scholarly journals Electrochemical Applications for the Antioxidant Sensing in Food Samples Such as Citrus and Its Derivatives, Soft Drinks, Supplementary Food and Nutrients

2021 ◽  
Author(s):  
Ersin Demir ◽  
Hülya Silah ◽  
Nida Aydogdu
Keyword(s):  
Antioxidant Capacity ◽  
Analytical Methods ◽  
High Sensitivity ◽  
Differential Pulse ◽  
Food Samples ◽  
Electrochemical Methods ◽  
General Description ◽  
Range Limit ◽  
Healthy Individuals ◽  
Limit Of Quantification

Although there are many definitions of antioxidants, the most general description; antioxidants are carried a phenolic function in their structure and prevent the formation of free radicals or intercept from damage to the cell by scavenging existing radicals. Moreover, they are one of the most effective substances that contain essential nutrients for healthy individuals. The importance of these antioxidants, which have an incredible effect on the body and increase the body’s resistance, is increasing day by day for healthy individuals. Numerous studies have been carried out for antioxidants with excellent properties and however new, reliable, selective, sensitive and green analytical methods are sought for their determination at trace levels in food samples. Along with the latest developments, electrochemical methods are of great interest in the world of science because they are fast, reliable, sensitive and environmentally friendly. Electrochemical methods have been frequently applied to analyze antioxidant capacity in many nutrients samples found in different forms such as solid, liquid without any pretreatment applications in the last decade. Furthermore, these methods are preferred because of the short analysis time, the ability to lower detection limits, reduction in a solvent, high sensitivity, portability, low sample consumption, wide working range, and more economical than existing other traditional analytical methods. The antioxidant sensing applications by modern electrochemical methods such as cyclic, square wave, differential pulse, and combined with stripping voltammetric techniques were used to deduce antioxidant capacity (AC) in critical nutrients. Moreover, this chapter includes a description of the classification of electrochemical methods according to the working electrode type, dynamic working range, limit of determination (LOD), limit of quantification (LOQ), sample type, and using standard analyte and so forth for each voltammetric methods. While many articles applied for the determination of antioxidant sensing by electrochemistry have gained momentum in the last two decades, we focused on the studies conducted over the last 4 years in this chapter.

scholarly journals Fabrication of Efficient and Selective Modified Graphene Paste Sensor for the Determination of Catechol and Hydroquinone

Surfaces ◽  
2020 ◽  
Vol 3 (3) ◽  
pp. 473-483
Author(s):  
Jamballi G. Manjunatha
Keyword(s):  
Modified Electrode ◽  
High Sensitivity ◽  
Differential Pulse ◽  
Official Method ◽  
Limit Of Quantification ◽  
Selective Determination ◽  
Graphene Paste Electrode ◽  
Modified Graphene ◽  
Paste Electrode

An electrochemical sensor, based on a graphene paste electrode (GPE), was modified with a polymerization method, and the electrochemical behavior of catechol (CC) and hydroquinone (HQ) was investigated using electroanalytical methods like cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The effect of CC at the modified electrode was evidenced by the positive shift of the oxidation peak potential of CC at the poly (rosaniline)-modified graphene paste electrode (PRAMGPE) and the nine-fold enhancement of the peak current, as compared to a bare graphene paste electrode (BGPE). The sensitivity of CC investigated by DPV was more sensitive than CV for the analysis of CC. The DPV method showed the two linear ranges of 2.0 × 10−6–1.0 × 10−5 M and 1.5 × 10−5–5 × 10−5 M. The detection limit and limit of quantification were determined to be 8.2 × 10−7 and 27.6 × 10−7 M, respectively. The obtained results were compared successfully with respect to those obtained using the official method. Moreover, this sensor is applied for the selective determination of CC in the presence of HQ. The high sensitivity, good reproducibility, and wide linear range make the modified electrode suitable for the determination of CC in real samples. The practical application of the sensor was demonstrated by determining the concentration of CC in water samples with acceptable recoveries (97.5–98%).

scholarly journals CUPRAC Voltammetric Determination of Antioxidant Capacity in Tea Samples by Using Screen-Printed Microelectrodes

