Adachi Kenta, Azakami Hiro, Yamauchi Miyuki, Koshoji Moeka, Yamamoto Asami, Tanaka Shohei
Department of Chemistry, Graduate School of Sciences & Technology for Innovation, Yamaguchi University, Yamaguchi 753-8512, Japan.
Department of Chemistry, Faculty of Science, Yamaguchi University, Yamaguchi 753-8512, Japan.
ACS Omega. 2024 Apr 15;9(17):18957-18972. doi: 10.1021/acsomega.3c09239. eCollection 2024 Apr 30.
Herein are presented the results of experiments designed to evaluate the effectiveness of host-guest interactions in improving the sensitivity of colorimetric detection based on surface-enhanced photochromic phenomena of tungsten(VI) oxide (WO) nanocolloid particles. The UV-induced photochromic coloration of WO nanocolloid particles in the presence of aromatic α-amino acid (AA), l-phenylalanine (Phe) or l-2-phenylglycine (Phg), and heptakis(2,3,6-tri--methyl)-β-cyclodextrin (TMβCDx) in an aqueous system was investigated using UV-vis absorption spectrometry. The characteristics of the adsorption modes and configurations of AAs on the WO surface have also been identified by using a combination of adsorption isotherm analysis and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR). A distinct linear relationship was observed between the concentration of AAs adsorbed on the WO nanocolloid particles and the initial photochromic coloration rate in the corresponding UV-irradiated colloidal WO in aqueous media, indicating that a simple and sensitive quantification of AAs can be achieved from UV-induced WO photochromic coloration without any complicated preprocessing. The proposed colorimetric assay in the Phe/TMβCDx/WO ternary aqueous system had a linear range of 1 × 10 to 1 × 10 mol dm for Phe detection, with a limit of detection of 8.3 × 10 mol dm. The combined results from UV-vis absorption, ATR-FTIR, and adsorption isotherm experiments conclusively indicated that the TMβCDx-complexed Phe molecules in the Phe/TMβCDx/WO ternary aqueous system are preferentially and strongly inner-sphere adsorbed on the WO surface, resulting in a more significant surface-enhanced photochromic phenomenon. The findings in this study provided intriguing insights into the design and development of the "label-free" colorimetric assay system based on the surface-enhanced photochromic phenomenon of the WO nanocolloid probe.
本文展示了一系列实验的结果,这些实验旨在评估主客体相互作用对基于氧化钨(WO)纳米胶体颗粒表面增强光致变色现象的比色检测灵敏度的提升效果。使用紫外可见吸收光谱法研究了在水性体系中,芳香族α-氨基酸(AA)、L-苯丙氨酸(Phe)或L-2-苯甘氨酸(Phg)以及七(2,3,6-三-O-甲基)-β-环糊精(TMβCDx)存在下,WO纳米胶体颗粒的紫外诱导光致变色着色情况。通过吸附等温线分析和衰减全反射傅里叶变换红外光谱(ATR-FTIR)相结合的方法,还确定了氨基酸在WO表面的吸附模式和构型特征。在水性介质中,观察到吸附在WO纳米胶体颗粒上的氨基酸浓度与相应紫外辐照的胶体WO中的初始光致变色着色速率之间存在明显的线性关系,这表明无需任何复杂的预处理,就可以通过紫外诱导的WO光致变色着色实现对氨基酸的简单而灵敏的定量分析。在Phe/TMβCDx/WO三元水性体系中提出的比色测定法用于检测Phe时,线性范围为1×10⁻⁶至1×10⁻⁵mol dm⁻³,检测限为8.3×10⁻⁷mol dm⁻³。紫外可见吸收、ATR-FTIR和吸附等温线实验的综合结果最终表明,在Phe/TMβCDx/WO三元水性体系中,与TMβCDx络合的Phe分子优先且强烈地以内层球的形式吸附在WO表面,从而导致更显著的表面增强光致变色现象。本研究的结果为基于WO纳米胶体探针表面增强光致变色现象的“无标记”比色测定系统的设计和开发提供了有趣的见解。