Multiple Assay Device
Abstract
Disclosed is an assay device for the determination of analyte in a liquid sample over an extended concentration range comprising a first assay and a second assay, wherein the first assay for an analyte comprises a first flow-path having a sole detection zone capable of immobilising a labelled binding reagent and the second assay for said analyte comprises a second flow-path having a sole detection zone capable of immobilising a labelled binding reagent, wherein the presence of labelled binding reagent at the detection zones provides an indication of the presence and/or extent of analyte in said liquid sample.
Claims
exact text as granted — not AI-modified1 . An assay device for determining the presence or concentration of an analyte in a liquid sample over an extended concentration range comprising:
a) a first flow-path having a sole detection zone capable of immobilising a labelled binding reagent, the first flow-path capable of providing an indication of the level of analyte in a first concentration range; and b) a second flow-path having a sole detection zone capable of immobilising a labelled binding reagent, the second flow-path capable of providing an indication of the level of analyte in a second concentration range; wherein the presence of labelled binding reagent at the detection zones provides an indication of the presence or concentration of analyte in said liquid sample.
2 . (canceled)
3 . The device according to claim 1 wherein the first and second concentration ranges overlap.
4 . The assay device according to claim 1 which is capable of providing an indication of the level of analyte with respect to one or more thresholds.
5 . The device according to claim 1 wherein the first and/or second flow-path comprises a porous carrier.
6 . (canceled)
7 . The device according to claim 1 wherein the first and/or second flow-path comprises a mobilisable labelled binding reagent for the analyte provided upstream from a detection zone.
8 . The device according to claim 1 wherein the detection zone of the first and/or second flow-path comprises an immobilised binding reagent for the analyte.
9 . The device according to claim 1 wherein the first flow-path defines a sandwich assay and the second flow-path defines a competition or inhibition assay.
10 . The device according to claim 9 wherein the first flow-path comprises a mobilisable labelled binding reagent for the analyte provided upstream from a detection zone, said detection zone comprising an immobilised binding reagent for the analyte and wherein the second flow-path comprises a mobilisable binding reagent for the analyte provided upstream from provided upstream from a detection zone, said detection zone comprising an immobilised analyte or analyte analogue for the mobilisable binding reagent.
11 . The device according to claim 9 wherein the first flow-path comprises a mobilisable labelled binding reagent for the analyte provided upstream from a detection zone, said detection zone comprising an immobilised binding reagent for the analyte and wherein the second flow-path comprises a mobilisable labelled analyte or analyte analogue provided upstream from an immobilised binding reagent for the analyte.
12 . (canceled)
13 . The device according to claim 1 wherein the first flow-path comprises a mobilisable labelled binding reagent for an analyte provided upstream from a detection zone, wherein the detection zone comprises an immobilised non-labelled binding reagent for the analyte; and wherein the second assay comprises a mobilisable labelled binding reagent for a first binding region of the analyte and a scavenger binding reagent for the analyte provided upstream from a detection zone, wherein said detection zone is capable of binding the labelled binding reagent.
14 . (canceled)
15 . (canceled)
16 . The device according to claim 13 wherein the mobilisable labelled binding reagent and the scavenger binding reagent of the second flow-path are for respectively a first and second binding region of the analyte, the detection zone comprising an immobilised binding reagent for a second binding region of the analyte.
17 . (canceled)
18 . (canceled)
19 . The device according to claim 13 wherein the mobilisable binding reagents and the scavenger reagent are provided on or in a first porous carrier material and the immobilised binding reagent provided at the detection zone is provided on and/or in a second porous carrier material.
20 . The device according to claim 19 wherein the first porous carrier material is glass-fibre and the second porous carrier material is nitrocellulose.
21 . (canceled)
22 . (canceled)
23 . (canceled)
24 . The device according to claim 1 wherein the fluid sample is urine.
25 . The device according to claim 1 wherein the binding reagent is labelled with an optically detectable particle.
26 . The device according to claim 25 wherein the optically detectable particle is a coloured polymer label.
27 . The device according to claim 1 , comprising a common sample application region which serves to supply liquid sample to both flow-paths.
28 . (canceled)
29 . An assay device for determining the presence or concentration of an analyte in a liquid sample comprising a first flow-path and a second flow-path wherein said first flow-path comprises a porous carrier having a detection zone comprising an immobilised binding reagent for an analyte and provided upstream from the detection zone is a mobilisable labelled binding reagent for said analyte; and wherein said second flow-path comprises a detection zone comprising an immobilised binding reagent for the analyte and a mobilisable labelled binding reagent upstream from the detection zone for the analyte and a scavenger reagent for said analyte, wherein detection of the presence of labelled binding reagent at the detection zone provides an indication of the presence or concentration of analyte in said liquid sample.
30 . (canceled)
31 . (canceled)
32 . The device according to claim 1 , wherein:
a) the first flow-path is capable of providing an indication of the level of hCG in the sample in a first range of less than or equal to a first threshold; and b) the second flow-path is capable of providing an indication of the level of hCG in the sample in a second range of above or equal to a second threshold; and c) the first and second flow-paths together are capable of providing an indication of the level of hCG in a third range of greater than the first threshold but less than the second threshold.
33 . (canceled)
34 . (canceled)
35 . An assay kit for determining the presence or concentration of an analyte in a liquid sample comprising an assay device comprising a first flow-path and a second flow-path wherein:
a) said first flow-path comprises:
i) a porous carrier having a detection zone comprising an immobilised binding reagent for an analyte; and
ii) a mobilisable labelled binding reagent for said analyte upstream from the detection zone; and
b) said second flow-path comprises:
i) a detection zone comprising an immobilised binding reagent for the analyte; and
ii) a mobilisable labelled binding reagent for the analyte and a scavenger reagent for said analyte upstream from the detection zone,
wherein detection of the presence of labelled binding reagent at the detection zones provides an indication of the presence and/or extent of the analyte in the sample.
36 - 38 . (canceled)Join the waitlist — get patent alerts
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