Immunochromatography Chip Electron Microscopy Sensitivity
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Solution Overview
Problem
Current immunochromatography methods face challenges in sensitivity and quantification, with conventional methods often resulting in false positives or negatives and difficulty in accurately measuring viral loads, especially when using visual observation for detection.
Innovation Solution
An immunochromatography measurement method utilizing an auxiliary liquid that prevents charging and heat generation under electron microscope conditions, allowing for high-resolution imaging and increased sensitivity by stabilizing samples and enhancing contrast, combined with an immunochromatography chip and kit for precise detection using metal nanoparticles and electron microscopy.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Speed
If immunochromatography is used for rapid detection, then detection speed is improved, but sensitivity is insufficient compared to PCR method
Solution Approach 1:
The invention changes the detection parameter from visual observation to electron microscope imaging, enabling detection at much lower viral loads (10-100 times higher sensitivity) while maintaining the rapid one-step operation characteristic of immunochromatography
Solution Approach 2:
The invention replaces the optical detection system (visual observation) with an electron microscope-based detection system, substituting the detection mechanism to achieve higher sensitivity while preserving the simplicity and speed of the immunochromatography process
2Ease of operation
If visual observation is used for immunochromatography, then operation simplicity is maintained, but quantification capability is insufficient
Solution Approach 1:
The invention replaces subjective visual observation with objective electron microscope imaging and image analysis, enabling accurate quantification of viral loads while maintaining operational simplicity through automated image processing
3Measurement precision
If electron microscope measurement is applied directly to immunochromatography chip, then high resolution imaging is achieved, but charging and heat generation deteriorate image quality
Solution Approach 1:
The invention introduces an intermediary substance (conductive coating or buffer solution) between the immunochromatography chip and the electron microscope beam, which dissipates charging effects and heat generation, enabling high-resolution imaging without degradation from these harmful factors
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
The method achieves a 10 to 100 times increase in sensitivity compared to conventional qualitative determination, enabling precise quantification of viral loads even at lower concentrations, with clear imaging of labeling substances on immunochromatography chips, thus improving diagnostic accuracy and efficiency.
Implementation Method 1
an auxiliary liquid other than a specimen undergoing immunochromatography is applied... having conductivity for preventing charging and heat generation
Implementation Method 2
having conductivity for preventing charging and heat generation which contributes to sharpness of images
Implementation Method 3
quantified by being identified with precision, high resolution, and increased contrast using an electron microscope... using metal nanoparticles
Implementation Method 4
A principle thereof is one that uses the antigen-antibody reaction... labeled antibody-object to be detected (antigen)-capture antibody
Data Source
AI summary
The present invention provides a highly sensitive immunochromatography measurement method in which a labeling substance for labeling an object to be detected in a specimen undergoing immunochromatography is quantified by being identified with precision, high resolution, and increased contrast using an electron microscope. An immunochromatography measurement method according to an embodiment of the present invention is characterized in that measurement is performed by an electron microscope after applying an auxiliary liquid other than a specimen in the immunochromatography.


