New portable smartphone-based PDMS microfluidic kit for the simultaneous colorimetric detection of arsenic and mercury

A smartphone-based microfluidic platform was developed for point-of-care (POC) detection using surface plasmon resonance (SPR) of gold nanoparticles (GNPs). The simultaneous colorimetric detection of trace arsenic and mercury ions (As³⁺ and Hg²⁺) was performed using a new image processing application (app). To achieve this goal, a microfluidic kit was fabricated using a polydimethylsiloxane (PDMS) substrate with the configuration of two separated sensing regions for the quantitative measurement of the color changes in GNPs to blue/gray. To fabricate the microfluidic kit, a Plexiglas mold was cut using a laser based on the model obtained from AutoCAD and Comsol outputs. The colorimetric signals originated from the formation of nanoparticle aggregates through the interaction of GNPs with dithiothreitol – 10,12-pentacosadiynoic acid (DTT-PCDA) and lysine (Lys) in the presence of As³⁺ and Hg²⁺ ions. This assembly exhibited the advantages of simplicity, low cost, and high portability along with a low volume of reagents and multiplex detection. Heavy Metals Detector (HMD), as a new app for the RGB reader, was programmed for an Android smartphone to quantify colorimetric analyses. Compared with traditional image processing, this app provided significant improvements in sensitivity, time of analysis, and simplicity because the color intensity is measured through a new normalization equation by converting RGB to an Integer system. As a simple, real-time, and portable analytical kit, the fabricated sensor could detect low concentrations of As³⁺ (710 to 1278 μg L⁻¹) and Hg²⁺ (10.77 to 53.86 μg L⁻¹) ions in water samples at ambient conditions.

A smartphone-based microfluidic platform was developed for point-of-care (POC) detection using surface plasmon resonance (SPR) of gold nanoparticles (GNPs).     

A novel dihydro phenylquinazolinone-based two-in-one colourimetric chemosensor for nickel(ii), copper(ii) and its copper complex for the fluorescent colourimetric nanomolar detection of the cyanide anion

Currently, considerable efforts have been devoted to the detection and quantification of hazardous multi-analytes using a single probe. Herein, we have developed a simple, environment-friendly colourimetric sensor for the sensitive, selective and rapid detection of Ni²⁺ and Cu²⁺ ions using a simple organic Schiff base ligand L in methanol–Tris–HCl buffer (1 : 1 v/v, 10 mM, pH = 7.2). The probe L exhibited a binding-induced colour change from colourless to yellow and fluorescence quenching in the presence of both Ni²⁺ and Cu²⁺ ions. The interactions between L and the respective metal ions were studied by Job''s plot, electrospray ionisation-mass spectrometry (ESI-MS), Fourier-transform infrared spectroscopy (FT-IR), density functional theory (DFT) and time-dependent density functional theory (TDDFT) calculations. The limit of detection (LOD) of L towards Ni²⁺ and Cu²⁺ was calculated to be 7.4 × 10⁻⁷ M and 4.9 × 10⁻⁷ M, respectively. Furthermore, the L–Cu²⁺ complex could be used as a new cascade fluorescent-colourimetric sensor to detect CN⁻ ions with a very low level of detection (40 nM). Additionally, L could operate in a wide pH range, and thus was successfully applied for the detection and quantification of Ni²⁺ and Cu²⁺ in environmental samples, and for building OR- and IMPLICATION-type logic gates.

A novel colorimetric chemosensor L has been developed for the detection of Ni²⁺ and Cu²⁺ ions. The obtained L–Cu²⁺ complex can be used as a new cascade fluorescent-colorimetric sensor for the nanomolar detection of CN⁻ ions. This chemosensor has practical application.     

A sensitive OFF–ON–OFF fluorescent probe for the cascade sensing of Al3+ and F− ions in aqueous media and living cells

A simple Schiff-base ligand 2-hydroxy-1-naphthaldehyde semicarbazone (HNS) was synthesized and characterized. Based on the combined effect of inhibition of CH N isomerization and chelation-enhanced fluorescence (CHEF), HNS functions as a fluorescence “turn on” sensor for Al³⁺ in buffered aqueous media. Based on the strong affinity of Al³⁺ to F⁻ ions, the in situ generated Al³⁺–HNS complex can also be utilized as an effective chemosensor for F⁻ sensing by metal displacement approach, ensuing quenching of fluorescence by the reversible return of HNS from Al³⁺–HNS complex. Thus a method using a single probe for the detection of both Al³⁺ and F⁻ ions is developed. The system exhibits high selectivity and sensitivity for Al³⁺ and F⁻ ions and the detection limits were found to be as low as 6.75 × 10⁻⁸ M and 7.89 × 10⁻⁷ M, respectively. Furthermore, the practical applicability of this probe has been examined in living cells.

