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Highly sensitive and selective label-free detection of dopamine in human serum based on nitrogen-doped graphene quantum dots decorated on Au nanoparticles: Mechanistic insights through microscopic and spectroscopic studies
摘要： A rapid, facile and label-free sensing strategy is developed for the detection of dopamine (DA) in the real samples by exploiting nitrogen-doped graphene quantum dots (N-GQDs) decorated on Au nanoparticles (Au@N-GQD). The as-grown Au@N-GQD exhibits strong blue fluorescence at room temperature and the fluorescence intensity is drastically quenched in presence of DA in neutral medium. The mechanistic insight into the DA sensing by Au@N-GQDs is explored here by careful monitoring of the evolution of the interaction of Au NPs and N-GQDs with DA under different conditions through electron microscopic and spectroscopic studies. The highly sensitive and selective detection of DA over a wide range is attributed to the unique core-shell structure formation with Au@N-GQD hybrids. The quenching mechanism involves the ground state complex formation as well as electron transfer from N-GQDs. The presence of Au NPs in Au@N-GQD hybrids accelerates the quenching process (~14 fold higher than bare N-GQDs) by the formation of stable dopamine-o-quinone (DQ) in this present detection scheme. The fluorescence quenching follows the linear Stern-Volmer plot in the range 0-100 μM, establishing its efficacy as a fluorescence-based DA sensor with a limit of detection (LOD) 590 nM, which is ~27 fold lower than the lowest abnormal concentration of DA in serum (16 μM). This sensing scheme is also successively applied to trace DA in Brahmaputra river water sample with LOD 480 nM including its satisfactory recovery (95-112%). Our studies reveal a novel sensing pathway for DA through the core-shell structure formation and it is highly promising for the design of efficient biological and environmental sensor.
关键词： Dopamine,Fluorescence quenching,Nitrogen-doped graphene quantum dots,Colorimetric sensing,Core-shell structure,Gold nanoparticles
更新于2025-11-21 11:01:37
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Gold nanoparticle-based plasmonic probe for selective recognition of adenosine
摘要： Adenosine, as an endogenous molecule in organisms, plays an essential role in biological processes. Here, a plasmonic probe, creatinine-Ag+/gold nanoparticle (AuNPs), is assembled for adenosine detection based on synergistic coordination on AuNPs. The A650 nm/520 nm values of AuNPs system change linearly with adenosine concentration over a range of 1.0–5.0 μM and the detection limits reached 45 nM. The adenosine detection is realized within 4 min. Furthermore, the quantitative detection of adenosine is realized by eyedropper (a function in Microsoft’s PowerPoint) for analyzing RGB value changes of colorimetric assay. Therefore, this sensor can provide accurate and rapid assay of adenosine in patients’ serum sample without complicated instrumentations.
关键词： colorimetric assay,adenosine detection,eyedropper function,gold nanoparticle,plasmonic probe
更新于2025-11-19 16:56:42
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A mitochondria-targeted ratiometric fluorescent probe for detection of SO2 derivatives in living cells and in vivo
摘要： A new near-infrared (NIR) ?uorescent probe for colorimetric and ratiometric detection of SO2 derivatives was developed based on conjugated hybrid coumarin-hemicyanine. The probe can detect HSO3?/SO32? in HEPES bu?er (10 mM, pH 7.4, with 10% DMF, v/v) with a large emission shift (259 nm). Importantly, it was successfully used for ?uorescence imaging of endogenous bisul?te in BT-474 cells and zebra?sh.
关键词： Near-infrared ?uorescent probe,SO2 derivatives,Mitochondria-targeted,Ratiometric,Colorimetric
更新于2025-11-19 16:56:35
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Proton Triggered Colorimetric and Fluorescence Response of a Novel Quinoxaline Compromising a Donor-Acceptor System
摘要： Quinoxaline-based novel acid-responsive probe Q1 was designed on the basis of a conjugated donor-acceptor (D-A) subunit. Q1 shows colorimetric and fluorometric changes through protonation and deprotonation in dichloromethane. With the addition of the trifluoroacetic acid (TFA), UV-vis absorption spectral changes in peak intensity of Q1 was observed. Moreover, the appearance of a new peaks at 284 nm 434 nm in absorption spectra with the addition of TFA indicating protonation of quinoxaline nitrogen and form Q1.H+ and Q1.2H+. The emission spectra display appearance of new emission peak at 515 nm. The optical property variations were supported by time resolved fluorescence studies. The energy band gap was calculated by employing cyclic voltammetry and density functional calculations. Upon addition of triethylamine (TEA) the fluorescence emission spectral changes of Q1 are found to be reversible. Q1 shows color changes from blue to green in basic and acidic medium, respectively. The paper strip test was developed for making Q1 a colorimetric and fluorometric indicator.
