Selective Detection Of Hydrogen Sulfide Research Articles

MOF-based ratiometric fluorescent nanoprobe for quantitative detection of hydrogen sulfide in acute pancreatitis

The timely detection of acute pancreatitis (AP) is crucial for mitigating its severe complications, including pancreatic necrosis and multi-system organ failure. In this work, we developed LMOF-BR, an innovative luminescent metal–organic framework (LMOF)-based ratiometric fluorescent nanoprobe, specifically designed for the sensitive and selective detection of hydrogen sulfide (H2S) in AP. This nanoprobe employs a synthesized LMOF to provide a stable reference signal, and a fluorescent dye (BR) as the target recognizer and signal output unit, enabling H2S detection through single-excitation dual fluorescence emission. The LMOF-BR nanoprobe demonstrates significant advantages, including improved water solubility, superior photostability, a high signal-background ratio, and a low limit of detection (LOD), all of which are crucial for accurate detection in complex biological environments. Successful quantification of H2S in serum samples and AP mouse plasma has been achieved by LMOF-BR nanoprobe, showcasing notable accuracy and precision. The LMOF-BR nanoprobe holds great promise in advancing biosensing technology, particularly for the timely and reliable diagnosis of AP.

Responsive luminescent silver-based metal-organic frameworks for highly sensitive and selective detection of hydrogen sulfide in biological system via a self-assembled headspace separation device

As a highly toxic gas pollutant and also an endogenous gaseous signaling molecule existing in a variety of physiological processes, the rapid and accurate in-field detection of hydrogen sulfide is of great concern. Nevertheless, two drawbacks as for the optical probes for H2S detection, taking about a long time to reach the optical signal balance or the low selectivity, always exist. Herein, by using a highly photoluminescent and H2S-stimuli responsive silver-based metal-organic frameworks (MOFs): Ag-BDC (BDC = 1, 4-benzene dicarboxylate), we demonstrated that the luminescence intensity of Ag-BDC MOFs was inversely proportional to the concentration of H2S due to the Ag–S coordination and the obstruction of ligand-to-metal charge transfer (LMCT) transition process, and there was a quick response time of below 3.0 min. Combined with a simple customized device to separate H2S from the sample, the selectivity of the method for H2S detection could be greatly improved, and no interference would be caused even if the other sulfur-containing species coexisted. The luminescence probe presented a favorable sensitivity within a linear range of 0.1–1000 μM along with a detection limit of 23.7 nM. When employed to assay the endogenous sulfide level in the human serum and mouse brain tissue, the approach showed recoveries from 96.3% to 102% with relative standard derivation (RSD) less than 2.0%. By the integration of the responsive luminescent silver-based MOFs with a simple self-assembled headspace separation device, obviously the present strategy could be beneficial to the development and design of the in-field fast H2S measurement, possessing particular advantages in biological systems to eliminate the potential interferences.

Liposome Based Near-Infrared Sensors for the Selective Detection of Hydrogen Sulfide.

Cyanine dye-based new amphiphilic compound NIR-Amp has been synthesised. NIR-Amp was embedded with phospholipids DOPC and DPPC to form liposomes based nanoscale chemical sensors NIR-Lip1 and NIR-Lip2. Here, two different phospholipids were used to demonstrate the influence of lipid structure, composition and fluidity on sensing of nanosensors. Both the probes show NIR absorption maximum at 790 nm and emission maximum at 815 nm. H2 S-triggered thiolation resulted a remarkable change in color from green to pale yellow. A decrease in UV-Vis absorption and emission in the NIR region was observed only with H2 S. NIR-Lip1 and NIR-Lip2 are highly selective for H2 S with a LOD of 0.57 μM and 1.24 μM, respectively. It was observed that in a solid-like gel state, NIR-Lip1 is slightly more sensitive towards H2 S than fluid-like NIR-Lip2. The H2 S sensing mechanism was confirmed by ESI-mass and infrared (IR) spectroscopic analysis. Based on the high sensitivity and selectivity, NIR-Lip1 was employed to detect H2 S in vegetable samples. Further, the probes are found to be non-toxic and established for H2 S fluorescence imaging in live cells.

