AccScience Publishing / IJB / Online First / DOI: 10.36922/IJB025420428
RESEARCH ARTICLE

Optimization of 3D bioprinting of mouse preosteoblasts using nanofibrillated cellulose hydrogels

Na Li1 Linge Wang2 Roxana Guillen De La Cruz1* Zhenyu Jason Zhang1*
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1 School of Chemical Engineering, University of Birmingham, Birmingham, UK
2 South China Advanced Institute for Soft Matter Science and Technology, School of Emergent Soft Matter, Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices, Guangdong Basic Research Centre of Excellence for Energy and Information Polymer Materials, South China University of Technology, Guangzhou, Guangdong, China
Received: 18 October 2025 | Accepted: 8 December 2025 | Published online: 16 December 2025
© 2025 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by/4.0/ )
Abstract

Development and optimization of advanced bioink formulations for living tissue-engineered scaffolds remain a challenging task. Herein, a nanofibrillated cellulose (NFC)-composited gelatin methacryloyl (G)/alginate (A) formulation (G/A/NFC100) was prepared for 3D bioprinting of mouse preosteoblasts MC3T3-E1, whereby the G/A formulations with a mixed NFC/microfibrillated cellulose and without NFC were included for comparison. The rheological properties of G/A formulation were enhanced by the addition of NFC, as evidenced by a decreased viscosity index characterizing shear thinning behavior from 0.52 (G/A) to 0.19 (G/A/NFC100). To construct 3D scaffolds with excellent shape fidelity while minimizing shear damage to cells during extrusion, the bioprinting conditions of the formulations were optimized based on the parameter optimization index. The G/A/NFC100 scaffold printed at a printing speed of 2 mm/s and a dispensing pressure of 30 kPa from a 27-gauge nozzle displayed a high shape fidelity (printability index of 0.883). The mechanical stability of the crosslinked 20-layered G/A/NFC100 structures were demonstrated by three consecutive press-relax cycles. The successful bioprinting of mouse preosteoblasts using the G/A/NFC100 formulation translated into an increased cell viability (above 97.64%) up to 21 days post-bioprinting. These results emphasize the exceptional potential of NFC-composited G/A formulation for bioprinting of bone tissue analogues for biomedical applications. In addition, the long-term controlled release of ampicillin (67.42% after 72 h) by G/A/NFC100 scaffolds demonstrates the feasibility of utilizing porous cellulose fibers as drug-delivery carriers to enable multifunctionality in bone tissue repair.

Graphical abstract
Keywords
3D bioprinting
Bioink formulation
Cell viability
Hydrogel
Nanofibrillated cellulose
Printability
Funding
We thank the financial support provided by the UKRI (Horizon Europe Guarantee scheme, 10066793), and FiberLean Technologies for kindly providing microfibrillated cellulose samples. Z.J.Z. thanks the financial support given by the Engineering and Physical Science Research Council (EP/V029762/1). N.L. acknowledges the Chinese Scholarship Council for the awarded scholarship (CSC201906950042).
Conflict of interest
The authors declare they have no competing interests.
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International Journal of Bioprinting, Electronic ISSN: 2424-8002 Print ISSN: 2424-7723, Published by AccScience Publishing