Microscopes TRIZ Cases

Adaptive optical correction elements reduce aberrations caused by oblique light passage through varying cover glass thicknesses and angles.

Coordinate transformed sinc filters constrain z frequency spectrum to reduce out-of-plane specimen damage.

A five-group immersion microscope objective corrects infrared aberrations and maintains high numerical aperture for deep tissue multiphoton imaging.

Virtual interface copies physical controls to resolve complexity contradictions while providing real-time adjustment feedback.

A gesture recognition system detects hand movements to control microscope alignment without physical contact.

Multi-view reflector microscope splits light beams to separate detection channels, resolving simultaneous position and orientation measurement limits.

Segmented lens groups with Gaussian structures resolve the trade-off between numerical aperture and working distance for living specimen imaging.

An autofocus mechanism detects focus position using illumination light output from a second region projected onto a light blocking area.

A holding system with a carrier module locked to a reference position on a holding module.

Bimetallic arms flex via Joule heating to assist electrostatic electrodes in orienting bistable micromirrors.

A five-lens microscope zoom system uses a stationary variable aperture stop between movable lens groups to control light transmission.

Suppressing highest diffraction orders reduces raw image requirements, lowering photodamage and increasing recording rates.

A segmented immersion microscope objective lens design corrects optical aberrations to maintain high resolution.

A multifaceted optical prism adapter tip realigns inspection light from angled-polished fiber endfaces to match the microscope objective lens axis.

Segmented galvo scanning and phase-locked SLM addressing overcome refresh rate limits for large-scale neural recording.

An inverted microscope merges total internal reflection fluorescence and disk scanning confocal optical systems to expand observation range.

A superimposing beam control splits excitation light into multiple beams with distinct polarization states and optical properties.

A spatial light modulator directs specific wavelengths to identified targets within a sample field of view.

A magnifying observation apparatus switches display modes automatically based on detected visual field changes.

A paraboloidal mirror focuses annularly collimated excitation light to generate a disc of light for 360-degree lateral sample illumination.

An imaging controller adapts operational parameters via machine learning from user discard signals, reducing manual adjustment time in microscopy workflows.

Electronic binning replaces complex zoom optics, reducing optical complexity while maintaining measurement precision.

Solidifies fluid material in pin bases to form elastomeric tips that prevent glass slides from slipping during high-speed stage movement.

Parallel line illuminations excite multiple dyes simultaneously, preventing image-capturing time increases from sequential wavelength switching.

A microscope controller transmits position signals to the table while it moves between sample regions.

Multi-branch bundle fiber divides light beams at the entrance end, eliminating high-precision mechanical alignment requirements.

A semi-submersible microscope objective uses a transparent protective coating to seal the optical outlet during imaging.

A scanning microscope directs light to an offset entrance pupil sub-region to generate inclined illumination foci for flexible specimen imaging.

Quantitative phase imaging tracks real-time cell mass dynamics to resolve the trade-off between measurement precision and dynamic single-cell response data.

A reflecting telescope design maintains a stationary eyepiece position while providing intrinsic zoom capability through integrated image correcting optics.

Two-dimensional CCD or CMOS sensor arrays capture specimen images to resolve noise and overexposure from varying fluorophore signal strengths.

A microscope scanner uses position feedback to trigger image capture at measured locations rather than assumed positions.

A focusing device uses a differential interference prism with an adjustable shearing amount to optimize error signal acquisition conditions.

A reflective Fresnel lens directs parallel light beams from annular LED arrays to enhance optical efficiency.

Side illumination enhances irradiance for scanning interferometry to simplify focus finding and identify regions of interest on measured samples.

Two orthogonal gradient-index lenses cancel position-dependent astigmatism in endoscopes.

An optical grating splits real image light beams by wavelength to enable multi-color fluorescence imaging under a single exposure.

A single LCOS modulates wavefronts to correct aberrations and form illumination patterns on specimens.

Liquid crystal lenses adjust focal length dynamically to resolve the trade-off between magnification flexibility and device size in conventional microscopes.

Laser fluorescence microscopy generates high resolution images of oil droplets in water using confocal optical sectioning.

Segmentation and intermediary principles isolate the sample from electronic components, preventing contamination while enabling precise imaging.

A microscope adjusts image generation parameters based on detected sample movement variables to maintain real-time image quality.

A lenslet array near the objective lens generates real images to capture angular data.

Liquid crystal display array generates scattered radiation patterns to enable quantitative phase imaging without precise optical control or moving parts.

An OCT microscopy system detects connected apparatuses to automatically adjust operational modes, eliminating manual readjustment time.

A microscope illumination method uses measurement radiation to adjust light source energy parameters for precise object targeting.

A chromatic confocal microscope system uses spatial filtering to remove stray light and dual color sensing units to detect RGB intensity signals.

Coordinate conversion tables translate between stage and sensor frames to reproduce observation positions with 0.1 µm accuracy.