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3D Bio-Based mRNA-Enriched Materials for Bone Regeneration: Optimizing Osteogenic Differentiation Using


Thesis topic details

General information

Organisation

The French Alternative Energies and Atomic Energy Commission (CEA) is a key player in research, development and innovation in four main areas :
• defence and security,
• nuclear energy (fission and fusion),
• technological research for industry,
• fundamental research in the physical sciences and life sciences.

Drawing on its widely acknowledged expertise, and thanks to its 16000 technicians, engineers, researchers and staff, the CEA actively participates in collaborative projects with a large number of academic and industrial partners.

The CEA is established in ten centers spread throughout France
  

Reference

SL-DRT-27-0005  

Direction

DRT

Thesis topic details

Category

Technological challenges

Thesis topics

3D Bio-Based mRNA-Enriched Materials for Bone Regeneration: Optimizing Osteogenic Differentiation Using AI-Based Methods

Contract

Thèse

Job description

This PhD project aims to develop bioresorbable scaffolds functionalized with mRNA using a polycation, poly(L-lysine), and hyaluronic acid, arranged in different structural architectures.
The originality of this approach lies in two key aspects. First, these biomaterials will incorporate mRNA sequences encapsulated within nanoparticles, encoding proteins that play a crucial role in bone regeneration, such as VEGF (Vascular Endothelial Growth Factor) and BMP (Bone Morphogenetic Proteins). Second, the project will investigate how the three-dimensional organization of the polymer network influences the biological performance of the scaffold.
The overall objective is to transform cells located at the injury site into localized therapeutic protein factories through in situ transfection, enabling sustained, localized production of the therapeutic proteins at physiological concentrations.
Artificial intelligence (AI) approaches will be used as computer-aided design tools to analyze and exploit the experimental data. These methods will guide the optimization of scaffold design—including composition, architecture, and mRNA loading—to maximize osteogenic differentiation while reducing the number of experimental iterations required.
This work is part of an interdisciplinary and collaborative research project. The PhD candidate will also contribute to data analysis, the writing of scientific publications, and the dissemination of research findings at national and international conferences.

University / doctoral school

Sciences de la Matière (ED482)
Université de Toulouse

Thesis topic location

Site

Grenoble

Requester

Position start date

01/10/2026

Person to be contacted by the applicant

SANCHEZ GONZALEZ Laura laura.sanchezgonzalez@cea.fr
CEA
DRT/DOCC//DOCC
51, rue de l'Innovation
31670 LABEGE
05.36.25.96.32

Tutor / Responsible thesis director

GIROD FULLANA SOPHIE
CIRIMAT UMR 5085 CNRS UT INP
CIRIMAT UMR 5085 CNRS UT INP

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