Cu-MOF-808 as a Sensing Material for Gaseous Hydrogen Sulfide.

The selective detection of hydrogen sulfide (H2 S) is an important task because of its potentially hazardous effects not only on the environment but also on human health. Here, we present the zirconium-based MOF-808, which was modified with copper salts, as a colorimetric sensor material for the visible, reversible and sensitive H2 S detection at room temperature. The copper cations, which are incorporated in the oxidation state +II, are installed at the inorganic building units (IBUs) of the framework so that they are accessible for interactions with H2 S. The activated copper doped MOF-808 powder shows significant and fast color change in the presence of H2 S, which can be detected by UV-vis spectroscopy. Moreover, the detection process is reversible by heating the material to 120 °C under ambient conditions leading to its decolorization. The detection performance of the material was studied by in situ UV-vis measurements in a reaction chamber. The material was able to respond to 100 ppm H2 S in several cycles of exposure and heating to 120 °C under moist air conditions in a defined wavelength range. This reversibility is very uncommon for copper-based H2 S sensing reactions and highlights the potential of MOFs as selective sensing materials.

Highly Selective Detection of Hydrogen Sulfide by Simple Cu-CNTs Nanocomposites

The presented work is devoted to the preparation of nanocomposites based on multiwall carbon nanotubes (MWCNTs) and copper (Cu) nanoparticles by a simple chemical method, and to study their sensing properties to hydrogen sulfide (H2S) gas. The Cu decorated multiwall carbon nanotubes (MWCNTs/Cu) were prepared by the deposition of very thin Cu layers on the pristine and functionalized multiwall carbon nanotubes (f-MWCNTs) using both physical (electron beam evaporation (EBE)) and chemical (electrochemical deposition) methods. MWCNTs/Cu prepared in the two above-mentioned ways, their sensing properties were studied, and the results were comparatively analyzed. The effect of the chemical functionalization of MWCNTs by oxygen-containing groups on the sensing properties of these f-MWCNT/Cu nanocomposites has been investigated. All the prepared sensors demonstrated high sensitivity and selectivity to H2S in the air at room temperature. The f-MWCNT/Cu structure obtained by the chemical method demonstrated about 5 times (~400%) higher sensitivity (∆R/R0) to H2S gas compared to the similar structure obtained by the physical method. The temperature effect on sensory characteristics (response and self-recovery time) of the f-MWCNTs/Cu structure was also studied.

A water-soluble NIR fluorescent probe capable of rapid response and selective detection of hydrogen sulfide in food samples and living cells

DDAO (1,3-Dichloro-7-hydroxy-9,9-dimethyl-2(9H)-acridone) is a near-infrared (NIR) fluorophore that has received increasing attention in recent years, exhibiting near-infrared emission at 658 nm, low pKa (∼5.0), good water solubility and high quantum yield (Φ = 0.39). The reported DDAO-based fluorescent probes can be applied to biological imaging ofenzymes and other substances in vivo with high sensitivity and selectivity. Herein, using –OCN as the detection group, a novel NIR H2S fluorescent probe DDAO-CN based on DDAO was designed and synthesized. In PBS buffer (10 mM, pH 7.4), probe DDAO-CN displayed specific selection, short response time (within 10 s) and low detection limit (4.3 nM) towards to H2S under the catalysis of CTAB. At the same time, the probe is able to sense H2S gas produced by food spoilage via the fluorescent test strip loaded with DDAO-CN. Moreover, since the probe has optimal pH range (6.0–9.0), it has been successfully used for bioimaging H2S in the HeLa cells with low cytotoxicity.

A fluorous-tag-assisted fluorescent probe for simple and selective detection of hydrogen sulfide: application for turbid dyeing solutions.

