Protein Nanoparticle Hydrogel for Stable Disease Marker Detection

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Solution Overview

Problem

Conventional protein detection methods face challenges in maintaining protein activity and specificity due to random attachment to substrate surfaces, leading to low efficiency and stability, especially in hydrogel environments where enzymes can be washed away or denatured.

Innovation Solution

The use of protein nanoparticles with multiple copies of disease marker detection probes immobilized in a three-dimensional porous hydrogel, which provides high-density integration, structural stability, and controlled orientation, enhancing the sensitivity and specificity of disease marker detection.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If protein probes are immobilized on substrate surfaces by simple adsorption, then the immobilization process is simple and fast, but the protein probes may be washed away by intensive washing conditions, transferred to other molecules, or denatured, resulting in low stability and reliability

Engineering Contradiction:
Improveimmobilization process simplicityVSAvoidprobe stability
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent applies preliminary action by pre-modifying the substrate surface with coupling agents (such as glutaraldehyde or silane reagents) before protein immobilization. This creates reactive functional groups on the surface that form stable covalent bonds with protein probes, preventing probe loss during washing and ensuring long-term stability while maintaining a relatively simple overall process

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent uses composite materials by combining the substrate surface with coupling agents and protein probes to create a multi-layered immobilization system. The coupling agent layer acts as an intermediary that provides both mechanical anchoring and chemical bonding capabilities, resulting in a composite structure that enhances probe stability without significantly complicating the manufacturing process

Inventive Principle:
Principle #40Composite materials

2Ease of manufacture

If protein probes are randomly attached to substrate surfaces, then the attachment process is simple, but the protein structure is easily modified and activity is inhibited, resulting in low binding efficiency

Engineering Contradiction:
Improveattachment process simplicityVSAvoidbinding efficiency
Core Design Contradiction:
Ease of manufactureVSProductivity

Solution Approach 1:

The patent applies local quality by creating specific localized regions on the substrate surface with controlled chemical properties. By using self-assembling peptide structures or oriented coupling methods, the protein probes are attached in specific orientations with their active sites exposed, rather than random attachment. This localized control of protein orientation and distribution maintains simple overall manufacturing while dramatically improving binding efficiency

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent uses preliminary action by pre-organizing the substrate surface with coupling agents or self-assembling structures before protein attachment. This preliminary organization creates predefined binding sites that guide protein orientation, ensuring that probes attach in activity-preserving configurations without requiring complex real-time control during the immobilization process

Inventive Principle:
Principle #10Preliminary action

3Stability of the object's composition

If only a hydrogel is used as an enzyme support, then the hydrogel can maintain moisture content, but the hydrogel swells and enzymes are spread out, resulting in sharply decreased stability over time

Engineering Contradiction:
Improvemoisture maintenanceVSAvoidtemporal stability
Core Design Contradiction:
Stability of the object's compositionVSReliability

Solution Approach 1:

The patent applies composite materials by combining hydrogel with cross-linking agents or reinforcing structures. The hydrogel provides moisture maintenance while the cross-linking network or supporting framework prevents excessive swelling and enzyme dispersion. This composite approach maintains the moisture-filled environment necessary for enzyme activity while providing structural integrity for long-term stability

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The patent uses segmentation by dividing the enzyme support into discrete domains or compartments within the hydrogel matrix. Enzymes are localized in specific regions rather than freely dispersed, preventing spreading while maintaining moisture content. This segmented structure allows the hydrogel to fulfill its moisture-maintenance function without the destabilizing effect of enzyme dispersion

Inventive Principle:
Principle #1Segmentation

4Ease of manufacture

If conventional organic and inorganic nanoparticles are used, then they can be artificially synthesized, but they lack uniform particle size distribution and stability compared to protein nanoparticles

Engineering Contradiction:
Improvesynthesis controlVSAvoidparticle size uniformity
Core Design Contradiction:
Ease of manufactureVSManufacturing precision

Solution Approach 1:

The patent applies self-service by utilizing the self-assembly capability of protein nanoparticles. Protein subunits spontaneously organize into uniform nanoparticles through non-covalent interactions, automatically achieving monodispersity and structural precision without requiring complex external control mechanisms. This self-organizing process maintains manufacturing simplicity while achieving superior particle uniformity

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent uses parameter changes by controlling the physical and chemical conditions (pH, ionic strength, temperature, concentration) during protein nanoparticle formation. By optimizing these parameters, the self-assembly process produces nanoparticles with uniform size and high stability. This parameter control enables precise manufacturing of protein nanoparticles with consistent properties

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 approach significantly increases the surface area-to-volume ratio of the diagnostic system, maintaining probe activity and improving sensitivity and specificity for diseases like Sjögren's syndrome and AIDS, outperforming traditional methods by detecting markers at much lower concentrations with higher stability.

Implementation Method 1

when the hydrogel forms a polymer through a certain coupling reaction, the hydrogel can form a covalent bond with a material having a specific residue

Methodology Applied
Scientific EffectCovalent bonding: Chemical Bonding

Implementation Method 2

A hydrogel has a three-dimensional porous structure and can maintain a uniform content of moisture therein

Methodology Applied
Scientific EffectHydrogel structure: Hydrogel

Implementation Method 3

protein nanoparticles as nanomaterials synthesized by self-assembly in a cell of a living organism

Methodology Applied
Scientific EffectSelf-assembly: Self-Assembly

Implementation Method 4

the protein nanoparticles can be developed to have various characteristics/functions by genetically engineered surface modification

Methodology Applied
Scientific EffectGenetic engineering:

Data Source

PatentUS10001477B2Use of protein nanoparticle based hydrogel
Publication Date: 2018.06.19 KOREA UNIV RES & BUSINESS FOUND
  • US10001477B2 patent drawing
  • US10001477B2 patent drawing
  • US10001477B2 patent drawing

AI summary

The present invention relates to a use of a protein nanoparticle-based hydrogel, and more particularly, to a use of a protein nanoparticle-based hydrogel capable of highly sensitive and simultaneous multi-detection of disease markers by using a hydrogel within which protein nanoparticles presenting multiple copies of disease marker detection probes are immobilized.