2019 ◽  
Vol 2019 ◽  
pp. 1-10 ◽  
Author(s):  
Alina Elena Trofin ◽  
Lucia Carmen Trincă ◽  
Elena Ungureanu ◽  
Adina Mirela Ariton
Keyword(s):  
Antioxidant Capacity ◽  
Differential Pulse Voltammetry ◽  
Low Cost ◽  
Differential Pulse ◽  
Food Samples ◽  
Open Circuit ◽  
Rapid Response ◽  
Detection Methods ◽  
Pulse Voltammetry ◽  
Screen Printed

Measurement of antioxidant capacity represents an analytical major challenge in terms of accuracy, efficiency, rapid response, or low cost of detection methods. Quantification of antioxidant capacity of food samples using disposable screen‐printed microelectrodes (SPMEs) was based on cyclic voltammetry versus open-circuit potential (CV vs OCP) and differential pulse voltammetry (DPV) as compared with spectrophotometric measurement of the CUPRAC reaction with 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (trolox). The SPMEs are organic‐resistant electrodes and thus compatible with food samples and organic solvents used to dissolve trolox. A micropipette was used to release a drop of 50 μL sample on the spotted surface of the SPME sensor/working electrode that was time programmed to function according to the working protocol. The SPME response was linearly correlated with trolox content. This preliminary demonstration was focused on the analysis of tea infusions, due to the simplicity and reproducibility of the samples’ preparations involved. Analytical results of the antioxidant capacity (expressed as mol·L−1 trolox equivalents) of the tea samples showed a good agreement in the case of spectrophotometry and differential pulse voltammetry (R2 > 0.998). DPV with SPME based on CUPRAC reactions was proven to be a promising approach for the characterization of antioxidant capacity of tea samples with rapid response, cost-effectiveness, and simplicity of operation.

scholarly journals A Dilute and Shoot Strategy for Determining Alternaria Toxins in Tomato-Based Samples and in Different Flours Using LC-IDMS Separation

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 1017
Author(s):  
Ádám Tölgyesi ◽  
Tamás Farkas ◽  
Mária Bálint ◽  
Thomas J. McDonald ◽  
Virender K. Sharma
Keyword(s):  
Matrix Effects ◽  
Internal Standard ◽  
High Sensitivity ◽  
Food Samples ◽  
Standard Samples ◽  
Limit Of Quantification ◽  
Enhanced Sensitivity ◽  
Alternaria Toxins ◽  
Sample Extraction ◽  
Liquid Chromatography Tandem Mass

Alternaria toxins are emerging mycotoxins whose regulation and standardization are in progress by the European Commission and the European Committee for Standardization. This paper describes a dilute and shoot approach to determine five Alternaria toxins in selected food samples using liquid chromatography–tandem mass spectrometry (LC-MS/MS). The strategy involves sample extraction with acidified aqueous methanol, followed by a solvent change accomplished via sample evaporation and reconstitution. The quantification is based on isotope dilution, applying all corresponding isotopically labeled internal standards to compensate possible matrix effects of the analysis. The main advantages of the present method over other existing methods includes simple and effective sample preparation, as well as detection with high sensitivity. The five-fold sample dilution can decrease matrix effects, which were evaluated with both external and internal standard methods. The results demonstrated a limit of quantification lower than 1.0 µg/kg for all five analytes for the first time. The newly presented method showed acceptable accuracy (52.7–111%) when analyzing naturally contaminated and spiked standard samples at the described levels. The method was validated for tomato-based and flour samples (wheat, rye, and maize). The absolute recovery ranged from 66.7% to 91.6% (RSD < 10%). The developed method could be an alternative approach for those laboratories that exclude sample cleanup and pre-concentration of state-of-the-art instruments with enhanced sensitivity.

scholarly journals DEVELOPMENT OF ELECTROCHEMICAL SENSORS FOR QUANTITATIVE ANALYSIS OF METHYLDOPA AT MODIFIED-GCE AND PGE ELECTRODES BY VOLTAMMETRY

2020 ◽  
Vol 4 (4) ◽  
pp. 223-236
Author(s):  
Suzan YANIK ◽  
Saliha B. KURT ◽  
Betul ARI ◽  
Sahin DEMIRCI ◽  
Selehattin YILMAZ
Keyword(s):  
Glassy Carbon ◽  
Sulfonic Acid ◽  
Electrochemical Sensors ◽  
Limit Of Detection ◽  
Modified Electrodes ◽  
Differential Pulse ◽  
Electrochemical Methods ◽  
Limit Of Quantification ◽  
Spectrophotometric Methods ◽  
Concentration Graphs

