DNA Tagged Microparticles for Safe Biosensor Calibration

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Solution Overview

Problem

Current biosimulants for testing biosensor networks are unsafe for public exposure, difficult to aerosolize, and lack controllable properties, making them unsuitable for real-world evaluation and calibration of biofluorescence detectors.

Innovation Solution

Development of microsphere simulants comprising a non-toxic carrier and DNA barcode, allowing for safe and controlled aerosolization, with tunable properties such as charge and size, enabling simultaneous multiple releases and unique identification.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If biosimulants are used for testing biosensor networks, then testing capability is provided, but safety for public exposure deteriorates

Engineering Contradiction:
Improvetesting capabilityVSAvoidsafety for public exposure
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent creates DNA-tagged microparticle simulants that copy the essential detection properties of biological agents without using actual pathogens. These simulants contain DNA barcodes that can be detected by biosensors, providing a safe alternative that maintains testing capability while eliminating public exposure risks associated with real biological agents

Inventive Principle:
Principle #26Copying

Solution Approach 2:

The microparticle simulants are designed as inexpensive, non-biological, biodegradable carriers that can be safely released and disposed of after use. They provide temporary testing capability without the long-term safety concerns of persistent biological agents, allowing public exposure without harm

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

2Ease of manufacture

If traditional simulants are used, then testing is possible, but ease of aerosolization deteriorates

Engineering Contradiction:
Improvetesting possibilityVSAvoidease of aerosolization
Core Design Contradiction:
Ease of manufactureVSEase of operation

Solution Approach 1:

The patent modifies the physical and chemical parameters of the simulants by using non-biological, biodegradable carrier materials with controlled size, shape, and surface properties. These parameter changes enable easy aerosolization while maintaining manufacturing feasibility, resolving the contradiction between ease of manufacture and ease of aerosolization

Inventive Principle:
Principle #35Parameter changes

3Productivity

If multiple releases are conducted simultaneously, then testing efficiency improves, but difficulty of identification deteriorates

Engineering Contradiction:
Improvetesting efficiencyVSAvoiddifficulty of identification
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent segments the identification system by assigning unique DNA barcodes to different microparticle simulants released from various locations. This segmentation allows simultaneous releases to be distinguished and tracked individually, improving testing efficiency while maintaining simple identification through unique genetic markers

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The DNA barcode acts as an intermediary that simplifies the identification process. Instead of directly tracking complex physical characteristics of multiple simultaneous releases, the system uses DNA barcodes as intermediate identifiers that can be easily detected and differentiated, resolving the contradiction between testing efficiency and identification difficulty

Inventive Principle:
Principle #24Intermediary (Mediator)

Data Source

PatentUS9290810B2DNA tagged microparticles
Publication Date: 2016.03.22 LAWRENCE LIVERMORE NAT SECURITY LLC
  • US9290810B2 patent drawing
  • US9290810B2 patent drawing
  • US9290810B2 patent drawing

AI summary

In one embodiment, a product includes a plurality of particles, each particle including: a carrier that includes a non-toxic material; and at least one DNA barcode coupled to the carrier, where the particles each have a diameter in a range from about 1 nanometer to about 100 microns.