Capillary Electrophoresis Albumin Separation

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Solution Overview

Problem

Conventional capillary electrophoresis methods for separating albumin and γ-globulin lack accuracy and efficiency, requiring longer analysis times and being prone to interference from interactions with other substances.

Innovation Solution

A capillary electrophoresis method using an alkaline solution with a non-surfactant-type sulfobetaine and a cationic polymer, which binds to albumin and γ-globulin, enhancing separation accuracy and speed by modifying their charge and reducing hydrophobic interactions.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If conventional capillary electrophoresis methods are used for separating albumin and γ-globulin, then the analysis can be performed with a small amount of sample, but the separation accuracy is insufficient and the analysis time is prolonged

Engineering Contradiction:
Improveseparation accuracyVSAvoidanalysis time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent changes the chemical parameters of the electrophoresis buffer by introducing a non-surfactant-type sulfobetaine substance. This substance modifies the electrophoretic mobility of albumin and γ-globulin through hydrophobic interactions and charge effects, enabling faster and more accurate separation. The specific parameter changes include pH adjustment to alkaline conditions and optimization of sulfobetaine concentration to achieve optimal separation within 10 minutes.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs a composite buffer system combining multiple components: a non-surfactant-type sulfobetaine substance, a cationic polymer, and other auxiliary substances. This composite formulation creates synergistic effects where the sulfobetaine provides hydrophobic interaction and charge modification, while the cationic polymer enhances separation through electrostatic interactions, collectively achieving high-accuracy separation in reduced time.

Inventive Principle:
Principle #40Composite materials

2Reliability

If conventional capillary electrophoresis methods are used, then the analysis can be performed with simple equipment, but the separation is prone to interference from interactions with other substances

Engineering Contradiction:
Improveseparation reliabilityVSAvoidbuffer system complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The non-surfactant-type sulfobetaine acts as an intermediary substance that mediates the interaction between the buffer and the proteins (albumin and γ-globulin). It provides hydrophobic interaction and charge modification without causing the unwanted interactions that plague conventional methods. The sulfobetaine shields the proteins from interfering interactions while maintaining their electrophoretic mobility, thereby improving separation reliability.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent optimizes specific parameters of the buffer system including pH (adjusted to alkaline range), ionic strength, and the concentrations of sulfobetaine and cationic polymer. These parameter changes create a controlled environment that enhances the specificity of protein-protein separation while minimizing non-specific interactions with other substances in the sample matrix.

Inventive Principle:
Principle #35Parameter changes

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 method effectively separates albumin and γ-globulin with higher accuracy and in shorter time compared to conventional methods, improving the separation process by leveraging the interactions between sulfobetaine and cationic polymer to enhance electrophoretic mobility.

Implementation Method 1

the alkaline solution contains a cationic polymer

Methodology Applied
Scientific EffectElectrostatic interaction: Ion Repulsion/Attraction

Implementation Method 2

separating albumin and γ-globulin from a sample containing albumin and γ-globulin, in an alkaline solution by capillary electrophoresis

Methodology Applied
Scientific EffectCapillary electrophoresis: Capillary Electrophoresis

Implementation Method 3

reducing hydrophobic interactions

Methodology Applied
Scientific EffectHydrophobic interaction: Hydrophobe

Implementation Method 4

modifying their charge and reducing hydrophobic interactions

Methodology Applied
Scientific EffectElectrophoretic mobility modification: Electrophoresis

Data Source

PatentUS20240159769A1SAMPLE ANALYSIS METHOD, SAMPLE PRODUCTION METHOD, DILUENT FOR DILUTING ALBUMIN- AND y-GLOBULIN-CONTAINING SAMPLE, AND SAMPLE ANALYSIS KIT
Publication Date: 2024.05.16 ARKRAY INC
  • US20240159769A1 patent drawing
  • US20240159769A1 patent drawing
  • US20240159769A1 patent drawing

AI summary

Provided is a sample analysis method, including separating albumin and γ-globulin from a sample containing albumin and γ-globulin, in an alkaline solution by capillary electrophoresis, in which the sample contains a non-surfactant-type sulfobetaine, and the alkaline solution contains a cationic polymer.