A compact hyperspectral imager adapted to operate in harsh environments and to conduct post acquisition signal processing to provide automated and improved hyperspectral processing results is disclosed. The processing includes luminance and brightness processing of captured hyperspectral images, hyperspectral image classification and inverse rendering to produce luminance invariance image processing.

According to some embodiments of the present invention, a fine focus microscope includes an objective lens for collecting light from an object being imaged, and a tube lens for forming a first image from light received from the objective lens. The fine focus microscope further includes a fine focus lens for forming a second image from the first image, and an eyepiece for forming a third image from the second image, wherein the third image is viewable by a user. The fine focus microscope further includes a field lens for directing light from the second image to the eyepiece, and a positioning system mechanically coupled to the fine focus lens, the eyepiece, and the field lens. The positioning system changes a position of the fine focus lens, the eyepiece, and the field lens with respect to the objective lens to provide a change in focus of the object being imaged.

Compact optical spectrometers are provided to measure optical spectral composition of light.

An interferometer includes a holding element having an actuation recess, a first mirror element arranged on the holding element opposite the actuation recess, and a second mirror element arranged opposite the first mirror element at a mirror distance, to form an optical slit. The first mirror element is arranged between the second mirror element and the holding element and the optical slit is spatially separated from the actuation recess by the first mirror element. The interferometer further includes an electrode pair including a first actuation electrode in one of the mirror elements and a second actuation electrode on a side of the actuation recess opposite the first actuation electrode. The mirror distance can be varied by applying an electrical voltage to the electrode pair.

An optical module includes a mirror unit and a beam splitter unit. The mirror unit includes a base with a main surface, a movable mirror, a first fixed mirror, and a drive unit. The beam splitter unit constitutes a first interference optical system for measurement light along with the movable mirror and the first fixed mirror. A mirror surface of the movable mirror and a mirror surface of the first fixed mirror follow a plane parallel to the main surface and face one side in a first direction perpendicular to the main surface. The movable mirror, the drive unit, and at least a part of an optical path between the beam splitter unit and the first fixed mirror are disposed in an airtight space.

The present invention provides a system for measuring concentrations of analytes. The system comprises a sampler (17) for taking at least one sample from each of one or more surfaces. The system also comprises an analyser (19) for analysing the at least one sample to determine the concentrations of the analytes on the sampled one or more surfaces. The system further comprises a management platform (43) for receiving the measured concentrations from the analyser and communicating the concentrations of the analytes on the one or more surface, wherein the system provides the results within a suitable time.

A Raman spectroscopy system is provided. The spectroscopy system includes an optical switch including a first side having a pump inlet and a return outlet, and a second side having a plurality of pump outlets and a plurality of return inlets. The spectroscopy system includes at least one radiation source optically coupled to the pump inlet and a detector optically coupled to the return outlet. The spectroscopy system further includes a pump filter module optically coupled between the at least one radiation source and the pump outlets and a return filter module optically coupled between the detector and the return inlets. The spectroscopy system further includes a plurality of probes, each probe optically connected to at least one of the plurality of pump outlets by at least one excitation fiber and optically coupled to one of the return inlets by at least one emission fiber.

An apparatus for providing temperature-dependent movement of an optical element, the apparatus comprising: a moveable mount for the optical element; a mount moving component attached to the moveable mount; and a guide attached to the mount moving component and configured to guide a movement of the moveable mount. The apparatus is configured such that a difference in thermal contraction or thermal expansion between the mount moving component and the guide in response to a change in temperature of the apparatus causes the mount moving component to move the moveable mount relative to the guide.

This far-infrared spectroscopy device is provided with: a variable wavelength far-infrared light source that generates first far-infrared light; an illuminating optical system that irradiates a sample with the first far-infrared light; a detecting nonlinear optical crystal that converts second far-infrared light into near-infrared light using pump light, said second far-infrared light having been transmitted from the sample; and a far-infrared image-forming optical system that forms an image of the sample in the detecting nonlinear optical crystal. The irradiation position of the first far-infrared light on the sample does not depend on the wavelength of the first far-infrared light.

A method of assessment of renal function by monitoring a time-varying fluorescence signal emitted from a fluorescent agent from within a diffuse reflecting medium with time-varying optical properties is provided that includes using a renal monitoring system comprising at least one light source, at least one light detector, at least one optical filter, and at least one controller to provide a measurement data set comprising a plurality of measurement entries, each measurement data entry comprising at least two measurements obtained at one data acquisition time from a patient before and after administration of the fluorescent agent.