A Julolidine Coupled Azine-based Reversible Chromo-fluorogenic Probe for Specific Detection of Cu2+ Ions.

Among the various essential trace elements for living organisms, the copper (Cu2+) ions are the most important. However, Cu2+ ions are vital for the human body and are associated with necessary physiological processes; insufficient or excessiveness has many hazardous effects on our bodies. In the present contribution, strategically, we have introduced a julolidine-coupled azine-based, 9,9'-((1E,1'E)-hydrazine-1,2-diylidene bis(methanylylidene)) bis(1,2,3,5,6,7-hexahydropyrido [3,2,1-ij] quinolin-8-ol) (HDBQ) reversible chromo-fluorogenic probe for specific detection of Cu2+ ions. Probe HDBQ exhibits observable orange colorimetric change from yellow, which is visible to the naked eye in daylight. The highly green fluorescence HDBQ becomes a non-fluorescent one with the incorporation of Cu2+ ions. Interestingly, the colorimetric change and non-fluorescent HDBQ-Cu2+ complex reverse to the original HDBQ in the presence of ethylenediamine tetraacetic acid (EDTA). The detection and quantification limit of HDBQ towards the detection of Cu2+ ions is found to be in the µM range, which is much lower than the limit (31.5 µM) recommended by WHO. We have also performed a colorimetric and fluorometric paper-based test strips-based experiment employing HDBQ for real-time on-site detection of Cu2+ ions. Using the reversibility characteristics of HDBQ for the consecutive addition of Cu2+ and EDTA, we have established the INHIBIT molecular logic gate. The present report brings a precise and sensitive probe for the detection of Cu2+ ions in real environmental and biological samples.

A Ratiometric Fluorescence Probe Based on Silver Nanoclusters and CdSe/ZnS Quantum dots for the Detection of Hydrogen Peroxide by Aggregation and Etching.

In this study, a ratiometric fluorescence nanoprobe is developed for the analysis of hydrogen peroxide (H2O2). Silver nanoclusters (AgNCs) were synthesized by chemical reduction method using sodium borohydride (NaBH4) as reducing agent, and were coupled with CdSe/ZnS quantum dots (QDs) to form the ratiometric fluorescence nanoprobe silver nanoclusters-quantum dots (AgNCs-QDs). The effect of the volume ratio of CdSe/ZnS QDs to AgNCs on the fluorescence ratio of AgNCs-QDs was investigated. The fluorescence characterization results show that two emission peaks of AgNCs-QDs are located at 473 nm and 661 nm, respectively. Transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS) results show that H2O2 can cause the fluorescence probe to aggregate, while etching AgNCs to produce silver ions, which together cause the fluorescence of the QDs in the ratiometric fluorescent probe to be quenched. Based on this strategy, the fluorescence intensity ratio of the two emission peaks F473/F661 exhibits a strong linear correlation with the concentration of H2O2. The detection range is 3.32 µM ~ 2.65 mM with a detection limit of 3.32 µM. In addition, the ratiometric fluorescence probe can specifically recognize H2O2 and has excellent anti-interference performance and good fluorescence stability. Importantly, the probe was utilized for the detection of H2O2 in serum, showing the possibility of the probe in clinical detection applications.

Highly Sensitive and Selective Fluorescence and Smartphone-Based Sensor for Detection of Rutin Using Boron Nitrogen Co-doped Graphene Quantum Dots.

This research explores the fluorescence properties and photostability of boron nitrogen co-doped graphene quantum dots (BN-GQDs), evaluating their effectiveness as sensors for rutin (RU). BN-GQDs are biocompatible and exhibit notable absorbance and fluorescence characteristics, making them suitable for sensing applications. The study utilized various analytical techniques to investigate the chemical composition, structure, morphology, optical attributes, elemental composition, and particle size of BN-GQDs. Techniques included X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The average particle size of the BN-GQDs was determined to be approximately 3.5 ± 0.3 nm. A clear correlation between the emission intensity ratio and RU concentration was identified across the range of 0.42 to 4.1 µM, featuring an impressively low detection limit (LOD) of 1.23 nM. The application of BN-GQDs as fluorescent probes has facilitated the development of a highly sensitive and selective RU detection method based on Förster resonance energy transfer (FRET) principles. This technique leverages emission at 465 nm. Density Functional Theory (DFT) analyses confirm that FRET is the primary mechanism behind fluorescence quenching, as indicated by the energy levels of the lowest unoccupied molecular orbitals (LUMOs) of BN-GQDs and RU. The method's effectiveness has been validated by measuring RU concentrations in human serum samples, showing a recovery range between 97.8% and 103.31%. Additionally, a smartphone-based detection method utilizing BN-GQDs has been successfully implemented, achieving a detection limit (LOD) of 49 nM.