A simple Schiff-base ligand 2-hydroxy-1-naphthaldehyde semicarbazone (HNS) was synthesized and applied to the sequential sensing of Al³⁺ and F⁻ ions in aqueous media and live cells.     

Determination of cesium ions in environmental water samples with a magnetic multi-walled carbon nanotube imprinted potentiometric sensor

A potentiometric sensor, based on the glassy carbon electrode (GCE) modified with a magnetic multi-walled carbon nanotubes/cesium ion-imprinted polymer composite (MMWCNTs@Cs-IIP), is introduced for the detection of cesium(i). The IIP was synthesized using cesium ions as the template ions, chitosan as the functional monomer and glutaraldehyde as the cross-linking agent. The membrane, which was coated on the surface of the GCE, was prepared using MMWCNTs@Cs(i)-IIP as the modifier, PVC as the neutral carrier, 2-nitrophenyloctyl ether as the plasticizer and sodium tetraphenylborate as the lipophilic salt. The proposed sensor exhibited a Nernstian slope of 0.05954 V dec⁻¹ in a working concentration range of 1 × 10⁻⁷ to 1 × 10⁻⁴ M (mol L⁻¹) with a detection limit of 4 × 10⁻⁸ M. The sensor exhibited high selectivity for cesium ions and was successfully applied for the determination of Cs(i) in real samples.

A Cs(i)-selective potentiometric microsensor based on the glassy carbon electrode (GCE) modified with a magnetic multi-walled carbon nanotubes/cesium ion-imprinted polymer has been developed.     

Robust colorimetric detection based on the anti-aggregation of gold nanoparticles for bromide in rice samples

Inorganic bromide (Br⁻) is an important contaminant ion as it can originate from the overuse of illegal methyl bromide as a fumigant in stored rice samples. Herein, we developed a simple and highly sensitive colorimetric sensor for bromide ion detection in rice samples. The sensor is based on the anti-aggregation of gold nanoparticles (AuNPs) by Br⁻ in the presence of Cr³⁺, which made the method more selective than other typical aggregations of nanoparticles. The AuNPs underwent an aggregation process as a result of the coordination of Cr³⁺ and the carboxylate group of a citrate ion stabilized the AuNPs, resulting in a red-to-blue color change. When Br⁻ was pre-mixed with the AuNPs and Cr³⁺ was added, the solution color changed from blue to red with an increase in the Br⁻ concentration. The anti-aggregation process can be detected with the naked eye and monitored using UV-vis spectrophotometry. The linear calibration curve ranged between 0.31 and 3.75 μM Br⁻ with a low LOD and LOQ of 0.04 and 0.13 μM. The recovery was excellent, ranging from 79.9–92.2% with an RSD of less than 4.0%. The good inter-day and intra-day precisions were 2.9–6.4% and 3.1–7.1%, respectively. The developed sensor has proved to provide a robust method for Br⁻ detection in rice samples.

In this work, we developed a AuNP colorimetric sensor for the facile, sensitive and selective detection of bromide ions in rice samples.     

Design and construction of an electrochemical sensor for the determination of cerium(iii) ions in petroleum water samples based on a Schiff base-carbon nanotube as an ionophore

