Microscopes TRIZ Cases

Synchronized stage motion and optical plane tracking enable artifact-free imaging of large or multiple samples at higher throughput.

A transparent-bottom dish with ceramic sidewalls applies TTFields to cell cultures without blocking the optical path for live microscopy.

High-index metamaterials create sub-diffraction speckle illumination, boosting nanoscopy resolution while lowering phototoxicity and enabling subsurface imaging.

Two-photon light-sheet autofluorescence imaging reduces out-of-focus photodamage while enabling deep, real-time embryo assessment.

An auxiliary focusing camera and calibration curve correct microscope defocus faster and more reliably than manual focusing.

Stored focus heights and observation settings let multiple target positions be replayed quickly with less manual focusing and setup.

Higher-NA microscope optics overcome the sub-0.1 limit of conventional 2× objectives to improve resolution and field of view with diffraction-limited imaging.

A micro-heater matrix and high-conductivity substrate shape local heat for fast, low-diffraction phase modulation in thermo-optical SLMs.

A positive first lens group bends principal rays inward, shrinking the beam splitter and epi-illumination optics while easing aberration correction.

Continuously tunable filter elements add spectral flexibility while a downstream compensator preserves focal position and spatial resolution.

A beam splitter and pupil image comparison track light sheet misalignment in real time, enabling continuous microscope alignment during acquisition.

Fixed-focal relay optics and xy-stage image stitching enable precise slide dissection with large field of view, high pixel density, and lower cost.

Asymmetric test illumination resolves position ambiguity in single-particle localization while avoiding mechanical repositioning and excess photon use.

Laser-synchronized pixel clocking and polygon scanning keep pulses per pixel uniform for faster multiphoton imaging with consistent intensity.

Multiple transverse light sheets image several z-planes at once, overcoming slow confocal scanning while preserving optical sectioning.

A tilted alignment unit keeps the intermediate image within depth of field, boosting light yield, signal-to-noise ratio, and cover-slip flexibility.

A rotating and linearly shifted microlens disk synthesizes focal-stack images to improve 3D microscopy resolution without shrinking sensor pixels.

A multi-group wafer inspection objective uses cemented and meniscus lenses to balance high resolution, wide field, long working distance, and aberration correction.

Relay optics laterally shift one ferrule image so both duplex fiber endfaces fit one microscope view with better focus alignment.

A non-orthogonal OTLS layout boosts imaging depth and resolution in thicker specimens while easing refractive index matching constraints.

Absorption saturation with a CW laser replaces pulse-laser nonlinear microscopy, improving S/N and resolution in diagnostic imaging.

A three-group image formation lens balances resolution, field of view, and aberration correction in microscope optical systems.

Beam switching across multiple scan paths keeps illumination away from polygon facet edges, enabling 100% duty cycle and high throughput.

Path planning across regions of interest cuts illumination time while preserving precise photolabeling and area coverage in spatial proteomics.

Movable negative and positive attachment optics correct chromatic and spherical aberrations across immersion liquids and observation depths.

Continuous slit illumination and synchronized scanning capture large samples faster, avoiding stop-go imaging and stitching delays.

A shared objective lens and dichroic path combine SLO and OCT to capture ultra-wide fundus and tomographic retinal images together.

Programmable illumination and sample motion create variable magnification with one objective, cutting mechanical complexity and imaging delays.

A 12-lens layout balances 50x magnification, optical length, and working distance while reducing aberrations and distortion.

Automated slide routing between multiple imaging units keeps processing running when one imager fails, reducing manual intervention and downtime.

Connected sample holes and bottom-side viewing let one holder image multiple cell samples at once while keeping the structure relatively simple.

A twelve-lens objective balances aberration correction, compact length, and working distance for high-resolution microscope imaging.

An aspherical correction plate at the pupil-conjugate position fixes high-NA spherical aberration, improving cytometer sensitivity and accuracy.

Elastic slide retention and nested stacking increase microscope slide storage while reducing reattachment work and limiting light interference.

Rapid VFL focus shifts and mirror-based field changes capture points-from-focus images for accurate 3D Z-height metrology without stage movement.

A ball-joint suspension with center-of-gravity balancing lets a medical microscope move freely in 3D while maintaining stable viewing orientation.

Separate excitation channels with shared de-excitation enable high-resolution multicolor scanning while reducing light-source cost and dye interference.

A variable detection pinhole widens detection depth during sample search, speeding focus finding while reducing illumination time and photobleaching.

Real-time slide imaging uses auto focus, stage motion, and ML artifact removal to avoid rescans and speed intraoperative tissue assessment.

A phase mask and spectral filter array capture spatial and spectral data in one microscope snapshot, avoiding scanning trade-offs and bulk.

User-defined areas of interest guide objective selection and stage scanning to balance assembled image quality with capture time.

Alternating micro-mirror positions across camera frame cycles reduces flicker and mechanical strain, extending spatial light modulator life.

Interchangeable optics, dual light sources, and motorized focusing solve portable microscope limits in magnification, field of view, and fine adjustment.

A tapered light pipe reshapes illumination cone angle to match objective NA, improving transmitted microscopy resolution without bulky condensers.

Optical markers embedded in specimen images enable fast, accurate microscope specimen identification without separate barcode scanning.

A split support layout uses outer balls and an inner roller bearing to improve objective switching accuracy while lowering machining cost.

A modular microscope switches between analog and digital viewing while sending images wirelessly to a smartphone for display and analysis.

A split beam path captures spatial intensity and spectral data together, enabling fluorophore differentiation without the light loss of prior ISM setups.