Validation of electrochemical device setup for detection of dual antibiotic drug release from hydrogel.

Due to antimicrobial resistance that occurs throughout the world, antibiotic-releasing hydrogel with at least two drugs that synergistically treat stubborn bacteria is preferable for infection prevention. Hydrogel can serve as a drug reservoir to gradually release drugs in a therapeutic window to effectively treat microorganisms with minimal side effects. The study and development of drug releasing hydrogels requires a reliable, straightforward, cost-effective, fast, and low labor-intensive drug detection technique. In this study, we validate the electrochemical technique and device setup for real-time determination of dual antibacterial drugs released from a hydrogel. Concentrations of two representative antibacterial drugs, tetracycline (TC) and chloramphenicol (CAP), were determined using square wave voltammetry (SWV) mode that yields the lower limit of detection at 2.5 µM for both drugs. Measurement accuracy and repeatability were verified by 36 known drug combination concentrations. Capability in long-term measurement was confirmed by the measurement stability which was found to last for at least 72 h. Stirring was revealed as one of the significant factors for accurate real-time detection. Real-time measurement was ultimately performed to demonstrate the determination of multiple drug releases from a drug releasing hydrogel and validated by high-performance liquid chromatography (HPLC). All the results support that the electrochemical technique with the proposed device design and setup can be used to accurately and simultaneously determine dual drugs that are released from a hydrogel in real-time.

Energy-efficient treatment of refractory industrial effluent using flow-through electrochemical processes: Oxidation mechanisms and reduction of chlorinated byproducts.

While flow-through anodic oxidation (FTAO) technique has demonstrated high efficiency to treat various refractory waste streams, there is an increasing concern on the secondary hazard generation thereby. In this study, we developed an integrated system that couples FTAO and cathodic reduction processes (termed FTAO-CR) for sustainable treatment of chlorine-laden industrial wastewater. Among four common electrode materials (i.e., Ti4O7, ß-PbO2, RuO2, and SnO2-Sb), RuO2 flow-through anode exhibited the best pollutant removal performance and relatively low ClO3 and ClO4 yields. Because of the significant scavenging effect of Cl- in real wastewater treatment, the direct electron transfer process played a dominant role in contaminant degradation for both active and nonactive anodes though active species (i.e., active chlorine) were involved in the subsequent transformation of the organic matter. A continuous FTAO-CR system was then constructed for simultaneous COD removal and organic and inorganic chlorinated byproduct control. The quality of the treated effluent could meet the national discharge permit limit at low energy cost (∼4.52 kWh m3 or ∼0.035 kWh g1-COD). Results from our study pave the way for developing novel electrochemical platforms for the purification of refractory waste streams whilst minimizing the secondary pollution.

Serotonin secretion by blood platelets: accuracy of high-performance liquid chromatography-electrochemical technique compared with the isotopic test and use in a clinical laboratory.

Background: Mild secretion defects are the most frequent and challenging blood platelet disorders to diagnose. Most δ-granule secretion tests lack validation, are not quantitative, or have unreliable response to weak platelet agonists. Objectives: To compare platelet serotonin secretion by HPLC-electrochemical detection technique (HPLC-ECD) with the reference isotopic test (3H-5-HT), evaluating its performance in clinical laboratories. Methods: The assay validation followed STARD-2015 recommendations. HPLC-ECD measured the nonsecreted serotonin remaining in platelet pellets after aggregation, comparing it with the reference 3H-5-HT assay. We studied subjects with inherited and aspirin-induced blood platelet disorders and assessed the HPLC-ECD operation for routine clinical diagnosis. Results: Calibration curves were linear (R2 = 0.997), with SD for residuals of 3.91% and analytical sensitivity of 5ng/mL. Intra- and interassay imprecision bias ranged between -8.5% and 2.1% and -9% and 3.1%, respectively. Serotonin recovery and stability were >95%, and the variability range of measurements was -5.5% to 4.6%. Statistical differences detected between tests were biologically irrelevant, with bias of 1.48% (SD, 8.43) and CI agreement of -18% to 15%. Both assays distinctly detected platelet secretion induced by 10 µM epinephrine and 4 µmM adenosine diphosphate. However, HPLC-ECD is quantitative and more sensitive to low serotonin content in blood platelets. Reference cutoffs for each agonist were determined in 87 subjects. Initially, the HPLC-ECD requires relatively expensive equipment and trained operators but has remarkably cheap running costs and a turn-around time of 24-36 hours. We have used this diagnostic tool routinely for >8 years. Conclusion: HPLC-ECD assay for platelet serotonin secretion is highly accurate, has advantages over the reference 3H-5-HT test, and is suitable as a clinical laboratory technique.