A carbon paste sensor (CPE) and screen-printed sensor (SPE) for Ce(iii)-selective determination were prepared using a 2,6-pyridine dicarbomethine-triethylene tetraamine macrocyclic Schiff base ligand (PDCTETA) and multi-walled carbon nanotubes (MWCNTs) as good sensing materials. With respect to most common cations, such as alkali, alkaline earth, transition, and heavy metal ions, the electrodes display high selectivity for the Ce(iii) ion. The sensors respond to Ce(iii) ions in a linear range of 1 × 10⁻⁷ to 1 × 10⁻¹ and 1 × 10⁻⁸ to 1 × 10⁻¹ mol L⁻¹ with a slope of 18.96 ± 0.73 and 19.63 ± 0.51 mV per decade change in concentration with a detection limit of 1.10 × 10⁻⁸ and 5.24 × 10⁻⁹ mol L⁻¹ for CPE (sensor IV) and SPE (sensor VIII), respectively. The sensors were found to have a lifetime of 102 and 200 days. The suggested electrodes performed well throughout the pH ranges of 3.5–8.0 and 3.0–8.5, with response times of 8 and 6 seconds for sensor IV and sensor VIII, respectively. The sensors have been used to measure Ce(iii) ions in water samples from several petroleum wells. They have also been utilized as indicator electrodes in Ce(iii) ion potentiometric titrations with EDTA. The results were quite similar to those obtained by employing atomic absorption spectrometry (AAS).

A carbon paste and screen-printed sensor for Ce(iii)-selective determination were prepared using a 2,6-pyridine dicarbomethine-triethylene tetraamine macrocyclic Schiff base ligand and multi-walled carbon nanotubes as good sensing materials.     

New sensing platform of poly(ester-urethane)urea doped with gold nanoparticles for rapid detection of mercury ions in fish tissue

A new electrochemical sensor has been fabricated based on the in situ synthesis of poly(ester-urethane) urea (PUU) doped with gold nanoparticles (AuNPs), and the obtained composite materials (PUU/AuNPs) were used as a new sensing platform for highly sensitive and selective detection of mercury(II) ions in fish tissue. PUU was synthesized and fully characterized by XRD, TGA, DSC, and FTIR to analyze the chemical structure, thermal stability, and morphological properties. As a polymeric structure, the PUU consists of urethane and urea groups that possess pronounced binding abilities to Hg²⁺ ions. SEM-EDX was carried out to confirm this kind of interaction. Using ferricyanide as the redox probe, PUU alone exhibited weak electrochemical signals due to its low electrical conductivity. Therefore, a new series of nanocomposites of PUU with different nanostructured materials were applied, and their electrochemical performances were evaluated. Among these materials, the PUU/AuNP-modified electrode showed high voltammetric signals towards Hg²⁺. Consequently, the parameters affecting the performance of the assay, such as electrode composition, scan rate, and sensing time, as well as the effect of electrolyte and pH were studied and optimized. The sensor showed a linear range of 5 ng mL⁻¹ to 155 ng mL⁻¹ with the regression coefficient R² = 0.986, while the calculated values of the limit of detection (LOD) and limit of quantification (LOQ) were 0.235 ng mL⁻¹ and 0.710 ng mL⁻¹, respectively. In terms of cross reactivity testing, the sensor exhibited a high selectivity against heavy metals which are commonly determined in seafood (Cd²⁺, Pb²⁺, As³⁺, Cr³⁺, Mg²⁺, and Cu²⁺). For real applications, total Hg²⁺ ions in fish tissue were determined with very high recovery and no prior complicated treatments.

A new electrochemical sensor based on poly(ester-urethane) urea doped with gold nanoparticles (PUU/AuNPs) for highly sensitive and selective detection of mercury(ii) ions in fish tissue.     

A highly specific and sensitive turn-on fluorescence probe for hypochlorite detection and its bioimaging applications

Development of high performance fluorescent chemosensors for the detection of ClO⁻in vitro and in vivo is very desirable, because many human diseases are caused by ClO⁻. In this paper, a highly selectivity and sensitive fluorescent probe, EDPC, based on 3-acetylcoumarin, was synthesized, which could respond to ClO⁻ and exhibit an “off–on” mode in Tris–HCl buffer (pH = 7.2, 10 mM, 50% C₂H₅OH) solutions. The detection limit of the EDPC probe for ClO⁻ was as low as 1.2 × 10⁻⁸ M. Moreover, the high selectivity and high sensitivity of EDPC towards ClO⁻ are attributed to the oxidation reaction between the C–O of the coumarin lactone and the C C formed by aldol condensation and the mechanism was further verified using ESI-MS and DFT. Additionally, the concentrations of ClO⁻ in real water were also calculated using the EDPC probe and showed good recovery. Finally, the distribution of intracellular endogenous ClO⁻ was gained by confocal fluorescence microscopy in living HEK293T cells.

