Lab-grown bone could change the way we test new medical treatments

Credit: Unsplash/CC0 Public Domain

A new technology that could be used to test new treatments for human organs and bone tissue—all whilst reducing the need for animal research—has been developed by engineers at the University of Sheffield.

The study, led by researchers from the University's Department of Materials Science and Engineering and the Insigneo Institute for in silico Medicine, along with collaborators from Universitat Ramon Llull, Spain, developed a -on-a-chip device containing mini scaffolding that can be used to grow human bone tissue in the laboratory.

In a new paper published in Frontiers in Bioengineering and Biotechnology, the researchers demonstrate how the bone-on-a-chip—a tiny chip containing living cells—can be used to grow bone tissue which can then be used to new potential treatments for diseased or damaged bones.

Testing new medicines usually requires extensive in vivo testing involving animal models. However, the new approach developed by the University of Sheffield-led team has been developed in vitro—entirely in the laboratory—and reduces the need to use in research.

The field of organ-on-a-chip aims to create small devices that contain miniature versions of organs such as bone, liver or lungs in the laboratory. By testing new medicines on small versions of rather than in animal models, the hope is that there will be a higher success rate of finding ones that work in humans.

The aim is that one day, the device developed by the Sheffield team could be connected to other organ-on-a-chip devices—such as the liver, heart, lungs, etc—to create a human-on-a-chip that would remove the need for animal research in the development of new medical treatments entirely.

In vitro testing of new treatments is normally done on cells grown on flat, two-dimensional surfaces. However, the team of researchers has created three-dimensional scaffold structures within their bone-on-a-chip that better resembles real bone.

The three-dimensional structures are developed using a material known as a polymerised high internal phase emulsion (polyHIPE) using a technique called emulsion templating. An emulsion is a mixture of oil and water which doesn't separate—like mayonnaise or milk. A polyHIPE is made using an oil that solidifies under ultraviolet light to create a plastic material which contains millions of tiny interconnected holes where the water used to be. These highly porous materials form a scaffold that helps cells create new bone tissue in 3-D.

Having produced the three dimensional scaffolds, the team inserted them into a mini bioreactor to create the bone-on-a-chip device and used in vitro techniques to assess its potential to reproducibly grow human from stem cells.

In the new paper, the researchers present findings demonstrating that organ-on-a-chip technologies have the potential to revolutionize pharmaceutical pre-clinical testing by increasing throughput whilst minimizing financial and ethical concerns associated with .

Dr. Frederik Claeyssens, Reader in Biomaterials from the University of Sheffield's Department of Materials Science and Engineering, said: "The introduction of microfluidic channels in a porous material allows us to mimic the natural 3-D environment of cells better than in standard microfluidics. This is, in my view, a great enabling technology to build complex 3-D tissues—or organs-on-a-chip—as testing platforms for pharmaceutical testing. These platforms have the potential to reduce the time and effort required for, and also reduce the use of animal models for preclinical drug testing."

Explore further

New miniature system to study kidney and intestine function

More information: Hossein Bahmaee et al. Design and Evaluation of an Osteogenesis-on-a-Chip Microfluidic Device Incorporating 3D Cell Culture, Frontiers in Bioengineering and Biotechnology (2020). DOI: 10.3389/fbioe.2020.557111
Citation: Lab-grown bone could change the way we test new medical treatments (2020, September 14) retrieved 23 January 2022 from
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Feedback to editors