Insights into the weathering behavior of pyrite in alkaline soil through electrochemical characterizations: Actual hazards or potentially benefits?

Pyrite is the most common metal sulfide mineral in the crust and readily weathers under natural circumstances to release H+ to acidify surrounding groundwater and soil, resulting in heavy metal ions in the surrounding environment (e.g., meadow and saline soils). Meadow and saline soils are two common, widely distributed alkaline soils and can affect pyrite weathering. Currently, the weathering behaviors of pyrite in saline and meadow soil solutions have not been systematically studied. Electrochemistry coupled with surface analysis methods were employed to study pyrite weathering behaviors in simulated saline and meadow soil solutions in this work. Experimental results suggest that saline soil and higher temperatures increase pyrite weathering rates due to the lower resistance and greater capacitance. Surface reactions and diffusion control the weathering kinetics, and the activation energies for the simulated meadow and saline soil solutions are 27.1 and 15.8 kJ mol-1, respectively. In-depth investigations reveal that pyrite is initially oxidized to Fe(OH)3 and S0, and Fe(OH)3 further transforms into goethite γ-FeOOH and hematite α-Fe2O3, while S0 ultimately converts into sulfate. When these iron compounds enter alkaline soils, the alkalinity of soil changes, and iron (hydr)oxides effectively reduce the bioavailability of heavy metals and benefit alkaline soils. Meanwhile, weathering of natural pyrite ores containing toxic elements (such as Cr, As, and Cd) makes these elements bioavailable and potentially degrades the surrounding environment.

Effect of marine microalgae Synechococcus sp., Chlorella sp., Thalassiosira sp. on corrosion behavior of Q235 carbon steel in f/2 medium.

The effect of marine microalgae on the corrosion behavior of carbon steel (CS) still needs further investigation due to their dual roles. In this study, the corrosion behavior of Q235 CS specimens in f/2 medium with absence and presence of three classes of marine microalgae Synechococcus sp., Chlorella sp., and Thalassiosira sp. was investigated during a 16-day immersion period by the weight loss, electrochemical impedance spectroscopy, potentiodynamic polarization curve, and surface analysis techniques. The biomass of the three microalgae was monitored at the same time. The results showed that the values of weight loss and corrosion current density decreased, and the values of charge transfer resistance increased in the CS specimens treated with these microalgae. On day 16, the inhibition efficiency of Thalassiosira sp. group was the highest (80.78%), followed by Chlorella sp. group (70.80%), and finally Synechococcus sp. group (69.38%). But the inhibition efficiency diminished with time. Furthermore, in these microalgal treatment groups, the passivation films were found to consist of a biofilm and a corrosion product film. This study revealed that the three microalgae can effectively strengthen the barrier of the CS specimens in the f/2 medium, leading to slow down their corrosion rates.

FeSO4·7H2O optimisation of earthed atomising corona discharge (Fe-EACD) a process for the pharmaceutical wastewater treatment.

