The lyocell process offers an environmentally friendly strategy to produce regenerated cellulose fibre from biomass. However, it is critical to recover and reuse the N-methyl-morpholine-N-oxide (NMMO) solvent to maximize the environmental benefits and lower the cost. This article reviews NMMO recovery and characterization techniques at the lab and industrial scales, and methods to limit the NMMO degradation during the process. The article also presents the results of a pilot study investigating the recovery of NMMO from lyocell manmade cellulosic fibre (L-MMCF) manufacturing wastewater. The work described includes the development of a calibration curve for the determination of NMMO content in aqueous solutions using Fourier Transform Infrared Spectroscopy (FTIR). Successful NMMO recovery from the wastewater was achieved using a rotary evaporator: the final NMMO concentration was 50, i.e., ready for use in the lyocell process, and no NMMO degradation was observed. The knowledge in this paper will support advances in L-MMCF manufacturing and the reduction in textile environmental footprint.

Chagas disease, a century-old disease that mainly affects the impoverished population in Latin America, causes high morbidity and mortality in endemic countries. The available drugs, benznidazole (Bz) and nifurtimox, have limited effectiveness and intense side effects. Drug repurposing, and the development of new chemical entities with potent activity against Trypanosoma cruzi, are a potential source of therapeutic options. The present study describes the biological activity of two new series of pyrazole-thiazoline derivatives, based on optimization of a hit system 5-aminopyrazole-imidazoline previously identified, using structure–activity relationship exploration, and computational and phenotype-based strategies. Promising candidates, 2c, 2e, and 2i derivatives, showed good oral bioavailability and ADMET properties, and low cytotoxicity (CC₅₀ > 100 µM) besides potent activity against trypomastigotes (0.4–2.1 µM) compared to Bz (19.6 ± 2.3 µM). Among them, 2c also stands out, with greater potency against intracellular amastigotes (pIC₅₀ = 5.85). The selected pyrazole-thiazoline derivatives showed good permeability and effectiveness in the 3D spheroids system, but did not sustain parasite clearance in a washout assay. The compounds’ mechanism of action is still unknown, since the treatment neither increased reactive oxygen species, nor reduced cysteine protease activity. This new scaffold will be targeted to optimize in order to enhance its biological activity to identify new drug candidates for Chagas disease therapy.