Ellagic Acid-Wrapped Gold Nanoparticles: Evaluation of Antimicrobial, Antioxidant, Anti-Inflammatory, and Cytotoxicity Effects of KB Cells

被引:1
作者
Soni, Muskan [1 ]
Ragavendran, Chinnasamy [1 ]
Imath, Mohamed [2 ]
Manoharadas, Salim [3 ]
Nakouti, Ismini [4 ]
机构
[1] Saveetha Inst Med & Tech Sci SIMATS, Saveetha Dent Coll & Hosp, Dept Cariol, Chennai 600077, India
[2] JKKMMRFS Annai JKK Sampoorani Ammal Coll Pharm, Dept Pharmacol, Namakkal, Tamil Nadu, India
[3] King Saud Univ, Coll Sci, Dept Bot & Microbiol, POB 2454, Riyadh 11451, Saudi Arabia
[4] Liverpool John Moores Univ, Ctr Nat Prod Discovery CNPD, Sch Pharm & Biomol Sci, Liverpool L3 3AF, England
关键词
Eco-friendly; Ellagic acid; Gold nanoparticles; Oral cancer properties; Antibacterial; GREEN SYNTHESIS; EXTRACTS;
D O I
10.1007/s10876-025-02852-9
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The green synthesis of metal nanoparticles using plant-based molecules is gaining attention for its potential in biomedical applications. The aim of present study the eco-friendly synthesis of gold nanoparticles (AuNPs) using ellagic acid, a natural antioxidant, which acted as both reducing and capping agent. The successful synthesized ellagic acid-coated AuNPs (EA-AuNPs) was indicated by a colour change to dark brown and confirmed through UV-visible spectroscopy with a peak at 587.5 nm. Transmission electron microscopy (TEM) revealed long rod-shaped nanoparticles ranging from 50 to 70 nm in size, and energy-dispersive X-ray spectroscopy (EDX) confirmed the presence of Au, C, Cl, and N elements. Zeta potential analysis showed a stable surface charge of -17.7 mV. EA-AuNPs exhibited strong antibacterial activity, including a 37.26 +/- 0.9 mm inhibition zone against Klebsiella pneumoniae at 100 mu g/mL and minimum inhibitory concentration (MIC) values below 1 mu g/mL against Staphylococcus aureus. The nanoparticles also demonstrated potent antioxidant activity, achieving 91% and 89% radical scavenging in DPPH and ABTS assays, respectively. Anti-inflammatory testing showed 78% membrane stabilization at 200 mu g/mL. Moreover, cytotoxicity studies revealed that EA-AuNPs had an IC50 of 59.58 mu g/mL against oral epidermoid carcinoma (KB) cells. In-silico analysis also demonstrated a promising binding affinity of -7.3 kcal/mol with Candida albicans, suggesting notable antifungal properties. The present study highlights the multi-functional therapeutic potential of EA-AuNPs in oral health care, offering a biocompatible approach to combat microbial infections, oxidative stress, inflammation, and oral cancer. The integration of both in-vitro and in-silico results supports their future application in dental and oral medicine.
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页数:26
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