A new probe, EDPC, was designed and synthesized for highly specific and sensitive detection of ClO⁻ with a fast response time in living cells.     

A facile fluorescent sensor based on nitrogen-doped carbon dots derived from Listeria monocytogenes for highly selective and visual detection of iodide and pH

Sensitive and visual analysis of iodide (I⁻) and pH is significant in environmental and food applications. Herein, we present a facile fluorescent sensor for highly selective and visual detection of I⁻ and pH based on nitrogen-doped carbon dots derived from Listeria monocytogenes (NCDs-LM). The NCDs-LM-based fluorescent sensor showed a good linear relationship to I⁻ concentrations, and the detection limit was calculated as 20 nmol L⁻¹. The developed sensor was successfully applied to the detection of I⁻ in drinking water and milk samples. Meanwhile, the as-synthesized NCDs-LM sensor can be used to detect pH, achieving a wide linear pH range. Furthermore, fluorescent test papers based on NCDs-LM were designed for semi-quantitative detection of I⁻ and pH via the naked-eye colorimetric assay. The present work indicates that the NCDs-LM-based fluorescent sensor has high potential for use in environmental monitoring and food analysis.

Listeria monocytogenes-derived nitrogen-doped carbon dots served as a facile fluorescent sensor with excellent sensing performances for iodide with low detection limit of 20 nmol L⁻¹ and wide pH range from 1.81 to 11.82.     

A simple hydrazone as a multianalyte (Cu2+, Al3+, Zn2+) sensor at different pH values and the resultant Al3+ complex as a sensor for F−

A new colorimetric and fluorescence molecular chemosensor based on triazole hydrazone can be used as a multi-probe for selective detection of Al³⁺, Zn²⁺, and Cu²⁺ by monitoring changes in the absorption and fluorescence spectral patterns. Results show that Al³⁺ and Zn²⁺ ions can induce remarkable fluorescence enhancement at pH 6.0 and pH 10.0, respectively, while the addition of Cu²⁺ ions leads to a significant UV-visible absorption enhancement in the visible range at pH 6.0. In addition, the resultant Al³⁺ complex could act as an ‘on–off’ fluorescence sensor for F⁻. The fluorescence sensor was also used to monitor intracellular Al³⁺, Zn²⁺, and F⁻ in Hela cells.

A fluorescent probe for Al³⁺ and Zn²⁺ was synthesised, and the resultant Al³⁺-complex was used for the detection of F⁻.     

A coumarin Schiff's base two-photon fluorescent probe for hypochlorite in living cells and zebrafish

Selective and sensitive fluorescent probes for ClO⁻ are desirable due to the importance of ClO⁻ in biological processes. Here, a coumarin Schiff''s base, compound 1, has been developed and successfully used as a one- and two-photon fluorescent probe for ClO⁻ with high selectivity. This probe can recognize ClO⁻ with obvious color change from yellow-green to colorless and green to blue fluorescence emission, which can be observed by the naked eye. The properties of low cytotoxicity and good cell permeability allow it to be used for ClO⁻ detection in living cells and zebrafish by both one- and two-photon microscopy imaging. All these results indicate that the compound is a sensitive probe with potential for analysis of ClO⁻ in biological samples. The mechanism by which probe 1 recognizes ClO⁻ is possibly nucleophilic addition followed by hydrolysis.

A coumarin Schiff''s base compound can selectively recognize ClO⁻ and can be successfully applied to the detection of ClO⁻ in living cells and zebrafish by one- and two-photon fluorescence modes.     

