Structured Illumination Microscopy Using Color CCD and DMD
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Solution Overview
Problem
Structured illumination microscopy (SIM) systems currently cannot achieve fast full-color three-dimensional optical sectioning imaging, limiting their application in fields requiring natural color information, such as biology, medicine, and materials science, due to the use of monochrome cameras and restricted imaging speed.
Innovation Solution
A full-color three-dimensional optical sectioning microscopic imaging system using a color CCD camera, a Digital Micro-mirror Device (DMD) for structured illumination, and image processing in the HSV color space to separate and combine images from different phases, allowing for accurate restoration of natural color information.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Loss of information
If monochrome CCD or CMOS cameras are used in SIM systems, then the imaging speed is fast, but the natural color information of the specimens cannot be acquired
Solution Approach 1:
The patent combines multiple color channel imaging capabilities into a single color CCD camera system. By integrating the imaging of different color channels (red, green, blue) into one camera sensor with appropriate optical filters, the system simultaneously captures full-color information without requiring sequential monochrome imaging, thus resolving the contradiction between color information acquisition and imaging speed.
2Loss of information
If multicolor fluorescent labeling and multi-channel integration is used, then color sectioned images can be obtained, but the imaging speed is limited and the configuration is complex
Solution Approach 1:
The patent employs a universal color CCD camera that can capture multiple color channels simultaneously through integrated optical filtering, replacing the need for separate monochrome cameras and complex multi-channel integration systems. This multi-functional approach maintains color imaging capability while significantly simplifying the overall system configuration and reducing the number of components required.
3Measurement precision
If laser scanning is used to obtain three-dimensional sectioned images, then high spatial resolution is achieved, but the imaging time is long and light damage to living cells is strong
Solution Approach 1:
The patent replaces the mechanical point-by-point scanning system with a wide-field optical sectioning approach using structured illumination. Instead of mechanically scanning laser focus through the sample, the system projects structured light patterns and uses computational algorithms to achieve optical sectioning, thereby eliminating mechanical scanning while maintaining spatial resolution and dramatically reducing imaging time.
4Measurement precision
If high power laser is used in scanning microscopy, then three-dimensional sectioning imaging capability is achieved, but phototoxicity to living cells and tissues is strong
Solution Approach 1:
The patent converts the harmful high-power laser scanning approach into a beneficial low-power wide-field illumination system. By using structured illumination patterns with much lower power requirements and combining them with computational optical sectioning algorithms, the system achieves the same sectioning capability without the phototoxic damage caused by high-power continuous laser exposure.
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 faster and more accurate restoration of true color information with increased gray scale and natural color representation, reducing light damage and phototoxicity, and providing a more compact system compared to multicolor fluorescent labeling methods.
Implementation Method 1
a dichroic prism 2 positioned at the illumination optical path
Implementation Method 2
a beam splitter 5 positioned at the optical path of 4
Data Source
AI summary
The present invention provides a full-color three-dimensional optical sectioning microscopic imaging system and method based on structured illumination, includes an illumination source, a dichroic prism positioned at the illumination optical path, a structured light generator positioned at the reflected optical path of the dichroic prism, a lens positioned at the transmitted optical path of the dichroic prism, a beam splitter positioned at the optical path of the lens, an objective lens and a sample stage positioned at the upper optical path of the beam splitter, a reflector mirror and a tube lens positioned at the lower optical path of the beam splitter and a CCD camera positioned behind the tube lens. The illumination source is an incoherent monochrome LED or a white light LED The structured light generator is a DMD (Digital Micro-mirror Device).


