Deep UV Pathogen Detection Using Fluorescence Spectral Signatures

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Solution Overview

Problem

Current pathogen testing methods are complex, expensive, and slow, often requiring hours to weeks for results, which can lead to widespread contamination in water, food, and healthcare settings due to delayed detection and reporting.

Innovation Solution

A portable system using deep ultraviolet (UV) light to excite biological substances, allowing for real-time detection and differentiation of pathogens through semiconductor photodetectors that analyze deep UV emission data for unique spectral signatures, enabling quick and affordable pathogen identification and quantification.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If traditional pathogen testing methods (filtering, culturing, incubation, staining) are used, then measurement precision is improved, but loss of time worsens significantly (24 hours to two weeks for results)

Engineering Contradiction:
Improvepathogen detection accuracyVSAvoidtesting duration
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent replaces mechanical/biological testing processes (filtering, culturing, incubation, staining) with optical detection using deep UV excitation and fluorescence emission measurement. This substitution enables real-time pathogen detection without requiring time-consuming biological culturing processes, resolving the contradiction between measurement precision and testing duration.

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

Solution Approach 2:

The patent changes the detection parameter from biological growth-based detection to optical fluorescence-based detection. By measuring fluorescence emission spectra of pathogens under deep UV excitation, the system achieves rapid detection (seconds to minutes) while maintaining precision through spectral analysis, thus resolving the time-precision contradiction.

Inventive Principle:
Principle #35Parameter changes

2Measurement precision

If complex laboratory testing processes are used, then measurement precision is improved, but device complexity worsens (requiring well-equipped laboratories and scientists)

Engineering Contradiction:
Improvepathogen detection accuracyVSAvoidtesting system complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent creates a universal detection platform that can identify and quantify multiple different pathogen types through their unique fluorescence spectral signatures. The system performs filtering, identification, and quantification functions in a single integrated device, eliminating the need for complex laboratory equipment and multiple specialized testing procedures.

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

Solution Approach 2:

The patent extracts the essential detection function from complex laboratory processes, isolating the key measurement (fluorescence emission) from the time-consuming preparatory steps (filtering, culturing, staining). This extraction enables pathogen detection to be performed with a simplified device that focuses only on the critical measurement aspect.

Inventive Principle:
Principle #2Taking out (Extraction)

3Measurement precision

If traditional testing methods are used, then measurement precision is improved, but ease of operation worsens (requiring scientists to perform multiple manual steps)

Engineering Contradiction:
Improvepathogen detection accuracyVSAvoidtesting procedure simplicity
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The patent enables the detection system to automatically perform identification and quantification of pathogens based on their intrinsic fluorescence spectral characteristics. The system self-calibrates and provides results without requiring scientists to perform manual filtering, culturing, or staining operations, thus dramatically improving ease of operation while maintaining precision.

Inventive Principle:
Principle #25Self-service

4Device complexity

If delayed testing results are accepted, then device complexity is reduced, but object-generated harmful factors worsen (widespread contamination, product recalls, infections)

Engineering Contradiction:
Improvetesting system simplicityVSAvoidcontamination spread
Core Design Contradiction:
Device complexityVSObject-generated harmful factors

Solution Approach 1:

The patent enables preliminary detection of pathogen contamination before it spreads widely through water supplies, food production lines, or healthcare facilities. By providing real-time detection capability, the system allows for immediate intervention to prevent contamination spread, product recalls, and infections, thus reducing harmful factors despite increased device complexity.

Inventive Principle:
Principle #10Preliminary action

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 rapid, cost-effective detection and quantification of pathogens in seconds, preventing contamination by providing real-time biological safety monitoring for water, food, and healthcare industries, complementing existing testing methods.

Implementation Method 1

pathogen in a medium auto-fluorescence when excited with ultraviolet light (e.g., deep ultraviolet light (deep UV))

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Implementation Method 2

detecting emission from the excited biological substance via a plurality of semiconductor photodetectors

Methodology Applied
Scientific EffectPhotoelectric Effect: Photoelectric Effect

Data Source

PatentUS12061150B2Detection of biological substances
Publication Date: 2024.08.13 ORB XYZ INC
  • US12061150B2 patent drawing
  • US12061150B2 patent drawing
  • US12061150B2 patent drawing

AI summary

The invention generally relates to detecting biological substances. In certain aspects, the invention is directed to a method directing one or more wavelengths of light within a deep ultraviolet (UV) spectrum into a medium to excite a biological substance in the medium, detect emission from the excited biological substance via a plurality of semiconductor photodetectors, and analyze the deep UV emission data for presence of a deep UV spectral signature indicative of the biological substance, wherein presence of the deep UV spectral signature indicates that the medium comprises a biological substance. The invention is also directed to identifying a pathogen in a medium comprising a pathogen and a non-pathogen biological substance.