Din Inam Ud, Ajaj Rahaf, Rauf Abdur, Ahmad Zubair, Muhammad Naveed, Ali Shahid, Hemeg Hassan A, Ullah Imran
Materials Research Laboratory, Department of Physics, University of Peshawar, Peshawar, Pakistan.
Department of Environmental and Public Health, College of Health Sciences, Abu Dhabi University, Abu Dhabi, United Arab Emirates.
PLoS One. 2025 Jul 1;20(7):e0326858. doi: 10.1371/journal.pone.0326858. eCollection 2025.
In this work, Silver (Ag) nanoparticles (NPs) were synthesized via green synthesis using Ficus benghalensis root extract (FBRE), serving as a capping and stabilizing agent. The synthesized Ag NPs were characterized via complementary characterization techniques, including SEM, XRD, EDS, UV-Vis, and FT-IR. SEM analysis revealed the fabrication of spherical NPs with an average size of 41.55 nm. A plasmon resonance peak was observed at 430 nm. FBRE effectively capped and stabilized the Ag NPs, ensuring their structural integrity over time, and is confirmed via FT-IR scan. DFT calculation revealed a thermodynamically and mechanically stable system. Moreover, optoelectronic properties confirmed the metallic behavior of Ag with a major contribution from 4d orbital near the fermi level and 5s orbital contribution to the conduction band with light absorption in the visible spectrum. Biological evaluations demonstrated significant enzyme inhibition. Ag NPs inhibited urease (80.76%), α-glucosidase (80.98%), carbonic anhydrase II (89.32%), and xanthine oxidase (49.9%), outperforming FBRE. In Vivo, Ag NPs exhibited dose-dependent analgesic (83.09% writhing inhibition at 10 mg/kg, similar to diclofenac) and sedative (16.09% locomotor reduction at 10 mg/kg) effects. Molecular docking confirmed strong enzyme-ligand interactions. These findings highlight the biomedical potential of FBRE-synthesized Ag NPs, particularly for enzyme inhibition and pharmacological applications.
在本研究中,通过绿色合成法利用孟加拉榕树根提取物(FBRE)合成了银(Ag)纳米颗粒(NPs),该提取物用作封端和稳定剂。通过包括扫描电子显微镜(SEM)、X射线衍射(XRD)、能谱分析(EDS)、紫外可见光谱(UV-Vis)和傅里叶变换红外光谱(FT-IR)在内的互补表征技术对合成的Ag NPs进行了表征。SEM分析显示制备出了平均尺寸为41.55nm的球形NPs。在430nm处观察到一个等离子体共振峰。FBRE有效地封端并稳定了Ag NPs,确保了它们随时间的结构完整性,这通过FT-IR扫描得到了证实。密度泛函理论(DFT)计算表明该系统在热力学和力学上是稳定的。此外,光电性质证实了Ag的金属行为,费米能级附近的4d轨道起主要作用,5s轨道对导带也有贡献,在可见光谱中有光吸收。生物学评估显示出显著的酶抑制作用。Ag NPs对脲酶(80.76%)、α-葡萄糖苷酶(80.98%)、碳酸酐酶II(89.32%)和黄嘌呤氧化酶(49.9%)具有抑制作用,优于FBRE。在体内,Ag NPs表现出剂量依赖性的镇痛作用(10mg/kg时扭体抑制率为83.09%,与双氯芬酸相似)和镇静作用(10mg/kg时运动减少率为16.09%)。分子对接证实了强烈的酶-配体相互作用。这些发现突出了FBRE合成的Ag NPs的生物医学潜力,特别是在酶抑制和药理学应用方面。