Facile hydrothermal synthesis of manganese sulfide nanoelectrocatalyst for high sensitive detection of Bisphenol A in food and eco-samples.

Bisphenol A (BPA) is a renowned plasticizer, and a key component of various plastics, resins, and food packaging materials. However, BPA have been identified as an endocrine disruption compound and cause severe consequences such as infertility, diabetic, obesity, carcinoma, and possess high risk of exposure in aquatic ecosystem. To this, we crafted an ultrasensitive electrochemical sensor based on the manganese sulfide nanoparticles (MnS NPs) catalyzed electrochemical oxidation of BPA, and its eventual application in rapid screening of BPA contamination. The physiochemical characteristics and electrocatalytic performance of the MnS nanocatalyst have been well studied and utilized in the fabrication of MnS/GCE based BPA sensor. The fabricated BPA sensor has shown a broad dynamic range (20 nM-2.15 mM), lower detection limits (6.52 nM) and promising towards rapid screening of BPA contaminations in food and environmental samples under mimicked real-world conditions with excellent accuracy and precision.

Rapid One-Pot Synthesis of Polydopamine Encapsulated Carbon Anchored with Au Nanoparticles: Versatile Electrocatalysts for Chloramphenicol and Folic Acid Sensors.

Designing and engineering nanocomposites with tailored physiochemical properties through teaming distinct components is a straightforward strategy to yield multifunctional materials. Here, we describe a rapid, economical, and green one-pot microwave synthetic procedure for the preparation of ternary nanocomposites carbon/polydopamine/Au nanoparticles (C/PDA/AuNPs; C = carbon nanotubes (CNTs), reduced graphene oxide (rGO)). No harsh reaction conditions were used in the method, as are used in conventional hydrothermal or high-temperature methods. The PDA unit acts as a non-covalent functionalizing agent for carbon, through π stacking interactions, and also as a stabilizing agent for the formation of AuNPs. The CNTs/PDA/AuNPs modified electrode exhibited excellent electrocatalytic activity to oxidize chloramphenicol and the resulting sensor exhibited a low detection limit (36 nM), wide linear range (0.1-534 µM), good selectivity (against 5-fold excess levels of interferences), appreciable reproducibility (3.47%), good stability (94.7%), and practicality (recoveries 95.0%-98.4%). Likewise, rGO/PDA/AuNPs was used to fabricate a sensitive folic acid sensor, which exhibits excellent analytical parameters, including wide linear range (0.1-905 µM) and low detection limit (25 nM). The described synthetic route includes fast reaction time (5 min) and a readily available household microwave heating device, which has the potential to significantly contribute to the current state of the field.

Ratiometric electrochemical molecular switch for sensing hypochlorous acid: Applicable in food analysis and real-time in-situ monitoring.

A ratiometric electrochemical molecular sensing platform for real-time quantification of extracellular hypochlorous acid (HClO) production has been developed based on a latent electrochemical probe aminoferrocene thiocarbamate (AFTC 3). The substrate AFTC consist of a masked redox reporter amino ferrocene (AF 4) linked with a dimethylthiocarbamate trigger via hydroxyl benzyl alcohol. The conceptual idea behind the probe design is based on a specific chemical interaction between HClO and dimethylthiocarbamate, which allows only HClO to unmask the probe to releases AF. The scheme was manipulated to establish a highly selective (in presence of various reactive oxygen species, anions and other biological interfering species) and sensitive (detection limit 75 nM) sensing platform not only in lab samples but also in real samples (food samples, and live cells). Real-time in situ quantification platform was developed to profile HClO productions in macrophages, and it did so with great consistency.

Electrochemical substrate for active profiling of cellular surface leucine aminopeptidase activity and drug resistance in cancer cells.

Leucine aminopeptidase (LAP) is an essential proteolytic enzyme and potential biomarker for liver malignancy. Overexpression of LAP is directly linked with some fatal physiological and pathological disorders. In this regard, we have designed an activity based electrochemical substrate leucine-benzyl ferrocene carbamate (Leu-FC) for selective profiling of LAP activity in live cells. In practice, LAP instantaneously hydrolyze the Leu residue of the substrate Leu-FC to eliminate the unmasked electrochemical reporter amino ferrocene via predefined self-immolative cascade. The electrochemical signal is distinctly specific for LAP and free of other electroactive biological interference. The substrate Leu-FC empowered sensor displayed broad dynamic range with admirable detection limits. On top of this, the probe Leu-FC was employed in real-time active profiling of cellular LAP activity in HepG2 cells and effect of LAP inhibitor. In extent, the substrate Leu-FC can effectively monitor cisplatin induced overexpression of LAP activity in HepG2 cells in presence and absence of bestatin. The sensor showcased an excellent reliability towards monitoring cellular LAP activity in HepG2 cells. Unlike the traditional antibody-based immunoassays, our approach is capable of monitoring in-situ activity of LAP in live cells.

Simplistic synthesis of ultrafine CoMnO3 nanosheets: An excellent electrocatalyst for highly sensitive detection of toxic 4-nitrophenol in environmental water samples.

