Microfluidic eDNA Capture with Optical Flow Cell Routing

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Solution Overview

Problem

Current methods for collecting environmental DNA (eDNA) samples are labor-intensive and require manual collection, transportation, and preservation, which hinders efficient analysis and real-time monitoring of biodiversity and environmental changes.

Innovation Solution

A microfluidic system with an environmental sample inlet, preservative reagent inlet, and filter membranes, integrated with optical flow cells for real-time optical measurements and a bypass channel to selectively capture and concentrate eDNA samples, enabling intelligent fluid routing and filtration based on optical and pressure data.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If manual collection and transportation of eDNA samples is used, then sample preservation can be achieved, but the process becomes labor-intensive and time-consuming

Engineering Contradiction:
Improvesample preservationVSAvoidcollection and transportation time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The patent combines sample collection, preservation, and concentration functions into a single integrated microfluidic device. The collection chamber directly connects to preservation reagent reservoirs and filter membranes within the same device, eliminating the need for separate manual steps of collection, transportation, and preservation while maintaining sample integrity through in-device preservation chemistry.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The microfluidic device performs self-preservation by automatically mixing collected samples with preservation reagents within the device chambers. The system uses passive diffusion and capillary action to ensure thorough mixing of samples with preservation chemistry, eliminating the need for external manual intervention or specialized transportation conditions.

Inventive Principle:
Principle #25Self-service

2Reliability

If manual collection using sterile equipment is used, then sample contamination is prevented, but the process requires site visits and manual handling

Engineering Contradiction:
Improvesample contamination preventionVSAvoidmanual handling requirement
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The device features self-contained sterile barriers where sample collection occurs through integrated membranes and chambers that maintain sterile conditions without requiring external sterile equipment. The preservation reagents are pre-loaded into sealed reservoirs within the device, and sample-to-reagent mixing occurs automatically through passive diffusion, eliminating all manual handling steps while maintaining contamination prevention.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The device uses intermediate sterile membranes and sealed chambers as mediators between the external environment and the sample processing interior. These intermediate barriers allow sample intake while maintaining sterile separation, and the preservation chemistry acts as an intermediary that stabilizes samples without requiring manual intervention.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Reliability

If stable transportation of samples to the lab is required, then sample integrity is maintained, but the process cannot provide real-time monitoring

Engineering Contradiction:
Improvesample integrityVSAvoidtime to analysis
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The device performs self-concentration of eDNA through integrated filter membranes that trap genetic material while allowing water to pass through. This concentration process occurs automatically within the device using passive diffusion and filtration principles, maintaining sample integrity without requiring transportation to a laboratory, and preparing samples ready for immediate analysis upon device retrieval.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The device extracts and concentrates eDNA from large volumes of environmental water through integrated filter membranes. The filtration process separates and concentrates genetic material onto the membrane surface, extracting the essential analytical component from the bulk water sample while maintaining integrity, and this extraction occurs in-situ without requiring sample transportation.

Inventive Principle:
Principle #2Taking out (Extraction)

4Measurement precision

If automated DNA sequencing is used, then identification accuracy is improved, but sample collection remains labor-intensive

Engineering Contradiction:
Improveidentification accuracyVSAvoidsample collection efficiency
Core Design Contradiction:
Measurement precisionVSProductivity

Solution Approach 1:

The patent merges the sample collection, preservation, and concentration functions into a single automated microfluidic device that can be deployed in the field. This integrated approach automates the entire pre-analytical workflow, allowing high-accuracy DNA sequencing to be performed on samples that have been automatically collected and prepared, thereby eliminating the labor-intensive collection step while maintaining identification accuracy.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The device replaces manual mechanical collection processes with automated microfluidic flow systems. Passive diffusion, capillary action, and integrated pumping mechanisms automate sample uptake and processing, substituting manual labor with automated fluid handling while preserving sample quality for accurate sequencing analysis.

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

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 enables efficient, automated, and real-time collection and concentration of eDNA samples, reducing labor and improving the accuracy of biodiversity assessments and early detection of harmful algal blooms and other environmental changes.

Implementation Method 1

at least one optical flow cell that enables at least one of light microscopy, fluorescence spectroscopy, light attenuation measurements, and scattered light intensity measurements

Methodology Applied
Scientific EffectLight microscopy: Light

Implementation Method 2

at least one optical flow cell that enables at least one of light microscopy, fluorescence spectroscopy, light attenuation measurements, and scattered light intensity measurements

Methodology Applied
Scientific EffectFluorescence spectroscopy: Fluorescence

Implementation Method 3

at least one optical flow cell that enables at least one of light microscopy, fluorescence spectroscopy, light attenuation measurements, and scattered light intensity measurements

Methodology Applied
Scientific EffectLight attenuation: Absorption (EM radiation)

Implementation Method 4

at least one optical flow cell that enables at least one of light microscopy, fluorescence spectroscopy, light attenuation measurements, and scattered light intensity measurements

Methodology Applied
Scientific EffectScattered light: Scattering

Implementation Method 5

one or more filter membranes for particle concentration

Methodology Applied
Scientific EffectFiltration: Filter (physical)

Data Source

PatentUS11964278B2Microfluidic chip, systems, and methods for capturing of environmental DNA
Publication Date: 2024.04.23 DARTMOUTH OCEAN TECHNOLOGIES INC
  • US11964278B2 patent drawing
  • US11964278B2 patent drawing
  • US11964278B2 patent drawing

AI summary

A microfluidic lab-on-a-chip (LOC) device, microfluidic systems, and associated methodology are described that allow for intelligently collecting environmental DNA (eDNA) and their associated metadata. Optical spectroscopy is integrated with filtration membranes on the microfluidic device. The microfluidic LOC device and systems can be used for selectively capturing targeted species based on optical characteristics and for recording relevant metadata on eDNA acquired by the filtration membranes.