Background: One of the most widely used metal nanoparticles in biological applications is gold, which has unique physicochemical characteristics. Strong localized surface plasmon resonance (LSPR) endows them with exceptional optical properties that facilitate the development of innovative methods for biosensing, bioimaging, and cancer research, particularly in the context of photothermal and photodynamic therapy. Methods: This study marked the first time that Mandragora autumnalis ethanolic extract (MAE) was utilized in the environmentally friendly synthesis of gold nanoparticles (AuNPs). Several characterization methods, including dynamic light scattering analysis (DLS), scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), and biological methods, were used to emphasize the anti-cancerous activity of the biogenic AuNPs. Results: MAE-AuNPs showed a surface plasmon resonance band at 570 nm. DLS and SEM demonstrated the synthesis of small, spherical AuNPs with a zeta potential of −19.07 mV. The crystalline nature of the AuNPs was confirmed by the XRD pattern, and data from FTIR and TGA verified that MAE-AuNPs played a part in stabilizing and capping the produced AuNPs. In addition, the MAE-AuNPs demonstrated their potential effectiveness as antioxidant and anticancer therapeutic agents by demonstrating radical scavenging activity and anticancer activity against a number of human cancer cell lines, specifically triple-negative breast cancer cells. Conclusions: Green synthesis techniques are superior to other synthesis methods because they are simple, economical, energy-efficient, and biocompatible, which reduces the need for hazardous chemicals in the reduction process. This article highlights the significance of characterizing MAE-AuNPs and evaluating their antioxidant and anticancer properties.

Gold nanoparticles (AuNPs) are promising materials for the development of novel anticancer agents, and their green synthesis has become essential because of their numerous advantages. This study aimed to synthesize AuNPs using an ethanolic extract of Scabiosa palaestina, characterize their physicochemical properties, and evaluate their anticancer properties and antioxidant potential. AuNPs were successfully synthesized and characterized using UV–visible spectroscopy, scanning electron microscopy (SEM), zeta potential analysis, thermogravimetric analysis (TGA), X-ray diffraction (XRD), and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR). The results indicated that the biosynthesized AuNPs were spherical and well-dispersed, exhibiting an absorption peak at 560 nm and an average size of 9.9 nm. Cytotoxicity assays demonstrated dose- and time-dependent inhibitory effects on MDA-MB-231, Capan-2, HCT116, and 22Rv1 cancer cell lines, with 22Rv1 and MDA-MB-231 cells showing the most potent responses. At the highest concentration tested (100 µg/mL), after 72 h, cell viability was reduced to 16.04 ± 1.8% for 22Rv1 and 17.48 ± 8.3% for MDA-MB-231 cells. Additionally, the AuNPs exhibited concentration-dependent antioxidant activity in both 2,2-diphenyl-1-picrylhydrazyl (DPPH) and hydrogen peroxide (H₂O₂) scavenging assays. In summary, the synthesized AuNPs demonstrated multifunctional properties that make them suitable for a wide range of biomedical and biotechnological applications.

Background: One of the most widely used metal nanoparticles in biological applications is gold, which has unique physicochemical characteristics. Strong localized surface plasmon resonance (LSPR) endows them with exceptional optical properties that facilitate the development of innovative methods for biosensing, bioimaging, and cancer research, particularly in the context of photothermal and photodynamic therapy. Methods: This study marked the first time that Mandragora autumnalis ethanolic extract (MAE) was uti-lized in the environmentally friendly synthesis of gold nanoparticles (AuNPs). Several characterization methods, including dynamic light scattering analysis (DLS), scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), and biological methods, were used to emphasize the anti-cancerous activity of the biogenic AuNPs. Results: MAE-AuNPs showed a surface plasmon resonance band at 570 nm. DLS and SEM demonstrated the synthesis of small, spherical AuNPs with a zeta potential of -19.07 mV. The crystalline nature of AuNPs was confirmed by the XRD pattern, and data from FTIR and TGA veri-fied that MAE-AuNPs played a part in stabilizing and capping the produced AuNPs. Al-so, the MAE-AuNPs demonstrated their potential effectiveness as antioxidant and anti-cancer therapeutic agents by demonstrating radical scavenging activity and anticancer activity against a number of human cancer cell lines, specifically triple-negative breast cancer cells. Conclusions: Green synthesis techniques are superior to other synthesis methods because they are simple, economical, energy-efficient, and biocompatible, which reduces the need for hazardous chemicals in the reduction process. This article highlights the significance of characterizing MAE-Au-NPs and evaluating their antioxidant and anticancer properties.

Gold nanoparticles (AuNPs) are promising materials for the development of novel anticancer agents, and their green synthesis has become essential due to their numerous advantages. This study aimed to synthesize AuNPs using an ethanolic extract of Scabiosa palaestina, characterize their physicochemical properties, and evaluate their anticancer properties as well as their antioxidant potential. AuNPs were successfully synthesized and characterized using UV–Visible spectroscopy, scanning electron microscopy (SEM), zeta potential analysis, thermogravimetric analysis (TGA), X-ray diffraction (XRD), and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR). The results indicated that the biosynthesized AuNPs were spherical and well-dispersed, exhibiting an absorption peak at 560 nm and an average size of 9.9 nm. Cytotoxicity assays demonstrated a dose- and time-dependent inhibitory effect on MDA-MB-231, Capan-2, HCT116, and 22Rv1 cancer cell lines, with 22Rv1 and MDA-MB-231 cells showing the most potent responses. At the highest concentration tested (100 µg/ml) after 72 hours, cell viability was reduced to 16.04 ± 1.8% for 22Rv1 and 17.48 ± 8.3% for MDA-MB-231 cells. Additionally, the AuNPs exhibited concentration-dependent antioxidant activity in both DPPH and H2O2 scavenging assays. In summary, the synthesized AuNPs demonstrated multifunctional properties that make them suitable for a wide range of biomedical and biotechnological applications.