Automated Whole Blood Analysis via Digital Imaging and Fluorescence

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Solution Overview

Problem

Current methods for performing a leukocyte differential count (LDC) on whole blood samples are labor-intensive, time-consuming, and reliant on operator skill, with limitations in accuracy and versatility, particularly due to the need for diluted samples and laborious blood smears.

Innovation Solution

An apparatus and method for analyzing whole blood samples within a chamber, using imaging and fluorescence techniques to identify and quantify features of white blood cells, such as monocytes, eosinophils, and neutrophils, through the use of colorants and programmable analysis, allowing for automated and accurate LDC without dilution.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If manual blood smear analysis is used, then operator flexibility is maintained, but labor intensity and time consumption increase significantly

Engineering Contradiction:
Improveoperator flexibilityVSAvoidanalysis speed
Core Design Contradiction:
Ease of operationVSProductivity

Solution Approach 1:

The patent replaces manual mechanical blood smear preparation and microscopic examination with an automated digital imaging system. The apparatus captures images of whole blood samples and uses computer algorithms to identify and classify white blood cells, eliminating the need for manual smear preparation while maintaining diagnostic accuracy and enabling high-throughput analysis.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Solution Approach 2:

The system enables self-service analysis by automating the entire leukocyte differential count process. The apparatus automatically captures images, processes them through algorithms that identify cell types based on morphological features, and generates results without requiring operator intervention for each sample, thereby increasing productivity while preserving flexibility through programmable analysis methods.

Inventive Principle:
Principle #25Self-service

2Extent of automation

If flow cytometry is used, then automation is achieved, but sample dilution and fluid handling equipment are required

Engineering Contradiction:
Improveanalysis automationVSAvoidfluid handling requirements
Core Design Contradiction:
Extent of automationVSDevice complexity

Solution Approach 1:

The patent extracts the essential function of white blood cell identification from the complex flow cytometry system. By removing the need for sample dilution and fluid handling equipment, the invention uses direct digital imaging of undiluted whole blood samples, capturing cellular images and using image processing algorithms to achieve automation without the cumbersome fluid handling requirements of flow cytometry.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The system replaces the mechanical fluid handling and serial cell passage requirements of flow cytometry with a static digital imaging approach. Whole blood samples are placed in a chamber and imaged directly, with automated analysis performed through computer vision algorithms that identify and classify white blood cells based on their visual characteristics, eliminating the need for complex fluid handling equipment.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

3Measurement precision

If traditional LDC methods are used, then white blood cell identification is achieved, but operator skill level significantly affects accuracy

Engineering Contradiction:
Improvecell identification accuracyVSAvoidoperator skill dependency
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The system incorporates feedback mechanisms where the automated image analysis algorithm continuously refines its cell identification and classification based on captured images. The programmable analyzer uses established algorithms to objectively measure cellular features and provide consistent, reproducible results that are independent of operator skill level, while allowing for validation and adjustment of results by trained personnel.

Inventive Principle:
Principle #23Feedback

Solution Approach 2:

The patent replaces the subjective human judgment required in traditional LDC with objective computer-based image analysis. The system captures high-resolution images of white blood cells and uses algorithms to automatically identify cell types based on morphological features, eliminating the variability introduced by different operator skill levels while maintaining high diagnostic accuracy.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

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 solution enables high-accuracy, automated analysis of whole blood samples, reducing operator dependency and time, while providing greater versatility and accuracy in distinguishing different types of white blood cells, as demonstrated by empirical data and comparison with manual hematological analysis.

Implementation Method 1

using imaging and fluorescence techniques to identify and quantify features of white blood cells

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentEP3388833B1Method and apparatus for automated whole blood sample analyses from microscopy images
Publication Date: 2021.12.29 ABBOTT POINT OF CARE INC
  • EP3388833B1 patent drawingFigure 1~2
  • EP3388833B1 patent drawingFigure 3~4
  • EP3388833B1 patent drawingFigure 5A~9D

AI summary

A method and apparatus for identifying one or more target constituents (e.g., white blood cells) within a biological sample is provided. The method includes the steps of: a) adding at least one colorant to the sample; b) disposing the sample into a chamber defined by at least one transparent panel; c) creating at least one image of the sample quiescently residing within the chamber; d) identifying target constituents within the sample image; e) quantitatively analyzing at least some of the identified target constituents within the image relative to one or more predetermined quantitatively determinable features; and f) identifying at least one type of target constituent within the identified target constituents using the quantitatively determinable features.