关键词： proton sensor,quinoxaline,fluorescent,colorimetric,reversible sensor
更新于2025-11-19 16:46:39
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A novel rhodamine-based turn-on probe for fluorescent detection of Au3+ and colorimetric detection of Cu2+
摘要： In this work, we design and synthesize the novel probe RC through introduction the 1-aza-4,13-dithia-15-crown-5 ring into the structure of rhodamine 6G hydrazide, where the N atom of crown ring is responsible for quenching of rhodamine fluorescence. The compound obtained behaves as multifunctional cation sensor providing selective fluorescent response to Au3+ and selective colorimetric response to Cu2+ ions in aqueous acetonitrile (1/1, v/v) at pH 7.0. The use of 10-5 M RC solution allowed reliable determination of target cations in the presence of a wide range of environmentally relevant ions with detection limits of 2×10-6 M and 5×10-7 M for gold and copper, respectively.
关键词： Colorimetric probe,Cu,Sensor,Rhodamine,Fluorescent probe,Au
更新于2025-11-19 16:46:39
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Non-enzymatic sensing of dopamine by localized surface plasmon resonance using carbon dots-functionalized gold nanoparticles
摘要： A highly selective, sensitive, and rapid colorimetric sensor for the determination of dopamine (DA) was developed using the color change of S-doped carbon dots functionalized gold nanoparticles (S-CDs@Au NPs). The base of the method is the formation of a complex between the amine groups of dopamine with carboxylic groups of S-CDs@Au NPs followed by their aggregation with Fe3+ ions which acts as the linkers causing a red shift from 520 to 670 nm in the localized surface plasmon peak of S-CDs@Au NPs. The ratio of absorbance intensity at 670 nm to 520 nm was monitored as the analytical signal for determination of dopamine. The parameters affecting the analytical signal including reaction time, solution pH, the concentration of Au NPs and concentration of Fe3+ were optimized. At optimized conditions, the calibration curve was linear in the concentration range of 0.81-16.80 μM of dopamine. The detection and quantification limits were 0.23 μM and 0.77 μM, respectively. The intra-day and inter-day relative standard deviation (RSDs) at 5.0 μM of DA were 3.9% and 5.6%, respectively (n = 5). The applicability of the method for determination of DA in dopamine ampoule, urine and serum human samples was investigated.
关键词： Carbon dots,Localized surface plasmon resonance,Colorimetric chemical sensor,Dopamine,Gold nanoparticles
更新于2025-11-14 15:18:02
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Colloidally Stable Monolayer Nanosheets with Colorimetric Responses
摘要： Despite the discovery of chromogenic-layered materials for decades of years, fabrication of colloidally stable monolayer organic 2D nanosheets in aqueous media with colorimetric responses is still challenging. Herein reported is the first solution synthesis of chromic monolayer nanosheets via the topochemical polymerization of self-assembled amphiphilic diacetylenes in aqueous media. The polydiacetylene (PDA) nanosheets are ≈3–4 nm thick in solution and only ≈1.9 nm thick in the dried state, while the lateral size can reach several micrometers. Moreover, the aqueous stability endows PDA nanosheets with excellent processability, which can further assemble into films via vacuum filtration or act as an ink for high-resolution inkjet printing. The filtrated films and printed patterns exhibit fully reversible blue-to-red thermochromism, and the film also displays an interesting reversible colorimetric transition in response to near-infrared light, which is not reported for other PDA-only systems. The present colloidal PDA nanosheets should represent a new kind of chromic organic 2D nanomaterials that may be applied as novel building blocks for developing intelligent hybrid materials and may also find diverse sensing, display and/or anticounterfeiting applications.
