Department of Biochemistry, PSG College of Arts and Science (Autonomous), Affiliated to Bharathiar University, Coimbatore 641014, Tamil Nadu, India.
Department of Nutrition, Dairy Science Division, National Institute of Animal Science, Rural Development Administration, Cheonan-si, Chungcheongnam-do 31000, Republic of Korea.
Int J Biol Macromol. 2020 Apr 15;149:844-852. doi: 10.1016/j.ijbiomac.2020.02.007. Epub 2020 Feb 3.
The biopolymer chitosan is currently in widespread use because of its nontoxicity, biocompatibility and biodegradability. Therefore, in this study, chitosan extracted from shrimp shells was used to synthesise biogenic silver nanoparticles (AgNPs). UV-visible spectrophotometry of reduced silver nanoparticles in the colloidal solution showed a single peak at 400 nm, confirming the formation of AgNPs. The presence of biomolecules responsible for reducing and capping the biogenic AgNPs was confirmed by FTIR. Surface morphology of the biosynthesised AgNPs was characterised using SEM, and TEM analysis showed the formation of spherical shapes 17-50 nm. The presence of elemental silver in the synthesised biogenic AgNPs was confirmed using EDX and the crystalline structure characterised by XRD. Cytotoxicity of biogenic AgNPs was determined using MTT and the trypan blue exclusion assay. Morphological changes in HepG2 cells were detected by analysis of the DNA ladder pattern via gel electrophoresis, and the IC of HepG2 cell inhibition by AgNPs was 48 μg/ml. The upregulated caspase 3 and 9 protein expression results confirmed cell death via apoptosis. In conclusion, chitosan has the ability to synthesise AgNPs with in vitro apoptotic activities.
由于壳聚糖具有无毒、生物相容性和可生物降解性,因此目前被广泛应用。在本研究中,我们使用从虾壳中提取的壳聚糖来合成生物银纳米粒子(AgNPs)。胶体溶液中还原银纳米粒子的紫外-可见分光光度法在 400nm 处显示出单一峰,证实了 AgNPs 的形成。傅里叶变换红外光谱(FTIR)证实了负责还原和包覆生物 AgNPs 的生物分子的存在。通过扫描电子显微镜(SEM)对生物合成 AgNPs 的表面形态进行了表征,透射电子显微镜(TEM)分析表明形成了 17-50nm 的球形。通过能谱仪(EDX)证实了合成的生物 AgNPs 中存在元素银,通过 X 射线衍射(XRD)对其晶体结构进行了表征。通过 MTT 和台盼蓝排除试验测定了生物 AgNPs 的细胞毒性。通过凝胶电泳分析 DNA 梯状图案检测 HepG2 细胞的形态变化,AgNPs 对 HepG2 细胞的抑制 IC 为 48μg/ml。上调的 caspase 3 和 9 蛋白表达结果证实了细胞通过凋亡而死亡。总之,壳聚糖具有体外诱导细胞凋亡活性的合成 AgNPs 的能力。