injectable hydrogels are increasingly used for in situ tissue regeneration and wound healing. ideally, an injectable implant should promote the recruitment of cells from the surrounding native tissue and allow cells to migrate freely as they generate a new extracellular matrix network. nanocomposite hydrogels such as carbon nanotube (cnt)-loaded hydrogels have been hypothesized to promote cell recruitment and cell migration relative to unloaded ones. to investigate this, cnt-glycol chitosan hydrogels were synthesized and studied. Chemoattractant-induced cell migration was studied using a modified Boyden Chamber experiment. Migrated cells were counted using flow cytometry. Cell adhesion was inferred from the morphology of the cells via an image segmentation method. cell migration and recruitment results confirmed that small concentrations of CNT significantly increase cell migration in hydrogels, thereby accelerating tissue regeneration and wound healing in situations where there is insufficient migration in the unloaded matrix. Hydrogels offer many advantages for biomedical applications due to their unique properties, in particular, their biocompatibility, biodegradation rate, mechanical stiffness, hydrophilicity, and porosity 1,2. Nanocomposite hydrogels have the potential to further improve upon these properties through the addition of nanoparticles to pure hydrogels. Such nanocomposite hydrogels have been reported to increase three-and four-dimensional printability, stiffness tunability, and electrical conductivity 3-9. For tissue engineering applications, composite hydrogels should allow sufficient cell adhesion and cell migration within its network. Such cell-biomaterial interaction is known to accelerate wound healing and tissue regeneration in the target region 10,11. Collagen, fibrin, fibronectin, nanoclays, cellulose nanocrystals, cellulose nanowhiskers, graphene oxide, and carbon nanotubes (CNTs) are among the many functional reinforcements available for fabricating bionanocomposite hydrogels 7,12-16. In our previous work, we found that the addition of CNTs to a glycol-chitosan matrix alters gelation time, porosity, and storage modulus 17. Since their discovery in 1991 by Iijima 18 , CNTs have been broadly used in biomedical applications. The CNTs can firmly attach to proteins and receptors on the cell membrane. The adherence between CNTs and cells is important. Firstly, single-walled carbon nanotubes (SWCNTs) may be employed for the purpose of drug delivery 19. Gangrade et al. took advantage of the thermal properties of the SWCNTs to obtain a temperature-dependent release of preloaded doxorubicin 20. Secondly, multiwalled carbon nanotubes (MWCNTs), which due to their size are more practical for tissue engineering applications, can be used as focal adhesion sites to enhance cell adhesion for anchorage-dependent cells such as fibroblasts 21,22. The latter may lead to an increased cell migration rate in CNT-loaded composite hydrogels. The larger diameter of MWCNTs with respect to SWCNTs approximates the p...