
Dora Maria Racca
BE PhD student
- Autoimmunity in Type I diabetes
- Diet and the intestine
© 2026 DAN HUH. All rights reserved.
MORPH LAB

an interdisciplinary research group with the mission of transforming the technological foundation of how we model human health and disease in biomedical research.
bioengineering design principles and methodologies to advance the frontiers of complex in vitro models and new approach methodologies (NAMs).
to evolving laboratory models of healthy and diseased human tissues into automated data engines and computational intelligence for the advancement of life science and technology.

Every hour, the human body runs experiments no instrument can fully record. Lungs stretch and recoil some twenty thousand times a day. A fresh film of tears spreads across the eye with every blink. In the placenta, a mother's blood flows past her child's, separated by a barrier only a few cells thick. Each of these exchanges carries information about how we stay healthy and how we become ill, yet almost none of it can be observed directly in a living person. For a century, medicine has filled that gap with laboratory animals and learned a great deal from them. It has also learned, often too late, that a mouse is not a human.

Anatomists once drew the human body from dissection, and microscopists from thin slices of fixed tissue. Every one of those portraits showed a body that had stopped working. We make portraits of human biology that are alive. In our laboratory at Penn, living human cells grow inside miniature engineered devices, where channels, membranes, and mechanical forces coax them into tissues that behave like their counterparts in the body.
Our lung chips breathe. Our eye chips blink. Our placenta chips carry nutrients from mother to fetus. Our bone marrow chip makes blood and mounts an immune defense, and our tumor chips resist the CAR T cells sent to destroy them. One of our systems has flown aboard the International Space Station. More and more, we build these tissues the way nature does, borrowing the rules of embryonic development and letting cells organize themselves.

A model that looks like an organ is only a beginning. We treat each chip as an instrument, a biological computer that takes precisely controlled inputs and returns detailed, quantitative human data. Paired with multi-omics, robotics and machine learning, these small worlds can be built reproducibly and at scale. They can then supply the causal, human-relevant data that computational models of our physiology will need.
Our aim is a science of the human body that we can observe, measure, and eventually simulate, so that we can predict how a drug, a disease, or an exposure will affect a patient before anyone is put at risk.
For recent examples of our work, see representative publications under Publications.
How does an organ-on-a-chip go from an elegant prototype to a tool that industry and regulators can rely on? We share our view in a Nature Communications Q&A, "5 perspectives on translating microphysiological systems from concept to application" (August 2026).
Read the Nature Communications Q&AMORPH LAB

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MORPH LAB
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October 2026 · Cover feature

Our paper about modeling placental exposure to cadmium has been selected as a cover article in Nature Biomedical Engineering.
October 2026 · Award feature

Vivodyne has been named one of Biopharma’s Most Promising Startups in 2026 by Endpoints 11.
Read story ↗June 2026 · Cover feature

Our paper on modeling CAR-T therapy for solid tumors has been selected as a cover article in Nature Biotechnology.
Read story ↗ Commentary by Gordana Vunjak-Novakovic ↗ Penn Today press release ↗October 2025 · Startup feature

Our spinout raised $40 million in its most recent financing round.
Read story ↗