Methyldopa is one of the important drugs used in the treatment of high blood pressure (hypertension). In addition to various methods such as chromatographic and spectrophotometric methods, electrochemical methods are used for the determination of methyldopa. However, poly (p-aminobenzene sulfonic acid), pen-tip graphite electrode (PGE) study was not found in the literature search. Modified electrodes are important because they increase the sensitivity of the analysis. Furthermore, electrochemical methods have advantages such as being faster and cheaper than other instrumental analysis methods, being more sensitive, not requiring long pretreatments in the preparation of samples. In this study, the glassy carbon electrode (GCE) was modified with poly(p-aminobenzene sulfonic acid) to prepare poly (p-aminobenzene sulfonic acid) -modified glassy carbon electrodes. Cyclic voltammetry (CV) technique was used for the electropolymerization process. Methyldopa was selected in various concentrations of phosphate pH 7.40 buffer, anodic and cathodic voltamograms were taken and oxidation and reduction properties were investigated. Measurements were taken at different scanning rates by CV technique and the current type of methyldopa was determined. Peak flow-concentration graphs were drawn from the measurements taken by Differential Pulse Voltammetry (DPV) technique and the linearity range was 0.020- 2.500 µM for modified-GCE and 0.020-2.820 µM for PGE. The limit of detection (LOD) was calculated as 0.006 µM for modified-GCE, 0.012 µM for PGE. The limit of quantification (LOQ) was calculated as 0.020 µM for modified-GCE and 0.040 µM for PGE.

scholarly journals A Fluidics-Based Biosensor to Detect and Characterize Inhibition Patterns of Organophosphate to Acetylcholinesterase in Food Materials

Micromachines ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 397
Author(s):  
Dang Song Pham ◽  
Xuan Anh Nguyen ◽  
Paul Marsh ◽  
Sung Sik Chu ◽  
Michael P. H. Lau ◽  
...  
Keyword(s):  
Room Temperature ◽  
Current Flow ◽  
Limit Of Detection ◽  
High Sensitivity ◽  
Food Samples ◽  
Side Chain ◽  
Limit Of Quantification ◽  
Activity Inhibition ◽  
Lysine Side Chain ◽  
Sensing Platform

A chip-based electrochemical biosensor is developed herein for the detection of organophosphate (OP) in food materials. The principle of the sensing platform is based on the inhibition of dimethoate (DMT), a typical OP that specifically inhibits acetylcholinesterase (AChE) activity. Carbon nanotube-modified gold electrodes functionalized with polydiallyldimethylammonium chloride (PDDA) and oxidized nanocellulose (NC) were investigated for the sensing of OP, yielding high sensitivity. Compared with noncovalent adsorption and deposition in bovine serum albumin, bioconjugation with lysine side chain activation allowed the enzyme to be stable over three weeks at room temperature. The total amount of AChE was quantified, whose activity inhibition was highly linear with respect to DMT concentration. Increased incubation times and/or DMT concentration decreased current flow. The composite electrode showed a sensitivity 4.8-times higher than that of the bare gold electrode. The biosensor was challenged with organophosphate-spiked food samples and showed a limit of detection (LOD) of DMT at 4.1 nM, with a limit of quantification (LOQ) at 12.6 nM, in the linear range of 10 nM to 1000 nM. Such performance infers significant potential for the use of this system in the detection of organophosphates in real samples.

Determination of Selected Phthalates in Some Commercial Cosmetic Products by HPLC-UV

2020 ◽  
Vol 23 (10) ◽  
pp. 1010-1022
Author(s):  
Emrah Dural
Keyword(s):  
High Performance ◽  
Phthalate Esters ◽  
High Sensitivity ◽  
Hplc Method ◽  
Cosmetic Products ◽  
Limit Of Quantification ◽  
Nail Polish ◽  
Accuracy And Precision ◽  
Butyl Phthalate