Nanochannel-based sensor for the detection of lead ions in traditional Chinese medicine

Lead ions (Pb²⁺) are used in the quality control of traditional Chinese medicine (TCM) preparations because they are highly toxic to human health. At present, sophisticated analytical instrumentation and complicated procedures for sample analysis are needed for the determination of Pb²⁺. Herein, a simple, fast, and sensitive peptide-modified nanochannel sensor to detect Pb²⁺ in TCM is reported, which is based on a Pb²⁺-specific peptide modified porous anodized aluminum membrane (PAAM). This peptide-based nanochannel clearly has the highest selectivity for Pb²⁺ when compared to other heavy metal ions, including As²⁺, Cd³⁺, Co²⁺, Cr²⁺, Cu²⁺, Fe³⁺, Hg²⁺, Mg²⁺, Mn²⁺, Ni²⁺, and Zn²⁺. Based on linear ranges from 0.01 to 0.16 μM and 10 to 100 μM, the detection limit was calculated to be 0.005 μM. Moreover, this peptide-based nanochannel sensor was successfully used to detect Pb²⁺ in complex TCM samples. In addition, when compared with the gold standard atomic absorption spectrophotometry (AAS) method, the recovery of the peptide-modified nanochannel sensor was between 87.7% and 116.8%. The experimental results prove that this new sensor is able to achieve accurate detection of Pb²⁺ in TCM samples. Thus, this sensor system could provide a simple assay for sensitive and selective detection of Pb²⁺ in TCM, thereby showing great potential in the practical application for the quality control of heavy metals in TCM.

The nanochannel-based sensor is able to achieve detection of Pb²⁺ in TCM samples.     

Selective and sensitive electrochemical sensors based on an ion imprinting polymer and graphene oxide for the detection of ultra-trace Cd(ii) in biological samples

New selective and sensitive electrochemical sensors were designed based on the deposition of a promising ion imprinted polymer (IIP) on the surface of glassy carbon electrode (GCE) for the detection and monitoring of Cd(ii) in different real samples. Herein, a highly selective Cd-imprinted polymer was successfully synthesized using a novel heterocyclic compound based on the benzo[f]chromene scaffold that acted as a complexing agent and a functional monomer in the presence of azobisisobutyronitrile (initiator) and ethylene glycol dimethacrylate (cross-linker). The characterization of the synthesized chelating agent and IIP was performed using FT-IR, SEM, ¹H-NMR, EIMS, and EDX analyses. After that, the voltammetric sensor was manufactured by introducing graphene oxide (GO) on the surface of GCE; then, the IIP was grown by a drop coating technique. The electrochemical characterization of the voltammetric sensor (IIP/GO@GCE) was performed by CV and EIS. For comparison, the potentiometric sensor was also prepared by embedding IIP in plasticized polyvinyl chloride and depositing it as one layer on the GCE surface. Anodic stripping voltammetry was used to construct the calibration graph; the IIP/GO@GCE exhibited a wider detection range (4.2 × 10⁻¹²–5.6 × 10⁻³ mol L⁻¹) and extremely low detection limit (7 × 10⁻¹⁴ mol L⁻¹) for Cd(ii). Meanwhile, the potentiometric sensor showed a linear calibration curve for Cd(ii) over a concentration range from 7.3 × 10⁻⁸ mol L⁻¹ to 2.4 × 10⁻³ mol L⁻¹ with a detection limit of 6.3 × 10⁻¹⁰ mol L⁻¹. Furthermore, both sensors offered outstanding selectivity for Cd(ii) over a wide assortment of other common ions, high reproducibility, and excellent stability.

New selective and sensitive electrochemical sensors were designed based on the deposition of a promising ion imprinted polymer (IIP) on the surface of glassy carbon electrode (GCE) for the detection and monitoring of Cd(ii) in different real samples.     

A sensitive and selective BINOL based ratiometric fluorescence sensor for the detection of cyanide ions

A highly selective, novel BINOL based sensor BBCN has been developed for the fluorescent ratiometric detection of cyanide ions (CN⁻). The optical study revealed that BBCN exhibited unique spectral changes only with cyanide ions in the presence of other competing ions. Besides, an apparent fluorescent colour change from green to blue was observed. A clear linear relationship was observed between the fluorescence ratiometric ratio of BBCN and the concentration of CN⁻ with a reasonably low detection limit (LOD) of 189 nM (507 ppb). The optical response was due to the nucleophilic addition of CN⁻ to the dicyanovinyl group of the sensor, which compromises the probe''s intramolecular charge transfer. This mechanism was well confirmed by Job''s plot, ¹H-NMR and ESI-MS studies. BBCN showed immediate spectral response towards (1 second) CN⁻ and detection could be realized in a broad pH window. Furthermore, the practical utility of BBCN was studied by test paper-based analysis and the detection of CN⁻ in various water resources.

