Embodiments herein provide a method and system for a non-invasive mechanism providing simultaneous determination of viscosity-temperature variation of a lubricant for predicting machine health using a Photo Acoustic (PA) sensing mechanism, Laser-enabled swept frequency acoustic interferometry (LE-SFAI), wherein the lubricant produces acoustic wave only if it absorbs the laser irradiation, thus overcomes the limitation of ultrasound based SFAI through optical absorption based contrast and proper selection of laser excitation wavelength. A PA signal received from the lubricant is processed by a Vector Network Analyzer (VNA), then converted to time domain to obtain normalized first peak that corresponds to the PA signal generated by the lubricant. A squared rise time of the first peak is indicative of viscosity of the liquid and shift in the first peak is indicative of variation of the viscosity as temperature of the lubricant varies.

In an embodiment, cross sectional image storage stores a cross sectional image group including multiple cross sectional images each of which is associated with time. Phase image storage stores a phase image group including multiple phase images each of which is associated with time. Blood flow information storage stores a blood flow information group including multiple blood flow information each of which is related to blood flow in a blood vessel of the living body and is associated with time. Display synchronously displays a cross sectional image included in the cross sectional image group and a phase image included in the phase image group using time associated with the cross sectional image and the phase image, and displays a blood flow image that expresses multiple blood flow information. The display performs the same change as the change to the cross sectional image, the phase image and the blood flow image.

Provided is a light scattering cell classification technology which can classify cells into various types and at the same time classify cells with very high accuracy despite the rotation of the cells. A cell analysis apparatus using a plurality of lasers, according to an embodiment of the present invention, comprises: a plurality of laser generators which are installed around a movement path through which cells to be classified are moved, and which irradiate laser beams at one measurement point on the movement path at different angles; a plurality of photodetectors, installed around the one measurement point, which collect a second laser beam, which is a laser beam generated as the laser beams irradiated from the laser generators are incident on the cells and then scattered; and a cell analysis unit which classifies the cells to be classified according to the second laser beam collected by the photodetectors.

Provided is a photonic device in which emission intensity in a short wavelength region is suppressed even in the case of increasing carrier injection density so as to obtain a wide spectrum half-maximum width as well as a high output. The photonic device includes: a first cladding layer; a second cladding layer; and an active layer including an emitting layer and a barrier layer and being provided between the first cladding layer and the second cladding layer, the emitting layer emitting light in a spectrum having a center wavelength λc and a spectrum half-maximum width Δλ, in which at least one of the first cladding layer and the second cladding layer includes a light absorbing part for absorbing light having a wavelength of λs or less represented by the following Expression (1):
λs<(λc−(Δλ/2))  (1).

A device includes an illumination device that casts light of a prescribed polarization direction on a scattering body, a camera that picks up images of the scattering body at a plurality of different polarization angles, and a processor that executes a process of generating and outputting an inner layer image, of an inner layer of an inside of the scattering body, in response to a depth from a surface of the scattering body on the basis of the images of the scattering body picked up at the plurality of different polarization angles.

A mammography device is disclosed. The mammography device includes a container configured to surround the breast and a plurality of optical fibers attached to be directed inward in the container and configured to perform radiation and detection of light. The container has a base member having an opening, a plurality of annular members continuously disposed to come in communication with the opening, and a bottom member disposed inside the annular member spaced the farthest distance from the base member. The annular members and the bottom member are configured to relatively displace the adjacent annular member on the side of the base member or the base member in a communication direction. Some of the plurality of optical fibers is attached to the plurality of annular members.

Disclosed herein are configurations for few-mode fiber optical endoscope systems employing distal optics and few-mode, double-clad or other optical fiber wherein the systems directing an optical beam to a sample via the optical fiber; collecting light backscattered from the sample; direct the backscattered light to a detector via the optical fiber; and detect the backscattered light; wherein the directed optical beam is single mode and the collected light is one or more higher order modes.

Exemplary embodiments of the present disclosure include apparatus and methods to identify endometrial tissue.

Imaging techniques of pharmaceutical preparations such as tablets are disclosed. The techniques combine the measurement of reflected/transmitted terahertz radiation originating from within the tablet and data analysis localized in frequency and time in order to enable a three dimensional image indicating composition to be obtained.

The present disclosure relates to a simple, fast, and low cost method for 3D microvascular imaging, termed “scatter labeled imaging of microvasculature in excised tissue” (SLIME). The method can include perfusing a contrast agent through vasculature of a tissue sample. The contrast agent can include colloids and a dispersant. After the contrast agent is perfused through the vasculature, the vasculature of the tissue sample can be treated with a molecule that cross links with at least a portion of the dispersant to form a sticky, non-Newtonian polymer that prevents leakage of the contrast agent out of the vasculature of the tissue sample. The tissue sample can then be immersed in a solution comprising a clearing agent and subsequently imaged.