Aim and scope: Due to the serious toxicological risks and their widespread use, quantitative determination of phthalates in cosmetic products have importance for public health. The aim of this study was to develop a validated simple, rapid and reliable high-performance liquid chromatography (HPLC) method for the determination of phthalates which are; dimethyl phthalate (DMP), diethyl phthalate (DEP), benzyl butyl phthalate (BBP), di-n-butyl phthalate (DBP), di(2- ethylhexyl) phthalate (DEHP), in cosmetic products and to investigate these phthalate (PHT) levels in 48 cosmetic products marketing in Sivas, Turkey. Materials and Methods: Separation was achieved by a reverse-phase ACE-5 C18 column (4.6 x 250 mm, 5.0 μm). As the mobile phase, 5 mM KH2PO4 and acetonitrile were used gradiently at 1.5 ml min-1. All PHT esters were detected at 230 nm and the run time was taking 21 minutes. Results: This method showed the high sensitivity value the limit of quantification (LOQ) values for which are below 0.64 μg mL-1 of all phthalates. Method linearity was ≥0.999 (r2). Accuracy and precision values of all phthalates were calculated between (-6.5) and 6.6 (RE%) and ≤6.2 (RSD%), respectively. Average recovery was between 94.8% and 99.6%. Forty-eight samples used for both babies and adults were successfully analyzed by the developed method. Results have shown that, DMP (340.7 μg mL-1 ±323.7), DEP (1852.1 μg mL-1 ± 2192.0), and DBP (691.3 μg mL-1 ± 1378.5) were used highly in nail polish, fragrance and cream products, respectively. Conclusion: Phthalate esters, which are mostly detected in the content of fragrance, cream and nail polish products and our research in general, are DEP (1852.1 μg mL-1 ± 2192.0), DBP (691.3 μg mL-1 ± 1378.5) and DMP (340.7 μg mL-1 ±323.7), respectively. Phthalates were found in the content of all 48 cosmetic products examined, and the most detected phthalates in general average were DEP (581.7 μg mL-1 + 1405.2) with a rate of 79.2%. The unexpectedly high phthalate content in the examined cosmetic products revealed a great risk of these products on human health. The developed method is a simple, sensitive, reliable and economical alternative for the determination of phthalates in the content of cosmetic products, it can be used to identify phthalate esters in different products after some modifications.

Recent Progress in the Analysis of Captopril Using Electrochemical Methods: A Review

2019 ◽  
Vol 15 (3) ◽  
pp. 198-206 ◽  
Author(s):  
Sarfaraz Ahmed Mahesar ◽  
Saeed Ahmed Lakho ◽  
Syed Tufail Hussain Sherazi ◽  
Hamid Ali Kazi ◽  
Kamran Ahmed Abro ◽  
...  
Keyword(s):  
Enzyme Inhibitor ◽  
Modified Electrodes ◽  
High Sensitivity ◽  
Pharmaceutical Formulations ◽  
Inorganic Materials ◽  
Electrochemical Methods ◽  
Nano Particles ◽  
Moderate Heart Failure ◽  
Analytical Instrumentation

Background: Captopril is the synthetic dipeptide used as an angiotensin converting enzyme inhibitor. Captopril is used to treat hypertension as well as for the treatment of moderate heart failure. Analytical instrumentation and methodology plays an important role in pharmaceutical analysis. Methods: This review presents some important applications of electrochemical modes used for the analysis of captopril. So far captopril has been analyzed by using different bare and modified working electrodes with a variety of modifiers from organic and inorganic materials to various types of nano particles/materials. Results: This paper presents some of the methods which have been published in the last few years i.e. from 2003 to 2016. This review highlights the role of the analytical instrumentation, particularly electrochemical methods in assessing captopril using various working electrodes. Conclusion: A large number of studies on voltammetry noted by means of various bare and modified electrodes. Among all of the published voltammetric methods, DPV, SWV, CV and miscellaneous modes were trendy techniques used to analyze captopril in pharmaceutical formulations as well as biological samples. Electrodes modified with nanomaterials are promising sensing tools as this showed high sensitivity, good accuracy with precision as well as selectivity. In comparison to chromatographic methods, the main advantages of electrochemical methods are its cheaper instrumentation, lower detection limit and minimal or no sample preparation.

scholarly journals Magnetoelastic Coupling and Delta-E Effect in Magnetoelectric Torsion Mode Resonators

Sensors ◽  
2021 ◽  
Vol 21 (6) ◽  
pp. 2022
Author(s):  
Benjamin Spetzler ◽  
Elizaveta V. Golubeva ◽  
Ron-Marco Friedrich ◽  
Sebastian Zabel ◽  
Christine Kirchhof ◽  
...  
Keyword(s):  
Low Frequency ◽  
High Sensitivity ◽  
Element Model ◽  
Mode Number ◽  
Frequency Change ◽  
General Description ◽  
Resonance Modes ◽  
Field Sensor ◽  
Magnetic Sensitivity ◽  
Bending Modes

