Optical Analysis Device Scanning Light Detection Region
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Solution Overview
Problem
Current optical analysis techniques using confocal microscopes struggle to detect and quantify light-emitting particles at low concentrations due to the need for statistical averaging, which requires high concentrations of fluorescent molecules and lengthy measurement times, limiting their sensitivity and sample efficiency.
Innovation Solution
An optical analysis device with a movable light detection region that scans the sample solution, allowing for individual detection of light-emitting particles by generating time series light intensity data, where the measuring unit time is set based on the size and speed of the light detection region to optimize signal detection and reduce data volume.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If statistical averaging is used to detect fluorescent molecules, then measurement reliability is improved, but measurement time increases and sensitivity to low concentrations deteriorates
Solution Approach 1:
The invention segments the detection process by moving the light detection region to scan through the sample solution, detecting individual light-emitting particles one by one rather than measuring bulk fluorescence statistically. This segmentation enables detection at low concentrations without requiring lengthy statistical averaging, thus reducing measurement time while maintaining reliability.
Solution Approach 2:
The light detection region is moved periodically through the sample solution at a controlled speed, creating a time-series detection pattern. This periodic scanning allows individual particles to be detected sequentially, enabling reliable detection at low concentrations without the need for prolonged statistical measurements.
2Reliability
If statistical averaging is used to detect fluorescent molecules, then measurement reliability is improved, but sensitivity to low concentrations deteriorates
Solution Approach 1:
The detection method is segmented into individual particle detection events, where the light detection region scans through and identifies each light-emitting particle separately. This approach maintains measurement reliability while achieving high sensitivity to low concentrations by counting individual particles rather than relying on statistical averaging of bulk signals.
Solution Approach 2:
The periodic movement of the light detection region creates systematic sampling of the sample solution, ensuring that even rare, low-concentration particles are detected with high reliability. The controlled scanning speed and detection timing enable precise sensitivity at low concentrations.
3Measurement precision
If high time resolution is used to detect individual particle signals, then signal detection accuracy is improved, but data volume increases
Solution Approach 1:
The light detection region moves periodically through the sample solution at a controlled speed, creating a time-series data pattern with inherent temporal structure. This periodic scanning approach achieves high signal detection accuracy through appropriate time resolution while reducing overall data volume by eliminating redundant measurements and focusing on particle passage events.
Solution Approach 2:
The system dynamically adjusts the detection process to match particle passage events, collecting high-resolution data only when particles are detected rather than continuously. This dynamic approach maintains signal detection accuracy while significantly reducing the total data volume that would result from continuous high-resolution monitoring.
4Productivity
If the light detection region is moved quickly through the sample, then measurement time is reduced, but signal detection accuracy deteriorates
Solution Approach 1:
The light detection region moves periodically through the sample solution at an optimized speed that balances measurement efficiency with detection accuracy. The periodic scanning pattern ensures that particles are detected with sufficient temporal resolution to maintain signal accuracy while keeping the overall measurement time short compared to statistical methods.
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
This approach enables the precise detection of light-emitting particles at lower concentrations, reducing measurement time and sample volume while maintaining signal accuracy and separating particle signals from noise, thus improving the efficiency and cost-effectiveness of optical analysis.
Implementation Method 1
the light emitted from a light-emitting particle may be fluorescence, phosphorescence, chemiluminescence, bioluminescence, scattered light, etc.
Implementation Method 2
the light emitted from a light-emitting particle may be fluorescence, phosphorescence, chemiluminescence, bioluminescence, scattered light, etc.
Implementation Method 3
the light emitted from a light-emitting particle may be fluorescence, phosphorescence, chemiluminescence, bioluminescence, scattered light, etc.
Implementation Method 4
the light emitted from a light-emitting particle may be fluorescence, phosphorescence, chemiluminescence, bioluminescence, scattered light, etc.
Implementation Method 5
the light emitted from a light-emitting particle may be fluorescence, phosphorescence, chemiluminescence, bioluminescence, scattered light, etc.
Data Source
AI summary
There is provided optical analysis techniques in the scanning molecule counting method using the light measurement with a confocal or multiphoton microscope in which the measuring unit time in the light measurement is set to an appropriate value in order to surely detect an approximately bell shape profile of the signal of a light-emitting particle and avoid excessive increase data volume of time series light intensity data. The inventive optical analysis technique of detecting light of a light-emitting particle in a sample solution generates time series light intensity data of light from a light detection region detected during moving the position of the light detection region of a microscope in the sample solution and detects in the data a signal indicating light from each light-emitting particle individually. The measuring unit time is determined based on the size and the moving speed of the light detection region.


