Abstract:
A spectrometry instrument with exchangeable accessories (34, 48, 50, 52) providing, for example, different sample presentation facilities. The accessories include a manually operable cam-lock facility (54, 68) for quick and easy attachment of an accessory to the instrument. The instrument also includes an electrical circuit (86-90), which is completed by a circuit portion (100) in an accessory when the accessory is attached to the instrument, for generating a unique identifying voltage (94) to thereby identify that accessory. This allows for automatic loading in a controlling computer of programs for setting up and running the instrument for measurement regimes using that accessory. The spectrometry instrument is preferably a spectrophotometer used for phosphorescence decay measurements in which sequential phosphorescence emission measurements data from each of a number of excitation cycles applied to a sample are taken and then reassembled into a correct time sequence to define a phosphorescence decay characteristic for the sample, that is, measured data points from a second (and subsequent) excitation cycle are interleaved with those from a first excitation cycle. This significantly reduces the time for establishing a phosphorescence decay characteristic.
Abstract:
Embodiments of the present disclosure include an oximeter sensor system including a reusable portion including a substantially rigid connector connected to an end of a cable. The substantially rigid connector includes an electronic element housing at least one electronic component of a probe. The system also includes a disposable portion including a flexible wrap comprising a substantially rigid connection port shaped to receive the substantially rigid connector in a releasably securable manner.
Abstract:
The present invention relates generally to the field of biochemical laboratory. More particularly the invention relates to the improved and more accurate instrumental features of equipment used as e.g. fluorometers, photometers and luminometers. The object of the invention is achieved by providing an optical measurement instrument where there is an interface (218, 223, 233a, 233b, 238) for a changeable optical module (240), and excitation and/or emission beam is guided through an aperture of the optical module. This allows performing various types of measurements by changing an optical module without a problem lenses becoming unclean due to manual handling of the optical modules. The invention also makes possible to achieve an accurate measurement location and area within a sample.
Abstract:
A coupling mechanism for mounting a sample accessory assembly into a spectrometer. The accessory assembly, on which is mountable a sample to be analyzed by a spectrometer, has connecter ends which are insertable into stirrups on the sample compartment of the spectrometer. The connector ends and the stirrups have elements that ensure that the accessory assembly is properly aligned in the sample compartment of the spectrometer. The accessory assembly also has an electronic component, such as a circuit or programmable microchip, that is connected to the spectrometer when the accessory is mounted in the spectrometer. The electronic component provides information to the spectrometer identifying the accessory assembly being used so that a diagnostic test of the spectrometer can be performed to ascertain, for example, proper mounting of the accessory assembly in the spectrometer.
Abstract:
An optical device for sensing a presence of an analyte in a person is provided. The optical device includes a light source, an optical stack, and a reader. The light source emits a first light having a first wavelength. The optical stack is placed on a skin of the person. The optical stack includes a sensor material and an optical filter. The sensor material emits a second light having a second wavelength when irradiated with the first light. An optical property of the second light is sensitive to the presence of the analyte. The optical filter is disposed on the sensor material and includes a plurality of microlayers numbering at least 10 in total. The optical filter has different first and second transmittances at the respective first and second wavelengths.
Abstract:
A hand held spectrometer is used to illuminate the object and measure the one or more spectra. The spectral data of the object can be used to determine one or more attributes of the object. In many embodiments, the spectrometer is coupled to a database of spectral information that can be used to determine the attributes of the object. The spectrometer system may comprise a hand held communication device coupled to a spectrometer, in which the user can input and receive data related to the measured object with the hand held communication device. The embodiments disclosed herein allow many users to share object data with many people, in order to provide many people with actionable intelligence in response to spectral data.
Abstract:
Provided is a portable biosensor that includes a sample filter cartridge, a filter collector, an optical sphere, an electromagnetic radiation emitter, a photo-detector, a processor, a signal display, a vacuum pump, and a power supply. The sample filter cartridge selectively removes small molecules to minimize spectral interference in the detection signal. The sample is concentrated onto the filter collector and subjected to illumination by the electromagnetic radiation emitter, producing Raman-scattering. The optical sphere collects and distributes the Raman-scattering shifts, which then pass through a spectral filter to produce spectral filtered scattering, which is then reflected by the concave holographic flat-field grating onto the photo-detector. The data is displayed graphically to provide the Raman-scattering shift data. The data is compared with a database for sample identification. The device is contained within a housing that is small enough to be easily transported for field use.
Abstract:
An electromagnetic radiation spectrum detection system including a sensor device and an electronic control and processing module. The sensor device may include two photodiodes. The sensor device may convert an incident electromagnetic radiation (EMR) into electrical current. The electronic control and processing module may store numerical calibration values representative of a responsivity matrix of the sensor device. The electronic control and processing module may selectively provide the sensor device with electrical control voltage values (VB). The electronic control and processing module may process the values of detected electric currents (Iph) and the numerical calibration values to obtain spectrum information related to incident electromagnetic radiation spectrums. The electronic control and processing module may determine power spectral density of incident electromagnetic radiation.
Abstract:
A system for non-invasively interrogating an in vivo sample for measurement of analytes comprises a pulse sensor coupled to the in vivo sample for detect a blood pulse of the sample and for generating a corresponding pulse signal, a laser generator for generating a laser radiation having a wavelength, power and diameter, the laser radiation being directed toward the sample to elicit Raman signals, a laser controller adapted to activate the laser generator, a spectrometer situated to receive the Raman signals and to generate analyte spectral data; and a computing device coupled to the pulse sensor, laser controller and spectrometer which is adapted to correlate the spectral data with the pulse signal based on timing data received from the laser controller in order to isolate spectral components from analytes within the blood of the sample from spectral components from analytes arising from non-blood components of the sample.
Abstract:
Systems and methods for characterizing biological specimens, which may involve identifying a cell type or state corresponding to a disease or health condition of a subject. A biological specimen is subjected to electromagnetic radiation for spectroscopic analysis such as Surface Enhanced Raman Spectroscopy (SERS) to determine the relative abundance of proteins or amino acids in the cells, which is used in a comparison to previously stored relative abundance data of a database to automatically identifies at least one of cell type and/or cell state of the cells (or the disease/health state of the subject with the disease state including the possibility of virus infection, or drug susceptibility of a subject to bacteria or fungus). The method may also be employed with biological entities or cellular structures such as exosomes and even protein or nucleic acid fragments to determine disease states or health states of the subject.