利用马兜铃生物合成纳米银。乙酸乙酯提取物:表征及体外抗肺腺癌细胞活性

H.S. Anil Kumar , Santosh Mallikarjun Bhavi , Sapam Riches Singh , Bothe Thokchom , Ramesh Babu Yarajarla , D. Kotresha
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引用次数: 0

摘要

肺癌仍然是癌症相关死亡的主要原因,需要新的治疗策略。马兜铃传统上对其在癌症治疗中的潜力进行了研究,本研究探索了用其乙酸乙酯提取物绿色合成银纳米颗粒(AgNPs),以评估其对人肺腺癌(NCIH-460)细胞的抗癌潜力。通过颜色变化证实AgNPs的生物合成,并通过UV-Vis光谱、FTIR、XRD、zeta势FE-SEM和TEM进行了表征。紫外可见光谱在450 nm处出现特征吸收峰,证实了纳米颗粒的形成。XRD分析表明AgNPs的晶体性质,FTIR光谱鉴定了参与纳米颗粒稳定的关键官能团,包括O-H, C-H, CC和C-O键。FE-SEM和TEM图像显示AgNPs多分散,大部分为球形,范围为4至171 nm, TEM衍生的平均尺寸为10 nm。Zeta电位分析显示电荷为−26 mV,表明溶液稳定性中等。AgNPs对NCIH-460细胞(IC₅₀= 13.44 µg mL - 1)表现出强大的细胞毒性,同时保留正常的L929细胞(IC₅₀= 196.05 µg mL - 1)。Annexin V/PI和TUNEL实验证实凋亡诱导,而细胞周期分析显示G0/G1期阻滞,支持caspase-3上调。这些发现表明,生物合成的AgNPs是一种很有前景的抗癌药物,能够诱导细胞凋亡和破坏癌细胞增殖,使其成为肺癌治疗的潜在候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biosynthesis of silver nanoparticles using Aristolochia bracteolata Lam. ethyl acetate extract: Characterization and In Vitro anticancer activity against lung adenocarcinoma cells
Lung cancer remains a leading cause of cancer-related mortality, necessitating novel therapeutic strategies. Aristolochia bracteolata Lam. has been traditionally studied for its potential in cancer treatment, and this study explores the green synthesis of silver nanoparticles (AgNPs) using its ethyl acetate extract to evaluate their anticancer potential against human lung adenocarcinoma (NCIH-460) cells. AgNPs biosynthesis was confirmed by a color change and characterized by UV-Vis spectroscopy, FTIR, XRD, zeta potential FE-SEM, and TEM. The UV-Vis spectrum exhibited a characteristic absorption peak at 450 nm, confirming nanoparticle formation. XRD analysis indicated the crystalline nature of AgNPs, while FTIR spectra identified key functional groups involved in nanoparticle stabilization, including O-H, C-H, CC, and C-O bonds. FE-SEM and TEM images showed polydispersed, mostly spherical AgNPs ranging from 4 to 171 nm, with an average TEM-derived size of 10 nm. Zeta potential analysis showed a charge of −26 mV, suggesting moderate stability in solution. The AgNPs exhibited potent cytotoxicity against NCIH-460 cells (IC₅₀ = 13.44 µg mL−1) while sparing normal L929 cells (IC₅₀ = 196.05 µg mL−1). Annexin V/PI and TUNEL assays confirmed apoptosis induction, while cell cycle analysis demonstrated G0/G1 phase arrest, supported by caspase-3 upregulation. These findings suggest biosynthesized AgNPs as promising anticancer agents, capable of inducing apoptosis and disrupting cancer cell proliferation, making them potential candidates for lung cancer therapy.
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