Chemiluminescence Sensor Research Articles

Solid-State Gas Sensors with Ni-Based Sensing Materials for Highly Selective Detecting NOx.

Precise monitoring of NOx concentrations in nitric oxide delivery systems is crucial to ensure the safety and well-being of patients undergoing inhaled nitric oxide (iNO) therapy for pulmonary arterial hypertension. Currently, NOx sensing in commercialized iNO instruments predominantly relies on chemiluminescence sensors, which not only drives up costs but also limits their portability. Herein, we developed solid-state gas sensors utilizing Ni-based sensing materials for effectively tracking the levels of NO and NO2 in the NO delivery system. These sensors comprised of NiO-SE or (NiFe2O4 + 30 wt.% Fe2O3)-SE vs. Mn-based RE demonstrated high selectivity toward 100 ppm NO under the interference of 10 ppm NO2 or 3 ppm NO2 under the interference of 100 ppm NO, respectively. Meanwhile, excellent stability, repeatability, and humidity resistance were also verified for the proposed sensors. Sensing mechanisms were thoroughly investigated through assessments of adsorption capabilities and electrochemical reactivity. It turns out that the superior electrochemical reactivity of NiO toward NO, alongside the NO2 favorable adsorption characteristics of (NiFe2O4 + 30 wt.% Fe2O3), is the primary reason for the high selectivity to NOx. These findings indicate a bright future for the application of these NOx sensors in innovative iNO treatment technologies.

Investigation of the chemiluminescence behavior of Ti3C2 MXene quantum dots as a sensing platform for uric acid

The current study explores the application of Ti3C2 MXene quantum dots (MQDs) as a chemiluminescent (CL) probe to determine uric acid (UA) in biological samples. The MQDs sensor was synthesized using ultrasonic-assisted hydrothermal method and characterized through Fourier transform infrared spectroscopy, Raman spectroscopy, scanning electron microscopy, energy dispersive X-ray analysis, high-resolution transmission electron microscopy, and X-ray diffraction. The presence of MQDs significantly enhances the ultra-weak Fe(II)–S2O82− CL system. Subsequently, quenching of the probe’s CL signal was observed in the presence of UA. Thus, the designed CL sensor offers an excellent analytical capability for determining UA in the 0.15–2.5 µM range, with a limit of detection of 0.093 µM. The method was effectively used to analyze UA in human serum and urine, yielding recovery rates between 94.4 % and 108.3 % with relative standard deviations (RSD) ranging from 1.9 % to 5.9 %.

Facile Synthesis and Characterization of Fluorescent Polystyrene Nanospheres for Homogeneous Light-Initiated Chemiluminescence Immunoassay.

Homogeneous light-initiated chemiluminescence technology (LICA) is widely used in clinical diagnostics due to the advantages of high sensitivity, minimal reagent usage, and no need for washing. Luminescent microspheres receive singlet oxygen emitted by photosensitive microspheres to generate optical signals. Therefore,1O2-initiated luminescent nanospheres are crucial, but there are few reports on the preparation of 1O2-initiated luminescent nanospheres. Herein, monodisperse luminescent Eu/C-28@PS (Eps) nanospheres were prepared and optimized using chelate Eu (TTA)3phen and 4-(2-phenyl-5,6-dihydro1,4-oxathiin-3-yl)-N, N-ditetradecylbenzenamine (C-28) as probe dye via THF/water swelling-shrinking procedure. Various swelling parameters were studied to obtain the swelling conditions that produce the minimum particle size and narrow size distribution, which shows good results in uniform particle size distribution (~ 250nm, a PDI of 0.03), surface carboxylate content (1.18mmol/g), and BSA loading capability (129.8mg/g) in the case of 20mg total probe dosage and 2h of incubation at 40°C using 14% THF/water mixture as a co-solvent system. The composition of the entrapped probe has a gain effect on the 1O2-initiated fluorescent signal and the optimal ratio of Eu (TTA)3phen: C-28 (1:1) was obtained on a commercial analyzer using IgG and anti-human IgG as models in PBS buffer. These results indicate that monodisperse luminescent Eps nanospheres are suitable as light-initiated chemiluminescence sensors and have great application potential in early detection, screening tests, and prognostic evaluation of patients.

