Panda Kamal K, Achary V Mohan M, Phaomie Ganngam, Sahu Hrushi K, Parinandi Narasimham L, Panda Brahma B
Molecular Biology and Genomics Laboratory, Department of Botany, Berhampur University, Berhampur 760 007, India.
Plant Molecular Biology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi 110067, India.
Mutat Res Genet Toxicol Environ Mutagen. 2016 Aug;806:11-23. doi: 10.1016/j.mrgentox.2016.05.006. Epub 2016 Jun 8.
The silver nanoparticles (AgNPs) were synthesized extracellularly from silver nitrate (AgNO3) using kernel extract from ripe mango Mengifera indica L. under four different reaction conditions of the synthesis media such as the (i) absence of the reducing agent, trisodium citrate (AgNPI), (ii) presence of the reducing agent (AgNPII), (iii) presence of the cleansing agent, polyvinyl polypyrrolidone, PVPP (AgNPIII), and (iv) presence of the capping agent, polyvinyl pyrrolidone, PVP (AgNPIV). The synthesis of the AgNPs was monitored by UV-vis spectrophotometry. The AgNPs were characterised by the energy-dispersive X-ray spectroscopy, transmission electron microscopy, X-ray diffraction, and small-angle X-ray scattering. Functional groups on the AgNPs were established by the Fourier transform infrared spectroscopy. The AgNPs (AgNPI, AgNPII, AgNPIII and AgNPIV) were spherical in shape with the diameters and size distribution-widths of 14.0±5.4, 19.2±6.6, 18.8±6.6 and 44.6±13.2nm, respectively. Genotoxicity of the AgNPs at concentrations ranging from 1 to 100mgL(-1) was determined by the Lathyrus sativus L. root bioassay and several endpoint assays including the generation of reactive oxygen species and cell death, lipid peroxidation, mitotic index, chromosome aberrations (CA), micronucleus formation (MN), and DNA damage as determined by the Comet assay. The dose-dependent induction of genotoxicity of the silver ion (Ag(+)) and AgNPs was in the order Ag(+)>AgNPII>AgNPI>AgNPIV>AgNPIII that corresponded with their relative potencies of induction of DNA damage and oxidative stress. Furthermore, the findings underscored the CA and MN endpoint-based genotoxicity assay which demonstrated the genotoxicity of AgNPs at concentrations (≤10mgL(-1)) lower than that (≥10mgL(-1)) tested in the Comet assay. This study demonstrated the protective action of PVPP against the genotoxicity of AgNPIII which was independent of the size of the AgNPs in the L. sativus L. root bioassay system.
利用成熟芒果(杧果)的果仁提取物,在四种不同合成介质反应条件下,从硝酸银(AgNO₃)中胞外合成了银纳米颗粒(AgNPs)。这四种条件分别为:(i)不存在还原剂柠檬酸三钠(AgNPI);(ii)存在还原剂(AgNPII);(iii)存在清洁剂聚乙烯基聚吡咯烷酮(PVPP,AgNPIII);(iv)存在封端剂聚乙烯基吡咯烷酮(PVP,AgNPIV)。通过紫外可见分光光度法监测AgNPs的合成过程。利用能量色散X射线光谱、透射电子显微镜、X射线衍射和小角X射线散射对AgNPs进行表征。通过傅里叶变换红外光谱确定AgNPs上的官能团。AgNPs(AgNPI、AgNPII、AgNPIII和AgNPIV)呈球形,直径分别为14.0±5.4、19.2±6.6、18.8±6.6和44.6±13.2nm,尺寸分布宽度各异。采用香豌豆根生物测定法以及包括活性氧生成与细胞死亡、脂质过氧化、有丝分裂指数、染色体畸变(CA)、微核形成(MN)和彗星试验测定的DNA损伤等多种终点测定法,确定了浓度范围为1至100mgL⁻¹的AgNPs的遗传毒性。银离子(Ag⁺)和AgNPs遗传毒性的剂量依赖性诱导顺序为Ag⁺>AgNPII>AgNPI>AgNPIV>AgNPIII,这与其诱导DNA损伤和氧化应激的相对效力相对应。此外,研究结果强调了基于CA和MN终点的遗传毒性测定法,该方法表明,在彗星试验中测试的浓度(≥10mgL⁻¹)以下的浓度(≤10mgL⁻¹)时,AgNPs具有遗传毒性。本研究证明了PVPP在香豌豆根生物测定系统中对AgNPIII遗传毒性的保护作用,且该作用与AgNPs的大小无关。