Pharmaceutical residues can cause serious water pollution problems, harm human health and destroy the ecological balance. FeSO4·7H2O optimisation of the earthed atomising corona discharge (Fe-EACD) process was used to dispose of pharmaceutical wastewater in this research. Experiments were analyzed by VI characteristic curves to optimise the electrode distance (20-50 mm) and wire electrode diameter (0.3-0.5 mm). The effects of discharging voltage (7-12 kV), time (0-54 min) and FeSO4 dosage (0.2-1.2 g/L) were investigated using the response surface methodology (RSM). According to the RSM results, the best removal efficiency of COD (89.6%) was detected at the optimal discharging voltage of 12 kV, time of 42 min and Fe2+ concentration of 0.4 g/L. The Fe-EACD process could work efficiently with BOD5/COD ratio moving to 0.49 in an acid environment. The kinetic analysis and mechanism study suggested that the Fe-EACD process was demonstrated well by the pseudo-first-order based on the correlation coefficient (R2). Active •OH producing in the EACD process is responsible for the COD removal and the FeSO4·7H2O as a catalyst can promote the formation of active hydroxyl. In other words, EACD with Fe2+ optimisation was an economic and feasible process for pharmaceutical wastewater treatment.

Green application of trimetallic nickel-cobalt-molybdenum nanocomposites on 3D graphene oxide as a powerful electrocatalyst for hydrogen evolution reaction.

In-situ designing of multiple metals electrocatalysts with high active sites and performance is the main challenge for hydrogen evolution reaction (HER). So in this work, 3D-rGO was easily obtained from 2D-graphene by a simple one-step hydrothermal method to create the interspace sites and active surface area. The Ni-Co-Mo tri-metallic@3D-rGO was synthesized and fully characterized by different techniques, e.g., FT-IR, XRD, Raman, FE-SEM, TEM, EDS, mapping, ICP-OES, AFM, voltammetry, and electrochemical impedance spectroscopy. According to the FE-SEM and TEM images, the Ni-Co-Mo tri-metallic@3D-rGO has a crumpled-formed structure. The as-prepared nanocomposite has high HER performance with a low potential of -0.11 (vs. RHE) to deliver 10 mA cm-2 and Tafel slope of 68 mV dec-1 for Pt and -0.25 V (vs. RHE) to deliver 10 mA cm-2 and Tafel slope of 110 mV dec-1 for graphite counter electrode. Furthermore, the 3D structure illustrates high long-term durability in the HER process for 1000 continuous cycles and 12 h operation at -0.42 V (vs. RHE) for Pt and graphite counter electrode. It's noticeable HER performance has the synergetic effect between 3D-rGO and tri-metallic structure with high porosity and electrical conductivity, enhancing HER kinetic.

The effect of a biofilm-forming bacterium Tenacibaculum mesophilum D-6 on the passive film of stainless steel in the marine environment.

The microbiologically influenced corrosion of 304 stainless steel in the presence of a marine biofilm-forming bacterium Tenacibaculum mesophilum D-6 was systematically investigated by means of electrochemical techniques and surface analyses to reveal the effect of the selective attachment and adsorption of the biofilms on the passivity breakdown of the stainless steel. It was found that the T. mesophilum D-6 was electroactive and could oxidize low valent cations and metal, facilitating the local dissolution of the passive film and the substrate in the film defects, nearly doubling the surface roughness. The biofilms of T. mesophilum D-6 with mucopolysaccharide secreta and chloride ions tended to preferentially adsorb at the defects of the passive film on the steel, yielding non-homogeneous microbial aggregates and local Cl- enrichment there. The adsorption of the bacteria and chloride ions reduced the thickness of passive film by 23.9%, and generate more active sites for pitting corrosion on the passive film and more semiconducting carrier acceptors in the film. The maximum current density of the 304 SS in the presence of T. mesophilum D-6 was over one order of magnitude higher than that in the sterile medium, and the largest pit was deepened 3 times.

Arsenopyrite weathering in acid rain: Arsenic transfer and environmental implications.

