A fluorescence photometer includes a photometer unit and an optical fiber unit. The photometer unit includes a light source, an excitation-side spectroscope for separating light emitted from the light source to generate excitation light, and a fluorescence-side spectroscope for separating fluorescent light emitted from a sample irradiated with the excitation light to generate monochromatic light. The optical fiber unit guides the excitation light to the sample placed outside the photometer unit and guides the fluorescent light emitted from the sample to the photometer unit and includes an image fiber for capturing an image of the sample, an excitation-side fiber arranged around the image fiber and for guiding the excitation light to the sample, and a fluorescence-side fiber arranged around the image fiber and to guide the fluorescent light emitted from the sample to the photometer unit. The excitation-side fiber and the fluorescence-side fiber are arranged to surround the image fiber.

The invention relates to a device for a light-spectroscopic analysis of a, for example, liquid sample. In particular, light should be guided through a sample and then detected and/or analyzed photometrically, spectrophotometrically, fluorometrically, spectrofluorometrically and/or by means of phosphorescence or luminescence.

A device for the in-ovo determination of the sex of a fertilized bird egg, having a light source for emitting excitation radiation for exciting fluorescence in a region inside the bird egg, a spectroscopic apparatus for analysing, in a temporally and/or spectrally-resolved manner, fluorescence radiation emitted from the region inside the bird egg, an evaluation unit for determining the sex from the data determined by means of the spectro-scopic apparatus and a measuring head for jointly transmitting the excitation radiation into the bird egg and receiving the fluorescence radiation from the bird egg. The measuring head has an optical fibre system with a head end for transmitting the excitation radiation and receiving the fluorescence radiation.

A combined capability sensor includes a first laser source and a second laser source. The first laser source is configured to emit light having a wavelength in at least one of an infrared spectrum and a visible spectrum and the second laser source is configured to emit light having a wavelength in a blue or ultraviolet spectrum. A director is configured to direct the first and second laser source to a detection zone. A first sensor is configured to detect scattered light originating from the first laser source, thereby detecting a presence of smoke in the detection zone. A second sensor is configured to detect fluoresced light originating from the second laser source, thereby detecting a presence of a biological agent in the detection zone.

The present disclosure relates to methods and systems for assessing the quality of a meat product. In certain embodiments, the present disclosure provides a method of assessing quality of a meat product, the method comprising receiving data representative of light emitted from the meat product upon application of incident light to the meat product, analysing the data to determine one or more parameters indicative of quality of the meat product, and assessing the quality of the meat product on the basis of the one or more parameters.

In a sensor unit, a sensor element having an optical behavior that depends on at least one analyte is in diffusive contact with an auxiliary medium, which is present in a reservoir in the sensor unit, via a membrane. The reservoir and the membrane, on the one hand, and sensor element, on the other hand, can be removed from one another in order to place the sensor unit in a measurement state. The auxiliary medium can serve to wet the sensor element during storage of the sensor unit or also for calibrating the sensor element.

The invention relates to an apparatus for simultaneously analysing luminescence of a plurality of samples. The apparatus comprises a fibre-optic plate.

Provided herein are devices, systems, and methods for characterizing a biological sample in vivo or ex vivo in real-time using time-resolved spectroscopy. A light source generates a light pulse or continuous light wave and excites the biological sample, inducing a responsive fluorescent signal. A demultiplexer splits the signal into spectral bands and a time delay is applied to the spectral bands so as to capture data with a detector from multiple spectral bands from a single excitation pulse. The biological sample is characterized by analyzing the fluorescence intensity magnitude and/or decay of the spectral bands. The sample may comprise one or more exogenous or endogenous fluorophore. The device may be a two-piece probe with a detachable, disposable distal end. The systems may combine fluorescence spectroscopy with other optical spectroscopy or imaging modalities. The light pulse may be focused at a single focal point or scanned or patterned across an area.

An optical measurement device is provided. The device includes first and second optical fibers; first and second reaction vessels, and a light guide stage coupled to the first and second optical fibers. The light guide stage is driven to simultaneously optically connect the first and second optical fibers with the first and second reaction vessels. The device includes a measurement device for receiving emissions from the first and second reaction vessels, and a connecting end arranging body that supports the first and second optical fibers along a path. The arranging body is driven along the path between a first position, in which the first optical fiber is optically connected with the measurement device so that light is transmittable from the first reaction vessel, and a second position, in which the second optical fiber is optically connected with the measurement device so that light is transmittable from the second reaction vessel.

An optical detection system for a capillary electrophoresis instrument is disclosed. The optical detection system comprises an ultraviolet (UV) source and an absorption measurement optical path. The optical path comprises a first plurality of optical elements comprising a first optical fiber array and other elements. The first plurality of optical elements are arranged to obtain a plurality of respective UV beamlets from a UV beam emitted by the UV source and to direct, at least partially using the first optical fiber array, the respective UV beamlets through respective capillaries of a plurality of capillaries and to an absorption detector positioned to detect respective signals for use in obtaining respective UV absorption measurements corresponding to the respective capillaries.