A highly selective, novel BINOL based sensor BBCN has been developed for the fluorescent ratiometric detection of cyanide ions (CN⁻).     

Direct and sensitive detection of sulfide ions based on one-step synthesis of ionic liquid functionalized fluorescent carbon nanoribbons

Despite widely reported fluorescence sensors for cations, direct detection of anions is nevertheless still rare. In this work, ionic liquid-functionalized fluorescent carbon nanoribbons (IL-CNRs) are one-step synthesized and serve as the fluorescent probes for direct and sensitive detection of sulfide ions (S²⁻). The IL-CNRs are synthesized based on electrochemical exfoliation of graphite rods in a water-IL biphasic system. The as-prepared IL-CNRs exhibit uniform structure, high crystallinity, strong blue fluorescence (absolute photoluminescence quantum yield of 11.4%), and unique selectivity towards S²⁻. Based on the fluorescence quenching of IL-CNRs by S²⁻, a fluorescence sensor is developed for direct, rapid and sensitive detection of S²⁻ in the range of 100 nM to 1 μM and 1–300 μM with a low detection limit (LOD, 85 nM). Moreover, detection of S²⁻ in a real sample (tap water) is also demonstrated.

Sensitive detection of sulfide ions is realized based on one-step synthesis of ionic liquid functionalized fluorescent carbon nanoribbons.     

A luminescent Cd(ii) coordination polymer as a multi-responsive fluorescent sensor for Zn2+, Fe3+ and Cr2O72− in water with fluorescence enhancement or quenching

A luminescent Cd(ii) coordination polymer, namely {[Cd(btic)(phen)]·0.5H₂O}_n (CP-1) (H₂btic = 5-(2-benzothiazolyl)isophthalic acid, phen = 1,10-phenanthroline), was constructed through the mixed-ligand method under solvothermal conditions. CP-1 manifests a chain structure decorated with uncoordinated Lewis basic N and S donors. CP-1 exhibits high sensing towards Zn²⁺, Fe³⁺ and Cr₂O₇²⁻ ions with fluorescence enhancement or quenching. CP-1 exhibited a fluorescence enhancement for Zn²⁺ ions through weak binding to S and N atoms, and a fluorescence quenching for Fe³⁺ and Cr₂O₇²⁻ ions by an energy transfer process. The binding constants were calculated as 1.812 × 10⁴ mol⁻¹ for Zn²⁺, 4.959 × 10⁴ mol⁻¹ for Fe³⁺ and 1.793 × 10⁴ mol⁻¹ for Cr₂O₇²⁻. This study shows CP-1 as a rare multi-responsive sensor material for the efficient detection of Zn²⁺, Fe³⁺ and Cr₂O₇²⁻ ions.

A luminescent Cd(ii) coordination polymer can act as a multi-responsive sensor for efficiently detecting Zn²⁺, Fe³⁺ and Cr₂O₇²⁻ ions.     

Facile synthesis of N,P-doped carbon dots from maize starch via a solvothermal approach for the highly sensitive detection of Fe3+

Nitrogen/phosphorus-doped carbon dots (N, P-CDs) with a quantum yield as high as 76.5% were synthesized by carbonizing maize starch via a facile ethanol solvothermal approach. Transmission electron microscopy (TEM) measurement shows that the as-prepared N, P-CDs displayed a quasi-spherical shape with a mean size of ca. 2.5 nm. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy disclosed the presence of –OH, –NH₂, –COOH, and –CO functional groups over the surface of N, P-CDs. On the basis of excellent fluorescent properties with strong blue fluorescence emission at 445 nm upon excitation at 340 nm, these N, P-CDs were adopted as a fluorescent probe towards the effective detection of Fe³⁺ ions in water. The limit of detection (LOD) was as low as 0.1 μmol L⁻¹ and showed a better linear relationship in the range of 0.1 ∼ 50 μmol L⁻¹. In conclusion, these synthesized N, P-CDs can be efficiently used as a promising candidate for the detection of Fe³⁺ ions in some practical samples.

Nitrogen/phosphorus-doped carbon dots (N, P-CDs) with a quantum yield as high as 76.5% were synthesized by carbonizing maize starch via a facile ethanol solvothermal approach and utilized for the detection of Fe³⁺.     

