Integrated Bioassay Sensor With Grating-Coupled Waveguides

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing bioassays require large, expensive laboratory equipment and trained personnel, and are typically performed in bulk, necessitating significant sample quantities, which limits accessibility and increases costs.

Innovation Solution

An integrated device with a pixelated sensor array and optical waveguides for parallel analysis of biological samples, utilizing luminescent markers to identify individual molecules or particles, enabling compact, high-speed, and cost-effective detection and quantitation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If conventional bioassays are performed using large laboratory equipment, then detection and analysis capability is achieved, but device size and cost increase significantly

Engineering Contradiction:
Improvedetection capabilityVSAvoidequipment size
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent combines multiple bioassay functions (sample processing, optical excitation, luminescence detection, and signal processing) into a single integrated device. The device integrates a light source, optical path, sample chamber, photodetector, and processing unit into one compact system, eliminating the need for separate laboratory equipment while maintaining detection precision.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The patent employs a nested structure where the sample chamber is positioned within the optical path, which is itself integrated within the housing. The photodetector is arranged to receive light through the sample chamber, creating a compact nested arrangement that reduces overall device size while preserving functional capabilities.

Inventive Principle:
Principle #7Nested doll (Nesting)

2Measurement precision

If conventional bioassays are performed in bulk, then detection is achieved, but sample quantity requirement increases

Engineering Contradiction:
Improvedetection capabilityVSAvoidsample quantity
Core Design Contradiction:
Measurement precisionVSQuantity of substance

Solution Approach 1:

The patent divides the sample analysis into individual processing units within the device. The sample chamber is designed to process samples in discrete amounts, and the device can perform multiple measurements sequentially or in parallel with different sample volumes, reducing the total sample quantity needed compared to bulk processing methods.

Inventive Principle:
Principle #1Segmentation

3Measurement precision

If luminescent markers are used to tag samples, then molecular identification is enabled, but detection system complexity increases

Engineering Contradiction:
Improvemolecular identification capabilityVSAvoiddetection optics complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent extracts and eliminates unnecessary optical components from the detection system. By using luminescent markers that emit light at specific wavelengths, the device can use simpler optical filters and detectors rather than complex spectroscopic systems, reducing overall detection system complexity while maintaining molecular identification capability.

Inventive Principle:
Principle #2Taking out (Extraction)

4Measurement precision

If expensive laser light sources are used to illuminate samples, then luminescence excitation is achieved, but device cost increases

Engineering Contradiction:
Improveluminescence excitation capabilityVSAvoiddevice cost
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent replaces expensive, long-lived laser light sources with more economical light sources such as LEDs or fluorescent lamps that have shorter operational lifetimes but sufficient durability for the device's intended use. This substitution significantly reduces device cost while maintaining the capability to excite luminescent markers effectively.

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

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

Facilitates low-cost, portable bioassays that can perform quantitative analysis of single molecules or particles, reducing the need for specialized laboratories and enabling widespread access to diagnostic tests.

Implementation Method 1

an integrated photodiode, the device comprising a plurality of chambers and a plurality of optical waveguides configured to couple excitation energy to the chambers

Methodology Applied
Scientific EffectOptical waveguide coupling: Waveguide (optics)

Implementation Method 2

Some bioassays are performed by tagging samples with luminescent markers that emit light of a particular wavelength. The markers are illuminated with a light source to cause luminescence

Methodology Applied
Scientific EffectLuminescence: Luminescence

Implementation Method 3

the luminescent light is detected with a photodetector to quantify the amount of luminescent light emitted by the markers

Methodology Applied
Scientific EffectPhotodetection: Photoelectric Effect

Implementation Method 4

a grating coupler configured to couple the excitation energy to the waveguides on the bio-optoelectronic chip

Methodology Applied
Scientific EffectGrating coupling: Diffraction Grating

Data Source

PatentEP4141416B1Integrated device and method of forming the same
Publication Date: 2025.10.08 QUANTUM SI INC
  • EP4141416B1 patent drawingFigure 1-1
  • EP4141416B1 patent drawingFigure 1-2A
  • EP4141416B1 patent drawingFigure 1-2B~1-2C

AI summary

An integrated device (1-102) comprising: a plurality of sample wells (1-108); a first optical waveguide (1-312) configured to couple excitation energy to a first portion of the plurality of sample wells; a second optical waveguide (1-312) configured to couple the excitation energy to a second portion of the plurality of sample wells; and a grating coupler (1-216) configured to receive the excitation energy from an optical source positioned outside the integrated device, and to couple the excitation energy to the first optical waveguide and to the second optical waveguide.