Sustainable synthesis of fluorescent polymer carbon dots@PVA for sensitive chlortetracycline detection.

Antibiotic residues persist in the environment and represent serious health hazards; thus, it is important to develop sensitive and effective detection techniques. This paper presents a bio-inspired way to make water-soluble fluorescent polymer carbon dots (PCDs@PVA) by heating biomass precursors and polyvinyl alcohol (PVA) together. For example, the synthesized PCDs@PVA are very stable with enhanced emission intensity. This property was observed in a wide range of environmental conditions, including those with changing temperatures, pH levels, UV light, and ionic strength. PCDs@PVA detected the antibiotic chlortetracycline (CTCs) with great selectivity against structurally related compounds and a low detection limit of 20 nM, demonstrating outstanding sensitivity and specificity. We confirmed the sensor's practical application through real sample analysis, yielding recovery rates of 98%-99% in samples of milk, honey, and river water. The synthesized PCDs@PVA fluorescence sensor was successfully used for CTCs detection in real samples.

Sensitive detection of choline and nicotine in real samples by switching upconversion luminescence.

Nicotine (3-(1-methyl-2-pyrrolidinyl)pyridine) is one of the most common addictive substances, causing the trace detection of nicotine to be very necessary. Herein, we designed and prepared a functionalized nanocomposite CS-PAA (NaYF4:19.5%Yb,0.5%Tm@NaYF4-PAA) using a simple method. The nicotine concentration was quantitatively detected through the inhibition of choline oxidase activity by nicotine and the luminescence intensity of CS-PAA being quenched by Fe3+. The mechanism of Fe3+ quenching CS-PAA emission was inferred by luminescence lifetime and UV-vis absorption spectra characterization. During the nicotine detection, both excitation (980 nm) and emission (802 nm) wavelengths of CS-PAA enable the avoidance of the interference of background fluorescence in complicated food objects, thus providing high selectivity and sensitivity with a linear range of 5-750 ng/mL and a limit of detection of 9.3 nM. The method exhibits an excellent recovery and relative standard deviation, indicating high accuracy and repeatability of the detection of nicotine.

Adaptation of Conductometric Monoenzyme Biosensor for Rapid Quantitative Analysis of L-arginine in Dietary Supplements.

The present study reports on the development, adaptation, and optimization of a novel monoenzyme conductometric biosensor based on a recombinant arginine deiminase (ADI) for the determination of arginine in dietary supplements with a high accuracy of results. Aiming for the highly sensitive determination of arginine in real samples, we studied the effect of parameters of the working buffer solution (its pH, buffer capacity, ionic strength, temperature, and protein concentration) on the sensitivity of the biosensor to arginine. Thus, it was determined that the optimal buffer is a 5 mM phosphate buffer solution with pH 6.2, and the optimal temperature is 39.5 °C. The linear functioning range is 2.5-750 µM of L-arginine with a minimal limit of detection of 2 µM. The concentration of arginine in food additive samples was determined using the developed ADI-based biosensor. Based on the obtained results, the most effective method of biosensor analysis using the method of standard additions was chosen. It was also checked how the reproducibility of the biosensor changes during the analysis of pharmaceutical samples. The results of the determination of arginine in real samples using a conductometric biosensor based on ADI clearly correlated with the data obtained using the method of ion-exchange chromatography and enzymatic spectrophotometric analysis. We concluded that the developed biosensor would be effective for the accurate and selective determination of arginine in dietary supplements intended for the prevention and/or elimination of arginine deficiency.

Nano solid phase micro membrane tip and electrochemical methods for vanillin analysis in chocolate samples.

