Propofol Extraction Apparatus with Integrated Lysis and Sorbent Filtration

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Solution Overview

Problem

Current methods for automating sample preparation in biological assays, such as propofol extraction from whole blood, are hindered by manual lysis and dilution steps that are prone to user error, biohazard risks, and inefficiencies in analyte recovery due to the need for precise metering and filtration, which restricts their use to specialized laboratories and limits their effectiveness in point-of-care settings.

Innovation Solution

An apparatus and method that combines osmotic and mechanical lysis within a fluidic system, using a sorbent material with affinity for the analyte to enhance extraction efficiency, allowing whole blood samples to be processed directly without pre-treatment, reducing the need for precise dilution and filtration, and incorporating a solid phase extraction cartridge for accurate analyte detection.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If manual lysis and dilution steps are performed by skilled laboratory personnel, then analyte extraction accuracy is maintained, but the complexity of operation increases and limits use to specialized laboratories

Engineering Contradiction:
Improveanalyte extraction accuracyVSAvoidoperational complexity
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The system performs automatic lysis and dilution through integrated fluidic pathways and pumping mechanisms, eliminating the need for manual intervention by skilled personnel while maintaining extraction accuracy through controlled automated processes

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

Manual mechanical lysis and dilution operations are replaced with automated fluidic systems including pumps, valves, and integrated mixing chambers that precisely control sample processing without requiring human manipulation

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

2Measurement precision

If precise metering and filtration are implemented in automated systems, then analyte recovery is improved, but the device complexity and cost increase

Engineering Contradiction:
Improveanalyte recoveryVSAvoidapparatus complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The system combines metering, lysis, and filtration functions into integrated fluidic modules where a single automated pathway performs multiple operations sequentially, reducing the number of separate components while maintaining analyte recovery through controlled processing

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The fluidic system is designed with multi-functional components that perform metering, mixing, and filtration through integrated pathways, allowing a single apparatus to handle various sample preparation steps without requiring specialized equipment for each function

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

3Measurement precision

If manual sample preparation steps are required, then analyte extraction accuracy is maintained, but productivity and efficiency decrease

Engineering Contradiction:
Improveextract ion accuracyVSAvoidsample processing efficiency
Core Design Contradiction:
Measurement precisionVSProductivity

Solution Approach 1:

The automated system enables continuous sample processing through integrated fluidic pathways where samples are automatically transported, lysed, diluted, and filtered in sequence without interruption, eliminating the time losses associated with manual transfer and preparation steps while maintaining extraction accuracy

Inventive Principle:
Principle #20Continuity of useful 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

This approach improves the accuracy and efficiency of propofol extraction by ensuring that the extracted amount reflects the original sample concentration, reduces the complexity and cost of the apparatus, and enables direct injection of whole blood samples, enhancing the reliability and precision of analyte measurement in clinical and point-of-care settings.

Implementation Method 1

a lysing agent, said lysing agent having an osmotic pressure lower than the osmotic pressure of the cellular material

Methodology Applied
Scientific EffectOsmotic lysis: Osmosis

Implementation Method 2

a filtering stage comprising a sorbent material for mechanically lysing the cellular material, said sorbent material having an affinity for binding Propofol

Methodology Applied
Scientific EffectAdsorption: Adsorption

Data Source

PatentUS9068997B2Analyte extraction apparatus and method
Publication Date: 2015.06.30 SPHERE MEDICAL
  • US9068997B2 patent drawing
  • US9068997B2 patent drawing
  • US9068997B2 patent drawing

AI summary

Disclosed is an apparatus for automatically extracting i2,6-diisopropylphenol (Propofol), from a complex sample matrix comprising cellular material, e.g. blood, the apparatus comprising a sample reception stage having on output for providing a defined quantity of the complex sample matrix; a mixing stage having a first input in fluidic connection with the output of the sample reception stage, a second input for receiving a lysing agent and an output for providing a mixture of the defined quantity of the complex sample matrix and the lysing agent; a delay stage having an input in fluidic connection with the output of the mixing stage and an output for providing the delayed mixture of the defined quantity of the complex sample matrix and the lysing agent; a filtering stage comprising a sorbent material for mechanically lysing the cellular material, said sorbent material having an affinity for binding Propofol, said filtering stage having an input in fluidic connection with the output of the delay stage; and a controller for controlling the flow rate of the mixture of the defined quantity of the complex sample matrix and the lysing agent through said delay stage. A method for such extraction is also disclosed.