein the plurality of analytical test devices are disposed parallel to each other.

19. The analytical test assembly according to claim 16, wherein the holder defines at least one external well dimensioned to receive the body fluid sample.

20. The analytical test assembly according to claim 16, wherein the holder defines a plurality of external wells each dimensioned to receive a portion of the body fluid sample, and each corresponding to one of the plurality of analytical test devices in the holder.

21. The analytical test assembly according to claim 16, wherein the holder defines a common reception cavity having means for communicating a portion of the body fluid sample introduced therein to each of the plurality of analytical test devices.

22. The analytical test assembly according to claim 21, wherein the plurality of analytical test devices are each disposed radially outwardly from the common reception cavity.

23. An analytical test device for competition assay for particular non-protein antigens representing drugs of abuse, consisting essentially of:

a test kit housing having means for introduction of a body fluid sample at a first end of said housing and means defining a flow path for the body fluid sample to a second end within said housing;

a supply of microscopic colored latex particles disposed adjacent to the means for introduction of the body fluid sample along the flow path, the colored latex particles becoming suspended in the body fluid sample and moving with flow of the body fluid sample along the flow path from said first end toward said second end, the colored latex particles being sensitized at least on a surface thereof with at least one of said antigens representing drugs of abuse and a functionally identical antigen conjugate;

a chromatographic membrane support disposed within the test kit housing and being impregnated at a first predetermined site along the flow path with an immobilized antibody responsive to said antigen and said antigen conjugate, and operable to complex therewith; and

means in proximity with said means for introduction of the body fluid, for allowing the colored latex particles and the body fluid sample to mix and for allowing the mixed colored latex particles and the body fluid sample to flow along the flow path from said first end toward said second end to the predetermined site such that the body fluid sample reaches the predetermined site prior to the colored latex particles, whereby presence of the antigen in the body fluid is indicated by lack of a colored mark at the predetermined site, due to exhaustion of said antibodies by binding with the antigen in the body fluid sample, and absence of the antigen in the body fluid sample is indicated by presence of the colored mark at the predetermined site due to binding of the latex particles to the antibodies the colored mark being of a same color as the colored latex particles.

24. The analytical test device according to claim 23, wherein said means for allowing the colored latex particles and the body fluid to mix and to flow toward the predetermined site includes a porous membrane between the means for introduction of the body fluid and the predetermined site, said body fluid sample traversing the porous membrane more quickly than the colored latex particles.