Dual-Objective Microscope for Simultaneous High-Low Magnification Imaging

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Solution Overview

Problem

Conventional optical and confocal microscopes cannot view a sample simultaneously at both high and low magnifications, nor can they achieve rapid switching between high and low magnification images, limiting real-time imaging capabilities.

Innovation Solution

A microscope configuration with a beam splitter and spatial light modulator that splits light paths to enable simultaneous or quasi-simultaneous high and low magnification imaging, using a detector with separate portions for transmitted and reflected light to generate confocal images, and a shutter mechanism for rapid objective switching.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Device complexity

If a single objective lens is positioned in the optical path at a time, then the microscope structure remains simple, but simultaneous high and low magnification imaging cannot be achieved

Engineering Contradiction:
Improvemicroscope structureVSAvoidsimultaneous multi-magnification imaging capability
Core Design Contradiction:
Device complexityVSAdaptability or versatility

Solution Approach 1:

The optical path is segmented into multiple independent channels, each equipped with its own objective lens (high magnification and low magnification). The beam splitter divides the light path into separate channels that can be independently controlled, allowing simultaneous operation of multiple objectives without increasing overall system complexity

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

A beam splitter acts as an intermediary device that receives light from the light source and directs it to multiple objective lenses simultaneously. This mediator enables the division of the optical path without requiring complex mechanical switching mechanisms, resolving the contradiction between structural simplicity and multi-magnification capability

Inventive Principle:
Principle #24Intermediary (Mediator)

2Device complexity

If conventional optical paths are used without beam splitting, then the optical configuration remains simple, but rapid switching between magnifications cannot be achieved

Engineering Contradiction:
Improveoptical configurationVSAvoidswitching speed between magnifications
Core Design Contradiction:
Device complexityVSSpeed

Solution Approach 1:

The system transitions from a static single-path optical configuration to a dynamic multi-path system controlled by shutters. The shutters can rapidly switch between different magnification channels, enabling quick transitions between high and low magnification imaging without mechanical repositioning of objectives

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The shutters implement periodic switching between different optical paths, alternating between high magnification and low magnification channels in a rhythmic manner. This periodic action enables rapid, repeated switching between magnifications for quasi-simultaneous viewing

Inventive Principle:
Principle #19Periodic action

3Device complexity

If a single detector is used, then the detector structure remains simple, but simultaneous detection of transmitted and reflected light cannot be achieved

Engineering Contradiction:
Improvedetector structureVSAvoidsimultaneous image capture capability
Core Design Contradiction:
Device complexityVSProductivity

Solution Approach 1:

The detector is segmented into multiple independent detection regions, each dedicated to detecting specific light paths (transmitted light and reflected light). This segmentation allows simultaneous detection of multiple signals without requiring complex signal processing or sequential scanning

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Multiple detection functions (detecting transmitted light and reflected light simultaneously) are merged into a single detector device. This combining approach enables simultaneous multi-channel detection while maintaining a relatively simple overall detector structure, improving productivity without excessive complexity

Inventive Principle:
Principle #5Merging (Combining)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Enables simultaneous or quasi-simultaneous viewing and capturing of high and low magnification images, allowing rapid switching without altering the optical configuration, and facilitates efficient image processing and storage.

Implementation Method 1

The beam splitter comprises a spatial light modulator comprising a plurality of transmissive and non-transmissive portions

Methodology Applied
Scientific EffectLight reflection and transmission: Reflection

Implementation Method 2

light from a light source is focused onto a single spot on the sample, and light emanating from that spot is then collected by an objective lens and focused onto a detector

Methodology Applied
Scientific EffectLight focusing: Focusing

Implementation Method 3

light emanating from that spot (for example, by reflection or fluorescence)

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentEP4204887B1microscope
Publication Date: 2025.10.08 AUROX LTD
  • EP4204887B1 patent drawingFigure 1
  • EP4204887B1 patent drawingFigure 2
  • EP4204887B1 patent drawing

AI summary

A microscope comprising: a sample stage for mounting a sample; a light source for illuminating the sample when mounted on the sample stage; a detector; a first objective disposed on one side of the sample stage; a second objective disposed on an opposite side of the sample stage; a first set of optical elements defining a first light path from the first objective to the detector; and a second set of optical elements defining a second light path from the second objective to the detector. The first objective and the second objective have a common optical axis and are configured to image a sample mounted on the sample stage in a common focal plane. Furthermore, the first objective is a high magnification objective and the second objective is a low magnification objective. The provision of such a microscope configuration enables a sample to be viewed simultaneously at both high and low magnifications and/or allows rapid switching between high and low magnification images, for example to provide quasi-simultaneous viewing at both magnifications.