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Organ-on-a-Chip: Driving the Future of Therapeutic Discovery and Precision Medicine
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Camilla Soragni

Camilla Soragni

Maastricht University

Dr. Camilla Soragni received her MSc in Chemistry from Ca’ Foscari University, Italy, in 2016, and an MRes in Chemical Biology from Imperial College London, UK, in 2018. She then pursued an industrial ITN–MSCA PhD in Biotechnology with Maastricht University and MIMETAS, where she developed scalable assays for on-a-chip models. After defending her thesis in 2023, she returned to academia, focusing on the use of pluripotent stem cells to generate 3D in vitro cardiac models for genetic studies.

Collection Overview

Organ-on-a-chip technologies enable researchers to recapitulate the complexity of human physiology in vitro, offering dynamic, microengineered environments that mimic in vivo structure and function. These systems are particularly powerful when generated from patient-derived cells, providing disease models that capture individual genetic backgrounds and overcoming the translational limitations of non-human animal models.


Versatile by design, organ-on-a-chip platforms can be applied across the drug development pipeline, from early-stage high-throughput screening to precision, patient-tailored therapeutic testing. In the drug discovery phase, the complexity and scalability of this technology allow for the tailored selection of hits based on multiple outcomes, such as efficacy and toxicity, at an early stage in development. This integrated approach improves candidate selection, steering it toward treatments with higher efficacy and safety profiles. In the clinical translation space, organ-on-a-chip devices enable personalised medicine strategies, predicting individual responses to therapy and identifying potential toxicities before administration, ultimately reducing adverse outcomes and improving patient care.


This JoVE collection will showcase state-of-the-art methodologies, protocols, and applications of organ-on-a-chip systems in therapeutic research and development. We aim to accelerate the adoption of organ-on-a-chip approaches, foster cross-disciplinary collaboration, and bridge the gap between basic research, translational studies, and clinical application, advancing the creation of safer, more effective treatments.

Articles

A Digital Microfluidic Electroporation Platform for Low-Input CRISPR Genome Editing and mRNA Transfection In Suspension T Cells and 3D Cell Models
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A Digital Microfluidic Electroporation Platform for Low-Input CRISPR Genome Editing and mRNA Transfection In Suspension T Cells and 3D Cell Models

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2026

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