Instant Medical Diagnostics, LLC

Other

Immunomatrix, Inc.

Bryan C Christiansen

Alan R Day

Allan M Weinstein

Lance A Liotta

Katherine Paweletz

Tabitha Harlacher

Disclosed is a test device and a method for qualitatively and/or quantitatively measuring the concentration of an analyte in a biological fluid sample. The test device includes a housing defining a sample port, a test well containing a stirrer and a conjugate, and a test strip disposed within the housing. The test well is also defined by being located between the sample port and the test strip. Fluid flows from the test well onto the test strip, which has a trapping zone which binds the analyte and allows for its detection. A control zone may also be included. The test device is generally adapted to use a sandwich assay. Also disclosed is a system comprising the test device and a signal sensing device; and a method for using the test device.

Device for detection of molecules in biological fluids

A light generating dry disposable device for determining the presence of analytes in a test sample is disclosed. The device comprises a first zone containing conjugated ligand which is capable of reacting with analytes in the test sample. The ligand is conjugated with a photoprotein or related enzyme. The device further comprises a second trapping zone comprising immobilized analyte. The device also includes a third zone containing a reporter system that activates light generation by the conjugate. The conjugates are maintained in the first zone such that they are removable from the first zone when reacted with the soluble analytes from the test sample passing through the first zone, but not removed from the second trapping zone in the absence of such analytes. The third zone contains material capable of reacting with the photoprotein- or enzyme-linked ligand to produce a light-emitting reaction which indicates the presence of the analyte being tested. The present invention provides dry flow through zones. The trapping zone is juxtaposed with the light activation zone such that only formed analyte conjugate complexes enter the light activation zone. Also disclosed is the use of a luminometer for measuring the amount of light generated from the assay device upon detection of analyte. Other provisions are disclosed for recording and quantifying the amount of analyte, such as for example, photographic film.

Light-emitting immunoassay

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Germantown, MD, United States of America

Bryan C Christiansen