A novel peptide fluorescent chemical sensor capable of detecting Cu2+, Zn2+, and S2.

A novel peptide-based chemical fluorescence sensor L (Dansyl-His-Pro-Thr-Cys-NH2) was designed and synthesized. This sensor exhibits an "On-Off-On" detection cycle to detect Cu2+, Zn2+, and S2- in solution. According to the chelation-enhanced fluorescence (CHEF) mechanism, when Zn2+ is present, the fluorescence is significantly enhanced and a blue shift occurs, representing a "Turn-On" phase of the fluorescence detection mode. Because copper ions (Cu2+) have a paramagnetic quenching sensing mechanism, the fluorescence of L quenches rapidly with the formation of the L-Cu system, representing the "Turn-Off" phase. The subsequent introduction of S2- to the L-Cu system results in the recovery of the L-fluorescence, thereby representing the second "Turn-On" phase. As a peptide molecule, the sensor L has several advantages over other types of sensors, including water solubility, high sensitivity, and good biocompatibility, with a very low detection limit. The detection lines of Zn2+ and Cu2+ are 97 nM (R = 0.993) and 75 nM (R = 0.995), respectively. Additionally, the sensor does not exhibit any obvious cell toxicity. These results indicate that this peptide chemiluminescent sensor has the potential to be applied in in vivo detection.

Amino-rich silicon quantum dots as efficient activator with intrinsic chemiluminescence for the detection of peroxydisulfate

The specific detection of peroxydisulfate (S2O82−, PDS) is significant and challenging due to the rapid development of PDS-related technologies and their widespread application in multiple fields. However, traditional analytical methods are mainly based on their strong oxidizing properties, making it difficult to simultaneously achieve specific identification and high sensitivity for PDS detection in complex water environments. Here, we purposely prepared amino-rich SiQDs (N-SiQDs) as an effective catalyst and introduced H2O2 acts as a co-reactant for PDS activation and determination with strong intrinsic chemiluminescence (CL) emission. High yield of reactive active oxygen (mainly O2˙− and ˙OH) were generated during CL process, which trigger electron-hole annihilation between the N-SiQDs˙+ and N-SiQDs˙− accounted for extraordinary CL emission. On this basis, a new CL assay for PDS detection was fabricated with broad linear range of 5 × 10−7M-5 × 10−5 M and low detection limit (3.2 × 10−7 M). Due to the absence of SO4˙− involvement during CL emission, the sensing platform is sensitive enough, satisfactory selectivity and does not respond to transition-metal ions and inorganic anions that have interferences in the PDS CL sensors reported before. This work not only deepens insight into the mechanisms of nanomaterials assisted PDS activation but also provides a new perspective on the modified metal-free QDs CL probe for chemical species detection.

Enhanced chemiluminescence by carbon dots for rapid detection of bisphenol A and nitrite

Herein, a novel chemiluminescence (CL) sensor was successfully developed based on chlorine doped carbon dots (Cl/CDs) for the rapid determination of bisphenol A (BPA) and nitrite. The Cl/CDs were synthesized through a hydrothermal method, using ascorbic acid as the precursor and hydrochloric acid as the dopant. It was found that Cl/CDs significantly enhanced the CL intensity of the acid-KMnO4 system, while BPA and nitrite quenched the CL intensity of the Cl/CDs-sensitized acid-KMnO4 system. Under optimal conditions, BPA exhibited a linear detection range of 0.05–10 μM, with limits of detection (LOD) and quantification (LOQ) of 0.86 nM and 2.8 nM, respectively. Nitrite showed a linear detection range of 0.7–100 μM, with LOD and LOQ of 22.5 nM and 75 nM, respectively. The CL sensor was successfully use to determine BPA in water samples and nitrite in pickles, ham and celery, with spike recovery rates of 96.3 %–104.8 % and 96.0 %–104.9 %, respectively.

