Solid phase multi-analyte assay
AssigneePsychemedics Corporation
InventorsVirginia Hill, Mohammad Atefi, Michael I. Schaffer
Life of this patent
Estimating the term…
Abstract
Compositions and methods for detecting the presence and/or amount of one or more analytes, including analytes such as drugs of abuse, are provided. The compositions include two or more analytes associated with a solid phase, e.g., a particle or a multiwell plate. The compositions and methods also allow the simultaneous, tandem, or serial determination of the presence and/or amount of two or more analytes of interest in a sample.
Claims18
A method for determining the amount of an analyte of interest in a sample, the method comprising contacting a solid phase composition with i) an antibody specific for the analyte of interest and ii) the sample under competitive binding conditions, and determining the amount of the analyte of interest in the sample;
- wherein:
- the solid phase composition comprises a polystyrene solid phase support and at least two different conjugates, wherein each conjugate comprises an albumin covalently conjugated to a drug of abuse or metabolite thereof selected from the group consisting of benzoylecgonine, an amphetamine, tramadol, PCP, morphine, oxycodone, methadone, cotinine, a benzodiazepine, buprenorphine, fentanyl, and a cannabinoid;
- wherein the antibody specific for the analyte of interest binds to one of the at least two different conjugates;
- the analyte is a drug of abuse or a metabolite thereof;
- the at least two different conjugates are bound noncovalently or via adsorption to the polystyrene solid phase support;
- the at least two different conjugates are randomly affixed as a mixture to a single solid phase component of the polystyrene solid phase support, wherein the polystyrene solid phase support comprises a plurality of single solid phase components, and each single solid phase component of the polystyrene solid phase support comprises the at least two different conjugates;
- and
- the antibody specific for the analyte of interest is labeled or a labeled secondary antibody is introduced which is specific for the antibody specific for the analyte of interest.
Dependencies are inferred from the claim text.