Optiscan Biomedical Corporation

Sony Pictures Entertainment, Inc.

Sony Corporation

Sony Electronics Inc

Sony Corporation of Japan

Ivac Medical Systems, Inc.

Casper W Barnes

James Roswell Braig

Peng Zheng

Daniel S Goldberger

Bernhard B Sterling

Arthur Melvin Shulenberger

Charles E Kramer

Richard A King

Rick P Trebino

Richard J Oliver

Paul M Embree

Rick Trembino

Robert Dwaine Butterfield

Jennifer H Gable

Gail Dawn Baura

Gregory I Voss

Laura Mercs

W Dale Hall

A method of determining the analyte concentration of a test sample is described. A temperature gradient is introduced in the test sample and infrared radiation detectors measure radiation at selected analyte absorbance peak and reference wavelengths. Reference and analytical signals are detected. In the presence of the selected analyte, parameter differences between reference and analytical signals are detectable. These parameter differences, having a relationship to analyte concentration, are measured, correlated, and processed to determine analyte concentration in the test sample. Accuracy is enhanced by inducing a periodically modulated temperature gradient in the test sample. The analytical and reference signals may be measured continuously and the parameter difference integrated over the measurement period to determine analyte concentration.

Method for determining analyte concentration using periodic temperature modulation and phase detection

A method and apparatus of determining the analyte concentration of a test sample is described. A temperature gradient is introduced into the test sample and infrared radiation detectors measure radiation at selected analyte absorbance peak and reference wavelengths. The modulation of the temperature gradient is controlled by a surface temperature modulation. A transfer function is determined that relates the surface temperature modulation to the modulation of the measured infrared radiation. Reference and analytical signals are detected. In the presence of the selected analyte, phase and magnitude differences in the transfer function are detected. These phase and magnitude differences, having a relationship to analyte concentration, are measured, correlated and processed to determine analyte concentration in the sample.

Method and apparatus for determining analyte concentration using phase and magnitude detection of a radiation transfer function

A device and method for determining analyte concentrations within a material sample are provided. A modulating temperature gradient is induced in the sample and resultant, emitted infrared radiation is measured at selected analyte absorbance peaks and reference wavelengths. The modulating temperature gradient is controlled by a surface temperature modulation. One embodiment provides a transfer function relating the surface temperature modulation to a modulation of the measured infrared radiation. Phase and magnitude differences in the transfer function are detected in the presence of the sought-after analyte. These phase and magnitude differences, having a relationship to analyte concentration, are measured, correlated and processed to determine analyte concentration in the material sample. Another embodiment provides a method for transforming thermal phase spectra to absorption spectra for consistent determination of analyte concentration within the sample.

Method for transforming phase spectra to absorption spectra

A method and apparatus of determining the analyte concentration of a test sample is described. A temperature gradient is introduced in the test sample and infrared radiation detectors measure radiation at selected analyte absorbance peak and reference wavelengths. The modulation of the temperature gradient is controlled by a surface temperature modulation. A transfer function is determined that relates the surface temperature modulation to the modulation of the measured infrared radiation. Reference and analytical signals are detected. In the presence of the selected analyte, phase and magnitude differences in the transfer function are detected. These phase and magnitude differences, having a relationship to analyte concentration, are measured, correlated, and processed to determine analyte concentration in the test sample.

Method for determining analyte concentration using periodic temperature

A system for processing audio samples, which compensates for any error between a future state of the system after a delay through a network and the predicted value of the input at that future time. The system synchronizes the motion of an audio transport to the motion of an audio input which has been delayed in processing through the network.

Audio sample tracker

A filter for a system for processing audio samples, which dynamically vaires its length responsive to a moving average of variations in an audio input rate. The filter lengthens at substantially constant input rate variations to reduce input noise, and shortens at rapid input rate variations to enhance responsiveness.

Variable-length moving-average filter

A decoder capable of decoding audio signals encoded using analog noise reduction techniques, particularly Dolby SR, is implemented by means of digital signal processing. The typical decoding paradigm used by analog Dolby SR decoders is modified to overcome the problems caused by delay which is introduced by the digital implementation. A gain factor is factored out of the feedback transfer function and is placed in the forward signal path of each stage of the digital decoder. A single control circuit can then be used to generate coefficients which define transfer functions of each filter stage of the signal path. Linear interpolation techniques are used to limit the number of coefficient entries necessary to emulate the transfer function of an analog Dolby SR decoder. The digital decoder structure can be inverted to produce a digital encoder which is capable of implementing any noise reduction standard desired, including Dolby SR.

DSP decoder for decoding analog SR encoded audio signals

Impedance to fluid flow in a fluid delivery line is measured. Two techniques are used depending on the flow rate selected. For high flow rates, the pump is controlled to vary the flow rate and the change in pressure is divided by the change in flow to directly determine the resistance. For low flow rates, a processor controls the pump to pump flow quantities in accordance with a pseudo-random binary code. The resulting pressure signal sensed at the conduit is decoded in accordance with that code. Pressures received during code periods of no flow are subtracted from pressures received during code periods of flow. Pressure offset is also removed and a least squares estimation approach is used with a linear prediction model to determine impedance. The coefficients determined in the model are used to calculate the resistance to fluid flow of the system. A quality supervisor monitors the resistance determination process and controls the display of resistance depending on the quality determined. A resistance display continuously displays the resistance of the system.

Fluid flow impedance monitoring system

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Murrieta, CA, United States of America

Casper W Barnes