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环糊精辅助的氧化钨纳米颗粒表面增强光致变色现象用于苯丙氨酸的无标记比色检测

Cyclodextrin-Assisted Surface-Enhanced Photochromic Phenomena of Tungsten(VI) Oxide Nanoparticles for Label-Free Colorimetric Detection of Phenylalanine.

作者信息

Adachi Kenta, Azakami Hiro, Yamauchi Miyuki, Koshoji Moeka, Yamamoto Asami, Tanaka Shohei

机构信息

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.

出版信息

ACS Omega. 2024 Apr 15;9(17):18957-18972. doi: 10.1021/acsomega.3c09239. eCollection 2024 Apr 30.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/611d/11064177/ea8145b9f43b/ao3c09239_0009.jpg

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