光谱学与光谱分析, 2011, 31 (5): 1371, 网络出版: 2011-05-30  

适配体修饰金硒纳米合金共振散射光谱法检测痕量Hg2+

Resonance Scattering Detection of Trace Hg2+ Using Aptamer Modified AuSe Nanoalloy
作者单位
广西师范大学环境与资源学院, 珍稀濒危动植物生态与环境保护省部共建教育部重点实验室, 广西 桂林 541000
摘要
用硼氢化钠还原法制备了金硒(AuSe)纳米合金。 用单链核酸适配体(aptamer)修饰AuSe纳米合金制备了汞离子的核酸适配体纳米探针(Apta-AuSe)。 在pH 6.8 Na2HPO4-NaH2PO4缓冲溶液中及NaCl存在下, Apta-AuSe纳米探针亦不聚集; 当Hg2+存在时, 它可以稳定aptamer序列中的T-T错配, 形成较稳定的双链T-Hg2+-T错配物, 从而使释放出来的AuSe纳米合金聚集形成较大的微粒, 导致590 nm处共振散射峰增强。 Hg2+浓度在1.3~1 466 nmol·L-1范围内与共振散射光强度呈良好线性关系, 其回归方程和检出限分别为ΔI590 nm=0.603c+2.0和0.74 nmol·L-1。 该方法用于水样中Hg2+的检测, 结果满意。
Abstract
Under the condition of sodium citrate as stabilizer, the gold-selenium (AuSe) nano-alloy was prepared by sodium borohydride reduction procedure, and was modified by single-strand aptamer to obtain an aptamer nano-alloy probe (apta-AuSe) for Hg(Ⅱ). In pH 6.8 Na2HPO4-NaH2PO4 buffer solution and in the presence of NaCl of 33 mmol·L-1, the Apta-AuSe probe is not aggregation. The apta-AuSe interacts with Hg2+ to form stable double-strand T-Hg(Ⅱ)-T mismatches and to release AuSe nano-alloy particles from the probe. The released AuSe nano-alloy particles (20∶1) aggregated to form bigger clusters that resulted in the resonance scattering (RS) intensity (I590 nm) increasing at 590 nm. The increased intensity ΔI590 nm was proportional to the Hg2+ concentration from 1.3 to 1 466 nmol·L-1, with a detection limit of 0.74 nmol·L-1.The regress equation was ΔI590 nm=0.603c+2.0. Thus, a new resonance scattering (RS) spectroscopy of apta-AuSe was applied to the analysis of trace mercury ion. This simple, rapid, selective and sensitive aptamer AuSe nano-alloy RS assay was applied to the determination of Hg2+ in wastewater, with satisfactory results.

蒋治良, 张轶, 覃惠敏, 周莲平, 梁爱惠, 王鹏飞, 欧阳辉祥. 适配体修饰金硒纳米合金共振散射光谱法检测痕量Hg2+[J]. 光谱学与光谱分析, 2011, 31(5): 1371. JIANG Zhi-liang, ZHANG Yi, QIN Hui-min, ZHOU Lian-ping, LIANG Ai-hui, WANG Peng-fei, OUYANG Hui-xiang. Resonance Scattering Detection of Trace Hg2+ Using Aptamer Modified AuSe Nanoalloy[J]. Spectroscopy and Spectral Analysis, 2011, 31(5): 1371.

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