Gatselou Vasiliki, Christodouleas Dionysios C, Kouloumpis Antonios, Gournis Dimitrios, Giokas Dimosthenis L
Department of Chemistry, University of Ioannina, 45110, Ioannina, Greece.
Department of Chemistry, University of Massachusetts Lowell, Lowell, MA 01854, United States.
Anal Chim Acta. 2016 Aug 17;932:80-7. doi: 10.1016/j.aca.2016.05.029. Epub 2016 May 25.
This work reports a new approach for the determination of phenolic compounds based on their interaction with citrate-capped rhodium nanoparticles. Phenolic compounds (i.e., catechins, gallates, cinnamates, and dihydroxybenzoic acids) were found to cause changes in the size and localized surface plasmon resonance of rhodium nanoparticles, and therefore, give rise to analyte-specific spectral and color transitions in the rhodium nanoparticle suspensions. Upon reaction with phenolic compounds (mainly dithydroxybenzoate derivatives, and trihydroxybenzoate derivatives), new absorbance peaks at 350 nm and 450 nm were observed. Upon reaction with trihydroxybenzoate derivatives, however, an additional absorbance peak at 580 nm was observed facilitating the speciation of phenolic compounds in the sample. Both absorbance peaks at 450 nm and 580 nm increased with increasing concentration of phenolic compounds over a linear range of 0-500 μM. Detection limits at the mid-micromolar levels were achieved, depending on the phenolic compound involved, and with satisfactory reproducibility (<7.3%). On the basis of these findings, two rhodium nanoparticles-based assays for the determination of the total phenolic content and total catechin content were developed and applied in tea samples. The obtained results correlated favorably with commonly used methods (i.e., Folin-Ciocalteu and aluminum complexation assay). Not the least, the finding that rhodium nanoparticles can react with analytes and exhibit unique localized surface plasmon resonance bands in the visible region, can open new opportunities for developing new optical and sensing analytical applications.
这项工作报道了一种基于酚类化合物与柠檬酸盐包覆的铑纳米颗粒相互作用来测定酚类化合物的新方法。发现酚类化合物(即儿茶素、没食子酸盐、肉桂酸盐和二羟基苯甲酸)会导致铑纳米颗粒的尺寸和局域表面等离子体共振发生变化,因此,在铑纳米颗粒悬浮液中产生分析物特异性的光谱和颜色转变。与酚类化合物(主要是二羟基苯甲酸酯衍生物和三羟基苯甲酸酯衍生物)反应时,在350nm和450nm处观察到新的吸收峰。然而,与三羟基苯甲酸酯衍生物反应时,在580nm处观察到一个额外的吸收峰,有助于样品中酚类化合物的形态分析。在0 - 500μM的线性范围内,450nm和580nm处的吸收峰均随酚类化合物浓度的增加而增加。根据所涉及的酚类化合物,检测限达到中微摩尔水平,且具有令人满意的重现性(<7.3%)。基于这些发现,开发了两种基于铑纳米颗粒的测定总酚含量和总儿茶素含量的方法,并应用于茶叶样品。获得的结果与常用方法(即福林 - 酚法和铝络合测定法)具有良好的相关性。最重要的是,铑纳米颗粒能够与分析物反应并在可见光区域呈现独特的局域表面等离子体共振带这一发现,为开发新的光学和传感分析应用开辟了新的机遇。