An ingenious chemiluminescence sensing strategy for recalcitrant triphenyl phosphate based on oxidant-free UV-activated MIL-100(Fe) gel system

BackgroundOrganophosphate flame retardants (OPFRs) are notorious emerging contaminants threatening the environment and human health. Triphenyl phosphate (TPHP), which has an extremely serious biotoxicity, is a typical harmful OPFR. Due to its wide use, TPHP has been discovered in various environmental mediums. Moreover, it is pretty recalcitrant to the removal process, resulting in the need for a technique to understand it better. Hence, accurate and quick discrimination of TPHP in the environment is critical to further evaluate its potential effect on ecosystems and human health. ResultsAn ingenious oxidant-free chemiluminescence (CL) sensor based on the oxidant-free UV/MIL-100(Fe) gel system was established for TPHP detection. The oxidation of luminol in the UV-activated MIL-100(Fe) gel has resulted in remarkable CL emission, which is contributed by reactive oxygen species (ROS) generated by it. Notably, the CL intensity was inhibited significantly after introducing TPHP. An investigation into the mechanism underlying the effect of CL suppression demonstrated that TPHP competed with luminol to consume ROS from UV-activated MIL-100(Fe) gel, contributing to CL inhibition. The subsequent sensing performance experiments demonstrated the advantages of environmentally friendly, economic efficiency, user-friendly operation, rapid determination, potential for compact size, high selectivity, and sensitivity. Additionally, these investigations confirmed the low limit of detection (210 ng L−1) and wide linear range (10–1000 μg L−1). SignificanceIn this paper, a green, economical, and oxidant-free CL sensing strategy for TPHP has been established. It has the advantage of being rapid, having the potential for compact size, high selectivity, and sensitivity. This ingenious method has promising applications in real-time and online environmental monitoring, and it paves the way for the rapid and environmentally friendly identification of emerging contaminants that are structurally stable and recalcitrant to remove.

Chemiluminescence detection of kanamycin by DNA aptamer regulating peroxidase-like activity of Co3O4 nanoparticles.

Kanamycin (KAN) is widely used as a growth hormone analog and an antibacterial agent. However, abuse of this substance has resulted in the accumulation of excessive residue levels in foods of animal origin, which presents a significant risk to human health. A chemiluminescent aptasensor was constructed for the rapid quantitative detection of KAN by combining the properties of Co3O4 nanoparticles (Co3O4 NPs) nanozyme activity and DNA aptamer with high specificity. The DNA aptamer/Co3O4 NPs nanozyme regulated the chemiluminescence signal by exploiting the chemiluminescent properties of luminol oxidation by H2O2. Specific binding of KAN to the aptamer led to the formation of a steric hindrance block in the solution, which inhibited the activity of nanozyme and reduced signal intensity. The degree of signal reduction is related to the concentration of KAN. Under optimal conditions, there was good linearity between KAN concentration and chemiluminescence signal intensity in the range of 0.5-8.0 μΜ, with a detection limit of 0.26 μΜ. The detection system performed well in the presence of competing antibiotics and was virtually unaffected. The method was also suitable for the detection of KAN in milk samples with sample recoveries of 97.8%-99.1%. The chemiluminescence sensor has the advantages of low cost, specificity, and sensitivity, and does not require an external light source or modification of the nucleic acid aptamer which makes it a promising candidate for applications in the field of food detection.

Highly sensitive chemiluminescent sensor for detecting o-toluenesulfonamide and sulfamethoxazole using Cu-doped carbon dots

In this study, Cu doped carbon dots (Cu-CDs) of uniform particle size and good water solubility was synthesized using Angelica Sinensis Radix as precursor materials through a one-step hydrothermal. The Lucigenin-(Cu-CDs) chemiluminescence sensor allows the simultaneous determination of o-toluenesulfonamide (TFA) and sulfamethoxazole (STZ) concentrations. Under optimal conditions, the sensor demonstrates the capability to detect TFA and STZ within the ranges of 50 μM–800 μM and 15 μM–120 μM, respectively. The limits of detection (LOD) for TFA and STZ are determined as 0.09 μM and 0.05 μM, respectively. While the limits of quantification (LOQ) are established at 0.3 μM and 0.17 μM, respectively. The feasibility of the method for determining TFA and STZ content in chicken samples was substantiated, demonstrating spiked recovery rates ranging from 97.5% to 102.3 % and 97.5%–99.8 %, respectively. The possible reaction mechanism was clarified based on chemiluminescence, UV–vis measurement and free radical analysis results. The newly established system is characterized by stability, convenience, and robust anti-interference capabilities, thus expanding the application of carbon dots and offering a promising strategy for the detection of TFA and STZ.