A polymer-based nanosensor and electrochemical methods were developed for the quantitative analysis of vanillin. The sample preparation was done using nano solid phase micro membrane tip extraction (NSPMMTE). A novel poly(phenylalanine)/TiO2/CPE sensor was built as the working electrode for the first time for the analysis of the vanillin substance. The electrochemical behavior and analytical performance of vanillin were examined in detail by cyclic voltammetry (CV) and differential pulse stripping voltammetry (DPSV) techniques via the oxidation process. The optimized modules of the DPSV technique that affected the vanillin peak current and peak potential were pH, pulse amplitude, step potential, and deposition time. The electroactive surface areas of bare CPE, TiO2/CPE, and poly(phenylalanine)/TiO2/CPE electrodes were found to be 0.135 cm2, 0.155 cm2, and 0.221 cm2, respectively. The limit of detection (LOD) was 32.6 µg/L in the 0.25-15.0 mg/L working range at pH 7.0. The selectivity of the proposed DPSV method for the determination of vanillin on the modified electrode was investigated in the presence of various organic and inorganic substances, and the determination of vanillin with high recovery was achieved with less than 5% relative error. The analytical application was applied in chocolate samples and the DPSV method was found highly efficient, reproducible, and selective.

A Carbazole-based Fluorescent Turn-off Chemosensor for Iron (II/III) Detection in a Dimethyl Sulfoxide.

We designed a novel carbazole-based chemosensor from 2-(N-hexylcarbazol-3'-yl)-pyridine-5-carbaldehyde which was named probe 7b. The main purpose of this study is to investigate whether metal ions in liquid media can be detected with probe 7b. The details were presented in this paper. First, the molecular absorption and fluorescence properties of probe 7b were characterized by spectrophotometers. Then, several methods were applied to check its sensing properties. The results showed that probe 7b has a sense towards Fe3+ ion than other interfering metal ions. The selectivity and sensitivity of probe 7b towards Fe3+ were very satisfactory to use in applications. Also, it was observed that when aqueous Fe3+ ion solutions were added to probe 7b in dimethyl sulfoxide (DMSO), the fluorescence intensity of probe 7b decreased. This situation (turn-off of emission) is due to the paramagnetic effect between probe 7b and Fe3+ ions. The limit of detection (LOD) value was found as 1.38 nM for probe 7b. This value is very small to compete with its counterparts in the literature. A real sample experiment indicated that probe 7b can detect Fe3+ ions more than other ions in real media, too. As a result, it was deduced that probe 7b is a very strong candidate to use in sensor technology.

Novel & Smart Sensing of Acetate and Hypochlorite Ions With Relay Recognition of Cr3+ Ion With Fluorescence Turn-on: Application in Bio-imaging & Real Sample Analysis.

The receptor-bearing anthraquinone chromophore was synthesized by a simple aldamine condensation reaction, and its anion sensing properties were investigated via colorimetric, UV-vis, photoluminescence, and DFT calculations. The synthesized receptor detects both acetate and hypochlorite ions, where remarkable colorimetric transitions were observed from pink to purple for the acetate ion and pink to blue for the hypochlorite ion. Moreover, in the occurrence of the acetate ion, it shows an admirable answer for the Cr3+ ion, which changes its purple color to pink, while no notable change was observed for other ions. The detection limits of receptors with acetate and hypochlorite are 7.1 × 10-7 M and 9.4 × 10-7 M, respectively. The DFT calculation was performed to better understand the sensing mechanisms of both AcO- and ClO- ions. Furthermore, receptors were effectively utilized in the preparation of optical sensors supported by silica gel for the detection of AcO- and ClO- ions. The receptor proved itself to be potentially useful for real-life application by sensing AcO - in vinegar and ClO - ions in ala. Furthermore, its preeminent detection properties enabled the successful labeling of the AcO- ion in living biological cells.

One Pot Hydrothermal Synthesis and Application of Bright-yellow-emissive Carbon Quantum Dots in Hg2+ Detection.

Carbon quantum dots (CQD) have drawn great interest worldwide for their extensive application as sensors due to their extraordinary physical and chemical characteristics, good biocompatibility, and high fluorescence in nature. Here, we demonstrate a technique for detecting mercury (Hg2+) ion using a fluorescent CQD probe. Ecology is concerned about the accumulation of heavy metal ions in water samples due to their harmful effects on human health. Sensitive identification and removal of metal ions from water samples are required to reduce heavy metals' risk. To find out Mercury in the water sample, carbon quantum dots were used and synthesized by 5-dimethyl amino methyl furfuryl alcohol and o-phenylene diamine through the hydrothermal technique. The synthesized CQD shows yellow emission when exposed to UV irradiation. Mercury ion was used to quench carbon quantum dots, and it was found that the detection limit was 5.2 nM with a linear range of 15-100 µM. The synthesized carbon quantum dots were demonstrated to efficiently detect Mercury ions in real water samples.