Arsenopyrite is widely distributed and weathers readily in the nature, releases As and pollutes the surrounding environment. Acid rain is acidic in nature as contains sulfur oxides (SOx) and nitrogen oxides (NOx), and is a typical hazardous material to human. When arsenopyrite encounters acid rain, their interaction effect may aggregate environmental degradation. In this work, the weathering behavior of arsenopyrite in simulated acid rain was studied using the electrochemical techniques and surface analysis. Cyclic voltammetry and Raman and XPS confirmed that FeAsS was oxidized to Fe2+, AsO33- and S0 at the initial phase, then, Fe2+ was converted to Fe3+, S0 transformed to SO32- and ultimately to SO42-, and AsO33- to AsO43- with the accumulation of H+. Polarization curve revealed higher temperature or higher acidity of acid rain increased the weathering trend and rate of arsenopyrite, and electrochemical impedance spectroscopic measurements showed the causes behind this to be smaller resistance and greater capacitance at the double layer and passivation film. Arsenopyrite weathering rate and temperature has a relationship: lnk = -3824.8/T + 10.305, via a transition state with activation enthalpy 29.37 kJ mol-1 and activation entropy - 167.40 J mol-1 K-1. This study provides a rapid and quantitative in-situ electrochemical method for arsenopyrite weathering and an improved understanding of arsenopyrite weathering in acid rain condition. The results have powerful implications for the remediation and management of As-bearing sites affected by mining activities in acid rain area.

Early-stage culprit in protein misfolding diseases investigated using electrochemical parameters: New insights over peptide-membrane interactions.

The dysfunctioning of ß-cells caused by the unspecific misfolding of the human islet amyloid polypeptide (hIAPP) at the membrane results in type 2 diabetes mellitus. Here, we report for the first time, the early-stage interaction of hIAPP oligomers on the DMPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine) lipid membrane using electrochemical parameters. Electrochemical techniques are better than other techniques to detect hIAPP at significantly lower concentrations. The surface level interactions between the peptide (hIAPP) and lipid membrane (DMPC) were investigated using atomic force microscopy (AFM), confocal microscopy (CM) and electrochemical techniques such as Tafel polarization, cyclic voltammetry (CV), differential pulse voltammetry (DPV), linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). Inserting IAPP into the fluid domains results in breaking the lipid-to-lipid interaction, leading to restriction of membrane mobility. The SLateral values of the liposome and IAPP co-solubilized liposome indicates the cooperative insertion of IAPP. Further, a new method of immobilizing a membrane to the gold surface has been employed, resulting in an electrical contact with the buffer, preventing the direct utilization of a steady-state voltage across the bilayer. The electrochemical studies revealed that the charge transfer resistance decreased for 3-mercaptopropanoic acid modified gold (MPA-Au) electrode coated with the liposome and after the addition of IAPP, followed by an increase in the capacitance. The present study has opened up new dimensions to the understanding of peptide-membrane interactions and shows different experimental approaches for the future researchers in this domain.

Plasmodium chabaudi Affects Mast Cell Degranulation as Measured by Carbon-Fiber Microelectrode Amperometry.

Mast cells (MCs) are effector cells of the immune system commonly known for their role in asthma and allergy. They are present throughout biological systems in various tissues, serving as an interface between the biological system and environment. Previous work characterizing the impact of malaria on MCs revealed contradictory results, showing minimal to strong correlation between MC degranulation and disease progression. This work seeks to reveal how MC degranulation is impacted in the presence of malaria, induced by Plasmodium chabaudi, using a mouse model and a single cell measurement technique that reveals exquisite biophysical detail about any impacts to the degranulation process. It was hypothesized that the malaria parasites would impact MC degranulation response during live infection, and the differences would be revealed via carbon-fiber microelectrode amperometry. In fact, the data collected show that different stages of malaria infection affect MC degranulation differently, affirming the importance of considering different infection stages in future studies of malarial immune response. Furthermore, a comparison of MC degranulation response to that measured from platelets under similar circumstances shows similar trends in quantitative degranulation, suggesting that MC and platelet exocytosis machinery are affected similarly despite their distinct biological roles. However, based on the small number of mouse replicates, the studies herein suggest that there should be further study about cellular and disease processes. Overall, the work herein reveals important details about the role of MCs in malaria progression, relevant during treatment decisions, as well as a potentially generalizable impact on chemical messenger secretion from cells during malarial progression.

