Lateral Flow IVTT Diagnostics for Multiplexed Point-of-Care Detection

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Conventional point-of-care diagnostic platforms are limited by their inability to multiplex effectively, requiring expensive equipment and complex procedures, making them unsuitable for low-cost, accessible healthcare solutions in resource-limited settings.

Innovation Solution

The MEDIFLOW platform integrates lateral flow assays with in vitro transcription and translation systems, utilizing synthetic biology detection mechanisms to produce unique single-stranded nucleic acid barcodes that generate distinct color changes upon target detection, enabling simultaneous, multiplexed detection without the need for expensive equipment or complex sample preparation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If conventional point-of-care diagnostic platforms are used, then simple biomarkers can be detected, but multiplexing capability is limited and expensive equipment is required

Engineering Contradiction:
Improvemultiplexing capabilityVSAvoidequipment complexity
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The detection system is segmented into multiple independent detection zones on the lateral flow strip, each zone containing specific capture probes for different targets. This allows simultaneous detection of multiple analytes without requiring complex multiplexed equipment, as each zone operates independently with its own signal transduction pathway

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

A universal in vitro transcription and translation system is implemented that can process multiple different nucleic acid templates simultaneously. This multi-functional system enables diverse target detection across multiple zones using a common biochemical platform, eliminating the need for target-specific equipment while maintaining multiplexing capability

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

2Measurement precision

If conventional point-of-care diagnostic platforms are used, then simple biomarkers can be detected, but complex procedures are required

Engineering Contradiction:
Improvedetection accuracyVSAvoidprocedure simplicity
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

Capture probes are pre-immobilized on the lateral flow strip in specific patterns, and the in vitro transcription and translation reagents are pre-formulated in a single master mix. This preliminary preparation eliminates complex step-by-step procedures during testing, as the system is designed to work with a single sample application followed by automated capillary flow

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The system utilizes capillary action for automatic sample and reagent flow through the lateral flow strip without requiring external pumps or complex fluid handling. The in vitro transcription and translation reactions proceed autonomously once initiated, with signal amplification occurring automatically through the biochemical reaction cascade, minimizing user intervention while maintaining detection precision

Inventive Principle:
Principle #25Self-service

3Adaptability or versatility

If synthetic biology detection mechanisms are used, then multiplexed detection capability is achieved, but low-resource reporters are needed

Engineering Contradiction:
Improvemultiplexed detection capabilityVSAvoidreporter availability
Core Design Contradiction:
Adaptability or versatilityVSEase of manufacture

Solution Approach 1:

The system changes the fundamental parameter of signal transduction by using in vitro transcription and translation to convert nucleic acid binding events into protein-based colorimetric signals. This parameter change enables the use of simple, stable, and inexpensive colorimetric reporters that can be manufactured without complex equipment, while maintaining multiplexed detection capability through spatially resolved signal patterns

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

MEDIFLOW enables scalable, cost-effective, and rapid multiplexed detection of multiple targets, enhancing healthcare diagnostics accessibility and efficacy globally by leveraging low-cost, stable, and rapid in vitro transcription and translation reactions.

Implementation Method 1

introducing an in vitro transcription and/or translation reagent to the in vitro transcription and/or translation area; and producing one or more reporters indicative of a presence of one or more targets

Methodology Applied
Scientific EffectIn vitro transcription:

Implementation Method 2

introducing an in vitro transcription and/or translation reagent to the in vitro transcription and/or translation area; and producing one or more reporters indicative of a presence of one or more targets

Methodology Applied
Scientific EffectIn vitro translation:

Implementation Method 3

each region comprising at least one distinct immobilized capture strand, each of the distinct immobilized capture strands configured to bind to a predetermined tail strand

Methodology Applied
Scientific EffectNucleic acid hybridization:

Data Source

PatentUS20250354200A1Multiplexed and sensitive point-of-care diagnostics via integrated lateral flow and in-vitro transcription and translation
Publication Date: 2025.11.20 GEORGIA TECH RES CORP
  • US20250354200A1 patent drawing
  • US20250354200A1 patent drawing
  • US20250354200A1 patent drawing

AI summary

Disclosed herein. is a method of detecting the presence of a target, the method comprising: providing an in vitro transcription and/or translation area comprising a plurality of regions, each region comprising at least one distinct immobilized capture strand, each of the distinct immobilized capture strands configured to bind to a predetermined tail strand; introducing one or more mobile tail strands to the in vitro transcription and/or translation area, the one or more tail strands generated due to the presence of a corresponding target; introducing an in vitro transcription and/or translation reagent to the in vitro transcription and/or translation area; and producing one or more reporters indicative of a presence of one or more targets.