Internal light-driven efficient chemiluminescence of graphitic carbon nitride quantum dots for improved carboxin sensing

Developing a new chemiluminescence (CL) sensor platform to achieve the identification of pollutants in the water environment is a significant and currently hot topic for researchers. Building on the effective development of a CL internal light source, this paper designed a direct, simple, and rapid pesticide identification strategy. Specifically, graphite carbon nitride quantum dots (CNQDs) with excellent optical properties were synthesized using a solvent heat treatment strategy. Acting as an energy acceptor, CNQDs triggered CL emission in the presence of singlet oxygen (1O2). The newly developed CNQDs/1O2 CL sensor exhibited a specific response toward carboxin (CBX) with high sensitivity. Based on this discovery, we have developed a highly selective, ultra-sensitive, and fast CL sensing platform for detecting CBX in water environments. Through numerous experiments, we attributed the CL emission of the CNQDs/1O2 system to the specific chemiluminescent resonance energy transfer (CRET) process between CNQDs and 1O2. Interestingly, the CL light of the CNQDs/1O2 system could serve as an internal light source to excite CBX generating a large amount of 1O2 through photosensitization, which was crucial for further enhancing the CL efficiency of the CNQDs/1O2/CBX system and also enabled the CL sensing of CBX. This study is the first to successfully identify CBX in water using CL sensors, showcasing the potential of CL internal light sources in regulating CL efficiency and offering new perspectives on detecting pollutants in complex environments.

Research progress in biosensors for adiponectin

Adiponectin, a cytokine associated with adipose tissue, is a recently defined adipocytokine involved in insulin, glucose, and adipocyte metabolism. Reduced adiponectin levels can increase the risk of developing metabolic syndrome (MS). Adiponectin is considered an important target for the treatment of type 2 diabetes mellitus (T2DM) and MS due to its anti-atherosclerotic and insulin-sensitizing effects. Therefore, the accurate determination of adiponectin concentrations in human plasma is necessary for the management of both T2DM and MS. A variety of biosensors have been developed for the detection of biomarkers such as adiponectin. This paper reviews the applications of electrochemical sensors, surface-enhanced Raman scattering sensors, and microfluidic chip-based chemiluminescence sensors in the detection of adiponectin and the recent research progress in the sensors for the detection of adiponectin, aiming to provide a reference for the research and application of sensors for adiponectin in the medical field.

Hydrogen peroxide enhanced glow-type chemiluminescence of hydrazine hydrate modified carbon quantum dots-potassium persulfate system

Most known chemiluminescence (CL) systems are flash-type that generate weak luminescence and decline quickly after dozens of seconds, while the glow-type CL systems have stable emission for an extended period to achieve accurate quantitation. In this work, a long-term CL system based on hydrazine-hydrate (N2H4·H2O) modified carbon quantum dots (N-CQDs) as a luminescent probe, with K2S2O8 and H2O2 as co-reactants, was proposed. The CL emission enhanced by H2O2 increased 18-fold more than that of N-CQDs and K2S2O8 direct reaction, and decayed by 5% of the maximum intensity over 700 s. In the reaction system, K2S2O8 and H2O2 co-reactants can promote each other to continuously generate corresponding radicals (•OH, O2•−, 1O2), which in turn trigger the CL emission of N-CQDs. This phenomenon was identified as the primary cause for the production of persistent CL. In addition, a stable and selective CL sensor based on the N-CQDs-K2S2O8-H2O2 CL enhancing system was developed for ascorbic acid quantitation in the linear range from 0.1 to 10.0 mM with a detection limit of 0.036 mM. The method has been applied to the analysis of tablet samples and holds potential in pharmaceutical analysis field.

Catalytic NIR chemiluminescence sensor with enhanced persistence and intensity for in vivo imaging

