Abstract: Compounds and methods of using said compounds, singly or in combination with additional agents, and pharmaceutical compositions of said compounds for the treatment of viral infections are disclosed.

Abstract: Spectroscopic systems and methods are disclosed for determining levels of at least one analyte in blood undergoing hemodialysis. In one aspect, the invention employs Raman spectroscopy to monitor and/or control hemodialysis. In one embodiment, the system uses a laser light directed to circulating blood from a patient undergoing dialysis to make Raman spectral measurements. For example, the laser light can be directed into a segment of the dialysis tubing. The system can utilize unique Raman spectroscopic signature of one or more analytes, e.g., urea, to identify and quantify such analytes against a whole blood background. Based on the spectral response, the concentration of the analytes can be monitored and/or used to control hemodialysis.

Abstract: The invention provides diagnostic apparatuses that are advantageously adapted for the Raman spectroscopic analysis of fluid samples, such as biological fluid samples, deposited on test strip substrates. The tests strips may be include a surface-enhanced Raman spectroscopy (SERS) surface for deposition and analysis of a sample and/or may be lateral flow binding assay type test strips.

Abstract: Methods and apparatus for in vitro detection of an analyte in a body fluid sample using low resolution Raman spectroscopy are disclosed. The body fluid analyzer includes a disposable strip for receiving a sample of body fluid on a target region, the target region including gold sol-gel to provide surface enhanced Raman scattering. A light source irradiates the target region to produce a Raman spectrum consisting of scattered electromagnetic radiation that is separated into different wavelength components by a dispersion element. A detection array detects at least some of the wavelength components of the scattered light and provides data to a processor for processing the data. The results of the processed data are displayed on a screen to inform a user about an analyte within the body fluid sample.

Abstract: Methods and apparatus for in vitro detection of an analyte in a blood sample using low resolution Raman spectroscopy are disclosed. The blood analyzer includes a disposable strip for receiving a sample of blood on a target region, the target region including gold sol-gel to provide surface enhanced Raman scattering. A light source irradiates the target region to produce a Raman spectrum consisting of scattered electromagnetic radiation that is separated into different wavelength components by a dispersion element. A detection array detects a least some of the wavelength components of the scattered light and provides data to a processor for processing the data. The results of the processed data are displayed on a screen to inform a user about an analyte within the blood sample.

Abstract: Spectroscopic systems and methods are disclosed for determining levels of at least one analyte in blood undergoing hemodialysis. In one aspect, the invention employs Raman spectroscopy to monitor and/or control hemodialysis. In one embodiment, the system uses a laser light directed to circulating blood from a patient undergoing dialysis to make Raman spectral measurements. For example, the laser light can be directed into a segment of the dialysis tubing. The system can utilize unique Raman spectroscopic signature of one or more analytes, e.g., urea, to identify and quantify such analytes against a whole blood background. Based on the spectral response, the concentration of the analytes can be monitored and/or used to control hemodialysis.

Abstract: Spectroscopic systems and methods are disclosed for determining levels of at least one analyte in blood undergoing hemodialysis. In one aspect, the invention employs Raman spectroscopy to monitor and/or control hemodialysis. In one embodiment, the system uses a laser light directed to circulating blood from a patient undergoing dialysis to make Raman spectral measurements. For example, the laser light can be directed into a segment of the dialysis tubing. The system can utilize unique Raman spectroscopic signature of one or more analytes, e.g., urea, to identify and quantify such analytes against a whole blood background. Based on the spectral response, the concentration of the analytes can be monitored and/or used to control hemodialysis.

Abstract: Production of oxygen-enriched gas streams is disclosed herein. Air streams contact an oxygen-selective mixed conductor particularly a perovskite material whereby oxygen is retained or adsorbed on the perovskite and can be employed in a variety of processes such as in combusting a fuel gas, heat recovery and boiler related operations.

Abstract: Raman spectroscopy probe assemblies are disclosed for use with portable and/or handheld analyzers. The probes are also adaptable to sample liquids, and/or powders, tablets and/or other solids and are capable of withstanding harsh environmental conditions. The probes include an optical head assembly, associated optical fibers and replaceable sampling tubes. In one aspect of the invention, a simple orthogonal optical head assembly is disclosed that does not require collinear optical paths. The orthogonal arrangement of input and captured light paths also reduces the need for precise alignment of the optical components. The orthogonal optical head assemblies of the present invention are well suited to accommodate the shutoff mechanisms of the present invention. In another aspect of the invention, sampling tubes, and replaceable end caps for such tubes, are disclosed that facilitate hand measurements of substances.

Abstract: A liquid can be marked for identification purposes with at least first and second miscible markers. The markers are mixed in the liquid so that the ratio of the concentration of the first marker to the concentration of the second marker is substantially equal to a predetermined value. Thus, by comparing the ratio of the measured concentration of the first marker to the measured concentration of the second marker with predetermined values the liquid can be uniquely identified. The detectors can be connected to a processor and control unit (22) for initiation of testing, for processing of detection signal from the detectors, and for display of readout information. Processor and control unit (22) can include a look up table (23) for storing information about marking patterns, a comparison element (35) for comparing measured values with values supplied by look up table (23), and a display (30).

Abstract: Spectroscopic systems and methods are disclosed for determining levels of at least one analyte in blood undergoing hemodialysis. In one aspect, the invention employs Raman spectroscopy to monitor and/or control hemodialysis. In one embodiment, the system uses a laser light directed to circulating blood from a patient undergoing dialysis to make Raman spectral measurements. For example, the laser light can be directed into a segment of the dialysis tubing. The system can utilize unique Raman spectroscopic signature of one or more analytes, e.g., urea, to identify and quantify such analytes against a whole blood background. Based on the spectral response, the concentration of the analytes can be monitored and/or used to control hemodialysis.

