Microfluidic Stereolithography for Multi-Material Bioprinting

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Solution Overview

Problem

Current 3D bioprinting techniques face challenges in fabricating cell-laden constructs with clinically relevant dimensions and high precision, particularly in managing material delivery for multicomponent constructs, which limits their clinical applicability.

Innovation Solution

A stereolithographic printing system integrated with a microfluidic device that allows for rapid and precise fabrication of biological constructs using a digital micromirror device (DMD) and a microfluidic chip with elastic membrane, enabling sequential injection and washing of multiple inks, including biologically active components, to form complex 3D structures.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If traditional 3D bioprinting techniques are used to fabricate cell-laden constructs, then biological materials can be incorporated into inks, but the fabrication speed and precision are insufficient for clinically relevant dimensions

Engineering Contradiction:
Improvefabrication speedVSAvoidprinting precision
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The printing process is divided into separate functional modules: a microfluidic device handles material delivery and mixing with high precision, while the stereolithographic printing device handles rapid photopolymerization. This segmentation allows each module to be optimized independently, achieving both high speed and high precision simultaneously.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

A microfluidic device is introduced as an intermediary component between the ink reservoirs and the printing zone. This intermediary enables precise control of multiple bioinks, their mixing ratios, and delivery timing, thereby achieving high manufacturing precision while maintaining rapid fabrication through automated fluid handling.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Adaptability or versatility

If multiple inks are used to fabricate multicomponent complex constructs, then material diversity is improved, but material delivery management becomes difficult

Engineering Contradiction:
Improvematerial diversityVSAvoidmaterial delivery management
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The microfluidic device performs multiple functions within a single integrated platform: it stores multiple inks in separate reservoirs, controls their individual delivery through dedicated channels, mixes them in precise ratios, and transports them to the printing zone. This multi-functionality reduces overall system complexity while enabling diverse material usage.

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

Solution Approach 2:

The system uses pneumatic pressure control through valves to regulate the flow of multiple inks through the microfluidic device. By controlling pressure differentials, the system can selectively deliver different inks, mix them in controlled proportions, and maintain precise material delivery management despite the complexity of using multiple materials.

Inventive Principle:
Principle #29Pneumatics and hydraulics

3Reliability

If sequential injection and washing of multiple inks is implemented, then decontamination efficiency is improved, but process time increases

Engineering Contradiction:
Improvedecontamination efficiencyVSAvoidprocess time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The microfluidic device maintains continuous flow of inks and washing buffers through its channels during the printing process. Rather than stopping to wash between ink injections, the system continuously circulates fluids, enabling decontamination to occur concurrently with material delivery and mixing operations, thereby eliminating idle time.

Inventive Principle:
Principle #20Continuity of useful action

Solution Approach 2:

The system pre-fills multiple ink reservoirs and prepares washing buffers in advance within the microfluidic device. By having all materials ready and positioned before the printing sequence begins, the system can execute rapid sequential injection and washing without interruption, maintaining both high decontamination efficiency and short process time.

Inventive Principle:
Principle #10Preliminary action

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 the rapid and precise fabrication of multi-material 3D constructs with high fidelity, overcoming the limitations of traditional bioprinting techniques by allowing for efficient switching between inks and decontamination, facilitating the creation of complex biological structures for clinical applications.

Implementation Method 1

a microfluidic chip with elastic membrane, enabling sequential injection and washing of multiple inks

Methodology Applied
Scientific EffectElasticity: Elasticity

Implementation Method 2

photocrosslinking the first ink in the printing region onto the deposition layer to form a first printed layer

Methodology Applied
Scientific EffectPhotocrosslinking: Photopolymerisation

Data Source

PatentUS12007687B2Microfluidics-enabled multimaterial stereolithographic printing
Publication Date: 2024.06.11 THE BRIGHAM & WOMEN S HOSPITAL INC
  • US12007687B2 patent drawing
  • US12007687B2 patent drawing
  • US12007687B2 patent drawing

AI summary

Described are systems and methods for multi-material printing. The systems and methods can utilize a stereolithographic printing device, a moving stage, and a microfluidic device. The microfluidic device can include a plurality of reservoirs, each reservoir housing a different ink for printing, and a microfluidic chip. The microfluidic chip can include a chamber that comprises a plurality of inlets, a printing region, and one or more outlets as well as an elastic membrane.