Chemiluminescence (CL) is a self-illumination phenomenon that involves the emission of light from chemical reactions, and it provides favorable spatial and temporal information on biological processes. However, it is still a great challenge to construct effective CL sensors that equip strong CL intensity, long emission wavelength, and persistent luminescence for deep tissue imaging. Here, we report a liposome encapsulated polymer dots (Pdots)-based system using catalytic CL substrates (L-012) as energy donor and fluorescent polymers and dyes (NIR 695) as energy acceptors for efficient Near-infrared (NIR) CL in vivo imaging. Thanks to the modulation of paired donor and acceptor distance and the slow diffusion of biomarker by liposome, the Pdots show a NIR emission wavelength (λ em, max = 720 nm), long CL duration (>24 h), and a high chemiluminescence resonance energy transfer efficiency (46.5 %). Furthermore, the liposome encapsulated Pdots possess excellent biocompatibility, sensitive response to H2O2, and persistent whole-body NIR CL imaging in the drug-induced inflammation and the peritoneal metastatic tumor mouse model. In a word, this NIR-II CL nanoplatform with long-lasting emission and high spatial-temporal resolution will be a concise strategy in deep tissue imaging and clinical diagnostics.

Bifunctional oxidase-peroxidase mimicking Fe–Ce MOF on paper-based analytical devices to intensify luminol chemiluminescence: Application for measuring different sugars with a smartphone readout

This study presents a potent paper-based analytical device (PAD) for quantifying various sugars using an innovative bi-nanozyme made from a 2-dimensional Fe/Ce metal-organic framework (FeCe-BTC). The MOF showed excellent bifunctional peroxidase-oxidase activities, efficiently catalyzing luminol's chemiluminescence (CL) reaction. As a peroxidase-like nanozyme, FeCe-BTC could facilitate the dissociation of hydrogen peroxide (H2O2) into hydroxyl radicals, which then oxidize luminol. Additionally, it was also discovered that when reacting with H2O2, the MOF turns into a mixed-valence MOF, and acts as an oxidase nanozyme. This activity is caused by the generated Ce4+ ions in the structure of MOF that can directly oxidize luminol. The MOF was directly synthesized on the PAD and cascaded with specific natural enzymes to establish simple, rapid, and selective CL sensors for the measurement of different sugars. A cell phone was also used to record light intensities, which were then correlated to the analyte concentration. The designed PAD showed a wide linear range of 0.1–10 mM for glucose, fructose, and sucrose, with detection limits of 0.03, 0.04, and 0.04 mM, respectively. It showed satisfactory results in food and biological samples with recovery values ranging from 95.8 to 102.4 %, which makes it a promising candidate for point-of-care (POC) testing for food control and medicinal purposes.

Green synthesized carbon quantum dots as chemiluminescence sensor for sulfanilamide detection

N–S co-doped quantum carbon dots (N–S-CQD) were synthesized using a hydrothermal method with Artemisia annua L. as a precursor and dl-cysteine as the nitrogen-sulfur source. N–S-CQD can enhance the chemiluminescence (CL) intensity of KMnO4 system, while sulfanilamide (SA) is capable of significantly inhibit the CL intensity of KMnO4-(N–S-CQD) system. Based on this finding, we developed a novel CL method for the determination of SA. Under the optimal conditions, SA could be accurately determined in the concentration range of 50–1600 μM with a limit of detection of 0.22 μM. The investigation of potential interferences and recovery rates confirmed the method's suitability for assessing biomass samples.

Dynamically regulating transient chemiluminescence of illuminated carbon nitride for simultaneous determination of ascorbic acid and dopamine

Developing a new strategy for a chemiluminescence (CL) sensor array to identify multiple biomarkers for psychiatric disorders simultaneously is a highly challenging task. This study designed a novel and straightforward strategy for simultaneous ascorbic acid (AA) and dopamine (DA) determination based on the interesting transient CL (TCL) kinetic curve tunability phenomenon on efficient graphite carbon nitride (CN) nanosheets. Advanced photoinduction strategies were introduced to synthesize light-illuminated CN nanosheets (L-CNNSs) as sensing materials with more negative reduction potential, excellent electron-hole separation, charge transfer capabilities, and high CL activity. Notably, using L-CNNSs as a sensing material could induce strong CL of alkaline lucigenin. This newly developed CL sensor exhibited high activity, excellent selectivity, and characteristic transient response toward AA and DA. Based on this finding, we developed a direct CL sensing platform for DA and AA discrimination in the urine of patients with mental disorders. Through many experiments, we attributed the CL recognition mechanism of the L-CNNSs/lucigenin system for DA and AA to the dynamic regulation of superoxide anions (O2·−) generation in the L-CNNSs solution. The different O2·− generation rates from L-CNNSs/lucigenin/AA and L-CNNSs/lucigenin/DA were regulated to obtain ‘flash-type’ and ‘sustained-type’ TCL curves, respectively, achieving simultaneous AA and DA discrimination and detection. This study provides insights for the simultaneous identification of multiple components based on CL sensors and offers new possibilities for practical analysis of sensor arrays.

