Microscopes TRIZ Cases

Taylor series coefficients correct chromatic dispersion in acousto-optic deflectors, enabling high-speed volumetric imaging.

A scanning probe microscope uses a reflective member and imaging device to capture wide-field views of the sample surface for precise positioning.

A microscopic measurement apparatus moves a measuring optical axis across sample areas using beam steering mirrors to acquire precise optical information.

A confocal scanner uses a linear light source and detector mounted on a moving mechanism to capture images.

A stereoscopic illumination system delivers two collimated light beams that overlap on the subject surface to enhance three-dimensional visualization.

Hydrophobic and lipophobic coatings on microscope objectives prevent incorrect immersion media application, maintaining imaging quality.

A surgical microscope uses digital image processing to generate a superimposition image that highlights eye lens pieces during cataract surgery.

An automated stereology system uses deep learning and extended depth of field imaging to segment biological samples.

A processor applies an inverse transformation matrix to digital detection signals from a photodetector.

A microscope stage sensor base uses low expansion material to stabilize position relative to the optical axis, reducing thermal drift errors in XY positioning.

Scanning a thin light sheet across a three-dimensional suspension medium captures spatial coordinates and morphology data without disrupting the sample.

A cooling microscope assembly uses a low thermal conductivity coupling medium to maintain temperature differentials between the objective lens and sample stage.

Adjustable correction optics reduce spherical aberration using quantitative phase contrast imaging.

AF circuit segments contrast into low and high frequency bands, resolving double peaks in transparent cell imaging.

A motor-driven adjusting device mounted on the objective housing converts rotational movement into linear lens displacement.

Elastic member secures lens on tubular shoulder, reducing part count and mechanical stress in fluorescence microscope lighting modules.

A scanning luminescence microscope uses optical gratings to form crossing line gratings of inhibition and excitation light.

Placing astigmatic optics between the tube lens and illumination objective prevents internal focus damage while enabling flexible light sheet adaptation.

A single scanning element in telecentric transport optics moves the light sheet laterally, reducing vibrations and increasing volume imaging frame rates.

A parabolic reflector captures emission light from above the illumination region and directs it to a detection system, increasing total collected signal volume.

A single-handed control apparatus integrates rotary controllers for stage movement and specimen review to streamline cytologist workflow.

Harmonics microscope measures glycated hemoglobin fraction in single red blood cells using laser-induced harmonic generation.

Circular light sources and shielding guide direct vertical excitation light through a prism, eliminating dichroic mirror reflections that reduce resolution.

Specimen-side objective guides obliquely inclined light sheets through a single optical path for simultaneous multi-directional illumination and detection.

A light microscope uses a dispersive element to spectrally split detection light into multiple line images.

Segmented sensor arrays resolve detection difficulty in high-density feature arrays by distributing the burden across specialized optical paths.

Rectilinear lens movement resolves the trade-off between high resolution and narrow visual field, enabling wide-field imaging with reduced apparatus size.

Spectral filtering separates light paths to distinct pixel groups, enabling simultaneous wide-field and detailed observation without mechanical movement.