Summary
Currently, 90% of the drugs fail to pass clinical trials1. One of the key reasons is that the animal models used in the preclinical phase poorly predict the human response to the drugs. Organ-on-a-Chip (OoC) is a game changing technology as one of the alternative methodolgies to animal models. The heart of an OoC system is an ‘Organ-chip’: cm-sized devices with micro-channels and -chambers in which human cells can be grown to closely mimic human tissues. More and more evidence shows that OoCs are more representative models than animals. However, the industry adoption of OoCs is still very limited. OoC users and developers simply have to choose between either OoCs with physiologically relevant flow but not fit for standard operating procedures in the pharmaceutical industry, or OoCs that are compatible but less physiological because of the absence or inadequacy of the flow.
The TOMAC project offer s novel a solution called “Magnetic Artificial Cilia (MAC) pump”: a chip-sized modular and tubeless flow system that on one hand, eliminates manual handling and enables automation, and on the other hand provides physiological flow for a range of organ models. The technology behind MAC is based on micrometer-sized magnetic hair-like structures called Magnetic Artificial Cilia (MAC), which are inspired by cilia occurring in nature. The MAC are flexible micro-actuators that respond to a varying magnetic field (created by the actuation system) by rotating or oscillating, and thus create a controlled fluid flow.
The TOMAC project offer s novel a solution called “Magnetic Artificial Cilia (MAC) pump”: a chip-sized modular and tubeless flow system that on one hand, eliminates manual handling and enables automation, and on the other hand provides physiological flow for a range of organ models. The technology behind MAC is based on micrometer-sized magnetic hair-like structures called Magnetic Artificial Cilia (MAC), which are inspired by cilia occurring in nature. The MAC are flexible micro-actuators that respond to a varying magnetic field (created by the actuation system) by rotating or oscillating, and thus create a controlled fluid flow.
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More information & hyperlinks
Web resources: | https://cordis.europa.eu/project/id/101155770 |
Start date: | 01-04-2024 |
End date: | 30-09-2025 |
Total budget - Public funding: | - 150 000,00 Euro |
Cordis data
Original description
Currently, 90% of the drugs fail to pass clinical trials1. One of the key reasons is that the animal models used in the preclinical phase poorly predict the human response to the drugs. Organ-on-a-Chip (OoC) is a game changing technology as one of the alternative methodolgies to animal models. The heart of an OoC system is an ‘Organ-chip’: cm-sized devices with micro-channels and -chambers in which human cells can be grown to closely mimic human tissues. More and more evidence shows that OoCs are more representative models than animals. However, the industry adoption of OoCs is still very limited. OoC users and developers simply have to choose between either OoCs with physiologically relevant flow but not fit for standard operating procedures in the pharmaceutical industry, or OoCs that are compatible but less physiological because of the absence or inadequacy of the flow.The TOMAC project offer s novel a solution called “Magnetic Artificial Cilia (MAC) pump”: a chip-sized modular and tubeless flow system that on one hand, eliminates manual handling and enables automation, and on the other hand provides physiological flow for a range of organ models. The technology behind MAC is based on micrometer-sized magnetic hair-like structures called Magnetic Artificial Cilia (MAC), which are inspired by cilia occurring in nature. The MAC are flexible micro-actuators that respond to a varying magnetic field (created by the actuation system) by rotating or oscillating, and thus create a controlled fluid flow.
Status
SIGNEDCall topic
ERC-2023-POCUpdate Date
12-03-2024
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