The Microfluidic Consortium, guided by Peter Hewkin for over 16 years, gathers international leading industrial players in microfluidics, from flow control and valve technologies to chip manufacturing. Its purpose is simple but impactful: create regular opportunities throughout the year, across different locations worldwide, for members to meet researchers, exchange ideas, explore market trends, and offer support to those venturing into microfluidics. This year marked our first participation, joining as a representative of flow control solutions. It was a great opportunity to connect with fellow members, share insights, and engage with a community that’s actively shaping the future of the field.
We had the chance to attend two fascinating presentations from local researchers. The first was by Johannes Bues from the Deplancke Lab at EPFL, who shared his work titled “High-throughput phenomics leveraging microfluidics for deterministic cell handling.” His talk focused on single-cell RNA sequencing (scRNA-seq), a powerful technique for studying gene expression at the level of individual cells within mixed populations. While scRNA-seq has become a standard in understanding tissue composition, it remains costly and inefficient, especially for small or precious samples like patient biopsies. Traditional methods often require thousands of cells for meaningful analysis, which leads to the need for bulk loading. This, in turn, generates confounding mosaic cell populations and obscures fine-grained insights.
To address these challenges, Johannes introduced DISCO, a Deterministic mRNA-capture bead and cell co-encapsulation system. Unlike conventional approaches that rely on passive cell capture, DISCO profit machine vision to actively detect and encapsulate individual cells and mRNA-capture beads into droplets. This not only enables continuous operation but also dramatically improves efficiency and scalability for processing low-input cell suspensions at high capture rates.
Building on this innovation, he presented the next phase of the work: IRIS (Integrated Robotic Imaging and Sorting). IRIS aims to push deterministic single-cell sequencing even further by replacing beads with precisely designed oligonucleotide barcodes, enabling the fusion of imaging and molecular profiling for each individual cell. Fully automated and high-throughput, the system envisions a future where identifying optimal cancer treatments could be as simple—and as fast—as visually inspecting a single cancer cell.
The second presentation was given by Christoph Merten, Associate Professor at EPFL and head of the Laboratory of Biomedical Microfluidics (LBMM). His talk focused on the challenges of antibody discovery, particularly the complexity of testing antibodies due to the variability in the cells that produce them. To address this, his team developed a microfluidic assay that encapsulates individual B-cells with their corresponding target cells in a single droplet, along with a fluorescent reporter. This reporter emits a signal when there is a functional interaction between the antibody and the target, enabling sorting and analysis of the droplets based on fluorescence. In a technique called fluorescence-activated droplet sequencing (FAD-seq), the droplets of interest are then picoinjected with a lysis and RT-PCR mixture to allow on-chip amplification of the antibody hits before transferring them off-chip. Even though a significant fraction of the material may be lost during this transfer, sufficient copy numbers of the target sequences can still be recovered for meaningful downstream analysis.
Christoph Merten also discussed the limitations of patient-derived organoids in drug testing and emphasized the potential of using single cells from patients, encapsulated alongside FDA-approved drugs, or combinations thereof, for more realistic and personalized drug screening. Yet, one fundamental question remains: how do we choose the right quantitative method to assess drug efficacy, especially when dealing with multiple drugs acting through different mechanisms?
To address this, he presented his team’s method published in Nature Communications: Combi-Seq—a scalable microfluidic workflow for screening hundreds of drug combinations in picoliter droplets, using transcriptomic changes as the readout. The approach employs a deterministic combinatorial DNA barcoding strategy to encode treatment conditions, allowing highly multiplexed gene expression-based analysis of drug effects.
He wrapped up his talk with an inspiring example of translational research, describing how a complex academic prototype was transformed into a refined, user-friendly instrument through the creation of Thera.me—a microfluidic platform that helps identify the most effective cancer therapies by testing them directly on live tumor samples from patients.
The application session by the Microfluidic Consortium members brought forward exciting innovations from several key industrial actors in microfluidics, each showcasing unique approaches and technologies that address current challenges in the field:
Two inspiring visits during our Lausanne trip around the Microfluidic Consortium showcased how researchers are using microfluidics to address both environmental and medical challenges.
The Microfluidic Consortium in Lausanne offered a clear reflection of the field’s momentum, highlighting the incredible range of applications microfluidics now touches, from single-cell sequencing and antibody discovery to mental health research and sustainable materials. The diversity of talks reminded us that microfluidics is more than a lab technique, it’s becoming an essential platform technology across healthcare, environmental science, and engineering.
Whether you’re prototyping a new method or industrializing an existing solution, choosing the right microfluidic tools can make all the difference. With customizable instruments and dedicated support that we provide at Elveflow, the transition from research to real-world application becomes faster, more accurate, and more impactful. With the right ecosystem in place, microfluidics is ready to move from concept to implementation at scale.
See you in the next Microfluidic Consortium event in Boston !
Written and reviewed by Louise Fournier, PhD in Chemistry and Biology Interface. For more content about Microfluidics, you can have a look here.
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