Galena weathering in simulated alkaline soil: Lead transformation and environmental implications.

Alkaline soils are widely distributed around the world. During the mining and transportation processes galena may be exposed to the alkaline soils. Weathering of galena may lead to the formation of different lead phases having higher bio-accessibility than galena, and thereby increasing the mobility and toxicity of lead. In this study, electrochemical techniques and Raman spectroscopic measurements were used for the evaluation of the interfacial processes that are involved in the galena weathering under the conditions of simulated saline soil and meadow soil solutions. The results showed that the release of Pb2+ and S0 took place during initial stage of the oxidation. Thereafter, further transformation to anglesite would take place, even leading to the transformation to ß-PbO and α-PbO at higher temperatures. Galena weathering prone to saline soil than that in meadow soil, and has a faster weathering rate in the saline soil at same ambient temperature. Higher temperatures was found to promote the weathering of galena, and the rate constant for the release of Pb (II) was approximate 10-9 to 10-8 mol∙m-2∙s-1, while surface reaction was found to control the weathering kinetics. Based on the surface characterization and evaluation of the thermodynamic and kinetic parameters, the weathering mechanism of galena in the alkaline soil and its environmental implications was suggested.

Identification of programmed death ligand-1 positive exosomes in breast cancer based on DNA amplification-responsive metal-organic frameworks.

Cancer-derived exosomes have recently emerged as potent candidates for diagnosis and prognosis of breast cancer. As an example, programmed death ligand-1 positive (PD-L1+) exosomes are found to be correlated with the progression and immunotherapy response of breast cancer, and therefore show great potential in liquid biopsy. Herein, we propose an electrochemical biosensing method for accurate identification of PD-L1+ exosomes by using DNA amplification-responsive metal-organic frameworks, PVP@HRP@ZIF-8. Specially, PD-L1+ exosomes are captured by anti-CD63 functionalized magnetic beads and bound with anti-PD-L1-linked capture probe. Then, in situ hyperbranched rolling circle amplification, a typical DNA amplification reaction, is conducted using the surface-attached capture probes as primers, which lows environmental pH. As a result, disassembly of PVP@HRP@ZIF-8 takes place, leading to the release of enzymes, which can arouse amplified electrochemical responses for the identification of target exosomes. Experimental results reveal that the biosensing method displays a linear range for PD-L1+ exosomes identification from 1 × 103 to 1 × 1010 particles/mL and the detection limit reaches 334 particles/mL. What is more, by using the method, elevated level of circulating PD-L1+ exosomes is found in the undiluted serum samples from patients with breast cancer, particularly for metastatic breast cancer, revealing a positive correlation of the PD-L1+ exosome level with the tumor staging and disease progression of breast cancer. Therefore, the biosensing method may be valuable for not only exosome identification but also providing reference information for diagnosis and real-time monitoring of breast cancer in the future.

Integrated Glycosylation Patterns of Glycoproteins and DNA Methylation Landscapes in Mammalian Oogenesis and Preimplantation Embryo Development.

