Hellany Heba, Badran Adnan, Albahri Ghosoon, Kafrouny Nadine, El Kurdi Riham, Maresca Marc, Patra Digambara, Baydoun Elias
Department of Biology, American University of Beirut, Beirut 1107, Lebanon.
Department of Nutrition, University of Petra, Amman 11196, Jordan.
Nanomaterials (Basel). 2025 Sep 4;15(17):1368. doi: 10.3390/nano15171368.
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 , 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 (HO) scavenging assays. In summary, the synthesized AuNPs demonstrated multifunctional properties that make them suitable for a wide range of biomedical and biotechnological applications.
金纳米颗粒(AuNPs)是开发新型抗癌药物的有前景的材料,由于其众多优点,其绿色合成已变得至关重要。本研究旨在使用 的乙醇提取物合成AuNPs,表征其物理化学性质,并评估其抗癌特性和抗氧化潜力。使用紫外可见光谱、扫描电子显微镜(SEM)、zeta电位分析、热重分析(TGA)、X射线衍射(XRD)和衰减全反射傅里叶变换红外光谱(ATR-FTIR)成功合成并表征了AuNPs。结果表明,生物合成的AuNPs呈球形且分散良好,在560 nm处有吸收峰,平均尺寸为9.9 nm。细胞毒性试验表明,对MDA-MB-231、Capan-2、HCT116和22Rv1癌细胞系有剂量和时间依赖性抑制作用,其中22Rv1和MDA-MB-231细胞反应最为强烈。在测试的最高浓度(100 µg/mL)下,72小时后,22Rv1细胞的细胞活力降至16.04±1.8%,MDA-MB-231细胞降至17.48±8.3%。此外,AuNPs在2,2-二苯基-1-苦基肼(DPPH)和过氧化氢(HO)清除试验中均表现出浓度依赖性抗氧化活性。总之,合成的AuNPs具有多功能特性,使其适用于广泛的生物医学和生物技术应用。