Zhang Ling Ling, Ma Fang Fang, Kuang Yang Fang, Cheng Shu, Long Yun Fei, Xiao Qiu Guo
Key Laboratory of Theoretical Chemistry and Molecular Simulation of Ministry of Education of China, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan, 411201, China; Hunan Xinshao Teachers Training College, China.
Key Laboratory of Theoretical Chemistry and Molecular Simulation of Ministry of Education of China, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan, 411201, China.
Spectrochim Acta A Mol Biomol Spectrosc. 2016 Feb 5;154:98-102. doi: 10.1016/j.saa.2015.10.019. Epub 2015 Oct 24.
A simple, fast and highly sensitive spectrophotometric method for the determination of bovine serum albumin (BSA) has been developed based on the interactions between triangular silver nanoplates (TAgNPs) and BSA in the presence of Britton-Robison buffer solution (BR). Particularly, the wavelength of absorption maximum (λ(max)) of TAgNPs is red shifted in the presence of BSA together with Britton-Robinson buffer solution (BR, pH=2.56), and the color of the solution changed from blue to light blue. This may be due to the interactions between BSA molecules on the surface of TAgNPs through electrostatic forces, hydrogen bonds, hydrophobic effects and van der Waals forces at pH2.56, which leads to the aggregation of TAgNPs. The determination of BSA was achieved by measuring the change of λ(max) corresponding to localized surface plasmon resonance (LSPR) from UV-visible spectrophotometry. It was found that the shift value in the wavelength of absorption maximum (Δλ, the difference in absorption maxima of the TAgNPs/BSA/BR mixture and the TAgNPs/BR mixture) was proportionate to the concentration of BSA in the range of 1.0 ng mL(-1) to 100.0 ng mL(-1) with the correlation coefficient of r=0.9969. The detection limit (3 σ/k) for BSA was found to be as low as 0.5 ng mL(-1).
基于三角形银纳米片(TAgNPs)与牛血清白蛋白(BSA)在 Britton-Robinson 缓冲溶液(BR)存在下的相互作用,开发了一种简单、快速且高度灵敏的分光光度法用于测定牛血清白蛋白(BSA)。特别地,在存在 BSA 和 Britton-Robinson 缓冲溶液(BR,pH = 2.56)的情况下,TAgNPs 的最大吸收波长(λ(max))发生红移,溶液颜色从蓝色变为浅蓝色。这可能是由于在 pH2.56 时,TAgNPs 表面的 BSA 分子通过静电力、氢键、疏水作用和范德华力相互作用,导致 TAgNPs 聚集。通过测量紫外可见分光光度法中对应于局域表面等离子体共振(LSPR)的λ(max)变化来实现 BSA 的测定。结果发现,最大吸收波长的位移值(Δλ,TAgNPs/BSA/BR 混合物与 TAgNPs/BR 混合物吸收最大值的差值)在 1.0 ng mL(-1)至 100.0 ng mL(-1)范围内与 BSA 的浓度成比例,相关系数 r = 0.9969。发现 BSA 的检测限(3σ/k)低至 0.5 ng mL(-1)。