A novel chemiluminescence sensor for alpha-fetoprotein detection based on an aptamer-luminol modified magnetic graphene oxide and copper-based MOF composite.

Herein, an aptamer-luminol modified magnetic graphene oxide and copper-based MOF composite was prepared and used to build a novel target-triggered "turn on" chemiluminescence (CL) sensor for alpha-fetoprotein (AFP) detection. Magnetic graphene oxide (MGO) was functionalized with the complementary sequence of the AFP aptamer (cDNA), and then MGO-cDNA was linked to aptamer modified luminol (Apt-luminol) through the complementary base pairing effect. The functionalized magnetic graphene oxide (MGO-cDNA/Apt-luminol) was prepared as a specific magnetic separation and signal switch material. ZnONPs-Au@CuMOFs shows excellent catalytic performance and was used as a catalyst for the luminol-H2O2 reaction. AFP will specifically recognize and bind to Apt on MGO-cDNA/Apt-luminol when AFP is present, which causes luminol release and triggers the CL reaction. The released luminol encounters ZnONPs-Au@CuMOFs and produces strong CL intensity. Therefore, a novel target-triggered "turn on" CL method with high selectivity and sensitivity for detecting AFP has been established. The linear range and detection limit were 1.0 × 10-4-50 ng mL-1 and 4.2 × 10-5 ng mL-1, respectively. The sensor also exhibited good selectivity, reproducibility and stability, and was finally used for AFP detection in serum samples.

Advances in MXene-based luminescence sensing strategies.

MXenes have attracted the attention of many researchers as one of the latest two-dimensional (2D) materials over the last decade. Their great potential for biosensing has also been fully exploited after the discovery of their unique properties such as superior optical properties, excellent hydrophilicity, good thermal stability, excellent mechanical property, high electrical conductivity, biocompatibility, large surface area, and ease of surface functionalization. In the MXene-based luminescence sensing strategy, MXenes typically appear in the form of nanosheets, quantum dots and modified MXene nanocomposites, and they are utilized as different sensing platforms or as a luminescence source. In this review, we focused on the MXene-based luminescence sensing strategies, including fluorescence, electrochemiluminescence and chemiluminescence sensors and the comparison of their performance. Finally, the perspectives of the MXene-based luminescence sensors are discussed.

Highly sensitive chemiluminescence sensors for the detection and differentiation of chemical warfare agents.

Highly sensitive chemiluminescence-based probes that effectively detect and differentiate between the extremely toxic real G- and V-type organophosphorus chemical warfare agents (OPCWAs) are presented. This straightforward approach does not require any instrumentation or light source; hence, it appears ideal for the future development of field colorimetric detectors.

Biotinylated Quinone as a Chemiluminescence Sensor for Biotin-Avidin Interaction and Biotin Detection Application

Biotin, or vitamin B7, is essential for metabolic reactions. It must be obtained from external sources such as food and biotin/vitamin supplements because it is not biosynthesized by mammals. Therefore, there is a need to monitor its levels in supplements. However, biotin detection methods, which include chromatographic, immune, enzymatic, and microbial assays, are tedious, time-consuming, and expensive. Thus, we synthesized a product called biotin-naphthoquinone, which produces chemiluminescence upon its redox cycle reaction with dithiothreitol and luminol; then it was used as a chemiluminescence sensor for biotin–avidin interaction. When a quinone biotinylated compound binds avidin, the chemiluminescence decreases noticeably due to the proximity between quinone and avidin, and when free biotin is added in a competitive assay, the chemiluminescence returns. The chemiluminescence is regained as the free biotin displaces biotinylated quinone in its complex with avidin, freeing biotin-naphthoquinone. Many experiments, including the use of a biotin-free quinone, proved the competitive nature of the assay. The competitive assay method used in this study was linear in the range of 1.0–100 µM with a detection limit of 0.58 µM. The competitive chemiluminescence assay could detect biotin in vitamin B7 tablets with good recovery of 91.3 to 110% and respectable precision (RSD < 8.7%).