Entrapping Magnetic Nanoparticles in Cross-Linked Protein Matrices

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Solution Overview

Problem

Current methods for immobilizing proteins on magnetic particles often require a pre-coating with polymers, which increases preparation time and can interfere with magnetism, and may affect the functional activity of the proteins or enzymes.

Innovation Solution

A method involving the direct entrapment of magnetic nanoparticles in a cross-linked matrix of proteins using a cross-linking agent like Epichlorohydrin, without a polymer coating, allowing for easy separation and maintaining the functional properties of the proteins.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If magnetic particles are pre-coated with polymers (dextran or agarose) for protein immobilization, then the particles become stable and easier to handle, but the preparation time increases and the magnetic properties may be interfered with

Engineering Contradiction:
Improvestability of magnetic particlesVSAvoidpreparation time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The invention removes the polymer coating step entirely from the traditional method. Instead of coating magnetic particles with dextran or agarose and then immobilizing proteins, the patent directly immobilizes proteins onto the surface of uncoated magnetic particles using carbodiimide chemistry, thereby eliminating the time-consuming pre-coating process while maintaining particle stability

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The magnetic particles are prepared in advance with surface functional groups (carboxyl or hydroxyl groups) that are ready for direct protein coupling. This preliminary surface preparation eliminates the need for subsequent polymer coating steps, allowing direct protein immobilization while maintaining particle stability

Inventive Principle:
Principle #10Preliminary action

2Ease of operation

If polymer coatings are used on magnetic particles, then the particles are easier to handle, but the magnetic properties are interfered with

Engineering Contradiction:
Improveease of handling magnetic particlesVSAvoidmagnetic response
Core Design Contradiction:
Ease of operationVSUse of energy by moving object

Solution Approach 1:

The invention removes the polymer coating that acts as a magnetic barrier. By directly immobilizing proteins on uncoated magnetic particles, the magnetic properties of the particles are preserved, allowing for efficient magnetic separation and handling without the interference of thick polymer layers

Inventive Principle:
Principle #2Taking out (Extraction)

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 reduces preparation time, preserves the magnetic properties, and maintains the functional activity of the proteins or enzymes, enabling efficient immobilization and purification of proteins, antibodies, and enzymes without the need for additional polymer coatings.

Implementation Method 1

easy separation under external magnetic fields

Methodology Applied
Scientific EffectMagnetic field: Magnetic Field

Implementation Method 2

treatment with a cross linking agent

Methodology Applied
Scientific EffectChemical bonding: Chemical Bonding

Data Source

PatentEP3314616B1Entrapment of magnetic nanoparticles in a cross-linked protein matrix without affecting the functional properties of the protein
Publication Date: 2021.08.25 MAGGENOME TECH PVT LTD
  • EP3314616B1 patent drawingFigure 1~2
  • EP3314616B1 patent drawingFigure 3~4
  • EP3314616B1 patent drawingFigure 5(a)~5(b)

AI summary

: Entrapped magnetic nanoparticles in a cross linked matrix of an intended protein, without having the functional properties of the protein affected, and a method for preparing the same is disclosed herein. Further, the use of entrapped magnetic nanoparticles in the protein matrix in diagnostic, immobilization and immunoprecipitation kits is described herein.