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一个检测痕量汞离子的鱼精DNA修饰纳米金共振散射光谱法
引用本文:凌绍明,李建福,梁爱惠,温桂清,康彩艳,蒋治良.一个检测痕量汞离子的鱼精DNA修饰纳米金共振散射光谱法[J].光谱学与光谱分析,2010,30(2).
作者姓名:凌绍明  李建福  梁爱惠  温桂清  康彩艳  蒋治良
作者单位:1. 广西师范大学,珍稀濒危动植物生态与环境保护教育部重点实验室,广西,桂林,541004;百色学院化学与生命科学系,广西,百色,533000
2. 桂林工学院材料与化学工程系,广西,桂林,541004
3. 广西师范大学,珍稀濒危动植物生态与环境保护教育部重点实验室,广西,桂林,541004
基金项目:国家自然科学基金项目(20667001,20965002);;广西自然科学基金项目(0832260,0991021Z)资助
摘    要:在pH 7.0 Tris-HCl缓冲溶液及0.017 mol.L-1NaCl介质中,鲱鱼精DNA与10 nm的金纳米粒子形成较稳定的结合物使得金纳米粒子不聚集,体系的散射信号较弱。当有Hg2+存在时,DNA与Hg2+形成更稳定的DNA-Hg2+结合物,金纳米粒子聚集导致572 nm处的共振散射峰增强。在3.87μg.mL-1金纳米粒子-11.7μg.mL-1DNA-pH 7.0~17 mmol.L-1NaCl条件下,Hg2+浓度c在3.3~3 333.3 nmol.L-1范围内与572 nm处的共振散射强度增强值ΔI572 nm成良好线性关系,其回归方程、相关系数、检出限分别为ΔI572 nm=0.019c+5.0,0.999 1,2.5 nmol.L-1。该法用于水样分析,结果与冷原子吸收光谱法一致,相对标准偏差为5.1%。

关 键 词:鱼精DNA修饰纳米金  汞离子  共振散射光谱法  

Resonance Scattering Detection of Trace Hg~(2+) Using Herring Sperm NDA Modified Nanogold
LING Shao-ming,LI Jian-fu,LIANG Ai-hui,WEN Gui-qing,KANG Cai-yan,JIANG Zhi-liang.Resonance Scattering Detection of Trace Hg~(2+) Using Herring Sperm NDA Modified Nanogold[J].Spectroscopy and Spectral Analysis,2010,30(2).
Authors:LING Shao-ming  LI Jian-fu  LIANG Ai-hui  WEN Gui-qing  KANG Cai-yan  JIANG Zhi-liang
Institution:LING Shao-ming1,3,LI Jian-fu2,LIANG Ai-hui1,WEN Gui-qing1,KANG Cai-yan1,JIANG Zhi-liang11.Key Laboratory of Ecology of Rare , Endangered Species , Environmental Conservation of Ministry of Education,Guangxi Normal University,Guilin 541004,China2.Department of Materials , Chemical Engineering,Guilin University of Technology,China3.Department of Chemistry , Life Science,Baise College,Baise 533000,China
Abstract:In pH 7.0 tris-HCl buffer solutions and in the presence of 0.017 mol·L~(-1) NaCl,herring sperm DNA was combined with gold nanoparticles in size of 10 nm to form stable complex,and the NaCl did not cause the aggregation of the gold nanopartielea.Upon addition of Hg~(2+),that reacted with DNA to form more stable complex of Hg~(2+)-DNA,and the gold nanoparticles aggregated to from larger nanogold clusters that led to considerable enhancement of the resonance scattering intensity at 572 nm enhanced considerably.The effect of GN concentration,DNA concentration,NaCl concentration,incubation time,and temperature,and ultrasonic irradiation was considered respectively,the conditions of 3.87 μg·mL~(-1) GN,11.7 μg·mL~(-1) DNA,pH 7.0 Tris-HC1 buffer solutions,17 mmol·L~(-1) NaCl,and incubation 10 min at 37℃ under the ultrasonic irradiation were chosen for use.Under the conditions,the enhanced resonance scattering intensity at 572 nm was linear to the Hg~(2+) concentration in the range of 3.3-3 333.3 nmol·L~(-1),with regress equation of △I_(572nm)=0.019c+5.0,coefficient of 0.999 1,and a detection limit of 2.5 nmol·L~(-1) Hg~(2+).Results of interference tests showed that 30 μmol·L~(-1) Mn~(2+),33 μmol·L~(-1) Mg~(2+) and Zn~(2+),100 μmol·L~(-1) Cd~(2+),200 μmol·L~(-1) Fe~(3+),and 420 μmol·L~(-1) Mo~(6+),Pb~(2+) and Cu~(2+) did not interfered with the determination of 0.33 μmol·L~(-1) Hg~(2+).That is,this resonance scattering spectral assay is of good selectivity.This assay was applied to the detection of Hg(Ⅱ)in water sample,with a relative standard deviation of 5.1%,and the results were in agreement with that of the cool vapor atomic absorption spectrophotometry.
Keywords:Herring sperm DNA modified nanogold  Hg2+  Resonance scattering spectrometry  
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