Disclosed is an assay for determining resistance in a target cell or tissue to a therapy associated with cellular stress using chemical microscopy and high-throughput single cell analysis to determine functional metabolic alteration, including determining metabolic reprogramming in a target cell or tissue to a therapy associated with cellular stress, and methods of using the assays.

A system for visualizing melanin present in tissue can include an imaging system to record a signal based on a presence of melanin in tissue and a display device to display an image based on the signal. A first laser source can emit a Stokes pulse train and a second laser source can emit a pump pulse train. Both the first laser source and the second laser source comprise a tunable center wavelength or frequency. An energy difference between a frequency of the Stokes pulse train and a frequency of the pump pulse train is from 1750 cm.sup.−1 to 2250 cm.sup.−1. The Stokes and the pump pulse train overlap in space and time. A scanning mechanism focuses the combined Stokes pulse train and pump pulse train within the tissue and scans across the tissue. A detector detects the signal based on a presence of melanin within the tissue.

Surface sensing methods for imaging a scanned surface of a sample via sum-frequency vibrational spectroscopy are disclosed herein. The methods include exposing a sampled location of the scanned surface to a visible light beam and exposing the sampled location to a tunable infrared beam such that the tunable infrared beam is at least partially coincident with the visible light beam. The methods also include varying a frequency of the tunable infrared beam an inducing optical resonance within an imaged structure that extends at least partially within the sampled location. The methods further include receiving at least a portion of an emitted light beam from the sampled location and scanning the visible light beam and the runnable infrared beam across the scanned portion of the scanned surface. The methods also include generating an image of the scanned portion of the scanned surface based upon the receiving and the scanning.

A stimulated Raman scattering (SRS) spectrometer for real-time, high-resolution molecular analysis of gases is based on two hollow-core fibres illuminated by a single high-power, short-pulse laser pump. The first fibre is prefilled with high-concentration target gases. Interaction of each target gas inside the first fibre, with the laser pump, generates Raman signals corresponding to the target gases. The combined beam of the Raman signals and the pump laser beam is directed into the second fibre containing the measured target gases. Interaction of each target gas with the combined beam generates the Stimulated Raman Growth (SRG), i.e., amplification of the Raman signal, which is proportional to the corresponding target gas concentration. A receiver subsystem receives the beam from the second fibre, spectrally separates it to wavelengths corresponding to each target gas, extracts the SRG value corresponding to each target gas and calculates the concentration of each target gas.

Provided is a light detection device having a laser light source, a splitting unit, a first modulation unit, a second modulation unit, a first detection unit and a second detection unit that detect light, and a control unit.

A spectrometry device includes a switch and a converter. The switch acquires a first reception signal and a second reception signal that respectively include information relating to an optical spectrum and switches between outputting the first reception signal and outputting the second reception signal based on control by a controller. The converter converts the first reception signal or the second reception signal output from the switch into a digital signal.

Disclosed is an assay for determining resistance in a target cell or tissue to a therapy associated with cellular stress using chemical microscopy and high-throughput single cell analysis to determine functional metabolic alteration, including determining metabolic reprogramming in a target cell or tissue to a therapy associated with cellular stress, and methods of using the assays.

A sensing device comprising: a light detection and ranging (LiDAR) sensor; and one or more optical spectroscopic sensors configured to extract biomarker information from one or more optical measurements of a user.

In a method for measuring at least two different components of a fluid, the fluid is to a first measuring cell and a second measuring cell. In the first measuring cell, a first component of the fluid is excited by a first excitation to trigger a first light emission, and in the second measuring cell, a second component of the fluid is excited by a second excitation which is different from the first excitation, thereby triggering a second light emission. The first light emission and the second light emission are captured by an optical system facility and guided by the optical system facility in a direction of a detector facility which measures the first light emission and the second light emission.

There is provided a light detecting device including: a laser light source generating light source pulse beam; a splitting section splitting the light source pulse beam into excitation beam, first probe beam and second probe beam; a first modulating section executing optical path length modulation that modulates a relative optical path length difference between the excitation beam, and the first probe beam and the second probe beam; a second modulating section phase-modulating the first probe beam; and a detecting section illuminating combined beam, in which the excitation beam, the first probe beam and the second probe beam are multiplexed, onto a sample, and detecting a stimulated Raman scattering signal that is generated.