Accurate hydrogen sulfide (H2S) detection has attracted much attention because its toxicity may affect aquatic environments and human health. However, recognizing H2S levels by conventional fluorescent probes in turbid wastewater has been challenging because the opaque environment interferes with their photophysical properties. To overcome this limitation, a fluorous-tagging strategy can be used for the development of fluorescent sensors to detect H2S in turbid solutions. The use of fluorescent probe assisted with fluorous-tag allowed for easy isolation of the probe using polytetrafluoroethylene (PTFE) material, while disturbing species were eliminated through a simple aqueous wash. This approach enabled the fluorescent probe to effectively quantify H2S, even in opaque solutions containing organic dyes that could interfere with fluorescence emission.

Planar carbon electrodes for real-time quantification of hydrogen sulfide release from cells.

A planar electrode system was developed to permit the real-time, selective detection of hydrogen sulfide (H2S) from stimulated cells. Planar carbon electrodes were produced via stencil printing carbon ink through a laser cut vinyl mask. Electrodes were preconditioned using a constant potential amperometry methodology to prevent sensor drift resulting from elemental sulfur adsorption. Modification with a bilaminar coating (electropolymerized ortho-phenylenediamine and a fluorinated xerogel) facilitated high selectivity to H2S. To demonstrate the biological application of this planar sensor system, H2S released from 17β-estradiol-stimulated human umbilical vein endothelial cells (HUVECs) was quantified in situ in real-time. Stimulated HUVECs released sustained H2S levels for hours before returning to baseline. Cellular viability assays demonstrated negligible cell cytotoxicity at the electrochemical potentials required for analysis.

A New Ratiometric Fluorescent Probe Based on BODIPY for Highly Selective Detection of Hydrogen Sulfide.

Hydrogen sulfide (H2S) as small molecular signal messenger plays key functions in numerous biological processes. The imaging detection of intracellular hydrogen sulfide is of great significance. In this work, a ratiometric fluorescent probe BH based on an asymmetric BODIPY dye for detection of H2S was designed and synthesized. After the interaction with hydrogen sulfide, probe display colorimetric and ratiometric fluorescence response, with its maximum emission fluorescence wavelength red-shifted from 542 nm to 594 nm, which is attributed to the sequential nucleophilic reaction of H2S leading to enhanced molecular conjugation after ring formation of the BODIPY skeleton. A special response mechanism has been fully investigated by NMR titration and MS, so that the probe has excellent detection selectivity. Furthermore, probe BH has low cytotoxicity and fluorescence imaging experiments indicate that it can be used to monitor hydrogen sulfide in living cells.

A hemicyanidin-based NIR fluorescent probe for detection of H2S and imaging study in cells and mice.

The selective detection of hydrogen sulfide in physiological and pathological processes has gained substantial attention in recent years. However, the real-time detection of hydrogen sulfide remains an elusive goal. In this work, a new type of hemicyanidin-based fluorescent "turn-on" probe NTR-HS (Ex = 680nm, Em = 760nm) was developed to detected H2S in a very short time (3min).Thefluorescence quantum yield is 0.15 and accompanied with a noticeable color change from violet to bluethatcan be used to detect H2S in the range 1.04 × 10-7-4 × 10-5Mwith a limit of detection of 1.04 x 10-7 M. TheNTR-HS probewas also used for imaging of endogenous hydrogen sulfide and mitochondrial localization in HCT116 and HeLa cells. The detection mechanism was studied through fluorescence, UV-Vis, NMR, and mass analysis. Notably, the probe was successfully used to imaging H2S in mice and locating hydrogen sulfide in the large intestine of mice.

