用D-A结构的亲脂性红色AIE荧光探针原位可视化3级lfp。

IF 2.6 4区 化学 Q2 BIOCHEMICAL RESEARCH METHODS
Qi Guo, Liqin Lu, Jiansen Wen, Guoxin Zhuang
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引用次数: 0

摘要

指纹是最常见的法医证据之一。然而,目前的数据库需要相对完整的指纹来提取足够的二级特征用于个体识别,从而限制了从犯罪现场收集的部分潜在指纹(lfp)的识别。因此,可视化lfp的3级特征(如宽度、间距、脊孔分布)至关重要。针对这一挑战,本研究开发了一种具有D-A结构的近红外AIE荧光探针(D-TPA-A-TXO)。在乙醇/水二元溶剂中,D-TPA-A-TXO能够快速、清晰地原位可视化各种底物的3级lfp特征。由于其亲脂性,D-TPA-A-TXO迅速从溶液中溶解到lfp的脂质成分中并不断聚集。通过聚集诱导发射(AIE)效应,标准相机可以直接捕获高分辨率的3级LFPs特征图像。这一进展为今后刑事侦查中提高部分指纹的匹配能力提供了重要的技术支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-situ Visualization of Level 3 LFPs Using a Lipophilic Red AIE Fluorescent Probe with a D-A Structure.

Fingerprints are among the most commonly encountered forms of forensic evidence. However, current databases require relatively complete fingerprints to extract sufficient level 2 features for individual identification, thereby limiting the recognition of partial latent fingerprints (LFPs) collected from crime scenes. Therefore, visualizing level 3 features of LFPs (such as width, spacing, and distribution of ridge and pore) is of critical importance. In response to this challenge, this study developed a near-infrared AIE fluorescent probe (D-TPA-A-TXO) with a D-A structure. In ethanol/water binary solvents, D-TPA-A-TXO enabled rapid and distinct in-situ visualization of level 3 LFPs features across various substrates. Owing to its lipophilic nature, D-TPA-A-TXO rapidly dissolved from the solution into the lipid components of LFPs and continuously aggregated. Through the aggregation-induced emission (AIE) effect, high-resolution images of level 3 LFPs features could be directly captured by a standard camera. This advancement provides crucial technical support for enhancing the matching capability of partial fingerprints in future criminal investigations.

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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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