In this paper, a facile and green approach for the synthesis of silver oxide nanoparticles Ag2O NPs was performed using the extract of the wild plant Herniaria hirsuta (H. hirsuta). Different spectral methods were used for the characterization of the biosynthesized Ag2O NPs, ultraviolet-visible (UV-Vis) spectroscopy gave a surface plasmon resonance (SPR) peak of Ag2O NPs is 430 nm, estimation of direct and indirect forbidden gap bands are respectively 3.76 eV and 3.68 eV; Fourier transform infrared (FTIR) spectral analysis revealed the groups responsible for the stability and synthesis of Ag2O NPs. The morphology of Ag2O NPs was studied by scanning electron microscopy (SEM) showing a nearly spherical shape of Ag2O NPs, and X-ray diffraction (XRD) study confirmed the crystallinity of Ag2O NPs with a crystallinity size of 15.51 nm. The catalytic activity of Ag2O NPs, as well as the rings number were studied by the degradation of methylene blue dye. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Taraxacum officinale (TO) has been historically used for medicinal purposes due to its biological activity against specific disorders. To investigate the antioxidant and the antiproliferativepotential of TO essential oil in vitro and in vivo, the chemical composition of the essential oil was analyzed by GC-MS. The in vivo antioxidant capacity was assessed on liver and kidney homogenate samples from mice subjected to acetaminophen-induced oxidative stress and treated with TO essential oil (600 and 12,000 mg/kg BW) for 14 days. The in vitro scavenging activity was assayed using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) and the reducing power methods. The cytotoxic effects against the HeLa cancer cell line were analyzed. The GC-MS analysis showed the presence of 34 compounds, 8 of which were identified as major constituents. The TO essential oil protected mice’s liver and kidneys from acetaminophen-induced oxidative stress by enhancing antioxidant enzymes (catalase, superoxide dismutase, and glutathione) and lowering malondialdehyde levels. In vitro, the TO essential oil demonstrated low scavenging activity against DPPH (IC50 = 2.00 ± 0.05 mg/mL) and modest reducing power (EC50 = 0.963 ± 0.006 mg/mL). The growth of the HeLa cells was also reduced by the TO essential oil with an inhibition rate of 83.58% at 95 µg/mL. Current results reveal significant antioxidant and antiproliferative effects in a dose-dependent manner and suggest that Taraxacum officinale essential oil could be useful in formulations for cancer therapy.