Abstract: A waveguide binding assay method involves detecting the scattering of light directed into the waveguide, the scattering being the result of scattering labels specifically bound to the waveguide within the penetration depth of an evanescent wave. The waveguide may be transparent plastic or glass and the binding is typically by oligonucleotide hybridization or immunological capture. Light scattering labels include colloidal metals or non-metals, including gold, selenium and latex. A light absorbing member consisting of dye or concentrated particles may also be employed to enhance signal. Real-time binding and dissociation can be monitored visually or by video imaging, such as with a CCD camera and frame grabber software. Hybridization mismatches of as few as one base can be distinguished by real-time melting curves.

Abstract: A device and method for quantitative determination of an analyte in a biological sample utilizes a non-transparent support medium for retaining a chromatogenic reaction product with the medium being exposed to a source of light for transmitting therethrough a scattered, uniform response light signal which is collected at a photosensitive device whereby the amount of the analyte is correlated to the intensity of the response light signal. The response light signal may be converted to a time-duration signal proportional to light intensity to facilitate the quantitative determination.