Functionalized organic–inorganic hybrid composites used as colorimetric chemosensors for hydrogen sulfide detection

AbstractDetection of trace‐level hydrogen sulfide (H2S) gas is of great importance both in industrial production and disease diagnosis. In this article, two simple but smart colorimetric chemosensors for H2S detection were designed based upon the principle of colorimetric reaction. Ag NPs, as the main detection agent was loaded onto the primary carrier, silica sulfonic acid. Thus, a silver‐modified silica sulfonic acid (Ag‐SSA) was prepared successfully. Then the Ag‐SSA was integrated with two kinds of secondary substrate materials. One is the cotton‐woven textile and the other one is polyvinyl alcohol (PVA) nanofibrous membrane. Finally, two functionalized organic–inorganic hybrid composite systems for H2S detection were formed. Both of them were able to exhibit a rapid visual color change in response to H2S. Ag‐SSA/cotton textile was tested in the aqueous state and the limit of detection (LOD) of H2S solution was around 10−6 mol/L. For the Ag‐SSA/PVA nanofibers membrane detected in the atmospheric condition, the LOD of H2S gas reached 6.5 ppm. This research has been successfully demonstrated for the application in sensitive and selective detection of hydrogen sulfide in aqueous solution and gaseous state.

A Water-Soluble NIR Fluorescent Probe Capable of Rapid Response and Selective Detection of Hydrogen Sulfide in Food Samples and Living Cells

A Water-Soluble NIR Fluorescent Probe Capable of Rapid Response and Selective Detection of Hydrogen Sulfide in Food Samples and Living Cells

A fluorescent Rhodol-derived probe for rapid and selective detection of hydrogen sulfide and its application

H2S has been reported to play essential roles in a variety of physiological and pathological procedures. In this work, a novel fluorescent probe, Rho-HS, for detecting H2S was developed by introducing the ortho-halogen to activate the least reactive recognition group 2,4-dinitrophenyl moiety. In combination of the structures from both Rhodamine B and fluorescein, Rho-HS could generate both the colorimetric and fluorescent responses. This feature was not frequently achieved and could lead to the quantitative and convenient for the end-user. In comparison with recent probes for H2S, the major advantages of Rho-HS included suiting wide pH range (6.0–10.0), relatively rapid response (within 15 min) and the high selectivity among the competing species including the biothiols. With low cytoxicity, Rho-HS was further applied in the biological imaging in living MCF-7 cells and Caenorhabditis elegans. We hope that the designing strategy in this work might provide useful information for more preferable implements in this field.

Selective and self-validating breath-level detection of hydrogen sulfide in humid air by gold nanoparticle-functionalized nanotube arrays

We demonstrate the selective detection of hydrogen sulfide at breath concentration levels under humid airflow, using a self-validating 64-channel sensor array based on semiconducting single-walled carbon nanotubes (sc-SWCNTs). The reproducible sensor fabrication process is based on a multiplexed and controlled dielectrophoretic deposition of sc-SWCNTs. The sensing area is functionalized with gold nanoparticles to address the detection at room temperature by exploiting the affinity between gold and sulfur atoms of the gas. Sensing devices functionalized with an optimized distribution of nanoparticles show a sensitivity of 0.122%/part per billion (ppb) and a calculated limit of detection (LOD) of 3 ppb. Beyond the self-validation, our sensors show increased stability and higher response levels compared to some commercially available electrochemical sensors. The cross-sensitivity to breath gases NH3 and NO is addressed demonstrating the high selectivity to H2S. Finally, mathematical models of sensors’ electrical characteristics and sensing responses are developed to enhance the differentiation capabilities of the platform to be used in breath analysis applications.

A new sensitive “turn-on” fluorescent probe based on naphthalimide: Application in visual recognition of hydrogen sulfide in environmental samples and living cells

The selective detection of hydrogen sulfide (H2S) in environmental and living systems has gained substantial attention in recent years. However, the identification of rapid and highly selective probes for the detection of H2S remains an elusive goal. This article presents the design and synthesis of a fluorescent “turn-on” probe based on the 1,8-naphthalimide framework (NAM-N3) to achieve this goal. H2S triggered reduction of NAM-N3 resulted in a remarkable ratiometric absorption enhancement alongside fluorescent “turn-on” response in the green region. The detection properties of NAM-N3 towards H2S were satisfactorily studied through fluorescence, UV–vis, 1H NMR, and mass analysis. The detection response was rapid, and the limit of detection (LOD) was calculated as 1.5 μM. The practical applicability of the probe was tested on various platforms.

