Project

InnovaTivE in situ 4D biopriNTing for regenerAtion of CoLorEctal mucosa and submucosa

Acronym
TENTACLE
Code
41F01225
Duration
01 January 2025 → 31 December 2028
Funding
European funding: framework programme
Research disciplines
  • Natural sciences
    • Macromolecular and materials chemistry not elsewhere classified
  • Medical and health sciences
    • Gastro-enterology
Keywords
bioprinter colonoscopic
Other information
 
Project description

Colorectal diseases are a cohort of pathologies that affect the mucosa and submucosa layers of the anus, rectum, and colon of more
than 2 million individual in the EU. Among them, familiar adenomatous polyposis (FAP) and ulcerative colitis (UC) seriously
compromise the patients’ quality of life. These pathologies could benefit from the removal of the intestinal mucosa and submucosa,
however no strategies exist nowadays for their replacement. Then, when their removal is necessary, the patients undergo a
proctocolectomy (i.e., surgical removal of the rectum and all or part of the colon) with a subsequent ileal pouch. Although preserving
the patient's continence, the procedure is burdened by significant complications.
In this scenario, TENTACLE pioneers a radically new strategy for the surgical treatment of UC and FAP, providing an innovative in situ
4D bioprinting strategy, for the regeneration of colorectal mucosa and submucosa. The TENTACLE in situ 4D bioprinting suite include:
i) a colonoscopic bioprinter, featuring an extrusion-based bioprinting unit, an valvejet printhead, a mesh delivery system and a
photocrosslinking device; ii) in silico tools for personalizing the bioprinting procedure; iii) two novel bespoken bioink formulations
containing patients’ cells, including suitable functionalization strategies. The mucosal formulation will feature a 4D shape morphing
behavior to recreate the colorectal mucosal crypts.
Within TENTACLE, the entire procedure will be validated ex vivo and in vivo, thus paving the way for translating the bioprinting suite
toward the clinics, by: i) identifying a GMP-compliant cell expansion protocol, ii) scaling up of the manufacturing routes, iii) promoting
involvement and acceptance of surgeons and patients, iv) aligning with the EU regulation. Collectively, our project will introduce a
minimally invasive alternative to proctocolectomy and is expected to have a high impact on the quality of life of patients affected by
FAP and UC.

 
 
 
Disclaimer
Funded by the European Union. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or the European Health and Digital Executive Agency (HADEA). Neither the European Union nor the authority can be held responsible for them.