New technique could make it easier to manufacture cell therapies

Publicly released:
International
Photo by National Cancer Institute on Unsplash
Photo by National Cancer Institute on Unsplash

Cell therapies - medicines made from human cells - are an important part of treating conditions including cancer, autoimmune diseases and infectious diseases, but current ways of manufacturing these medicines are generally slow or expensive. International researchers have developed a prototype for a new technique which they say can process cells at a faster rate at a low cost. The researchers tested their prototype, and say their experiments showed processing the cells at the forces required to operate at the higher speed did not impact the health of the cells compared to cells processed using conventional methods.

Media release

From: The Royal Society

  • Cell therapy manufacturing – A new approach for separating cells holds promise for cheaper and more efficient manufacture of cell therapies to treat disease. A prototype 'inertial focusing microfluidic device', which filters cells through a spiral of microchannels, effectively separated target cells quickly without damage. This could reduce the time, cost and complexity of clinical cell therapy manufacturing over conventional methods like centrifuging. Interface

 

Human leukocytes processed by fast-rate inertial microfluidics retain conventional functional characteristics

Journal of the Royal Society Interface

Cell therapies are medicines made from human cells. Often, scientists use a process called centrifugation in manufacturing of cell therapies, but this can be slow and other alternatives are expensive. We made a new prototype ‘inertial focusing microfluidic device’ that has the potential to be integrated into cell therapy manufacturing procedures. Our device processes cells at a very fast rate and at low cost. It was previously unknown if cells tolerate the large forces experienced in similar devices, but our experiments showed that the cells appeared to be as healthy as centrifuged cells.

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conference:
Royal Society Interface
Research:Paper
Organisation/s: Heriot-Watt University, UK
Funder: This work was supported by Medical Research Scotland (grant no. 50167-2019) and internal research funding from NHS National Services Scotland.
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