Abstract: The invention is directed to a method of making and using a porous solid matrix for trapping metal nanoparticles for use in detection, identification and quantification of trace levels of water contaminants using surface enhanced Raman scattering (SERS). The metal nanoparticles are polydispersed in the porous solid matrix, sufficiently separated to prevent conduction, in creating a broad area of excited electrons in response to applied radiation. In one aspect, the metal nanoparticles may be derived from gold, silver or platinum. In another aspect, the porous solid matrix is a sol-gel embedded with a polydispersion of metal for use in SERS detection. This metal nanoparticle substrate can be used on-site, is highly sensitive and easy to use for an immediate and accurate result.

Abstract: Raman spectroscopy probe assemblies are disclosed for use with portable and/or handheld analyzers. The probes are also adaptable to sample liquids, and/or powders, tablets and/or other solids and are capable of withstanding harsh environmental conditions. The probes include an optical head assembly, associated optical fibers and replaceable sampling tubes. Safety shut-off mechanisms are provided to reduce the risk of inadvertent exposure to radiation. In one embodiment, the shut-off switch is a spring-biased shutter that is opened by a solenoid only under predefined proper operating conditions. In another aspect of the invention, a simple orthogonal optical head assembly is disclosed that does not require collinear optical paths. The orthogonal arrangement of input and captured light paths also reduces the need for precise alignment of the optical components. The orthogonal optical head assemblies of the present invention are well suited to accommodate the shutoff mechanisms of the present invention.

Abstract: Production of oxygen-enriched gas streams is disclosed herein. Air streams contact an oxygen-selective mixed conductor particularly a perovskite material whereby oxygen is retained or adsorbed on the perovskite and can be employed in a variety of processes such as in combusting a fuel gas, heat recovery and boiler related operations.

Abstract: The present invention provides low resolution Raman spectroscopic systems and methods for in-vivo detection and analysis of a lesion in a lumen of a subject. The system uses a multi-mode laser attached to a catheter in making in-vivo Raman spectroscopic measurements of the lumen. The system includes a light collector and/or a light dispersion element as well as a detector to measure spectral patterns that indicate the presence of the lesion. Based on the spectral response of the lumen, the presence (or absence) of a lesion can be determined. In addition, the components of the lesion can also be identified based on the unique Raman spectrum associated with each component.

Abstract: The present invention provides an apparatus for measuring a property of a sample using low resolution Raman spectroscopy. The apparatus includes a multi-mode laser element, a wavelength dispersion element, a detector, and a processor. The multi-mode laser element irradiates a sample with laser radiation to produce a Raman spectrum. The collection element collects the radiation scattered from the molecules of the sample and transmits the scattered radiation to the dispersion element. The dispersion element disperses the scattered radiation into different wavelength components. The detection array detects the different wavelength components. A processor processes data from the detector array to identify a constituent or to measure a property of the sample. The apparatus preferably has a resolution of between 30 cm.sup.-1 and 50 cm.sup.-1. The resolution of the apparatus being determined in part by the spectral full width at half maximum of the multi-mode laser, and, in part, by the dispersion element.

Abstract: Methods for marking a liquid and methods and systems for identifying marked liquids. A liquid can be marked for identification purposes with at least a first marker and a second marker. Each of the markers is miscible with the liquid. The markers are mixed in the liquid so that the ratio of the concentration of the first marker to the concentration of the second marker is substantially equal to a predetermined value. Thus, when a system according to the invention measures the concentrations of the first and second markers, the system can compare the ratio of the measured concentration of the first marker to the measured concentration of the second marker with a look up table of the predetermined values to provide information concerning the identity of the liquid. In a preferred embodiment, the concentration of the markers is measured using an absorption spectrometer.

Abstract: Method and devices for fuel characterization and optimization on-site at a fuel delivery dispenser are disclosed. Fuel properties associated with a fuel sample of a fuel can be measured by mid-infrared analysis and displayed. Pre-determined preferred values for the fuel properties for the particular vehicle can be determined by inputting the model and type of vehicle into a processing means and correlating the vehicle information with the preferred values. The preferred and measured values can be compared and the comparison displayed. A fuel sample rating for the vehicle can be performed based this comparison and displayed. An optimal dispenser fuel for the vehicle can be identified based on a comparison between the preferred values and the values for the fuel properties for each of the dispenser fuels. In one embodiment, driveability index can be the fuel property determined in situ and in real time. In other embodiments, octane number, and Reid vapor pressure can be similarly determined.

Abstract: Method and apparatus for diagnosing fuel-related problems at the site of vehicle servicing and matching fuels to new engine designs. Fuel properties associated with a fuel sample can be measured with mid-infrared analysis. The measured fuel property values can be compared with pre-determined preferred values for the fuel properties for the particular type of vehicle. Fuel-related problems can then be identified and diagnosed based upon this comparison, and the diagnosis can be immediately displayed for the operator. In one embodiment, driveability index can be determined in situ and in real time. In other embodiments, octane number, and Reid vapor pressure can be similarly determined.

Abstract: Method and apparatus for detecting and/or monitoring the presence of hydrocarbons in a fluid medium at a remote location, by sensing the presence of hydrocarbon-based fluid in the fluid medium in the remote location, generating a signal indicative of the sensed fluid, and transmitting the signal to monitoring means for indication of hydrocarbon contamination. The apparatus has multiple sensors at different vertical levels for sensing the fluid medium at a plurality of levels within the fluid.