Summary
Off late, there has been a tremendous surge in the cost of bringing new drugs to the market. The rising costs and ethical concerns related to screening with animal models have led to the development of alternate approaches for drug discovery. Owing to the advantages of high physiological relevance and predictive value, Micro-physiological systems (MPSs) (also referred to as Organ-on-chips (OoC)) are gradually taking over as powerful and cost-effective alternative to animal model-based drug screening. However, OoCs have yet to cross certain key barriers, before they are adopted as an industry standard for drug screening. The current state-of-the-art in OoCs suffer from a low standardization level, low throughput workflow, in comparison to conventional cell culture-based methods. The main objective of the project is to design and develop a library of inter-lockable hard-soft hybrid components, which can be used to construct any given organ-on-chip at the required physiological/functional scale. Each part of the library would serve to enable a certain physicochemical stimulus/structure warranting its use in the design of a specific type of organ-on-chip. The overall library would contain all the required parts to enable implementation of different microenvironments from different organs of the human body. The development of such parts would enable a standardized approach to OoC development and testing across the industry. The project will have a preliminary focus on demonstrating the proof-of-concept for assembling a lung-on-chip OoC from the developed modular components. Followed by integration of different organ-on-chips with functional scaling and parallelization for high-throughput. The project has a strong multi-disciplinary nature with expertise involved from fields of engineering/mechanical design, microfluidics, biological cell culture/microbiology.
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More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/840231 |
| Start date: | 11-10-2019 |
| End date: | 10-10-2021 |
| Total budget - Public funding: | 196 707,84 Euro - 196 707,00 Euro |
Cordis data
Original description
Off late, there has been a tremendous surge in the cost of bringing new drugs to the market. The rising costs and ethical concerns related to screening with animal models have led to the development of alternate approaches for drug discovery. Owing to the advantages of high physiological relevance and predictive value, Micro-physiological systems (MPSs) (also referred to as Organ-on-chips (OoC)) are gradually taking over as powerful and cost-effective alternative to animal model-based drug screening. However, OoCs have yet to cross certain key barriers, before they are adopted as an industry standard for drug screening. The current state-of-the-art in OoCs suffer from a low standardization level, low throughput workflow, in comparison to conventional cell culture-based methods. The main objective of the project is to design and develop a library of inter-lockable hard-soft hybrid components, which can be used to construct any given organ-on-chip at the required physiological/functional scale. Each part of the library would serve to enable a certain physicochemical stimulus/structure warranting its use in the design of a specific type of organ-on-chip. The overall library would contain all the required parts to enable implementation of different microenvironments from different organs of the human body. The development of such parts would enable a standardized approach to OoC development and testing across the industry. The project will have a preliminary focus on demonstrating the proof-of-concept for assembling a lung-on-chip OoC from the developed modular components. Followed by integration of different organ-on-chips with functional scaling and parallelization for high-throughput. The project has a strong multi-disciplinary nature with expertise involved from fields of engineering/mechanical design, microfluidics, biological cell culture/microbiology.Status
TERMINATEDCall topic
MSCA-IF-2018Update Date
28-04-2024
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