Micro-Bioelectrochemical Cell Layout for High-Throughput Microbial Imaging

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Solution Overview

Problem

Current devices and methods lack the ability to visualize microbial interactions with charged surfaces at the microscopic level and have low throughput capacity for studying genetic mutant strains or varying conditions, preventing the demonstration of statistical significance and high-resolution imaging of live microbes.

Innovation Solution

A micro-bioelectrochemical cell (μ-BEC) device with multiple chambers, each containing a working electrode, counter electrode, and reference electrode, compatible with confocal and super-resolution imaging, allowing for high-throughput electrochemical and bioimaging analyses of microbial interactions with charged surfaces.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If bulk reactor studies are used to study microbial interactions, then the overall electrochemical output can be monitored, but the ability to visualize processes at the microscopic level is lost

Engineering Contradiction:
Improvemicroscopic visualization capabilityVSAvoiddevice structure
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The device is divided into multiple individual chambers (e.g., 96 chambers) instead of using a single bulk reactor. Each chamber can be independently imaged and analyzed, enabling microscopic visualization while maintaining manageable device complexity through modular design

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The invention transitions from bulk-scale analysis to micro-scale analysis by creating miniaturized chambers that are optically accessible. This dimensional reduction enables confocal and super-resolution imaging while maintaining electrochemical measurement capabilities

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

2Measurement precision

If confocal and super-resolution imaging of live microbes is performed, then high-resolution visualization is achieved, but the throughput capacity for comparing multiple strains or conditions is reduced

Engineering Contradiction:
Improveimaging resolutionVSAvoidthroughput capacity
Core Design Contradiction:
Measurement precisionVSProductivity

Solution Approach 1:

Multiple chambers are arranged in parallel within a single device, allowing simultaneous imaging of multiple microbial strains or conditions. This segmentation enables high-throughput experimentation while maintaining the optical quality needed for confocal and super-resolution imaging

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The device design integrates multiple functions: electrochemical measurements, confocal imaging, and super-resolution imaging capabilities within the same chamber structure. This multi-functionality allows a single device to perform comprehensive analyses without requiring separate specialized equipment for each technique

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

3Reliability

If multiple genetic mutant strains or physical/chemical conditions are studied simultaneously, then statistical significance can be demonstrated, but the device complexity and data analysis burden increase

Engineering Contradiction:
Improvestatistical significanceVSAvoidexperimental setup
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

Each chamber is designed as an independent experimental unit that can contain a different genetic mutant strain or physical/chemical condition. This segmentation allows systematic variation of parameters across multiple chambers while maintaining identical imaging and measurement protocols, facilitating statistical analysis

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The device enables systematic variation of experimental parameters (genetic mutations, chemical conditions, physical conditions) across different chambers while maintaining consistent measurement and imaging protocols. This standardized approach to parameter variation facilitates robust statistical analysis

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

Enables high-throughput, high-resolution imaging and electrochemical analysis of microbial interactions with charged surfaces, facilitating the study of electron flow and extracellular electron transfer processes, and overcoming limitations of bulk reactor studies.

Implementation Method 1

Each chamber includes one well sealed between one portion of the working electrode layer and one portion of the electrical layer containing one counter electrode and one reference electrode. The one portion of the working electrode layer, the one counter electrode, and the one reference electrode are in electrical contact with the volume of the chamber.

Methodology Applied
Scientific EffectElectrochemical reactions:

Implementation Method 2

The first surface is bonded to the support contact surface and the second surface is bonded to the electrical contact layer in alignment to form the plurality of chambers.

Methodology Applied
Scientific EffectAdhesion bonding: Adhesive

Data Source

PatentUS20250360505A1Micro-bioelectrochemical cell devices and methods of detecting electron flows
Publication Date: 2025.11.27 WASHINGTON UNIV IN SAINT LOUIS
  • US20250360505A1 patent drawing
  • US20250360505A1 patent drawing
  • US20250360505A1 patent drawing

AI summary

A micro-bioelectrochemical cell (μ-BEC) device is disclosed that includes from 4 to 96 microfluidically connected chambers, in which each chamber encloses a volume of about 1 μL to 2 μL. A working electrode, reference electrode, and counting electrode contacts each volume. The μ-BEC device includes a support layer coated with a working electrode layer, a microfluidics layer containing a plurality of wells, and an electrical layer containing the reference and counter electrodes. Methods of using the μ-BEC device to perform bioelectrochemical measurements of cells are also disclosed.