Akshay Kodiyawala, Arindam Mondal, Suban K. Sahoo, Subrata Dutta
{"title":"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","authors":"Akshay Kodiyawala, Arindam Mondal, Suban K. Sahoo, Subrata Dutta","doi":"10.1016/j.jlumin.2024.120982","DOIUrl":null,"url":null,"abstract":"<div><div>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⁻/SO₃<sup>2</sup>⁻ 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 (λ<sub>em</sub> = 488 nm) and HSA (λ<sub>em</sub> = 720 nm). It also distinguishes between nucleophilic attacks by HSO₃⁻/SO₃<sup>2</sup>⁻ on free AHN probe (λ<sub>em</sub> = 488 nm) and HSA-bound AHN (λ<sub>em</sub> = 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, HSO<sub>3</sub><sup>−</sup> can be detected by using simple cotton wool or filter paper.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"277 ","pages":"Article 120982"},"PeriodicalIF":3.3000,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A dual channel NIR-fluorescence probe for simultaneous and independent sensing of SO2 and HSA\",\"authors\":\"Akshay Kodiyawala, Arindam Mondal, Suban K. Sahoo, Subrata Dutta\",\"doi\":\"10.1016/j.jlumin.2024.120982\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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⁻/SO₃<sup>2</sup>⁻ 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 (λ<sub>em</sub> = 488 nm) and HSA (λ<sub>em</sub> = 720 nm). It also distinguishes between nucleophilic attacks by HSO₃⁻/SO₃<sup>2</sup>⁻ on free AHN probe (λ<sub>em</sub> = 488 nm) and HSA-bound AHN (λ<sub>em</sub> = 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, HSO<sub>3</sub><sup>−</sup> can be detected by using simple cotton wool or filter paper.</div></div>\",\"PeriodicalId\":16159,\"journal\":{\"name\":\"Journal of Luminescence\",\"volume\":\"277 \",\"pages\":\"Article 120982\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-11-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Luminescence\",\"FirstCategoryId\":\"101\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022231324005465\",\"RegionNum\":3,\"RegionCategory\":\"物理与天体物理\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OPTICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231324005465","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
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.
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.