Microfluidic Plasma Layer Optical Analyte Detection
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Solution Overview
Problem
Current methods for determining analyte concentration in whole blood are hindered by hemolysis, which alters blood plasma composition and requires time-consuming plasma separation, making it difficult to detect analytes like extracellular hemoglobin efficiently.
Innovation Solution
A method utilizing the Fahraeus effect to generate a plasma layer in a microfluidic channel, where light is directed and reflected, allowing for the analysis of analyte concentration without separating blood plasma from whole blood, using index matching substances to ensure light interaction with the plasma layer and not the channel surface, and capturing the reflected light to determine the analyte concentration.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Measurement precision
If plasma separation is performed to detect analyte concentration, then measurement precision is improved, but loss of time increases
Solution Approach 1:
The invention segments the whole blood sample into different layers (plasma layer and cell layer) using the Fahraeus effect in a microfluidic channel. This segmentation allows direct optical measurement of the plasma layer without requiring complete separation, thus reducing time loss while maintaining measurement precision for analyte concentration detection.
Solution Approach 2:
The invention extracts only the necessary plasma layer containing the analyte from the whole blood sample using the Fahraeus effect, rather than performing complete plasma separation. This extraction approach enables direct measurement of analyte concentration in the plasma layer while minimizing time consumption associated with full separation procedures.
2Quantity of substance
If hemolysis occurs in whole blood, then analyte concentration changes, but measurement reliability deteriorates
Solution Approach 1:
The invention converts the harmful effect of hemolysis (which releases intracellular contents into plasma) into a beneficial measurement opportunity. By using the Fahraeus effect to separate and measure the plasma layer optically, the system can detect and quantify hemolysis-induced changes in analyte concentration, transforming a quality degradation into a measurable signal for reliability assessment.
3Measurement precision
If light is directed through whole blood, then analyte detection is possible, but light scattering from blood cells interferes with measurement
Solution Approach 1:
The invention segments the whole blood into a plasma layer and a cell layer using the Fahraeus effect in a microfluidic channel. By directing light through only the plasma layer (which is free of blood cells), the measurement achieves high precision for analyte concentration detection without interference from light scattering caused by blood cells.
Solution Approach 2:
The microfluidic channel structure acts as an intermediary that uses the Fahraeus effect to create a cell-free plasma layer at the channel walls. This intermediary structure enables light to interact with the plasma layer without encountering blood cells, thereby eliminating light scattering interference while maintaining measurement precision.
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 fast, cost-effective detection of analyte concentration in whole blood samples with minimal sample volume and no additional reagents required, allowing for accurate measurement of hemolysis without interference from blood cells.
Implementation Method 1
exposing the plasma layer to light. Furthermore, the method includes capturing light reflected from the plasma layer
Implementation Method 2
A method utilizing the Fahraeus effect to generate a plasma layer in a microfluidic channel
Data Source
Figure 1
Figure 2A~2B
Figure 3A~3B
AI summary
A device for determining the concentration of an analyte in whole blood is disclosed. A plasma layer (302, 308) is generated in the whole blood sample. Furthermore, the the plasma layer (302) is exposed to light (303, 304). Light (305) reflected from the plasma layer (302) is captured. Additionally, the reflected light (305) is analyzed to determine the concentration of the analyte. A device for determining the concentration of an analyte in a whole blood sample comprises a channel (309) configured to carry whole blood; a light source configured to direct light (303) on the channel (309); and an optical fiber (301), wherein within the optical fiber (301) the light (303) is reflected multiple times to form reflected light (304), the optical fiber (301) being located inside the channel (309) and extending in parallel with the channel (309).