Nitrogen and sulfur co-doped photoluminescent carbon dots for highly selective and sensitive detection of Ag+ and Hg2+ ions in aqueous media: Applications in bioimaging and real sample analysis.

In this study, we report the synthesis of photoluminescent (PL) nitrogen (N) and sulfur (S) co-doped carbon dots (NS-CDs) from nitazoxanide and 3-mercaptopropionic acid as a precursors via a one-pot hydrothermal methods. N and S co-doped materials allows more active sites in the CDs surface resulting in an enhancement of their PL properties. NS-CDs show bright blue PL, excellent optical properties, good water solubility, and a high quantum yield (QY) of 32.1%. The as-prepared NS-CDs were confirmed by UV-Visible, photoluminescence, FTIR, XRD and TEM analysis. An optimized excitation at 345 nm, the NS-CDs exhibited strong PL emission at 423 nm with an average size of 3.53 ± 0.25 nm. Under optimized conditions, the NS-CDs PL probe shows high selectivity with Ag+/Hg2+ ions detected, while other cations no significant changes the PL signal. The PL intensity of NS-CDs linearly quenching and enhancement with Ag+ and Hg2+ ions from 0 to 50 × 10-6 M, with the detection limit of 2.15 × 10-6 M and 6.77 × 10-7 M (S/N = 3). More interestingly, as-synthesized NS-CDs shows a strong binding to Ag+/Hg2+ ions with the PL quenching and enhancement to precise and quantitative detection of Ag+/Hg2+ ions in living cells. The proposed system was effectively utilized for the sensing of Ag+/Hg2+ ions in real samples resulting in high sensitivity and good recoveries (98.4-109.7%).

Fabrication of Carbon Nanofiber Incorporated with CuWO4 for Sensitive Electrochemical Detection of 4-Nitrotoluene in Water Samples.

In the current work, copper tungsten oxide (CuWO4) nanoparticles are incorporated with carbon nanofiber (CNF) to form CNF/CuWO4 nanocomposite through a facile hydrothermal method. The prepared CNF/CuWO4 composite was applied to the electrochemical detection of hazardous organic pollutants of 4-nitrotoluene (4-NT). The well-defined CNF/CuWO4 nanocomposite is used as a modifier of glassy carbon electrode (GCE) to form CuWO4/CNF/GCE electrode for the detection of 4-NT. The physicochemical properties of CNF, CuWO4, and CNF/CuWO4 nanocomposite were examined by various characterization techniques, such as X-ray diffraction studies, field emission scanning electron microscopy, EDX-energy dispersive X-ray microanalysis, and high-resolution transmission electron microscopy. The electrochemical detection of 4-NT was evaluated using cyclic voltammetry (CV) the differential pulse voltammetry detection technique (DPV). The aforementioned CNF, CuWO4, and CNF/CuWO4 materials have better crystallinity with porous nature. The prepared CNF/CuWO4 nanocomposite has better electrocatalytic ability compared to other materials such as CNF, and CuWO4. The CuWO4/CNF/GCE electrode exhibited remarkable sensitivity of 7.258 µA µM-1 cm-2, a low limit of detection of 86.16 nM, and a long linear range of 0.2-100 µM. The CuWO4/CNF/GCE electrode exhibited distinguished selectivity, acceptable stability of about 90%, and well reproducibility. Meanwhile, the GCE/CNF/CuWO4 electrode has been applied to real sample analysis with better recovery results of 91.51 to 97.10%.

Uracil-Appended Fluorescent Sensor for Cu2+ and Hg2+ Ions: Real-Life Utilities Including Recognition of Vitamin B2 (Riboflavin) in Milk Products and Invisible Ink Applications.

A simple uracil-appended fluorescent sensor (1) has been developed by one pot reaction and characterized by using common spectroscopic methods such as UV-vis, Fluorescence, HRMS and FT-IR analyses. Upon addition of various metal ions to the CH3CN solution of sensor 1, the fluorescence was quenched in the presence of Cu2+ / Hg2+ ions. The limit of detection for Cu2+ and Hg2+ was calculated to be 3.31 and 0.316 µM, respectively. Further, the sensor was applied for real-life applications in the determination of Vitamin B2 (riboflavin) and its presence in milk products. With the incorporation of different sources of vitamin-B to acetonitrile solution of it, there was discernible fluorescence enhancement only in the presence of vitamin B2. Also, it has been successfully applied for the detection of Vitamin B2 (riboflavin) in milk and curd. Moreover, based on the fluorescent color changes, the sensor was utilized for invisible ink applications.

