Borrowing from clinical laboratory methods, rapid-screening tests based on immunochemical or nucleic acid technologies have been developed for food testing. These tests can provide results in 8 to 48 hours.The three types of rapid-test methods are manual, semiautomated, and fully automated. Manual rapid-test methods include lateral-flow tests and dipstick immunoassays. Semiautomated methods include ELISA tests and enzyme-linked hybridization tests. Fully automated systems include instrumentation to perform either immunoassays or PCR methodologies.
Researchers have developed some new rapid technology that can detect food borne pathogens, such as electroimmunoassay technology and live cells technology.
Electroimmunoassays couple specific antibody-antigen binding to the production of an electrical signal. The technology is comprised of a circuit with a capture antibody attached to the solid surface in the area of the electrode gap Upon addition of sample, the target antigen binds to the capture antibody. In the next step, a colloidal gold–labeled detection antibody is bound, creating a capture-target-detector sandwich. The final step is the deposition of silver ions onto the colloidal gold, which produces a conductive silver bridge, closing the circuit and resulting in a measured drop in resistance. This detection technology can also be applied to nucleic acid hybridization assays.
In addition, the live cells technique utilizes live mammalian cells that release a measurable amount of a signaling chemical when harmed. Optical equipment and computer software can then analyze this quantity to estimate the amount of harmful microbes present, Bhunia said. The technology can recognize very small amounts of Listeria monocytogenes, a bacterium that kills one in five infected and is the leading cause of food-borne illness. It also recognizes several species of Bacillus, a non-fatal but common cause of food-poisoning. The cells are suspended in collagen gel, a useful substance for capturing particles of a desired size, and put into small wells within multi-well plates. Each well can test one sample, so tests can be expanded to quickly analyze as many samples as desired.
http://www.purdue.edu/UNS/x/2008a/080228BhuniaBiosensor.html
http://www.devicelink.com/ivdt/archive/01/06/003.html