Department of Nutrition, Dairy Science Division, National Institute of Animal Science, Rural Development Administration, Cheonan-si, Chungcheongnam-do 31000, Republic of Korea.
Department of Biochemistry, PSG College of Arts and Science (Autonomous), Affiliated to Bharathiar University, Coimbatore 641014, Tamil Nadu, India.
Int J Biol Macromol. 2020 Dec 15;165(Pt A):1402-1409. doi: 10.1016/j.ijbiomac.2020.10.032. Epub 2020 Oct 9.
In this study, a well-organized, simplistic, and biological route of AgNPs (AgNPs) was synthesized using shrimp shell extracted chitin as reducing, capping and stabilizing factor under the optimized conditions. Also, the anticancer potential of synthesized biogenic AgNPs was evaluated against human hepatocarcinoma (HepG2) cells. Ultraviolet visible spectroscopy (UV-Vis spec) study indicated that the development of AgNPs present in the colloidal solution was single peak at 446 nm. FTIR results showed a strong chemical interaction between the chitin and biogenic AgNPs; whereas, XRD studies confirmed AgNPs presence in the composites. The SEM TEM analytical studies confirmed the synthesized AgNPs had a spherical shape crystalline structure with size ranges from 17 to 49 nm; EDX study also confirmed the percentage of weight and atomic elements available in the colloidal mixture. Furthermore, the synthesized AgNPs showed significant cytotoxic effect on the HepG2 cells with an IC value shown at 57 ± 1.5 μg/ml. The apoptotic and necrotic cell death effects of AgNPs were also confirmed by flow cytometry. The upregulated apoptotic related proteins Bax, cytochrome-c, caspase-3, caspase-9, PARP and downregulated anti-apoptotic related proteins Bcl-2 and Bcl-xl in cancer cells, confirmed the anticancer potential of AgNPs. These findings suggest that the AgNPs possess significant anticancer activity against HepG2 cells which could play major role in the therapeutic drug development to treat cancer in future.
在这项研究中,使用虾壳提取的壳聚糖作为还原剂、封端剂和稳定剂,在优化条件下,通过一种组织良好、简单且具有生物学意义的路线合成了 AgNPs(银纳米粒子)。此外,还评估了合成的生物源 AgNPs 对人肝癌(HepG2)细胞的抗癌潜力。紫外可见光谱(UV-Vis spec)研究表明,胶体溶液中存在的 AgNPs 的发展呈现出 446nm 处的单一峰。FTIR 结果表明壳聚糖和生物源 AgNPs 之间存在强烈的化学相互作用;而 XRD 研究则证实了复合材料中 AgNPs 的存在。SEM TEM 分析研究证实,合成的 AgNPs 具有球形结晶结构,尺寸范围为 17 至 49nm;EDX 研究还证实了胶体混合物中存在的重量和原子元素的百分比。此外,合成的 AgNPs 对 HepG2 细胞表现出显著的细胞毒性作用,IC 值为 57±1.5μg/ml。通过流式细胞术还证实了 AgNPs 的凋亡和坏死细胞死亡效应。凋亡相关蛋白 Bax、细胞色素-c、caspase-3、caspase-9、PARP 的上调和抗凋亡相关蛋白 Bcl-2 和 Bcl-xl 的下调,证实了 AgNPs 的抗癌潜力。这些发现表明,AgNPs 对 HepG2 细胞具有显著的抗癌活性,这可能在未来治疗癌症的治疗药物开发中发挥重要作用。