Ultrasensitive electrochemical detection of furazolidone in biological samples using 1D-2D BiVO4@MoS2 hierarchical nano-heterojunction composites armed electrodes.

In this work, the hydrothermally synthesized of BiVO4@MoS2 hierarchical nano-heterojunction composite is employed as a novel electrocatalyst for electrochemical sensing of Furazolidone (FZE) drug by modifying the glassy carbon electrodes (GCE). The Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy and transmission electron microscopy are used to thoroughly investigate the functional groups, vibrational modes, crystal structure, elemental composition and surface topography of the heterojunction composite. The physical characterization results revealed the successful construction of 1D-2D BiVO4@MoS2 hierarchical nano-heterojunction composite. When these unique architectures are reinforced on GCE surface, we achieved an enhanced electroactive surface area of 0.154 cm2. The electrochemical performance of 1D-2D BiVO4@MoS2 is examined though cyclic voltammetry and differential pulse voltammetry (DPV) analysis. The BiVO4@MoS2 composites exhibited an excellent electrocatalytic activity in sensing of FZE with superior linear detection ranges of 0.01-14 and 14-614 µM. The limit of detection (LOD) of the BiVO4@MoS2 based sensor is determined to be 2.9 nM which is far superior than other reported FZE sensors. Consequently, it is evident from the investigation that the BiVO4@MoS2 based FZE sensor can be recommended for analyzing real time samples like human urine and blood serum with appreciable recovery.

Near-infrared fluorogenic receptor for selective detection of cysteine in blood serum and living cells.

A novel near-infrared fluorescent probe, namely propane-2,2-diylbis(2-((E)-2-(benzo[d]thiazol-2-yl)-2-cyanovinyl)-4,1-phenylene) diacrylate (BTA), was synthesized for selective detection of cysteine over other biologically significant amino acids. Upon addition of cysteine, the probe BTA displays a dramatic increase in fluorescence intensity at 715 nm along with a fast response time (4 min). The limit of detection (LOD) was calculated as 0.12 µM. In addition, the synthesized probe BTA was effectively utilized for the recognition of cysteine in blood serum and living cells.

A 1-Hydroxy-2,4-Diformylnaphthalene-Based Fluorescent Probe and Its Detection of Sulfites/Bisulfite.

A novel 1-hydroxy-2,4-diformylnaphthalene-based fluorescent probe L was synthesized by a Knoevenagel reaction and exhibited excellent sensitivity and selectivity towards sulfite ions (SO32-) and bisulfite ions (HSO3-). The detection limits of the probe L were 0.24 µM using UV-Vis spectroscopy and 9.93 nM using fluorescence spectroscopy, respectively. Furthermore, the fluorescent probe L could be utilized for detection in real water samples with satisfactory recoveries in the range 99.20%~104.30% in lake water and 100.00%~104.80% in tap water by UV-Vis absorption spectrometry, and in the range 100.50%~108.60% in lake water and 102.70%~103.80% in tap water by fluorescence spectrophotometry.

Real Sample Consistency Regularization for GANs.

Mode collapse has always been a fundamental problem in generative adversarial networks. The recently proposed Zero Gradient Penalty (0GP) regularization can alleviate the mode collapse, but it will exacerbate a discriminator's misjudgment problem, that is the discriminator judges that some generated samples are more real than real samples. In actual training, the discriminator will direct the generated samples to point to samples with higher discriminator outputs. The serious misjudgment problem of the discriminator will cause the generator to generate unnatural images and reduce the quality of the generation. This paper proposes Real Sample Consistency (RSC) regularization. In the training process, we randomly divided the samples into two parts and minimized the loss of the discriminator's outputs corresponding to these two parts, forcing the discriminator to output the same value for all real samples. We analyzed the effectiveness of our method. The experimental results showed that our method can alleviate the discriminator's misjudgment and perform better with a more stable training process than 0GP regularization. Our real sample consistency regularization improved the FID score for the conditional generation of Fake-As-Real GAN (FARGAN) from 14.28 to 9.8 on CIFAR-10. Our RSC regularization improved the FID score from 23.42 to 17.14 on CIFAR-100 and from 53.79 to 46.92 on ImageNet2012. Our RSC regularization improved the average distance between the generated and real samples from 0.028 to 0.025 on synthetic data. The loss of the generator and discriminator in standard GAN with our regularization was close to the theoretical loss and kept stable during the training process.

