Blood Sample Microscopy for Optical Measurement Error Correction

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Solution Overview

Problem

Optical measurement systems for biological samples, such as blood samples, suffer from errors due to sample degradation, environmental factors, and equipment malfunctions, leading to inaccurate results.

Innovation Solution

Implementing a method to identify and account for errors by analyzing microscopic images of blood samples within a sample chamber, including determining cell settling dynamics, identifying specific cell types, and calibrating measurements based on image analysis to ensure accurate optical density and concentration calculations.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If optical measurements are performed on blood samples in sample carriers, then diagnostic information can be obtained, but measurement accuracy deteriorates due to sample degradation, environmental factors, and equipment malfunctions

Engineering Contradiction:
Improvemeasurement accuracyVSAvoidsample degradation and environmental interference
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The system performs preliminary error identification by analyzing microscopic images of the sample before final optical density measurements are taken. This allows detection of settling artifacts, bubbles, and other sample issues that would compromise measurement accuracy, enabling corrective actions to be taken beforehand

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The system implements a feedback mechanism where microscopic image analysis results are used to determine whether optical density measurements should be performed or invalidated. The computer processor uses the image analysis feedback to make intelligent decisions about measurement validity and triggers appropriate actions such as repeating the measurement or invalidating results

Inventive Principle:
Principle #23Feedback

2Adaptability or versatility

If multiple measurement methods (microscopic imaging and optical density) are used on blood samples, then comprehensive analysis is achieved, but system complexity increases

Engineering Contradiction:
Improvemeasurement comprehensivenessVSAvoidsystem configuration
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The system combines microscopic imaging capabilities and optical density measurement capabilities into a single integrated sample carrier system. Both measurement modes can be performed on the same sample using the same physical carrier, eliminating the need for separate sample preparation and reducing overall system complexity

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The sample carrier is designed as a multi-functional device that can accommodate both microscopic imaging and optical density measurements. The carrier structure and sample chamber are configured to support both measurement modalities, allowing a single carrier to serve multiple diagnostic purposes

Inventive Principle:
Principle #6Universality (Multi-functionality)

3Measurement precision

If error identification and calibration procedures are implemented, then measurement precision is improved, but analysis time increases

Engineering Contradiction:
Improveoptical measurement accuracyVSAvoidsample analysis time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The system performs partial error checking by analyzing only key features in microscopic images (such as presence of bubbles, settling patterns, and sample quality indicators) rather than conducting exhaustive analysis. This selective approach provides sufficient error detection without requiring excessive processing time

Inventive Principle:
Principle #16Partial or excessive action

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

Enhances the accuracy of optical measurements by identifying and correcting errors, ensuring reliable results by invalidating or calibrating measurements based on image analysis, thereby improving the precision of blood sample analysis.

Implementation Method 1

the concentration and/or density of a component may be measured by performing optical absorption, transmittance, fluorescence, and/or luminescence measurements upon the sample

Methodology Applied
Scientific EffectOptical absorption: Absorption (EM radiation)

Implementation Method 2

the concentration and/or density of a component may be measured by performing optical absorption, transmittance, fluorescence, and/or luminescence measurements upon the sample

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Implementation Method 3

the concentration and/or density of a component may be measured by performing optical absorption, transmittance, fluorescence, and/or luminescence measurements upon the sample

Methodology Applied
Scientific EffectLuminescence: Luminescence

Implementation Method 4

a microscope system is used that is generally similar to the microscope system described in US 2014/0347459 to Greenfield

Methodology Applied
Scientific EffectLight refraction and focusing: Refraction

Implementation Method 5

the optical measurement unit includes a microscope system configured to perform microscopic imaging of a portion of the sample

Methodology Applied
Scientific EffectOptical imaging: Lens

Implementation Method 6

each of which is configured to emit light at a respective wavelength or at a respective band of wavelengths

Methodology Applied
Scientific EffectLight emission from LEDs: Light Emitting Diode

Data Source

PatentUS12498325B2Accounting for errors in optical measurements
Publication Date: 2025.12.16 S D SIGHT DIAGNOSTICS LTD
  • US12498325B2 patent drawing
  • US12498325B2 patent drawing
  • US12498325B2 patent drawing

AI summary

Apparatus and methods are described including preparing a blood sample for analysis by depositing the blood sample within a sample chamber (52), and placing the sample chamber, with the blood sample deposited therein, within a microscopy unit (24). One or more microscopic images of the sample chamber (52) with the blood sample deposited therein are acquired, using a microscope of the microscopy unit. Based upon the one or more images, an amount of one or more cell types within the sample chamber that had already settled within the sample chamber, prior to acquisition of the one or more microscopic images is determined. A characteristic of the sample is determined, at least partially in response thereto. Other applications are also described.