Microchip Optical Tweezers for Forensic Cell Separation

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Solution Overview

Problem

Forensic biologists face challenges in analyzing DNA mixtures from mixed biological samples, as existing methods are subjective, complex, and not easily transferable to forensic lab settings, leading to inefficiencies and potential biases in DNA identification.

Innovation Solution

A microfluidic-based approach using a microchip and optical tweezers for cell separation, allowing for the precise and accurate isolation of cells from mixed samples, enabling reliable transition to downstream processing and reducing the need for complex bioinformatics solutions.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If manual interpretation procedures are used to analyze DNA mixtures, then flexibility in handling different mixture types is maintained, but objectivity and reliability deteriorate due to subjectivity and potential bias

Engineering Contradiction:
Improveflexibility in handling different mixture typesVSAvoidobjectivity of mixture interpretation
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The patent replaces manual mechanical interpretation procedures with an optical trapping system that uses laser beams to physically manipulate and separate cells. This substitution eliminates human subjectivity while maintaining the ability to handle different mixture types through automated optical manipulation and sorting procedures.

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

Solution Approach 2:

The patent introduces optical tweezers as an intermediary system between the mixed cell sample and the analysis process. This intermediary automatically performs cell manipulation and separation, serving as an objective mediator that eliminates direct human interpretation while preserving adaptability through programmable optical control.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If complex bioinformatics software solutions are implemented to address DNA mixtures, then objectivity is improved, but device complexity and cost increase

Engineering Contradiction:
Improveobjectivity of mixture analysisVSAvoidcomplexity of bioinformatics solutions
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent extracts the cell separation step from the complex bioinformatics workflow and performs it physically at the cellular level using optical tweezers. By separating cells before DNA extraction and analysis, the system eliminates the need for complex computational deconvolution of mixed DNA profiles, simplifying the overall process while maintaining objectivity.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent performs cell separation as a preliminary action before DNA extraction and analysis. By physically separating individual cells from mixed samples prior to molecular analysis, the system prevents the formation of complex DNA mixtures that would require sophisticated bioinformatics software, thereby reducing device and computational complexity.

Inventive Principle:
Principle #10Preliminary action

3Manufacturing precision

If optical tweezers are used to trap and separate spermatozoa from mixed samples, then cell separation capability is improved, but ease of operation deteriorates due to complex droplet formation and capillary positioning steps

Engineering Contradiction:
Improvecell separation capabilityVSAvoidease of transfer to forensic lab setting
Core Design Contradiction:
Manufacturing precisionVSEase of operation

Solution Approach 1:

The patent designs the optical trapping system with universal features that can handle multiple cell types and sample configurations using the same basic platform. The system performs droplet formation, cell trapping, manipulation, and transfer using integrated microfluidic channels and standardized protocols, making it easily transferable to forensic laboratories without requiring multiple specialized devices.

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

4Ease of operation

If pipetting is used to transfer samples containing low quantities of cells, then sample transfer is simplified, but cell loss increases due to pipetting-associated losses

Engineering Contradiction:
Improvesimplicity of sample transferVSAvoidcell loss during transfer
Core Design Contradiction:
Ease of operationVSLoss of substance

Solution Approach 1:

The patent uses microfluidic hydraulic principles to transfer cells through integrated channels within the device. This hydraulic transport system eliminates the need for external pipetting operations, preventing cell loss associated with pipette tips and manual transfer while maintaining ease of operation through automated fluid flow control.

Inventive Principle:
Principle #29Pneumatics and hydraulics

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

This method enables more accurate DNA identification of perpetrators, reduces case backlogs, and simplifies the processing of evidentiary cell mixtures by providing a reliable, objective, and intuitive solution for cell separation, compatible with forensic lab procedures.

Implementation Method 1

microchip and optical tweezing (OT) for separation of different cells from a cell mixture

Methodology Applied
Scientific EffectOptical tweezers: Optical Tweezers

Data Source

PatentUS20230338955A1Microdevices and processes to separate and process mixed forensic biological samples
Publication Date: 2023.10.26 VIRGINIA COMMONWEALTH UNIV
  • US20230338955A1 patent drawing
  • US20230338955A1 patent drawing
  • US20230338955A1 patent drawing

AI summary

Microdevices and methods provide for separating cells of a single type from a mixed biological sample containing multiple types of cells. A single microdevice may be configured to allow for separating out cells into multiple groupings, each grouping containing cells of only one cell type. Transfer of separated cells off the microdevice is performed by physical separation of part of the microdevice from a remainder of the microdevice. This step advantageously minimizes accidental cell losses in the transfer. Subsequent analysis may then be performed using non-microfluidic equipment and techniques.