3D Plasmonic Biosensor for Low-Concentration Optical Detection

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Solution Overview

Problem

Existing plasmonic biosensors face challenges in detecting hazardous substances and biomolecules at very low concentrations, requiring complex and costly laboratory procedures, limited interaction surface areas, and high fabrication costs, which hinder sensitivity and selectivity.

Innovation Solution

A method and device utilizing plasmonic nanostructures that emit radiation through non-radiative plasmon resonance modes, allowing for differential measurement of light properties under on- and off-resonance conditions to detect and quantify chemical and biological agents, with a 3-D free-form design and low-cost fabrication.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If conventional plasmonic biosensors use absorption spectroscopy or total internal reflection arrangements, then detection capability is achieved, but the devices require complex and costly laboratory procedures, high capital cost instrumentation, and limited interaction surface areas

Engineering Contradiction:
Improvedetection sensitivityVSAvoidcomplexity of detection procedure
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent replaces complex mechanical/optical systems (total internal reflection arrangements, orthogonal prisms, spectroscopic analysis instruments) with a simpler plasmonic resonance-based system using 3D nanostructures that directly convert chemical/biological interactions into measurable optical signals, eliminating the need for complex laboratory instrumentation

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Solution Approach 2:

The patent transitions from 2D planar surfaces to 3D nanostructures with free-form surfaces, increasing the interaction surface area and enabling more effective plasmonic resonance. This dimensional change allows for enhanced sensitivity without requiring complex multi-component systems

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

2Reliability

If conventional biosensors use label-free spectral absorption, then detection is achieved, but the detectivity is reduced and requires complex chemical functionalization processes for amplification

Engineering Contradiction:
ImprovedetectivityVSAvoidcomplexity of functionalization process
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The patent changes the fundamental detection parameter from absorption intensity to emitted radiation intensity under plasmonic resonance conditions. This parameter change inherently provides signal amplification without requiring complex chemical functionalization or labeling processes, as the 3D plasmonic nanostructures themselves generate the enhanced signal

Inventive Principle:
Principle #35Parameter changes

3Productivity

If conventional methods use small spatial extend interaction regions in optical waveguides or microring resonators, then integrated device fabrication is achieved, but the sensitivity and selectivity are limited

Engineering Contradiction:
Improveintegration capabilityVSAvoidsensitivity
Core Design Contradiction:
ProductivityVSMeasurement precision

Solution Approach 1:

The patent employs 3D nanostructures with extended surface areas and complex geometries that provide larger interaction regions compared to planar waveguide surfaces. This three-dimensional configuration maintains integrability while significantly enhancing sensitivity and selectivity through increased analyte-nanostructure interaction volume

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

Solution Approach 2:

The patent integrates plasmonic nanostructures within optical waveguide or microring resonator systems, creating a nested configuration where the 3D nanostructures are positioned within or on the surface of the integrated photonic device, combining the benefits of both approaches

Inventive Principle:
Principle #7Nested doll (Nesting)

4Measurement precision

If conventional nanohole biosensors use extraordinary optical transmission, then detection is achieved, but the fabrication requires very high cost methods such as electron-beam or ion-beam lithography

Engineering Contradiction:
Improvedetection capabilityVSAvoidfabrication cost
Core Design Contradiction:
Measurement precisionVSEase of manufacture

Solution Approach 1:

The patent changes the detection mechanism from relying on transmission through nanoholes to utilizing emitted radiation from plasmonic resonance in 3D nanostructures. This parameter change enables the use of simpler, lower-cost fabrication methods such as standard lithography or self-assembly techniques, eliminating the need for expensive electron-beam or ion-beam lithography

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

Enables fast, accurate, and sensitive detection of toxins and biological agents at low concentrations without complex labeling processes, offering high sensitivity and selectivity with reduced operational costs.

Implementation Method 1

the nanostructure is forced to plasmonic resonance and emits radiation by its non-radiative plasmon resonance modes

Methodology Applied
Scientific EffectPlasmon resonance: Resonance

Implementation Method 2

The interaction of optical radiation with nanoparticles of mainly noble metals results in the coupled vibration of the electron plasma that defines the physical concept of 'plasmon'. The Localized Surface Plasmon Resonance (LSPR) is achieved in a specific spectral region and results in absorption of radiation.

Methodology Applied
Scientific EffectLocalized Surface Plasmon Resonance (LSPR):

Data Source

PatentEP4660612A1Plasmonic radiation biosensor
Publication Date: 2025.12.10 UNIVERSTY OF PATRAS
  • EP4660612A1 patent drawingFigure 1A~1B
  • EP4660612A1 patent drawingFigure 2A~2B
  • EP4660612A1 patent drawingFigure 3A~3D

AI summary

Method for the detection with high accuracy, sensitivity and selectivity of chemical and biological agents, wherein an exogenous chemical and/or biological agent is trapped in a plasmonic nanostructure and changes its physical and/or chemical environment, so that upon optical interrogation with radiation of distinct wavelengths and polarization properties, the nanostructure is forced to emit optical radiation from non-radiative plasmon resonance modes, thereby altering the properties of the transmitted, reflected and diffracted radiation. The differential variation of any property of the light constitutes the measurable signal for the quantification of the chemical/biological agent to be detected. Also provided is a plasmonic radiation biosensor device for implementing the method, incorporating a free-form free-space or optical waveguide sensor head equipped with designed three-dimensional plasmonic diffractive nanostructures of large surface area and free stereometric form, or multiple nanostructures, incorporating molecular or atomic functionalizers capable of trapping and detecting the chemical/biological agent through the propagation and/or reflection and/or diffraction of optical radiation.