Dopamine-induced photoluminescence quenching of bovine serum albumin-capped manganese-doped zinc sulphide quantum dots.

The direct detection of dopamine (DA) in human body fluids is a great challenge for medical diagnostics of neurological disorders like Parkinson's disease, Alzheimer's disease, senile dementia, and schizophrenia. In this work, a simple and turn off luminescence sensing of DA based on bovine serum albumin (BSA)-capped manganese-doped zinc sulphide quantum dots (Mn:ZnS/BSA QDs) is developed. The Mn:ZnS/BSA QDs were synthesized by a chemical co-precipitation method. Due to the special interaction of DA with BSA and metal ions, Mn:ZnS/BSA QDs can serve as an effective sensing platform for DA. The luminescence of Mn:ZnS/BSA QDs decreased linearly with increasing concentration of DA in the range from 6.6 to 50.6 nM. The limit of detection is 2.02 nM. The driving force for the luminescence quenching is partly provided by ground-state complex formation of QDs with DA. The photo-induced electron transfer from the conduction band of QDs to oxidized dopamine (quinone) also favors quenching. The Mn:ZnS/BSA QDs are barely interfered with by other competing biomolecules except catecholamine neurotransmitter like epinephrine. Moreover, this method is used in the analysis of DA-spiked human serum and human urine samples and good recovery percentages are found. To assess the utility of the developed sensor, paper strip assay was also successfully conducted. Graphical abstract.

Determination of Alternaria Toxins in Sunflower Oil by Liquid Chromatography Isotope Dilution Tandem Mass Spectrometry.

Alternaria toxins have gained attention as a potential health risk and can be classified as emerging mycotoxins. As a result, they are candidates to be regulated by the European Commission. This paper describes a liquid chromatography tandem mass spectrometric (LC-MS/MS) method for analyzing five Alternaria toxins in sunflower oil, which is a rather different type of sample to those matrices investigated in earlier published papers. An optimal sample preparation condition was achieved when samples were dissolved in n-hexane and extracted with methanol/water mixture, followed by sample pre-concentration with solvent evaporation. This study is the first focusing only on this lipophilic matrix and in using all corresponding isotopically labeled internal standards (ISTD) to compensate the matrix effect that strongly influences the LC-MS/MS analysis of toxins. Target compounds were separated on Zorbax Extend C-18 column enabling the analysis at alkaline pH of 8.8 that was necessary to obtain appropriate peak shape of tenuazonic acid and to separate the analytes at baseline. The method was validated according to the EU 2002/657/EC Decision and all the analytical performance characteristics met the requirements. The recovery was between 74% and 122% in fortified sunflower oil samples and the precision varied from 9% to 22%. The method was successfully demonstrated for sunflower seed quality check (QC) samples. Finally, 16 different sunflower oil samples were measured; and tenuazonic acid and tentoxin toxins were detected at levels close to LOQ concentrations.

A novel dye-based colorimetric chemosensors for sequential detection of Cu2+ and cysteine in aqueous solution.

An IDAs based chemosensing ensembles for sensitive and selective sequential detection of Cu2+ and cysteine (Cys) in 100% aqueous solution was designed on the basis of the complex formation between 4-(2-Pyridylazo)resorcinol (PAR). In the first step, PAR was used for colorimetric detection of Cu2+ in aqueous solution by the obvious color change. The detection limit (31.0 nmol L-1) for Cu2+ much lower than the guideline (31.5 µmol L-1) of WHO in drinking water. In the second step the produced ensemble (PAR-Cu2+), sensitively and selectively detected a low concentration of Cys via indicator displacement assay system. The detection limit for Cys was determined to be 72 nmol L-1. The colorimetric detection operation is low-cost using PAR and copper ion and has a simple operation without any further modifications. Any enzymatic reactions, separation processes, chemical modifications, and sophisticated instrumentations are also not required in this experiment. It could find applications for the detection of analytes in environmental, biological samples based on these results, dual logic gates (IMPLICATION and INHIBIT) were obtained by controlling the chemical inputs.