Effective screen-printed potentiometric devices modified with carbon nanotubes for the detection of chlorogenic acid: application to food quality monitoring

All-solid state screen-printed electrodes were fabricated for chlorogenic acid (CGA) detection. The screen-printed platforms were modified with multi-walled carbon nanotubes (MWCNTs) to work as a lipophilic solid-contact transducer. The sensing-membrane was plasticized with a suitable solvent mediator and incorporating [Ni^II(bathophenanthroline)₃][CGA]₂ complex as a sensory material. In a 30 mM phosphate solution (buffer, pH 6), the sensor revealed a Nernstian-response towards CGA ions with a slope of −55.1 ± 1.1 (r² = 0.9997) over the linear range 1.0 × 10⁻⁷ to 1.0 × 10⁻³ (0.035–354.31 μg mL⁻¹) with a detection limit 7.0 × 10⁻⁸ M (24.8 ng mL⁻¹). It revealed a stable potentiometric response with excellent reproducibility and enhanced selectivity over several common ions. Short-term potential stability and the interfacial sensor capacitance was estimated using both electrochemical-impedance spectroscopy (EIS) and chronopotentiometry techniques. The presented electrochemical platform revealed the merits of design simplicity, ease of miniaturization, good potential-stability, and cost-effectiveness. It is successfully applied to CGA determination in different coffee beans extracts and juice samples. The data obtained were compared with those obtained by liquid chromatography reference method (HPLC).

All-solid state screen-printed electrodes were fabricated for chlorogenic acid (CGA) detection.     

Electro-spinning fabrication of nitrogen,phosphorus co-doped porous carbon nanofiber as an electro-chemiluminescent sensor for the determination of cyproheptadine

Nitrogen, phosphorus co-doped porous carbon nanofiber (N, P-PCNF) is prepared by electrospinning the mixed solution of polyacrylonitrile (PAN), polyvinylpyrrolidone (PVP) and phosphoric acid followed by carbonization. The N, P-PCNF as a modified electrode material is directly used to fabricate an electro-chemiluminescent sensor for determination of cyproheptadine, and owing to the large specific area, more active sites and promotion of electron transfer, the sensor exhibits high electro-catalytic activity, high sensitivity, a good linear relationship ranging from 1.0 × 10⁻⁷ to 1.0 × 10⁻⁵ mol L⁻¹ and a low detection limit (2.89 × 10⁻⁸ mol L⁻¹). In addition, the good recoveries indicate that the sensor is a promising device for the detection of cyproheptadine in real samples.

Nitrogen, phosphorus co-doped porous carbon nanofiber is as electrode modified material to fabricate an electro-chemiluminescent sensor for detecting cyproheptadine.     

Acridinedione as selective flouride ion chemosensor: a detailed spectroscopic and quantum mechanical investigation

The use of small molecules as chemosensors for ion detection is rapidly gaining popularity by virtue of the advantages it offers over traditional ion sensing methods. Herein we have synthesized a series of acridine(1,8)diones (7a–7l) and explored them for their potential to act as chemosensors for the detection of various anions such as fluoride (F⁻), acetate (OAc⁻), bromide (Br⁻), iodide (I⁻), bisulfate (HSO₄⁻), chlorate (ClO₃⁻), perchlorate (ClO₄⁻), cyanide (CN⁻), and thiocyanate (SCN⁻). Acridinediones were found to be highly selective chemosensors for fluoride ions only. To investigate in detail the mechanism of selective fluoride ion sensing, detailed spectroscopic studies were carried out using UV-visible, fluorescence and ¹H NMR spectroscopy. Fluoride mediated (NH) proton abstraction of acridinedione was found to be responsible for the observed selective fluoride ion sensing. Quantum mechanical computational studies, using time dependent density functional theory (TDDFT) were also carried out, whereupon comparison of acridinedione interaction with fluoride and acetate ions explained the acridinedione selectivity for the detection of fluoride anions. Our results provide ample evidence and rationale for further modulation and exploration of acridinediones as non-invasive chemosensors for fluoride ion detection in a variety of sample types.

The use of small molecules as chemosensors for ion detection is rapidly gaining popularity by virtue of the advantages it offers over traditional ion sensing methods.