关键词： colorimetric responses,monolayer nanosheets,colloidal stability,polydiacetylene
更新于2025-09-23 15:23:52
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A Simple Colorimetric and Fluorescent Sensor to Detect Organophosphate Pesticides Based on Adenosine Triphosphate-Modified Gold Nanoparticles
摘要： A simple and dual modal (colorimetric and fluorescent) sensor for organophosphate pesticides with high sensitivity and selectivity using adenosine triphosphate (ATP)- and rhodamine B-modified gold nanoparticles (RB-AuNPs), was successfully fabricated. This detection for ethoprophos afforded colorimetric and fluorescence imaging changes visualization. The quantitative determination was linearly proportional to the amounts of ethoprophos in the range of a micromolar scale (4.0–15.0 μM). The limit of detection for ethoprophos was as low as 37.0 nM at 3σ/k. Moreover, the extent application of this simple assay was successfully demonstrated in tap water samples with high reliability and applicability, indicating remarkable application in real samples.
关键词： multimodal assay,ethoprophos detection,gold nanoparticles,colorimetric and fluorescent sensor,organophosphate pesticides
更新于2025-09-23 15:23:52
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A Simple Rhodanine-Based Fluorescent Sensor for Mercury and Copper: The recognition of Hg2+ in aqueous solution, and Hg2+/Cu2+ in organic solvent
摘要： Detection of copper and mercury attracts important in most environmental and biological systems. In this study, the simple probe 2-OxI-Rh containing rhodanine core was synthesized by a green approach and sensing properties were studied using colorimetric and fluorometric detection. The research indicated that the specific ion affinity for Hg2+ ions in aqua systems and the multi-ion affinity for Hg2+ and Cu2+ in organic solvent results in drastic color and spectral changes. According to the data obtained, while the peak intensity increases at 390 nm, the peak intensity decreased at 272 nm in the absorption spectrum of 2-OxI-Rh and an increase in fluorescence intensity of 2-OxI-Rh were observed in the presence of Hg2+ and Cu2+ ions. The binding ratio of 2-OxI-Rh to Hg2+ and Cu2+ were found to be 1:1 according to Job's plot experiments. The binding constants were calculated using the Benesi-Hildebrand equation and found to be 2.15×104 M?1 for Hg2+ and 1.21×104 M?1 for Cu2+. Based on these concentration dependent fluorescence changes, the limit of detection (LOD) values were also calculated and found to be 3.36 μM for Hg2+ and 2.31 μM for Cu2+, which is the range of copper that should be in the blood (11.8–23.6 μM). As a result of all these studies, we can understand that prove 2-OxI-Rh, which is non-toxic, is a good selective candidate turn-on sensor that can be used for Hg2+ and Cu2+ detection in different solvent systems.
关键词： oxindole,Rhodanine,colorimetric,turn-on sensor.,mercury,chemosensor,copper
更新于2025-09-23 15:23:52
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Sensitive detection and imaging of endogenous peroxynitrite using a benzo[d]thiazole derived cyanine probe
摘要： Peroxynitrite is a short-lived endogenous reactive species and plays important roles in many physiological and pathological processes. In this work, we synthesized a near-infrared probe based on the structure of benzothiazole derived cyanine for determination of peroxynitrite (ONOO-). The designed probe specifically reacted with ONOO- through oxidative cleavage of conjugated C?C double bonds and generating the non-fluorescent product. Meanwhile, the characteristic absorption of the probe at 630 nm greatly decreased after reaction with ONOO-, accompanied by drastic color change from bright blue to green yellow, which exhibited a distinct visual feature. It was demonstrated that the probe could be used to measure ONOO- in a dose-response manner and had a detection limit lower as 26 nM. Furthermore, the probe Cy-SN was applied for the imaging of endogenous ONOO- in living cells by confocal microscopy, which showed good cell permeability and low cytotoxicity. Successful application of probe for exogenous colorimetric detection and endogenous fluorescence imaging of ONOO- is suggesting its great potential applications in biological analysis.
关键词： Colorimetric,Peroxynitrite,Benzothiazole derived cyanine,Fluorescent probe,Endogenous fluorescence imaging
更新于2025-09-23 15:23:52