Visual Detection of Cadmium and Glutathione by Dicyanoisophorone Fluorescent Probe and its Portable Application.

IF 3.1 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Panru Zu, Yanchao Yu, Bolin Li, Jun You, Wenju Wu, Mianyuan Wu
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引用次数: 0

Abstract

A novel fluorescent probe XL derived from dicyanoisophorone was designed and synthesized, achieving successful sequential detection of Cd2+ and GSH. As probe XL interacted with Cd2+, the emission wavelength redshifted from 565 nm to 650 nm, accompanied by enhanced red fluorescence, which realising a fluorescence turn-on response in the near-infrared region. A large Stokes shift (121 nm) combined with low detection limit (0.484 µmol/L) were key advantages of the detection process. However, due to high affinity of GSH for Cd2+, as addition of GSH to complex XL-Cd2+, fluorescence response in NIR region was switched off and emission peak was blue-shifted back to 565 nm. Detection limit for GSH was calculated as 0.784 µmol/L, a value significantly lower than its normal intracellular concentration, and the assay process with good sensitivity. Notably, probe XL showed an immediate response (3 s) to Cd2+ and GSH, with a clear visual detection in natural light. In addition, XL could be used to detect Cd2+ and GSH in real samples and achieve linked applications with smartphones.

双氰异膦酮荧光探针视觉检测镉和谷胱甘肽及其便携式应用。
设计并合成了一种新型的双氰异佛酮荧光探针XL,成功实现了Cd2+和GSH的序列检测。当XL探针与Cd2+相互作用时,发射波长从565 nm红移到650 nm,并伴有增强的红色荧光,在近红外区域实现荧光开启响应。大Stokes位移(121 nm)和低检出限(0.484µmol/L)是该检测方法的主要优点。然而,由于GSH对Cd2+的高亲和力,在配合物XL-Cd2+中加入GSH后,近红外区的荧光响应被关闭,发射峰蓝移回565 nm。计算出谷胱甘肽的检出限为0.784µmol/L,显著低于胞内正常浓度,具有良好的灵敏度。值得注意的是,XL探针对Cd2+和GSH表现出即时反应(3 s),在自然光下具有清晰的视觉检测。此外,XL可用于检测真实样品中的Cd2+和GSH,并实现与智能手机的链接应用。
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来源期刊
Journal of Fluorescence
Journal of Fluorescence 化学-分析化学
CiteScore
4.60
自引率
7.40%
发文量
203
审稿时长
5.4 months
期刊介绍: Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.
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