Glycosylation is one of the most fundamental post-translational modifications. However, the glycosylation patterns of glycoproteins have not been analyzed in mammalian preimplantation embryos, because of technical difficulties and scarcity of the required materials. Using high-throughput lectin microarrays of low-input cells and electrochemical techniques, an integration analysis of the DNA methylation and glycosylation landscapes of mammal oogenesis and preimplantation embryo development was performed. Highly noticeable changes occurred in the level of protein glycosylation during these events. Further analysis identified several stage-specific lectins including LEL, MNA-M, and MAL I. It was later confirmed that LEL was involved in mammalian oogenesis and preimplantation embryogenesis, and might be a marker of FGSC differentiation. Modified nanocomposite polyaniline/AuNPs were characterized by electron microscopy and modification on bare gold electrodes using layer-by-layer assembly technology. These nanoparticles were further subjected to accuracy measurements by analyzing the protein level of ten-eleven translocation protein (TET), which is an important enzyme in DNA demethylation that is regulated by O-glycosylation. Subsequent results showed that the variations in the glycosylation patterns of glycoproteins were opposite to those of the TET levels. Moreover, analysis of correlation between the changes in glyco-gene expression and female germline stem cell glycosylation profiles indicated that glycosylation was related to DNA methylation. Subsequent integration analysis showed that the trend in the variations of glycosylation patterns of glycoproteins was similar to that of DNA methylation and opposite to that of the TET protein levels during female germ cell and preimplantation embryo development. Our findings provide insight into the complex molecular mechanisms that regulate human embryo development, and a foundation for further elucidation of early embryonic development and informed reproductive medicine.

Monitoring Oxidative Status in Winemaking by Untargeted Linear Sweep Voltammetry.

An electrochemical portable device based on linear sweep voltammetry was evaluated for studying the redox behavior of polyphenolic compounds in industrial scale winemaking to infer the effects of selected early processing steps on the vinification trials of Pinot gris, Chardonnay, Vermentino and Sangiovese grapes. For each sample, the redox behavior showed a distinctive voltammetric signal pattern related to the processing step during winemaking, therefore being useful as a potential fingerprint for wine identification and to provide insights about the phenolic content. For instance, there was a high correlation (R2 = 0.72) between the total phenolic compounds (PhenOx) and the easily oxidizable compounds (EasyOx), the latter representing approx. 30% on average of the total phenolics. Furthermore, the maceration of red grapes was concluded after 29 days based on information driven by the phenolics pattern. As expected, during alcoholic fermentation, white wines showed a lower content of phenolic compounds than those found in red wines, with an average ratio PhenOx/EasyOx of about 4.7, 5.0 and 3.6 for Chardonnay, Pinot gris and Vermentino, respectively. The portable tool with miniaturized disposable electrodes showed interesting analytical features that can be exploited for on-site and real-time quality control for monitoring change in phenolic composition during wine processing and storage, and for tailoring winemaking practices to enhance the color stability of products.

Evaluation of pectin isolated from tomato peel waste as natural tin corrosion inhibitor in sodium chloride/acetic acid solution.

The pectin from tomato peel waste (TPP) was employed as tin corrosion inhibitor with the aim to enhance the knowledge regarding the application of natural inhibitors, instead synthetic, and reducing the waste disposal for value-added biopolymers production. To evaluate the TPP anticorrosion activity the commercial apple pectin (CAP) was also utilised. The gravimetric tests show that the highest inhibitive impact (η) of 75.9 % (CAP) and 73.9 % (TPP) are gained at concentration of 20 g L-1. By electrochemical, potentiodynamic polarization and impedance spectroscopy measurements, the maximum η (60.05-65.5 %) are reached at lower concentration (4 g L-1), due to tendency of pectins to form viscous solution. The prominent decreases in current density with the shifts of potential in the cathodic direction revealed that pectins provided cathodic protection of tin surface. Similar inhibition impact of pectins, and fine agreement between applied methods confirmed their suitability against tin corrosion.

The influence of humic acids on the weathering of pyrite: Electrochemical mechanism and environmental implications.