A fuel cell type gas sensor based on Pt/NbN for highly selective detection of hydrogen sulfide

Hydrogen sulfide (H2S) is considered a highly hazardous toxic gas. H2S sensors are therefore of paramount significance for real-time leak detection. However, existing solutions do not meet the strict performance targets set by stakeholders, while deactivation due to surface area of sensing materials decrease and contamination is a widely unsolved problem. Presented here is a new support material, mesoporous niobium nitride (NbN), which improve the long-term stability largely via enhancing the interaction between metal and support. Simultaneously, sensor devices using NbN as support show enlarged sensitivity, enhanced limit of detection and well repeatability when compared with these sensors using traditional carbon black support. In a wider perspective, our work suggests strategies for enhancing long-stability of next-generation chemical gas sensors by optimizing metal-support interaction.

A Near-infrared Benzothiazole-based Chemodosimeter for Rapid and Selective Detection of Hydrogen Sulfide

Hydrogen sulfide (H2S) is a biologically relevant gaseous molecule, which involves in a wide variety of physiological and pathological processes. Thus, detection of H2S is highly valuable in order to clarify its complex roles. In this study, a new benzothiazole-based donor-acceptor type H2S selective chemodosimeter (HP-1) was synthesized and its H2S detection capabilities were investigated in aqueous solutions. HP-1 exhibited a red-shifted absorption signal at 530 nm and a near-infrared (NIR) fluorescence peak at 680 nm as a result of enhanced intramolecular charge transfer (ICT) in the presence of H2S, which enabled a selective and very rapid ratiometric fluorescent detection. HP-1 was also showed to be highly sensitive toward H2S with a very low limit of detection value.

A near infrared fluorescent probe for naked eye visualization and selective detection of hydrogen sulfide

A napthofluoresciene based NIR fluorescent probe for sulfide was synthesized and characterized by nmr and ESI-MS spectrometry. The present probe can act as rapid, colorimetric and NIR fluorescent turn on sulfide sensor at nano molar levels. It is highly selective to sulfide over other reducing agents like sulfate, sulfite and also thiol moieties. It has been successfully applied for the determination of sulfide in various environmental water samples.

Design and Synthesis of a Fluorescent Probe Based on Copper Complex for Selective Detection of Hydrogen Sulfide

A novel fluorescence probe NA-LCX was rationally designed and synthesized for the sequential recognition of Cu2+ and H2S by the combination of hydroxyl-naphthalene and diformylphenol groups. The response properties of NA-LCX for Cu2+ ions and H2S with “on-off-on” manner were investigated by fluorescence emission spectra. A highly selective and sensitive response of complex NA-LCX-Cu2+ for H2S over other competing amino acids was observed with a limit of detection at 2.79 μM. The stoichiometry of NA-LCX toward Cu2+ ions was determined to be 1 : 1 by the UV-Vis absorption spectrum, and the coordination configuration was calculated by density functional theory (DFT) calculations. Moreover, probe NA-LCX was applied successfully for the recognition of Cu2+ ions and H2S in living cells.

A coumarin-based "off-on" fluorescent probe for highly selective detection of hydrogen sulfide and imaging in living cells.

Hydrogen sulfide (H2S), as a significant signaling molecule, is associated with diverse physiological and pathological processes. However, it's still a challenge to explore outstanding tools for detecting endogenous H2S in vivo. Thus, a simple "off-on" H2S fluorescent probe CMHS has been reasonably designed, and it is based on coumarin as the fluorophore group. The probe CMHS displayed a crucial turn-on fluorescence enhancement (180-fold), rapid reaction time, high selectivity, and a low limit of detection (2.31 × 10-7 M). Additionally, probe CMHS could be applied to visualize exogenous and endogenous H2S successfully in HeLa cells with low cytotoxicity and good permeability.