pH-Buffering Reagent Layer for Durable Continuous Biosensing

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Solution Overview

Problem

Conventional biosensors struggle with continuous and direct monitoring of samples without continuous buffer solution feed, lacking pH buffering ability in their reagent layers.

Innovation Solution

A reagent layer containing a polymer with a proton accepting group in its repeating unit, combined with an oxidoreductase, provides pH buffering ability and maintains optimal reaction conditions.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If a conventional biosensor without pH buffering ability in the reagent layer is used, then the device complexity is reduced, but the reliability deteriorates due to inability to maintain pH stability during continuous monitoring

Engineering Contradiction:
ImprovepH stabilityVSAvoiddevice complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent combines the pH buffering function with the reagent layer by incorporating a polymer containing proton-accepting groups (such as imidazole, pyridine, or carboxyl groups) directly into the reagent layer matrix. This merging of buffering capability into the existing reagent layer structure eliminates the need for separate buffering systems while maintaining pH stability during continuous analyte monitoring.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The reagent layer becomes self-sufficient by containing an embedded pH buffering system through the polymer with proton-accepting groups. This allows the reagent layer to autonomously maintain optimal pH conditions for enzyme activity without requiring external buffer solution feeds or additional pH control mechanisms, thereby improving reliability while avoiding increased device complexity.

Inventive Principle:
Principle #25Self-service

2Reliability

If continuous buffer solution feed is implemented, then the pH buffering ability is improved, but the device complexity increases due to additional feed systems

Engineering Contradiction:
ImprovepH buffering abilityVSAvoiddevice complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent extracts the pH buffering function from the external buffer solution feed system and relocates it directly into the reagent layer through the incorporation of polymers with proton-accepting groups. This extraction eliminates the dependency on continuous buffer feeding while preserving the essential pH buffering ability, thereby reducing device complexity without sacrificing reliability.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The polymer containing proton-accepting groups acts as an intermediary buffering agent within the reagent layer. This intermediary substance provides pH buffering capacity locally at the enzyme active site without requiring external buffer solution feeds, thus maintaining pH buffering ability while avoiding the complexity of continuous feed systems.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Duration of action of stationary object

If the reagent layer lacks pH buffering ability, then the ease of manufacture is improved, but the duration of action deteriorates due to enzyme deactivation

Engineering Contradiction:
Improvesensor durabilityVSAvoidease of manufacture
Core Design Contradiction:
Duration of action of stationary objectVSEase of manufacture

Solution Approach 1:

The patent merges the pH buffering function with the reagent layer fabrication process by incorporating polymers containing proton-accepting groups (such as polyvinylimidazole, poly-L-histidine, or carboxymethyl cellulose) directly into the reagent layer matrix during manufacturing. This integration extends sensor durability by preventing enzyme deactivation through pH stabilization while maintaining ease of manufacture through a unified fabrication approach.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The patent modifies the chemical composition parameters of the reagent layer by incorporating polymers with specific proton-accepting functional groups. This parameter change introduces pH buffering capability into the reagent layer, thereby extending the operational duration and durability of the biosensor without significantly complicating the manufacturing process, as these polymers can be integrated using standard reagent layer fabrication techniques.

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

The reagent layer maintains pH stability, preventing enzyme deactivation and enhancing sensor durability during continuous analyte monitoring.

Implementation Method 1

a polymer containing a proton accepting group in a repeating unit and having a pH buffering ability

Methodology Applied
Scientific EffectpH buffering:

Implementation Method 2

an oxidoreductase that oxidizes or dehydrogenates an analyte

Methodology Applied
Scientific EffectOxidation: Oxidation

Implementation Method 3

an oxidoreductase that oxidizes or dehydrogenates an analyte

Methodology Applied
Scientific EffectDehydrogenation:

Data Source

PatentUS20260015649A1Reagent layer and biosensor comprising reagent layer
Publication Date: 2026.01.15 PHC HLDG CORP
  • US20260015649A1 patent drawing
  • US20260015649A1 patent drawing
  • US20260015649A1 patent drawing

AI summary

In an embodiment of the present invention, there is provided a reagent layer comprising a polymer containing a proton accepting group in a repeating unit and having a pH buffering ability, and an oxidoreductase that oxidizes or dehydrogenates an analyte.