Pyrite weathering often occurs in nature and causes heavy metal ion pollution and acid mine drainage during the process. Humic acid (HA) is a critical natural organic material that can bind metal ions, thus affecting metal transfer and transformation. In this work, in situ electrochemical techniques combined with spectroscopic analysis were adopted to investigate the interfacial processes involved in pyrite weathering with/without HA. The results showed that the pyrite weathering mechanism with/without HA is FeS2 → Fe2+ + 2S0 + 2e-. The presence of HA did not change the pyrite weathering mechanism, but HA adsorbs on the pyrite surface and inhibits the further transformation of sulfur. Furthermore, HA and Fe(II) ions can form complex at 45.0 °C. Increased concentration of HA, decreased HA solution acidity or decreased environmental temperature would all weaken the pyrite weathering, for the above conditions cause pyrite weathering to have a larger resistance of the double layer and a larger passive film resistance. Pyrite will release 73.7 g m-2·y-1 Fe2+ to solution at pH 4.5, and the amount decreases to 36.8 g m-2·y-1 in the presence of 100 mg/L HA. This study provides an in situ electrochemical method for the assessment of pyrite weathering.

Insight into the Effects of Plasmodium chabaudi on Platelets Using Carbon-Fiber Microelectrode Amperometry.

Platelets are anuclear circulating cell bodies within the bloodstream commonly known for their roles in clot formation during vascular injury to prevent blood loss. They also have significant impact in a range of diseases, including malaria. However, the role of platelets in malaria is controversial, with contradicting evidence suggesting either that they assist in destruction of malarial parasites or facilitate a severe form of malaria. Precedent work suggests that the timing of infection is critical in determining whether platelets switch roles from being protective to deleterious. As such, the work herein makes use of the unique mechanistic perspective offered by carbon-fiber microelectrode amperometry (CFMA) to understand how platelet secretion is impacted in malarial infection stages (ascending parasite count versus descending parasite count). Malarial platelet behavior was compared to platelets from noninfected control mice by probing their exocytotic function. Results suggest that mouse malaria caused by the parasite Plasmodium chabaudi, during both ascending and descending infection stages, reduces platelet exocytotic events and delays platelet granule fusion; in addition, platelets are more impacted by the disease early in the infection stages. In all, understanding platelet behavior in the malarial context may present new therapeutic routes to treat or cure malaria.

Food Safety Analysis Using Electrochemical Biosensors.

Rapid and precise analytical tools are essential for monitoring food safety and screening of any undesirable contaminants, allergens, or pathogens, which may cause significant health risks upon consumption. Substantial developments in analytical techniques have empowered the analyses and quantitation of these contaminants. However, conventional techniques are limited by delayed analysis times, expensive and laborious sample preparation, and the necessity for highly-trained workers. Therefore, prompt advances in electrochemical biosensors have supported significant gains in quantitative detection and screening of food contaminants and showed incredible potential as a means of defying such limitations. Apart from indicating high specificity towards the target analytes, these biosensors have also addressed the challenge of food industry by providing high analytical accuracy within complex food matrices. Here, we discuss some of the recent advances in this area and analyze the role and contributions made by electrochemical biosensors in the food industry. This article also reviews the key challenges we believe biosensors need to overcome to become the industry standard.

Multiplexed electrochemical detection of three cardiac biomarkers cTnI, cTnT and BNP using nanostructured ZnO-sensing platform.

AIM: Development of a label-free multiplexed point-of-care diagnostic device for a panel of cardiac biomarkers - cardiac troponin-T (cTnT), troponin-I (cTnI) and B-type natriuretic peptide (BNP). METHODS: A nonfaradaic electrochemical immunoassay designed with anisotropic high surface area ZnO nanostructures grown using low-temperature hydrothermal methods was selectively immobilized with capture antibodies. Multiplexed detection in human serum using ZnO nanostructures based on complementary electrochemical measurement techniques - electrochemical impedance spectroscopy and Mott-Schottky. RESULTS: Linear signal response for detection of three biomarkers in human serum with dynamic range of 1 pg/ml-100 ng/ml and limit of detection at 1 pg/ml and low signal response to background interferences was achieved. CONCLUSION: First demonstration of simultaneous detection of three cardiac biomarkers in clinically relevant range with sensor's analytical performance and linear response of detection showed potential utility in screening clinical samples for early diagnosis of acute myocardial infarction and chronic heart failure.