One pot Hypnea valentiae mediated synthesis of silver doped curcumin nanoparticles and their evaluation of antibacterial, anti-inflammatory and anticancer activity

被引:1
作者
Surya, Muthuvel [1 ]
Kumar, Aswin S. [2 ]
Sankar, Muthupandi [3 ]
Moses, Victor Antony Raj [4 ]
Mahendran, Karthikeyan [5 ]
Muthupandian, Saravanan [1 ,6 ,7 ]
机构
[1] Saveetha Dent Coll & Hosp, Saveetha Inst Med & Tech Sci SIMATS, Dept Pharmacol, AMR & Nanotherpeut Lab, Chennai 600077, Tamil Nadu, India
[2] Saveetha Univ, Saveetha Med Coll & Hosp, Saveetha Inst Med & Tech Sci SIMATS, Dept Pharmacol, Chennai 602105, Tamil Nadu, India
[3] Saveetha Univ, Saveetha Med Coll & Hosp, Saveetha Inst Med & Tech Sci SIMATS, Ctr Global Hlth Res, Chennai 602105, Tamil Nadu, India
[4] Univ Madras, Loyola Coll, Dept Phys, Chennai 600034, India
[5] PSG Coll Arts & Sci, Dept Microbiol, Coimbatore 641014, Tamil Nadu, India
[6] Univ Tabuk, Fac Appl Med Sci, Dept Med Lab Technol, Tabuk 71491, Saudi Arabia
[7] Univ Tabuk, Prince Fahad Bin Sultan Chair Biomed Res, Tabuk 71491, Saudi Arabia
关键词
Green synthesis; AgNPs; Curcumin; Antibacterial; Anti-inflammatory; Cytotoxicity; GREEN SYNTHESIS; BIOSYNTHESIS; ANTIOXIDANT; EXTRACT;
D O I
10.1016/j.jiec.2025.01.051
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, extracts of the red algae Hypnea valentiae were utilized as capping and reducing agents for the biosynthesis of silver-doped curcumin nanoparticles (Cur-AgNPs). The physicochemical properties, cytotoxicity, anti-inflammatory, and antibacterial activities of the synthesized Cur-AgNPs were systematically evaluated. UV-Vis spectroscopy revealed a characteristic peak at 446 nm for the algal-extract-capped Cur-AgNPs, accompanied by a visually detectable color change. Scanning electron microscopy (SEM) confirmed a nearly hexagonal structure with nanoscale diameters ranging from 200 to 400 nm. Fourier transform infrared (FTIR) spectroscopy identified molecular bonds associated with C-X, C-O, N-O, C=C, C equivalent to C and C-H groups in the Cur-AgNPs. The nanoparticles demonstrated potent antibacterial activity against multidrug-resistant bacterial strains, including Enterococcus faecalis, Pseudomonas aeruginosa, methicillin-resistant Staphylococcus aureus, and Klebsiella pneumoniae, with the significant inhibition zone observed at an 80 mu g/mL concentration. Cur-AgNPs showed a peak anti-inflammatory activity of 84 % at a concentration of 100 mu g/mL, whereas diclofenac displayed a superior activity of 94.7 %, and the IC50 value for Cur-AgNPs was determined to be 52.9 mu g. Cytotoxicity studies revealed an IC50 value of 44 mu g/mL against the A549 lung cancer cell line, highlighting the potential of CurAgNPs in biomedical efficacy studies. To increase the stability and efficacy of the Cur-AgNPs, more research might focus on improving the synthesis procedure. To clarify the precise interactions and processes by which these nanoparticles exhibit their biological efficiency, in-depth mechanistic studies are necessary. Furthermore, to confirm the therapeutic potential and evaluate the drug viability of Cur-AgNPs, in vivo study and clinical trials would be needed.
引用
收藏
页码:374 / 385
页数:12
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