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Materials Science & Engineering C-Materials for Biological Applications

Publication date: 2019-05-01
Volume: 98 Pages: 1133 - 1144
Publisher: Elsevier

Author:

Van den Broeck, Laurien
Piluso, Susanna ; Soultan, Al Halifa ; De Volder, Michael ; Patterson, Jennifer

Keywords:

Science & Technology, Technology, Materials Science, Biomaterials, Materials Science, Cytocompatibility, Mechanical properties, Hydrogel swelling, Multi-walled carbon nanotubes, PEGylation, MECHANICAL-PROPERTIES, MATRIX ELASTICITY, PEG HYDROGELS, IN-VITRO, SCAFFOLDS, TOUGH, FUNCTIONALIZATION, DIFFERENTIATION, BIODEGRADATION, NANOCOMPOSITES, Animals, Biocompatible Materials, Cell Proliferation, Cell Survival, Cells, Cultured, Fibroblasts, Hydrogels, Mice, Nanocomposites, Nanotubes, Carbon, Polyethylene Glycols, Polymers, Tissue Engineering, Tissue Scaffolds, 0903 Biomedical Engineering, 0912 Materials Engineering, Biomedical Engineering, 4003 Biomedical engineering, 4016 Materials engineering

Abstract:

Hydrogels are attractive materials for stimulating 3D cell growth and tissue regeneration, and they provide mechanical support and physical cues to guide cell behavior. Herein, we developed a robust methodology to increase the stiffness of polyethylene glycol (PEG) hydrogels by successfully incorporating carbon nanotubes (CNTs) within the polymer matrix. Interestingly, hydrogels containing pristine CNTs showed a higher stiffness (1915 ± 102 Pa) than both hydrogels without CNTs (1197 ± 125 Pa) and hydrogels incorporating PEG-grafted CNTs (867 ± 103 Pa) (p < / 0.005). The swelling ratio was lower for hydrogels with pristine CNTs (45.4 ± 3.5) and hydrogels without CNTs (46.7 ± 5.1) compared to the hydrogels with PEG-grafted CNTs (62.8 ± 2.6). To confirm that the CNT-reinforced hydrogels were cytocompatible, the viability, proliferation, and morphology of encapsulated L929 fibroblasts was investigated. All hydrogel formulations supported cell proliferation, and the addition of pristine CNTs increased initial cell viability (83.3 ± 10.7%) compared to both pure PEG hydrogels (51.9 ± 8.3%) and hydrogels with PEG-CNTs (63.1 ± 10.9%) (p < / 0.005). Altogether, these results demonstrate that incorporation of CNTs could effectively reinforce PEG hydrogels and that the resulting cytocompatible nanocomposites are promising scaffolds for tissue engineering.