Amphiphilic Polymer Biosensor Coatings for Rapid Protein Aggregate Detection

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Solution Overview

Problem

Existing biosensors are limited by traditional biochemistries such as antigen-antibody or ligand-receptor interactions, which are time and labor-intensive for measuring critical quality attributes like protein aggregation, and there is a need for biosensors that can detect a variety of compounds through expanded classes of coating chemistries.

Innovation Solution

Biosensors coated with amphiphilic polymers that utilize hydrophobic interactions to capture protein aggregates, optionally with fluorescent labeling for quantitation, using a core component with amphiphilic polymers having hydrophilic and hydrophobic portions to facilitate capture and signal generation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If traditional antigen-antibody or ligand-receptor interactions are used for biosensing, then specific binding can be achieved, but the measurement process becomes time and labor intensive

Engineering Contradiction:
Improvedetection accuracyVSAvoidmeasurement time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent changes the fundamental interaction parameter from specific biological recognition (antigen-antibody) to universal hydrophobic interactions. By coating the biosensor with amphiphilic polymers that present hydrophobic groups, the system detects protein aggregates through hydrophobic effects rather than specific binding, dramatically reducing measurement time while maintaining detection capability

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The amphiphilic polymer coating provides universal detection capability for various protein aggregates regardless of their specific identity. The hydrophobic groups on the polymer can interact with any aggregated protein structure, making the biosensor broadly applicable to different analytes without requiring specific antibody development for each target

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

2Adaptability or versatility

If traditional biosensor coating chemistries are used, then specific analyte binding is achieved, but the biosensor cannot detect a variety of compounds through expanded classes of interactions

Engineering Contradiction:
Improvedetection rangeVSAvoidcoating chemistry complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The amphiphilic polymer coating enables the biosensor to detect multiple types of compounds including protein aggregates, lipids, and other hydrophobic molecules through a single universal mechanism. This expands the detection range from specific antigen-antibody pairs to a broad class of hydrophobic analytes

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

Solution Approach 2:

The biosensor uses composite amphiphilic polymer coatings that combine hydrophilic and hydrophobic segments in a single material system. This composite structure allows the sensor to interact with diverse hydrophobic analytes while maintaining stability in aqueous environments, simplifying the overall coating chemistry

Inventive Principle:
Principle #40Composite materials

3Measurement precision

If fluorescent labeling is used for analyte detection, then quantitation capability is improved, but interference and reduced accuracy occur

Engineering Contradiction:
Improvequantitation accuracyVSAvoidlabel interference
Core Design Contradiction:
Measurement precisionVSObject-affected harmful factors

Solution Approach 1:

The biosensor system uses the inherent fluorescent properties of the protein aggregates themselves for detection. The aggregated proteins exhibit intrinsic fluorescence or can be detected through label-free optical methods, eliminating the need for external fluorescent labels and avoiding the interference problems associated with labeling

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent removes the fluorescent labeling step entirely from the detection process. By using label-free detection methods or detecting intrinsic fluorescence of the analyte, the system eliminates the harmful effects of label interference while maintaining quantitation capability

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

Enables efficient and rapid detection and quantitation of protein aggregates without the need for traditional labeling, reducing interference and improving accuracy through hydrophobic interactions and fluorescent dye binding.

Implementation Method 1

one or more hydrophobic groups of the amphiphilic polymer is capable of binding to protein aggregates based on hydrophobic effects

Methodology Applied
Scientific EffectHydrophobic interactions: Hydrophobe

Implementation Method 2

In certain embodiments, a fluorescent dye is bound to the captured protein aggregates of each amphiphilic polymer

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentUS20260043808A1Biosensors comprising amphiphilic polymers and use thereof
Publication Date: 2026.02.12 SARTORIUS BIOANALYTICAL INSTRUMENTS INC
  • US20260043808A1 patent drawing
  • US20260043808A1 patent drawing
  • US20260043808A1 patent drawing

AI summary

Biosensors for detecting and analyzing protein aggregates in a sample are provided. A biosensor may be coated with an amphiphilic polymer having one or more hydrophobic groups for binding to protein aggregates, based on hydrophobic effects. An outer surface of a protein aggregate may be generally non-polar and hydrophobic and, thus, drawn to and captured by hydrophobic groups of the amphiphilic polymer. The biosensor may detect the binding of an analyte directly, without use of a detectable label attached to the analyte. In certain embodiments, the biosensor may detect the binding of the analyte based on indirect detection of a fluorescent label that binds to the analyte after capture by the biosensor.