Johns Hopkins University

David R Kohler

Harvey Wayne Ko

Micah A Carlson

George M Murray

Michael P McLoughlin

Jennifer L Sample

Terry E Phillips

Protagoras N Cutchis

Adam K Arabian

Charles W Anderson

Allan B Fraser

Richard C Benson

Jennifer A Nix

C Brent Bargeron

Cheryl S Schein

Paul T Strickland

John D Groopman

A method and apparatus for evaluating a bioaerosol sample is provided which includes detecting frequency and/or time resolution factors that allow discriminate between a plurality of signals emitted by the bioaerosol to selectively detect biological materials contained in the bioaerosol sample from materials of non-biological origin and potentially associated with a pathogenic bioaerosol.

Method and apparatus for detection of bioaerosols

A hand held, self-contained, automatic, low power and rapid sensor platform for detecting and quantifying a plurality of analytes. A sample solution potentially containing an unknown amount of an analyte is passed through an affinity column which contains antibodies to which the analyte binds thereby extracting the analyte. The affinity column is then rinsed to remove any other chemicals that may fluoresce. The rinsed affinity column is then eluted with a known volume of elution fluid causing the analyte to release from the antibody and dissolve in the fluid (eluant). The eluant is then placed in the quartz cuvette of a fluorometer. The analyte suspended in the eluant fluoresces at a waveband which is different than that of the light source that excites it. The amount of fluorescence is measured and the level of analyte determined. The rinsing and elution fluids, and/or the affinity column can be placed in a module for easy insertion and removal from the sensor when depleted or when the sensor is to be used against a different analyte.

Miniature immuno-optical rapid analyte sensor platform

Growing community of inventors

Ocean Pines, MD, United States of America

David R Kohler