Abstract:
Methods and apparatus for detecting biological activity within a sample are disclosed. The present invention provides a combination of a first and a second infrared light source arranged on the side of a sample vial, and a first and a second narrow-band infrared detector similarly arranged on the side of the vial approximately opposite the sources. The disclosed arrangement cancels the sources of error while measuring the carbon dioxide content of the headspace gas above the sample. In operation, the present invention sequentially measures the photocurrents generated at each detector with no source turned on, with the first source turned on, and with the second source turned on and the first source turned off. The C0 2 absorption coefficient of the vial headspace gas is then calculated based on the photocurrents measured. This present invention allows compensation for source aging, detector aging, and vial wall thickness changes. Moreover, the present invention permits a determination of the absolute absorption coefficient at a selected wavelength, most preferably about 4.26 µm, which is the C0 2 absorption characteristic wavelength. The determination of the absolute C0 2 concentration within the headspace permits the detection of bacterial growth processes. Additionally, the disclosed source/detector combination can be produced at low cost. Thus, in preferred embodiments, the apparatus of the present invention comprises a plurality of vials that are simultaneously monitored by providing each of the plurality of vials with its own source/detector combination and activating and deactivating the sources and detectors using a multiplexer/demultiplexer arrangement.
Abstract:
An assay result reading device for reading the result of an assay performed using a test strip, the device comprising: a light source or sources, said light source(s) emitting light incident upon at least two, spatially separated zones of the test strip; and a photodetector which detects light emanating from each of the two said zones; in a further aspect is disclosed an assay result reading device for reading the result of an assay performed using a test strip, the device comprising: at least one light source incident upon a zone of the test strip; and at least two photodetectors both of which are able to detect some of the light emanating from the zone of the test strip illuminated by the light source.
Abstract:
Disclosed is an assay result reading device for reading the result of an assay performed using a liquid transport carrier, the device comprising: at least one light source capable of emitting light incident upon at least one of two or more spatially separated zones of the carrier; a photodetector so positioned as to be capable of detecting light emanating from each of the two said zones and generating signals representing the presence or absence of a fluid sample in the respective zone; and a computation circuit responsive to the signals to: calculate a flow rate for a fluid flowing along the carrier; compare the calculated flow rate to upper and lower limits; and reject the assay result if the calculated flow rate is outside the upper and lower limits
Abstract:
An assay result reading device for reading the result of an assay performed using a liquid transport carrier may include at least one light source capable of emitting light incident upon at least one of two or more spatially separated zones of the carrier, a photodetector so positioned as to be capable of detecting light emanating from each of the two said zones and generating signals representing the presence or absence of a fluid sample in the respective zone, and a computation circuit. The computation circuit may be responsive to the signals to calculate a flow rate for a fluid flowing along the carrier, compare the calculated flow rate to upper and lower limits, and reject the assay result if the calculated flow rate is outside the upper and lower limits.
Abstract:
Methods and apparatus for detecting biological activity within a sample are disclosed. The present invention provides a combination of a first and a second infrared light source arranged on the side of a sample vial, and a first and a second narrow-band infrared detector similarly arranged on the side of the vial approximately opposite the sources. The disclosed arrangement cancels the sources of error while measuring the carbon dioxide content of the headspace gas above the sample. In operation, the present invention sequentially measures the photocurrents generated at each detector with no source turned on, with the first source turned on, and with the second source turned on and the first source turned off. The C0 2 absorption coefficient of the vial headspace gas is then calculated based on the photocurrents measured. This present invention allows compensation for source aging, detector aging, and vial wall thickness changes. Moreover, the present invention permits a determination of the absolute absorption coefficient at a selected wavelength, most preferably about 4.26 µm, which is the C0 2 absorption characteristic wavelength. The determination of the absolute C0 2 concentration within the headspace permits the detection of bacterial growth processes. Additionally, the disclosed source/detector combination can be produced at low cost. Thus, in preferred embodiments, the apparatus of the present invention comprises a plurality of vials that are simultaneously monitored by providing each of the plurality of vials with its own source/detector combination and activating and deactivating the sources and detectors using a multiplexer/demultiplexer arrangement.
Abstract:
PROBLEM TO BE SOLVED: To provide a method for deciding optimal read time to address a situation where a flow rate of a liquid flowing along a porous carrier fluctuates for every inspection in a manner that a convection current surface moves along the carrier at a faster rate than usual in one inspection and at a slower rate than usual in the other inspection causing optimal read time to be fluctuated accordingly.SOLUTION: An analysis result reading device to read a result of an analysis performed with a liquid transfer carrier comprises: at least one light source to radiate light incident on at least one of two or more spatially isolated regions in the carrier; a light detector which is positioned to receive light emitted from each of the two or more regions and generates a signal to indicate whether or not a liquid sample is present in each of the region; and a calculation circuit. The calculation circuit calculates a flow rate of a fluid stream along the carrier in response to the signal, compares the calculated flow rate with an upper limit and a lower limit, and rejects an analysis result when the calculated flow rate is outside a range between the upper limit and the lower limit.