Multi-branched Waveguide for Real-time PCR Detection

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Solution Overview

Problem

Current optical detection systems for polymerase chain reactions (PCR) face challenges in efficiently detecting stationary samples with reduced sample read time and simultaneous reading of multiple light wavelengths, often requiring complex alignments and direct fiber optic connections.

Innovation Solution

A modular PCR device with integrated light emitting diodes, photodiodes, and a multi-branched waveguide system that allows for real-time detection of nucleic acid amplification, eliminating the need for precise alignments and direct fiber optic connections, and enabling simultaneous reading of multiple wavelengths.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Use of energy by moving object

If direct fiber optic connections are used between light source and sample holder, then light transmission efficiency is improved, but device complexity and alignment requirements increase

Engineering Contradiction:
Improvelight transmission efficiencyVSAvoidalignment requirements
Core Design Contradiction:
Use of energy by moving objectVSDevice complexity

Solution Approach 1:

The patent introduces a multi-branched waveguide as an intermediary component between the light source and sample holder. This waveguide system transmits light without requiring direct fiber optic connections, thereby maintaining light transmission efficiency while eliminating complex alignment requirements. The waveguide acts as a mediator that couples the light source to the sample through a flexible, alignment-tolerant pathway.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Device complexity

If sequential reading of samples is used, then device simplicity is maintained, but sample throughput and read time are reduced

Engineering Contradiction:
Improvedevice simplicityVSAvoidsample throughput
Core Design Contradiction:
Device complexityVSProductivity

Solution Approach 1:

The patent segments the optical detection system into multiple independent detection channels, each capable of simultaneously reading different samples or wavelengths. This segmentation allows parallel processing of multiple samples rather than sequential reading, significantly increasing sample throughput while keeping each individual detection channel relatively simple.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent transitions from sequential reading (one-dimensional time-based approach) to simultaneous multi-wavelength reading (multi-dimensional approach). By adding the wavelength dimension to the detection process, the system can read multiple samples or features at the same time, thereby increasing productivity without proportionally increasing device complexity.

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

3Speed

If multiple light wavelengths are read simultaneously, then detection speed is improved, but hardware requirements and space occupation increase

Engineering Contradiction:
Improvedetection speedVSAvoidhardware space
Core Design Contradiction:
SpeedVSArea of stationary object

Solution Approach 1:

The patent merges multiple light sources and detection channels into a single integrated optical detection system. By combining multiple wavelengths and detection functions into one unified system with shared optical pathways and compact components, the patent achieves simultaneous multi-wavelength reading while minimizing the overall hardware footprint and space requirements.

Inventive Principle:
Principle #5Merging (Combining)

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 system achieves high-speed PCR amplification and detection with reduced sample read time, improved reliability, and increased sample throughput, while minimizing hardware requirements and maintaining minimal space occupation.

Implementation Method 1

at least one light emitting diode device (device being an integrated assembly of light emitting diodes or a compact group of light emitting diodes) that is carried on at least one support substrate, is in electrical communication with a power source, and is adapted to emit light at a plurality of different wavelengths

Methodology Applied
Scientific EffectLight emitting diode: Light Emitting Diode

Implementation Method 2

at least one photodiode detector device (the device being an integrated assembly of photodiodes (e.g. photodiode array), an individual photodiode or compact group of photodiodes) may also be included such that the detector is adapted to issue signals based upon intensity of light it receives

Methodology Applied
Scientific EffectPhotoelectric effect: Photoelectric Effect

Implementation Method 3

a light transmission assembly that includes at least one multi-branched waveguide and at least one manifold (e.g., a fiber optics block) that is configured to support the waveguide between the sample holder and both the at least one light emitting diode device and the at least one photodiode detector device

Methodology Applied
Scientific EffectTotal internal reflection: Total Internal Reflection

Implementation Method 4

receives a biological sample having a nucleic acid to be amplified and at least one fluorescing agent that interacts with the nucleic acid during amplification and that emits light upon excitation by light of a known wavelength

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentUS9932632B2Real-time optical system for polymerase chain reaction
Publication Date: 2018.04.03 STRECK LLC
  • US9932632B2 patent drawing
  • US9932632B2 patent drawing
  • US9932632B2 patent drawing

AI summary

An improved device and system for facilitating polymerase chain reaction including a light source, detector, waveguide, and filters that occupy minimal space and facilitate reduced sample read time and rapid reading of multiple light wavelengths.