Abstract:
Method and apparatus for spectroscopic measurement of the concentration of a gas in a sample where you detect the intensity of light from a light source (1) passed through the sample (4) and through a reference cell (5) and generates a signal which represents the concentration of the gas. A laser diode (1) constitutes the light source which is locked to the absorption line of the gas at known concentration and pressure contained in a reference cell (5). The laser light with the properly selected wavelength is distributed via optical fibres (2, 3, 6) and/or glass prisms (19, 20) to the reference cell (5) and the sample (4). Non-gas-related transmission variations in the measurement path or in the optics is automatically compensated for by a special laser modulation which generates a time multiplexed reference. The measurement can be performed in a measurement cell incorporating several reflective mirrors (30) to reflect the laser beam several times inside the measurement cell thereby increasing the effective length of the measurement path. The measurement can also be performed using an optical fiber designed so that the surrounding gas or fluid via the evanescent field affects the laser light so that the concentration of the substance in question in the surrrounding fluid or gas can be determined.
Abstract:
A method and apparatus for measuring the oxygen saturation level and hematocrit of human blood in real time. A catheter having a notch in its tip is inserted into a blood vessel and guided to a desired location in the body of a patient. Bursts of light at each of three wavelengths are transmitted through the blood in the notch. The intensities of the bursts of light after transmission are utilized along with a set of molecular exinction coefficients and optical scattering coefficients to calculate the oxygen level and hermatocrit. The light is provided by a set of LEDs in a housing connected to the catheter and the intensity of the transmitted light is measured by a photocell in the same housing. Optical fibers transmit the light through the catheter between the housing and the notch. Characterization resistors in the housing are encoded with characteristics such as the wavelengths of the LEDs and the width of the notch. In an alternate embodiment blood circulating through a loop out of the patient's body is passed through a chamber and is exposed to the light.
Abstract:
This invention pertains to a method and an apparatus for determining concentration of solid particles of interest in a sample in the presence of at least one other type of solid particle by measuring light scatter at a wavelength which is independent of solid particle concentration which is not of interest and related to solid particle concentration of interest. Preferably, solid particles of interest are cells grown in cell culture medium comprising a solid substrate.
Abstract:
Concentration gradients in samples to be evaluated are detected by measuring the deflection of a probe light beam passed through the sample using the principals of Schlieren optics. Specific chemical compounds in a sample can be detected and identified by supplying excitation energy to the sample where such energy is selected to be absorbed by the chemical compound to be specifically identified and not by other compounds in the sample. The absorption of the excitation energy by the absorbing compound produces a temperature gradient within the sample which causes deflection of the probe light beam and signals representative of such deflection may be separated from signals representative of deflections caused by other refractive index gradient present in the sample. A light emitting diode may be used to generate the probe light beam. Rather than detecting movement of the probe light beam caused by an unknown gradient, by passing the probe light beam through a known gradient, with or without excitation energy present, the light beam can be deflected in a controlled manner.
Abstract:
In an optical instrument, fiber optics are employed to receive light from a linear filament. The fiber optics are arranged into a plurality of light receiving bundle ends distributed around the linear filament and shaped into narrow rectangular slits aligned with the filament. The fibers from each of the receiving ends are equally distributed between two transmitting ends which direct the light through cylindrical lenses to opposite sides of a rotating filter wheel in a paddle wheel configuration. Light beams from the transmitting ends of the fiber optic bundles pass through filters on the filter wheel to additional fiber optic bundles which carry the received light to a probe.
Abstract:
A system for coupling photometers to an incubation ring for use in in vitro diagnostics comprises one or more light sources, and an incubation ring assembly, and two photometers. An incubation ring assembly comprises an internal trough and an external trough. Each trough comprises (a) an internal wall comprising an internal aperture and (b) an external wall comprising an external aperture. A first photometer comprises: a first optics housing directing light from the light sources through the external aperture of the internal trough, and a first detector positioned to receive the light through the internal aperture of the internal trough. A second photometer comprises a second optics housing directing the light from the light sources through the internal aperture of the external trough, and a second detector positioned to receive the light through the external aperture of the external trough.
Abstract:
A spectroscopic system may include: a probe having a probe tip and an optical coupler, the optical coupler including an emitting fiber group and first and second receiving fiber groups, each fiber group having a first end and a second end, wherein the first ends of the fiber groups are formed into a bundle and optically exposed through the probe tip; a light source optically coupled to the second end of the emitting fiber group, the light source emitting light in at least a first waveband and a second waveband, the second waveband being different from the first waveband; a first spectrometer optically coupled to the second end of the first receiving fiber group and configured to process light in the first waveband; and a second spectrometer optically coupled to the second end of the second receiving fiber group and configured to process light in the second waveband.
Abstract:
An apparatus and method of use are provided; the apparatus having at least a degasser, a hollow core fiber HCF, an optical mechanism, a detector, and circuitry. The degasser enables gasses to permeate out of a liquid into the degasser interior. The propagator establishes a low-pressure area that helps to pull the gas from the degasser interior into the HCF interior, where the optical mechanism delivers electromagnetic radiation EMR that interacts with the gas. The detector determines EMR absorption, producing output signals which are sent to the circuitry. Circuitry controls the optical mechanism and analyzes the output signals to quantify the concentration of gas in the HCF and in the liquid.
Abstract:
The present invention is directed to an assembly for use in detecting an analyte in a sample based on thin-film spectral interference. The assembly includes a light source to emit light signals; a light detector to detect light signals; a coupler to optically couple the light source and the light detector to a waveguide tip; a monolithic substrate having a coupling side and a sensing side; and a lens between the waveguide tip and the monolithic substrate. The lens relays optical signals between the waveguide tip and the monolithic substrate.