Microscopes TRIZ Cases

Lateral optical path deflection improves user access to objective lens controls, resolving compactness versus operability trade-offs.

Automated digital rock analysis determines representative elementary volume through computational convergence.

Automated optical switching directs emissions between two detectors, reducing dead time and missed sample events in high-throughput flow cytometry.

A detection unit illuminates a sample carrier with a predetermined pattern to determine focus position changes along the optical axis.

A confocal OCT imaging system uses a mask with transmissive portions to generate non-overlapping light beams for parallel scanning.

A non-concentric reflective microscope objective lens directs light along an asymmetric path to improve transmission efficiency.

Multi-plane optical assembly directs light from multiple depths to distinct pixel sections for simultaneous volumetric imaging.

A microscope targeting light projects a crosshair pattern onto the stage to align the subject, eliminating iterative objective swapping and re-focusing.

An electronically tunable lens in an optical relay varies the focal plane without mechanical motion to capture multiple images simultaneously.

Centralized server analysis of remote sensor data eliminates costly on-site engineer visits by enabling automated diagnostic execution.

An imaging optical system with an inclined observation axis captures partial image data during continuous sample scanning.

A 3D interferometric lattice light-sheet imaging system combines orthogonal excitation with opposed detection lenses to achieve high-resolution volumetric capture.

Offset pixel lines on a tilted sensor enable simultaneous multi-depth capture, resolving the trade-off between light sensitivity and tilting capability.

Multiple peak value memories track distinct signal amplitudes to resolve the contradiction between measurement precision and multi-peak versatility.

Scanning coaxial beam arrays create discontinuous light sheets that reduce tiling positions, decreasing raw data size while maintaining spatial resolution.

Integrating the chip onto the upper cover removes manual handling, resolving the trade-off between chip replaceability and operation convenience.

Greenough stereomicroscope uses asymmetric optical diameters to vary numerical aperture across two monocular channels.

A microscope apparatus adjusts astigmatic difference via a cylindrical lens unit to capture high-resolution sample images across varying objective lenses.

A microscopy imaging system uses an off-axis laser beam to detect upper surface reflections for precise objective focusing.

A microscope control unit adjusts electric zoom magnification to maintain total magnification during objective lens switching.

Motor-driven lens group mechanism converts rotational motion into precise axial translation, eliminating optical system soiling from spring abrasion.

A phase mask encodes wavelength and three-dimensional position data directly into the point spread function shape within a single optical channel.

A microscope objective cover houses the lens with an aperture to extend liquid between sample and cover.

An observation device merges illumination and object optical systems on one side of the sample using diagonal light paths.

An adjustable divergence angle mechanism in a light sheet microscope bypasses shading portions to reduce shadow bands while maintaining longitudinal resolution.

Moving imaging optics stabilizes magnification during focus changes, keeping lateral variation under five percent.

A speckle-modulated line illumination unit uses a moving diffuser to create temporally varying light patterns.

Automated confocal aperture alignment uses the Nelder-Mead simplex algorithm to optimize optical positioning.

Segmenting the detector into four elements reduces device complexity while maintaining high imaging resolution through asymmetric placement.

A fluorescence lifetime detection method measures photon counts within varying temporal windows to characterize decay behavior.

Segmented microscope design replaces cable routing with wireless signals to maintain stability during portable observation.

Stiffening wires on the flow chamber retain immersion oil, resolving leakage and fragility while maintaining high imaging resolution.

A fluorescence imaging device positions the light source on-axis between the objective lens and subject to increase excitation intensity.

A high-speed data stream transmits measurement and control information using compact packets with type bits.

A diffractive optical element positioned near the principal ray crossing point corrects chromatic aberration in an objective lens design.

An optical distance measuring apparatus uses coherent light scanning and photoelectric conversion to detect phase information.

Modifying the liquid-liquid interface via adaptive optical elements reduces wavefront aberrations, improving the Strehl ratio and resolution.

Aperture stop positioned at focal distance maintains uniform numerical aperture across the field of view, resolving resolution versus equipment size trade-offs.

A microscope uses a microlens array to subdivide the detection aperture into individual sub-apertures for capturing light field images.

A microscope illumination apparatus uses a reflecting spatial modulation element to control light intensity and polarization for precise specimen targeting.

A method determines sample holder thickness using reflected illumination radiation measurements.

Adaptive STED microscopy modulates de-excitation light intensity based on preliminary low-resolution overview scans to preserve sample integrity.

A parallel sort-and-compression algorithm uses multiple mobile optical tweezers to reduce rearrangement time and complexity in large-scale atom array assembly.

A surgical microscope optical structure uses a right-angle roof prism to shorten the internal light path and simplify the binocular unit design.

Segmented rotary wheel limits zoom range per objective, maintaining parfocal alignment and compact construction.

A laser scanning microscope optical assembly uses nested pupil planes and variable beam deflection to switch between excitation and manipulation radiation paths.