Design and fabrication of cost effective analytical tools to monitor toxic organic emissions in eco system is of a great necessity. Nitrophenols are a class of widespread toxic organic pollutant lead to serious adverse effects in biosphere on its consumption. This article reports a high sensitive, cost effective, robust electrochemical sensor for 4-nitrophenol (4-NP) in environmental water samples. A novel sheet like CoMnO3 (CMO Ns) nanocatalyst was synthesized via oxalic acid assisted co-precipitation technique and employed as electrocatalyst for the high sensitive detection of 4-NP. The physiochemical properties of CMO Ns are studied in detail via XRD, FTIR, TEM, TGA, and XPS. TEM results reviled the protocol is an excellent way for synthesis of a uniformly distributed CMO Ns with lathery surface. Evident to the surface and other physiochemical studies the CMO Ns based sensor holds superior electrocatalytic activity towards 4-NP detection with excellent sensitivity (2.458 µA µM-1 cm-2) coupled with nanomolar detection (10 nm) limits. Moreover, the constructed sensor holds reliable long-term durability, good reproducibility, and excellent working stability. The practical applicability of the developed sensor was evaluated by determination of 4-NP in samples acquired from water resources with RSD ± 3.3%.

Ultrasonic energy-assisted preparation of ß-cyclodextrin-carbon nanofiber composite: Application for electrochemical sensing of nitrofurantoin.

A simple ultrasonic energy assisted synthesis of ß-cyclodextrin (ß-CD) supported carbon nanofiber composite (CNF) and its potential application in electrochemical sensing of antibiotic nitrofurantoin (NFT) is reported. The elemental composition and surface morphology of the ß-CD/CNF composite was validated through Field emission scanning electron microscopy, energy dispersive X-ray microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis. The uniform enfolding of hydrophilic ß-CD over CNF enhance the aqueous dispersion and offer abundant active surface to the ß-CD/CNF composite. Further, the electrocatalytic efficacy of the ß-CD/CNF composite is utilized to fabricate an electrochemical sensor for the high sensitive quantitative detection of NFT. Under optimized analytical conditions, the sensor displays a broad working range of 0.004-308 µM and calculated detection limit of 1.8 nM, respectively. In addition, the sensor showcased a good selectivity, storage, and working stability, with amiable reproducibility. The point-of-care applicability of the sensor was demonstrated with NFT spiked human blood serum and urine sample with reliable analytical performance. The simple, cost-effective NFT sensor based on ß-CD/CNF offered outstanding analytical performance in real-world samples with higher reliability.

Facile Solvothermal Preparation of Mn2CuO4 Microspheres: Excellent Electrocatalyst for Real-Time Detection of H2O2 Released from Live Cells.

Hydrogen peroxide (H2O2) is an eminent biomarker in pathogenesis; a selective, highly sensitive real-time detection of H2O2 released from live cells has drawn a significant research interest in bioanalytical chemistry. Binary transition-metal oxides (BTMOs) displayed a recognizable benefit in enhancing the sensitivity of H2O2 detection; although the reported BTMO-based H2O2 sensor's detection limit is still insufficient, it is not appropriate for in situ profiling of trace amounts of cellular H2O2. In this paper, we describe an efficient, reliable electrochemical biosensor based on Mn2CuO4 (MCO) microspheres to assay cellular H2O2. The Mn2CuO4 microspheres were prepared through a superficial solvothermal method. It is obvious from impedance studies, introduction of manganese into copper oxide lattice significantly improved the ionic conductivity, which is beneficial for the electrochemical sensing process. Thanks to the distinct microsphere structure and excellent synergy, MCO-modified electrode exhibited excellent nonenzymatic electrochemical behavior toward H2O2 sensing. The MCO-modified electrode delivered a broad working range (36 nM to 9.3 mM) and an appreciable detection limit (13 nM), with high selectivity toward H2O2. To prove its practicality, the developed sensor was applied in the detection of cellular H2O2 released by RAW 264.7 cells in presence of CHAPS. These results label the possible appliance of the sensor in clinical analysis and pathophysiology. Thus, BTMOs are evolving as a promising candidate in designing catalytic matrices for biosensor applications.

Electrochemical Molecular Switch for the Selective Profiling of Cysteine in Live Cells and Whole Blood and for the Quantification of Aminoacylase-1.

A first-of-a-kind latent electrochemical redox probe, ferrocene carbamate phenyl acrylate (FCPA), was developed for the selective detection of cysteine (Cys) and aminoacylase (ACY-1). The electrochemical signal generated by this probe was shown to be highly specific to Cys and insensitive to other amino acids and biological redox reactants. The FCPA-incorporated electrochemical sensor exhibited a broad dynamic range of 0.25-100 µM toward Cys. This probe also proficiently monitored the ACY-1-catalyzed biochemical transformation of N-acetylcysteine (NAC) into Cys, and this proficiency was used to develop an electrochemical assay for quantifying active ACY-1, which it did so in a dynamic range of 10-200 pM (0.1-2 mU/cm3) with a detection limit of 1 pM (0.01 mU/cm3). Furthermore, the probe was utilized in real-time tracking and quantification of cellular Cys production, specifically in Escherichia coli W3110, along with a whole blood assay to determine levels of Cys and spiked ACY-1 in blood with a reliable analytical performance.