Magnetoelectric resonators have been studied for the detection of small amplitude and low frequency magnetic fields via the delta-E effect, mainly in fundamental bending or bulk resonance modes. Here, we present an experimental and theoretical investigation of magnetoelectric thin-film cantilevers that can be operated in bending modes (BMs) and torsion modes (TMs) as a magnetic field sensor. A magnetoelastic macrospin model is combined with an electromechanical finite element model and a general description of the delta-E effect of all stiffness tensor components Cij is derived. Simulations confirm quantitatively that the delta-E effect of the C66 component has the promising potential of significantly increasing the magnetic sensitivity and the maximum normalized frequency change ∆fr. However, the electrical excitation of TMs remains challenging and is found to significantly diminish the gain in sensitivity. Experiments reveal the dependency of the sensitivity and ∆fr of TMs on the mode number, which differs fundamentally from BMs and is well explained by our model. Because the contribution of C11 to the TMs increases with the mode number, the first-order TM yields the highest magnetic sensitivity. Overall, general insights are gained for the design of high-sensitivity delta-E effect sensors, as well as for frequency tunable devices based on the delta-E effect.

scholarly journals Ag nanoparticles outperform Au nanoparticles for the use as label in electrochemical point-of-care sensors

2021 ◽  
Author(s):  
Franziska Beck ◽  
Carina Horn ◽  
Antje J. Baeumner
Keyword(s):  
Limit Of Detection ◽  
Point Of Care ◽  
Automatic Measurement ◽  
High Sensitivity ◽  
Differential Pulse ◽  
Small Sample ◽  
Blood Protein ◽  
User Friendliness ◽  
Response Curves ◽  
Assay Protocol

AbstractElectrochemical immunosensors enable rapid analyte quantification in small sample volumes, and have been demonstrated to provide high sensitivity and selectivity, simple miniaturization, and easy sensor production strategies. As a point-of-care (POC) format, user-friendliness is equally important and most often not combinable with high sensitivity. As such, we demonstrate here that a sequence of metal oxidation and reduction, followed by stripping via differential pulse voltammetry (DPV), provides lowest limits of detection within a 2-min automatic measurement. In exchanging gold nanoparticles (AuNPs), which dominate in the development of POC sensors, with silver nanoparticles (AgNPs), not only better sensitivity was obtained, but more importantly, the assay protocol could be simplified to match POC requirements. Specifically, we studied both nanoparticles as reporter labels in a sandwich immunoassay with the blood protein biomarker NT-proBNP. For both kinds of nanoparticles, the dose-response curves easily covered the ng∙mL−1 range. The mean standard deviation of all measurements of 17% (n ≥ 4) and a limit of detection of 26 ng∙mL−1 were achieved using AuNPs, but their detection requires addition of HCl, which is impossible in a POC format. In contrast, since AgNPs are electrochemically less stable, they enabled a simplified assay protocol and provided even lower LODs of 4.0 ng∙mL−1 in buffer and 4.7 ng∙mL−1 in human serum while maintaining the same or even better assay reliability, storage stability, and easy antibody immobilization protocols. Thus, in direct comparison, AgNPs clearly outperform AuNPs in desirable POC electrochemical assays and should gain much more attention in the future development of such biosensors.

scholarly journals Bioactivity and Bioavailability of the Major Metabolites of Crocus sativus L. Flower

Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2827 ◽  
Author(s):  
Moratalla-López ◽  
Bagur ◽  
Lorenzo ◽  
Salinas ◽  
Alonso
Keyword(s):  
Antioxidant Capacity ◽  
Critical Review ◽  
Analytical Methods ◽  
Mechanisms Of Action ◽  
Crocus Sativus ◽  
Crocus Sativus L ◽  
Identification And Quantification

Crocus sativus L. has been cultivated throughout history to obtain its flowers, whose dried stigmas give rise to the spice known as saffron. Crocetin esters, picrocrocin, and safranal are the main metabolites of this spice, which possess a great bioactivity, although the mechanisms of action and its bioavailability are still to be solved. The rest of the flower is composed by style, tepals, and stamens that have other compounds, such as kaempferol and delphinidin, which have an important antioxidant capacity, and these can be applied in foods, phytopharmaceuticals, and cosmetics. The aim of this work was to provide an updated and critical review of the research on the main compounds of Crocus sativus L. flower, including the adequate analytical methods for their identification and quantification, with a focus on their bioactivity and bioavailability.

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