Project description
New generation of CMOS-based neural probes
The introduction of high-density implantable neural probes based on complementary metal–oxide semiconductor (CMOS) technology is a big step forward in neuroscience. These new probes provide simultaneous access to thousands of single neurons in different brain circuits, introducing hundreds of closely spaced microelectrodes into the substrate for recording extracellular bioelectrical signals. Current CMOS probes are not suitable for stable chronic implants and potential clinical applications in brain–machine interfaces or neuroprosthetics. To achieve this, a proposed solution is to minimise tissue reactions and improve the stability of implantable probes based on downscaling the sizes of the probes and the overall system. The EU-funded ChroMOS project will therefore work towards the exploitation of the key advantages of CMOS neural probes together with the optimisation of circuits, materials and microfabrication processes.
Objective
The recent advent of active high-density implantable neural probes based on CMOS technology is a big leap forward in neuroscience. Unprecedentedly, these new probes provide simultaneous access to several thousands of single-neurons in different brain circuits. Although realized with different circuit’s architectures, such devices combine the use of standard CMOS and MEMS technologies to realize monolithic active dense probes that integrate into the same substrate hundreds of closely spaced microelectrodes together with electronic circuits for recording extracellular bioelectrical signals. However, despite their unique value, current CMOS-probes are not yet adapted for chronically stable implants and this is a major drawback both for neuroscience research as well as for growing potential clinical applications in fields such as brain-machine-interfaces or neuroprosthetics.
An emerging hypothesis to minimize tissue-reactions and improve chronic stability of implantable probes consists in downscaling the cross-sectional sizes of their shafts as well as the overall system size. This fellowship proposes a deep study of this hypothesis by exploiting key advantages of monolithic CMOS based neural probes together with the optimization of circuits, materials and microfabrication processes. I will exploit my background in MEMs technologies and acquire new expertise in neuroscience to evaluate solutions for reducing CMOS shanks dimensions (20-80 µm width, 15-30 µm thick), strategies to improve tissue-materials interfaces, and to assess the effects of these features on brain tissue responses and recording performances. This will lead to ChroMOS probes with a very thin and uniform width (tens of microns) through all the shaft, and with electrode densities up to 1000 sites/mm2. This can lead to remarkably stable probe’s implants with large-scale single-neuron recording capabilities, far behind current technologies.
Fields of science (EuroSciVoc)
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
- natural sciences biological sciences neurobiology
- medical and health sciences medical biotechnology implants
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Keywords
Project’s keywords as indicated by the project coordinator. Not to be confused with the EuroSciVoc taxonomy (Fields of science)
Project’s keywords as indicated by the project coordinator. Not to be confused with the EuroSciVoc taxonomy (Fields of science)
Programme(s)
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
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H2020-EU.1.3. - EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions
MAIN PROGRAMME
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H2020-EU.1.3.2. - Nurturing excellence by means of cross-border and cross-sector mobility
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Topic(s)
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Funding Scheme
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)
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Call for proposal
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
(opens in new window) H2020-MSCA-IF-2019
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Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.
16163 GENOVA
Italy
The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.