Multiwell stat test

Claim 1

A kit for performing a diagnostic assay, said kit comprising: (1) a collector-dilutor-dispenser device useful for processing a sample for a diagnostic assay and quantitatively measuring a sample volume, said device comprising: a compressible tube enclosed at one end; a cover mounted over the open end of said tube and comprising at least one aperture; a liquid medium in said tube; at least one frangible barrier separating said medium from said aperture; and at least one absorbent nib in said tube above said barrier and extending through said aperture, said nib comprising means for preventing said nib to pass through said aperture, providing substantially quantitative release of said sample into said liquid medium for allowing for quantitative determination of an analyte in said sample; (2) a diagnostic device for measuring an analyte which is a member of a specific binding pair, where a label is employed for said measuring which label provides for a visual detectable signal, said device comprising: a housing comprising an upper reservoir portion and a lower casing portion for holding at least one layer; in said casing in the direction of flow: a porous reactive filter as the floor of said reservoir component comprising a measurement circle of a member of a specific binding pair immobilized to said filter and defining a concentration gradient comprising an inner circle at an elevated concentration and an outer contiguous circle at a substantially lower concentration; and fluid receiving means for receiving fluid from said porous reactive filter; and (3) reagents for performing said assay.

Claim 3

A method for detecting the presence of an analyte in a sample, said method employing a reagent system which produces a visual signal for detecting the formation of specific binding pair member complexes, and a collector-dilutor-dispenser device useful for processing a sample for a diagnostic assay and measuring a sample volume, said device comprising: a compressible tube closed at one end; a cover mounted over the open end of said tube and comprising at least one aperture; a liquid medium for use in said diagnostic assay is said tube as the assay medium; a least one frangible barrier separating said medium from said aperture; and at least one absorbent nib in said tube above said barrier and extending through said aperture, said nib comprising means for preventing said nib to pass through said aperture, wherein said nib is supported by said frangible barrier and becomes at least partially immersed in said medium upon breaking of said frangible barrier, said nib being capable of absorbing a predetermined liquid volume and substantially quantitatively releasing said sample into said liquid medium; said method comprising: contacting said sample with said nib, wherein said nib absorbs said sample in a predetermined volume; breaking said frangible barrier, whereby said nib is combined with said liquid medium and said sample is dispensed into said liquid medium, wherein said liquid medium optionally includes at least one reagent of said reagent system; transferring said liquid medium through said aperture in the absence of said nib to the reservoir of a diagnostic device for measuring an analyte which is a member of a specific binding pair, said device comprising: a housing comprising an upper reservoir portion and a lower casing portion for holding at least one layer; in said casing in the direction of flow: a porous reactive filter as the floor of said reservoir component comprising a measurement circle of a member of a specific binding pair immobilized to said filter and defining a concentration gradient comprising an inner circle at an elevated concentration and an outer contiguous circle at a substantially lower concentration; and fluid receiving means for receiving fluid from said porous reactive filter; allowing said liquid medium to pass through said porous reactive filter into said fluid receiving means; adding any additional reagents of said reagent system to said porous reactive filter; and detecting the presence of said visual signal in relation to a visual signal obtained with a sample having a known amount of analyte.

Claim 4

A method for detecting the presence of an analyte in a sample, said method employing a reagent system which produces a visual signal for detecting the formation of specific binding pair member complexes, and a collector-dilutor-dispenser device useful for processing a sample for a diagnostic assay and measuring a sample volume, said device comprising: a compressible tube closed at one end; a cover mounted over the open end of said tube and comprising at least one aperture; a liquid medium for use in said diagnostic assay is said tube as the assay medium; a least one frangible barrier separating said medium from said aperture; and at least one absorbent nib in said tube above said barrier and extending through said aperture, said nib comprising means for preventing said nib to pass through said aperture, wherein said nib is supported by said frangible barrier and becomes at least partially immersed in said medium upon breaking of said frangible barrier, said nib being capable of absorbing a predetermined liquid volume and substantially quantitatively releasing said sample into said liquid medium; said method comprising: contacting said sample with said nib, wherein said nib absorbs said sample in a predetermined volume; breaking said frangible barrier, whereby said nib is combined with said liquid medium and said sample is dispensed into said liquid medium, wherein said liquid medium optionally includes at least one reagent of said reagent system; transferring said liquid medium through said aperture in the absence of said nib to the reservoir of a diagnostic device for measuring an analyte which is a member of a specific binding pair, said device comprising: a housing comprising an upper reservoir portion and a lower casing portion for holding at least one layer; in said casing in the direction of flow: a porous reactive filter as the floor of said reservoir component comprising a measurement circle of a member of a specific binding pair immobilized to said filter and defining a concentration gradient comprising an inner circle at an elevated concentration and an outer contiguous circle at a substantially lower concentration; and fluid receiving means for receiving fluid from said porous reactive filter; allowing said liquid medium to pass through said porous reactive filter into said fluid receiving means; adding any additional reagents of said reagent system to said porous reactive filter; and detecting the presence of said visual signal in relation to a visual signal obtained with a sample having a known amount of analyte.