Biosensing Apparatus Using Grating-Coupled Localized Plasmon Resonance

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Solution Overview

Problem

Standard SPR biosensors are expensive, inconvenient, and difficult to miniaturize due to their reliance on bulky optics for measuring surface plasmon resonance, limiting their ability to probe bio-molecular interactions effectively.

Innovation Solution

A bio-sensing apparatus utilizing localized plasmon resonance coupled with diffraction, featuring a substrate with a grating, nanoparticles functionalized with molecular recognition units, and a cover plate, which detects changes in refractive index and bio-molecular interactions using a simple optical setup, allowing for label-free and miniaturized bio-sensing.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If standard SPR biosensor configuration is used, then surface plasmon resonance measurement is achieved, but the device becomes expensive, bulky, and difficult to miniaturize

Engineering Contradiction:
Improvesurface plasmon resonance measurementVSAvoidoptical setup complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent replaces the complex mechanical optical system (prism, mirrors, beam splitters) with a simplified optical configuration using a diffraction grating and localized surface plasmon resonance on metal nanoparticles. This substitution maintains measurement precision while dramatically reducing device complexity and enabling miniaturization.

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

Solution Approach 2:

The patent changes the operational parameters from conventional SPR (measuring reflected light intensity at a specific angle) to localized SPR coupled with diffraction (measuring diffraction pattern shifts). This parameter change allows the use of simpler optical components while achieving equivalent or superior sensing performance.

Inventive Principle:
Principle #35Parameter changes

2Reliability

If conventional SPR optical setup is used, then bio-molecular interaction probing is achieved, but the system becomes expensive and inconvenient

Engineering Contradiction:
Improvebio-molecular interaction detectionVSAvoidsystem convenience
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The complex mechanical optical bench is replaced with a compact integrated device using diffraction grating and localized SPR, making the system more convenient for operation and potential on-site deployment while maintaining reliable bio-molecular interaction detection.

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

Solution Approach 2:

The simplified optical setup using diffraction grating and localized SPR can serve multiple functions including detection, miniaturization, and potential integration with portable platforms, making the system universally applicable for various bio-sensing scenarios.

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

3Measurement precision

If standard SPR configuration is used, then label-free bio-sensing is achieved, but miniaturization is difficult

Engineering Contradiction:
Improvelabel-free detection capabilityVSAvoiddevice size
Core Design Contradiction:
Measurement precisionVSLength of moving object

Solution Approach 1:

The replacement of bulky optical components with a compact diffraction grating-based localized SPR system enables label-free detection capability to be maintained while reducing device size for miniaturization and portability.

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

Solution Approach 2:

The patent transitions from measuring reflected light intensity in one dimension to analyzing diffraction pattern shifts in angular space, enabling compact device design while maintaining detection precision for label-free bio-sensing.

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

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 enables highly sensitive, cost-effective, and portable bio-sensing with potential for on-site and disposable devices, capable of real-time detection of bio-interactions without the need for bulky optics, and allows for multiplex detection through an array format.

Implementation Method 1

A bio-sensing apparatus and a system using localized plasmon resonance coupled with diffraction

Methodology Applied
Scientific EffectDiffraction: Diffraction

Implementation Method 2

localized plasmon resonance coupled with diffraction

Methodology Applied
Scientific EffectLocalized plasmon resonance: Surface Acoustic Wave

Data Source

PatentUS8068995B2Biosensing apparatus and system
Publication Date: 2011.11.29 NATIONAL CHUNG CHENG UNIV
  • US8068995B2 patent drawing
  • US8068995B2 patent drawing
  • US8068995B2 patent drawing

AI summary

A bio-sensing system comprises a light source, a bio-sensing apparatus, a detecting platform, and a processing unit. A bio-sensing apparatus further comprising a substrate, a sample with at least one analyte, at least one grating bound on the substrate for diffracting a light beam in a reflection mode and outputting at least one output light beam, a plurality of nanoparticles being bound on one side of the grating, a molecular recognition unit bound on said nanoparticle surface, and a cover plate covering the nanoparticle-modified side of the substrate. The detecting platform receives a signal while the at least one output light beam passing through the bio-sensing apparatus. The processing unit couples with the detecting platform for receiving and analyzing the signal. Wherein when the analyte passes through the microfludic channel to contact with said nanoparticles, the at least one output light beam changes in accordance with the refractive index of the sample or in accordance with the interaction of the analyte with said molecular recognition unit bound on said nanoparticle surface.