用于同时独立检测二氧化硫和氢氧化钠的双通道近红外荧光探头

IF 3.3 3区 物理与天体物理 Q2 OPTICS Journal of Luminescence Pub Date : 2024-11-09 DOI:10.1016/j.jlumin.2024.120982
Akshay Kodiyawala, Arindam Mondal, Suban K. Sahoo, Subrata Dutta
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引用次数: 0

摘要

现有的近红外荧光探针只能单独检测 SO₂或 HSA,为了解决这种探针的局限性,我们开发了一种近红外荧光探针(AHN),它能够在 PBS 缓冲液(pH 7.4,10 mM)中同时单独检测 SO₂ 和 HSA。AHN 通过亲核加成碳碳双键来检测 HSO₃-/SO₃2,通过与 HSA 的疏水口袋结合来检测 HSA。探针发出不同的荧光信号,以区分 SO₂(λem = 488 nm)和 HSA(λem = 720 nm)。它还能区分 HSO₃-/SO₃2- 对游离 AHN 探针的亲核攻击(λem = 488 nm)和与 HSA 结合的 AHN(λem = 465 nm)。SO₂ 和 HSA 的检测限分别为 124 nM 和 20.5 nM,SO₂ 在 HSA 存在下的检测限为 22.4 nM。药物竞争研究表明,AHN 特别针对 HSA 蛋白的 I 位点。该探针还能成功检测人工尿液中的 HSA 和实际样品(如水、糖、无酒精葡萄酒和饼干)中的 HSO₃-。此外,使用简单的棉絮或滤纸也能检测到 HSO3-。
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A dual channel NIR-fluorescence probe for simultaneous and independent sensing of SO2 and HSA
To address the limitations of existing NIR-fluorescent probes that only detect either SO₂ or HSA individually, we have developed a NIR-fluorescent probe (AHN) capable of detecting both SO₂ and HSA independently and concurrently in PBS buffer (pH 7.4, 10 mM). AHN detects HSO₃⁻/SO₃2⁻ via nucleophilic addition to a carbon-carbon double bond and HSA via binding to a hydrophobic pocket of HSA. The probe emits distinct fluorescence signals to differentiate between SO₂ (λem = 488 nm) and HSA (λem = 720 nm). It also distinguishes between nucleophilic attacks by HSO₃⁻/SO₃2⁻ on free AHN probe (λem = 488 nm) and HSA-bound AHN (λem = 465 nm). The detection limits for SO₂ and HSA are 124 nM and 20.5 nM, respectively, and a detection limit of 22.4 nM for SO₂ in the presence of HSA. Drug competition studies reveal that AHN specifically targets the site-I of the HSA protein. The probe also successfully detects HSA in artificial urine and HSO₃⁻ in real samples, such as water, sugar, non-alcoholic wine, and biscuits. Furthermore, HSO3 can be detected by using simple cotton wool or filter paper.
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
期刊介绍: The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid. We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.
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