Hydrogels of TEMPO-oxidized nanocellulose (TO-CNF) were stabilized for dry-jet wet spinning using a shell of cellulose dissolved in 1,5-diazabicyclo[4.3.0]non-5-enium propionate ([DBNH][CO2Et]), a protic ionic liquid (PIL). Coagulation in an acidic water bath resulted in continuous core-shell filaments (CSF) that were tough and flexible: average dry (and wet) toughness of ~11 (2) MJ . m -3 and elongation of ~9 ( 14) %. CSF morphology, chemical composition, thermal stability, crystallinity, and bacterial activity were assessed using scanning electron microscopy with energy dispersive X-ray spectroscopy, liquid-state nuclear magnetic resonance, Fourier transform infrared spectroscopy, thermogravimetric analysis, pyrolysis gas chromatography-mass spectrometry, wide angle X-ray scattering and bacterial cell culturing, respectively. The coaxial wet spinning yields PIL-free systems carrying on the surface the cellulose II polymorph, which not only enhances the toughness of the filaments but facilities their functionalization.apply a strategy based on the principles of the circular economy. Bio-based materials and, in particular, cellulose nanomaterials (CNMs) have become excellent candidates in this regard, as they could partially replace materials based on non-renewable resources. Indeed, CNMs enable high-performance, green functional materials with a broad spectrum of applications, e.g., electronics, biomedical and tissue engineering scaffolds, coatings, food, textiles, and even in daily use goods [1][2][3][4][5][6][7][8] .Cellulose resources have the potential of becoming a platform to develop novel CNMs with high mechanical performance since nanocellulose, in its cellulose I crystalline phase, possess an elastic modulus of about 150 GPa and 18-50GPa in the longitudinal and transverse directions, respectively 9,10 . The regioselective C6 oxidation of nanocellulose fibers can be additionally catalyzed by the use of the 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) nitroxyl radical to produce hydrogels with high transparency 11 , an extensive degree of fibrillation 12 , and low cytotoxicity 13 . These TEMPO-oxidized cellulose nanofibers (TO-CNF) are suitable for applications in diverse fields such as packaging 3,4,[14][15][16] , textiles [17][18][19][20] , biosensing and bioelectronics 21,22 , fire retardancy 23 , wound dressing and cell delivery [24][25][26] , among others 3 . Despite its excellent mechanical properties, materials derived from nanocellulose and, in particular, TEMPO-oxidized nanocellulose, have several drawbacks inherent to its nature. For instance, these materials are mostly hydrophilic owing to the high concentration of hydroxyl and carboxylate groups; this causes mechanical instability of the formed materials under wet/humid conditions, and exhibit rather low aspect ratios compared to dissolved polymers. The limited aspect ratio makes it difficult to create oriented structures of cellulose nanofibrils by drawing 27,28 . Many attempts to overcome hydrophilicity challenges have been made through appr...