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Inorganic Sol-Gel Polymerization for Hydrogel Bioprinting
Titouan Montheil1, Marie Maumus2, Laurine Valot1,3
1IBMM, University of Montpellier, CNRS, ENSCM, Montpellier, France.
ACS Omega
|February 26, 2020
Summary
This study introduces a novel bioink for 3D bioprinting using hydroxypropyl methyl cellulose (HPMC) cross-linked via sol-gel polymerization. This method enables the creation of functional hydrogel scaffolds for cell encapsulation and tissue engineering.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Polymer Chemistry
Background:
- Three-dimensional (3D) bioprinting requires advanced bioinks for fabricating functional tissue scaffolds.
- Hydrogels offer promising biomaterial properties but often lack the mechanical stability and printability needed for complex structures.
- Developing biocompatible and tunable hydrogel systems is crucial for regenerative medicine applications.
Purpose of the Study:
- To develop a novel bioink for 3D bioprinting using an inorganic sol-gel polymerization process.
- To create a hydroxypropyl methyl cellulose (HPMC)-based hydrogel precursor for extrusion-based bioprinting.
- To investigate the physicochemical properties and functionalization capabilities of the resulting hydrogel scaffolds.
Main Methods:
- An inorganic sol-gel polymerization was employed as a cross-linking reaction for hydrogel formation.
- Hybrid hydroxypropyl methyl cellulose (HPMC) with controlled silylation was synthesized as a 3D-network precursor.
- The bioink, containing human mesenchymal stem cells, was extruded and polymerized in situ at physiological pH (7.4) using biocompatible catalysts (NaF and glycine).
- Rheological and viscosity measurements were performed to determine the printing window.
- Physicochemical properties of the hydrogels were analyzed.
- Covalent functionalization was demonstrated using a triethoxysilyl-containing fluorescent molecule.
Main Results:
- A stable, printable bioink was successfully formulated using silylated HPMC and sol-gel polymerization.
- The sol-gel process occurred under biocompatible conditions (pH 7.4, NaF/glycine catalysis), suitable for cell encapsulation.
- Rheological analysis defined the optimal printing parameters for the bioink.
- The resulting hydrogels exhibited tunable physicochemical properties.
- Covalent functionalization of the hydrogel network was achieved, demonstrated by incorporating a fluorescent molecule.
Conclusions:
- The developed HPMC-based bioink, cross-linked via inorganic sol-gel polymerization, is a promising material for 3D bioprinting of cell-laden scaffolds.
- The biocompatible and tunable nature of this system supports its potential application in tissue engineering and regenerative medicine.
- The demonstrated covalent functionalization opens avenues for creating advanced, multi-functional biomaterials.

