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Active HORIZON European Commission

Holographic Optical Tweezing Bioprinting (HOTB): Towards precise manipulation of cells for artificial multi-scaled vascularized tissues/organ printing.

€1.97M EUR

Funder European Commission
Recipient Organization Universidade Da Coruna
Country Spain
Start Date Feb 01, 2024
End Date Jan 31, 2029
Duration 1,826 days
Number of Grantees 1
Roles Coordinator
Data Source European Commission
Grant ID 101125172
Grant Description

Because current limitations in 3D bioprinting for tissue engineering stem from the fact that the multi-scaled vasculature associated to the human microtissues and organs cannot be replicated.

The overarching aim of the HOT-BIOPRINTING project is to deliver a methodology enabling the manufacturing of a new generation of tissue-like structures with properties mimicking more closely the complexity of biological tissues and organs.

The innovation of HOT-BIOPRINTING lies on the development of a disruptive technology named Holographic optical tweezing bioprinting (HOTB) for single and automatized multiple cell 3D bioprinting.

The non-contact nature of light will eliminate the fails on bioprinting associated to instrumentation, which along with the HOTB capabilities for manipulating single cells for printing will drive a new paradigm shift: “resolution will be dictated by the cell size instead of by the mechanical component of the instrumentation”.

This new technological advancement for resolution enhancement while maintaining bioprinting speed using holographic automatization can open new opportunities to the tissue engineering and regenerative medicine community.

I propose the following general objectives that go beyond the state of the art in bioprinting human mimetic tissue:1) Generate the knowledge and develop a Holographic Optical tweezer bioprinter (HOTB) for high-definition single/multiple cell bioprinting. 2) Demonstration and automatization for 3D multicellular printing for large area tissue generation. 3) Overcome the challenges associated with existing biofabrication techniques (limited multi-scaled vascularization and oversimplified structures).4) Demonstrating lymph-node bioprinting with integrated vasculature.

This represents a big challenge, if achieved, will revolutionize the bioprint technology by increasing the tissue complexity and by responding to the demand of biofabricating multi-scale vascularized complex tissues and organs.

All Grantees

Universidade Da Coruna

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