Sivakumar Allur Subramaniyan, Krishnaraj Chandran, Sheet Sunirmal, Rampa Dileep Reddy, Kang Da Rae, Belal Shah Ahmed, Kumar Abhay, Hwang In Ho, Yun Soon-Il, Lee Yang Soo, Shim Kwan Seob
Department of Animal Biotechnology, Chonbuk National University, Jeonju, 561-756, Republic of Korea.
Department of Food Science and Technology, Chonbuk National University, Jeonju, 561-756, Republic of Korea.
In Vitro Cell Dev Biol Anim. 2017 Aug;53(7):632-645. doi: 10.1007/s11626-017-0150-5. Epub 2017 May 1.
The present study evaluates in vitro cytotoxic effects and the mode of interaction of biologically synthesized Ag and Au nanoparticles (NPs) using Brassica oleracea L. var. capitata f. rubra (BOL) against HT-1080 cancer cells and bacterial cells as well as their wound healing efficacy using a mouse model. UV-visible spectroscopy, scanning electron microscopy, high-resolution transmission electron microscopy, and energy-dispersive X-ray analysis have ascertained the formation of nano-sized Ag and Au particles. Fourier transform infrared analysis has confirmed that polyphenol and amide groups in BOL act as capping as well as reducing agents. The free radical scavenging activity under in vitro conditions is found to be higher for the Ag NPs when compared to the Au NPs. Acridine orange-ethidium bromide dual staining and comet assay have indicated that the cytotoxic effects are mediated through nuclear morphological changes and DNA damage. The intracellular localization of Ag and Au NPs in HT-1080 cells and their subsequent effect on apoptosis and necrosis were analyzed by flow cytometry while the mode of interaction was established by scanning electron microscopy under field emission mode and by bio-transmission electron microscopy. These methods of analysis clearly revealed that the Ag and Au NPs have easily entered and accumulated into the cytosol and nucleus, resulting in activation of inflammatory and apoptosis pathways, which in turn cause damage in DNA. Further, mRNA and protein expression of caspase-3 and caspase-7, TNF-α, and NF-κB have provided sufficient clues for induction of intrinsic and extrinsic apoptosis and inflammatory pathways in Ag NP- and Au NP-treated cells. Evaluation of wound healing properties of Ag and Au NPs using a mouse model indicates rapid healing of wounds. In addition, no clear toxic effects and no nuclear abnormalities in peripheral blood cells are observed. Ag NPs appear to be a better anticancer therapeutic agent than Au NPs. Nonetheless, both Ag NPs and Au NPs show potential for promoting topical wound healing without any toxic effects. Graphical abstract Schematic representation of biological synthesis of Ag and Au NPs and its application on cancer and wound healing.
本研究评估了利用红甘蓝(Brassica oleracea L. var. capitata f. rubra,BOL)生物合成的银和金纳米颗粒(NPs)对HT-1080癌细胞和细菌细胞的体外细胞毒性作用及相互作用模式,以及使用小鼠模型评估它们的伤口愈合功效。紫外可见光谱、扫描电子显微镜、高分辨率透射电子显微镜和能量色散X射线分析已确定了纳米尺寸银和金颗粒的形成。傅里叶变换红外分析证实,BOL中的多酚和酰胺基团充当封端剂和还原剂。体外条件下,银纳米颗粒的自由基清除活性高于金纳米颗粒。吖啶橙-溴化乙锭双重染色和彗星试验表明,细胞毒性作用是通过核形态变化和DNA损伤介导的。通过流式细胞术分析了银和金纳米颗粒在HT-1080细胞中的细胞内定位及其对细胞凋亡和坏死的后续影响,同时通过场发射模式下的扫描电子显微镜和生物透射电子显微镜确定了相互作用模式。这些分析方法清楚地表明,银和金纳米颗粒很容易进入并积聚到细胞质和细胞核中,导致炎症和细胞凋亡途径的激活,进而造成DNA损伤。此外,半胱天冬酶-3和半胱天冬酶-7、肿瘤坏死因子-α和核因子-κB的mRNA和蛋白质表达为银纳米颗粒和金纳米颗粒处理的细胞中内源性和外源性细胞凋亡及炎症途径的诱导提供了充分线索。使用小鼠模型评估银和金纳米颗粒的伤口愈合特性表明伤口愈合迅速。此外,未观察到明显的毒性作用,外周血细胞也未出现核异常。银纳米颗粒似乎比金纳米颗粒是更好的抗癌治疗剂。尽管如此,银纳米颗粒和金纳米颗粒都显示出促进局部伤口愈合且无任何毒性作用的潜力。图形摘要 银和金纳米颗粒生物合成及其在癌症和伤口愈合中的应用示意图