Analytical Parameters Research Articles

Micro-RNA Signature in CSF Before and After Autologous Hematopoietic Stem Cell Transplantation for Multiple Sclerosis.

MicroRNAs (miRNAs) are regulators of gene expression and have been reported to be dysregulated in people with multiple sclerosis (pwMS). Autologous hematopoietic stem cell transplantation (aHSCT) is an immune-ablative treatment intervention for pwMS. Currently, it is unknown if aHSCT affects expression levels of miRNAs in CSF. We explored the ability of circulating miRNA to discriminate between pwMS and healthy controls (HCs) and investigated whether these miRNAs were affected by treatment with aHSCT. Using quantitative reverse transcription PCR, 87 miRNAs were analyzed in CSF samples of a discovery cohort (baseline: 4 & HC: 4). The top 22 miRNAs discriminating between pwMS and HCs were then analyzed in 187 CSF samples of a validation cohort (pwMS: 50, HC: 32). Samples, failing quality control or being follow-ups to baseline samples with quality control issues, were excluded from further analyses. The remaining 133 samples (HC: 29, MS: baseline: 33, 1 year: 30, 2 years: 26, 3-5 years: 15) were analyzed for expression of the top 22 miRNAs. Twelve miRNAs were dysregulated in pwMS compared with HC (q < 0.05). Associations with clinical and analytical parameters were observed in relation to all 12 miRNAs; however, a cluster of 4 miRNAs (miR-16-5p, miR-21-5p, miR-150-5p, and miR-146a-5p) with strong correlations (r > 0.60, p < 0.001) with multiple parameters was identified. Of the 12 miRNAs, 8 were differentially expressed in pwMS with gadolinium-enhancing lesions at baseline and 4 by prior disease-modifying treatment class (p < 0.05). These 4 miRNAs correlated strongly with each other, decreased after aHSCT, and remained low throughout the follow-up period (p < 0.05). Target and pathway analysis of these revealed association with biological processes affecting cytokine production, inflammatory response, and regulation of myelin maintenance. miRNAs are dysregulated in CSF from pwMS and particularly in patients with less effective treatments and/or higher inflammatory disease activity. A 4-miRNA signature with elevated expression of miR-16-5p, miR-21-5p, miR-150-5p, and miR-146a-5p was recurring in multiple analyses. After intervention with aHSCT, the expression levels approached the levels of the HCs, suggesting a potent treatment effect.

Layered triple hydroxide (NiCoFe-LTH) with g-C3N4 hybrid nanocomposite as an adsorbent for Pb(II) extraction.

Hybrid graphitic carbon nitride (g-C3N4) with layer triple hydroxide (LTH) nanocomposite synthesized using the hydrothermal procedure has been investigated as a novel adsorbent g-C3N4@NiCoFe-LTH in the dispersive solid phase microextraction (DSp-ME) for Pb(II) determination in the food and water samples. The nanocomposite was characterized using FTIR, SEM, SEM-EDX, and XRD techniques. Several analytical parameters were adjusted, including pH, adsorbent quantity, adsorption and elution time, sample and eluent volume, and elution solvent concentration, and found as 8.0, 7.5mg, 60, and 30s, 40mL, 2mL, and 0.5mol/L, respectively. The method's accuracy was also evaluated using matrix effects. The results indicated the LOD as 0.163μg/L, LOQ as 0.54μg/L, and PF as 20. The percent relative standard deviation (%RSD)<10%, and the coefficient of determination (R2) was 0.999, demonstrating excellent precision and linearity. The method's effectiveness was also validated by analyzing certified reference materials (CRMs).

Polycatechol coated cigarette filter as a sorbent for microextraction by packed sorbent of acidic non-steroidal anti-inflammatory drugs (NSAIDs) from wastewater samples

In this study, we employed microextraction by packed sorbent (MEPS) using polycatechol-coated cigarette filters (PCCFs) as a sorbent to extract acidic non-steroidal anti-inflammatory drugs (NSAIDs) from water samples, followed by high-performance liquid chromatographic analysis. The formation of coating on cigarette filter was confirmed by Fourier transform infrared (FT-IR) spectroscopy, UV–vis diffuse reflectance spectroscopy (DRS) and scanning electron microscopy (SEM). The effect of coating parameters on extraction efficiency of acidic NASIDs were investigated and 106.0 mg of Na2CO3, 30.0 mg of catechol and 3 h coating time were selected as optimum conditions. Additionally, other factors affecting the analyte extraction efficiency were optimized including a sample solution pH of 2.0, 700.0 µL of methanol as the elution solvent, 3 sorption cycles, 2 desorption cycles, and a 1.5 ml sample volume. Under the optimum conditions the calibration curves for all three analytes were draw and the analytical performance parameters including linear dynamic range (50.0–1000.0 µg.L−1 for naproxen and diclofenac and 100.0–500.0 µg.L−1 for ibuprofen) with R2 > 0.9982, limit of detection (LOD < 45.3 µg.L−1), precision (RSD% < 6.5), accuracy (recovery% > 90.1) and enrichment factor (EF > 2.7) were evaluated. Finally, this method was successfully used to extract and determine the amount of selected acidic NSAIDs in wastewater samples. The sorbent was cheap, easily prepared, efficient, and even reusable.

Assessment of raw milk and skimmed milk through analytical parameters

Milk, a cornerstone of global nutrition, plays a vital role in human diets due to its rich nutritional profile. Quality assurance of milk, whether raw or skimmed, is critical for ensuring public health and meeting regulatory standards. This review provides a detailed examination of the key parameters for assessing milk quality, focusing on physical, chemical, microbiological, and nutritional aspects. Advanced analytical techniques and their relevance in modern dairy science are discussed, emphasizing their application in detecting adulteration, ensuring safety, and meeting consumer demands. Through an in-depth exploration of each parameter, this article underscores the importance of milk quality assessment in the dairy industry.

Spectrophotometric determination of quercetin using micelles of cetyltrimethylammonium bromide in a low ratio methanol–water mixture

A simple and achievable UV-Vis spectrophotometric method for the micro-quantitative determination of quercetin has been developed and validated. This method relies on the formation of supramolecular assemblies of quercetin (QR) and the cationic surfactant cetyltrimethylammonium bromide (CTAB) in a 5 % methanolic aqueous solution. In this solvent medium, CTAB in the presence of QR has a critical micelle concentration of 1.2·10-3 mol l-1 at 24 °C, determined through conductometry. Important analytical parameters such as wavelength, composition of methanol-water mixture, CTAB concentration (cCTAB), and pH were optimized. Under the optimum experimental conditions (l = 397 nm, 5 % methanol as solvent, cCTAB = 2.0·10-3 mol l-1, and pH = 6.0), Beer's law was valid for QR concentrations up to 16.9 mg ml-1. The Ringbom optimum QR concentration range was 1.0 - 16.9 mg ml-1. The method sensitivity was 2.03·104 l mol-1 cm-1 (the molar absorptivity) and 0.13 mg ml-1 (limit of detection). The applicability of the proposed method for quantifying QR in pharmaceutical formulations was demonstrated. Furthermore, the proposed UV-Vis spectrophotometric method was successfully applied to the reliably assay of QR, even in the presence of vitamin C.

ORACLE: An analytical approach for T1, T2, proton density, and off-resonance mapping with phase-cycled balanced steady-state free precession.

To develop and validate a novel analytical approach simplifying , , proton density (PD), and off-resonance quantifications from phase-cycled balanced steady-state free precession (bSSFP) data. Additionally, to introduce a method to correct aliasing effects in undersampled bSSFP profiles. Off-resonant-encoded analytical parameter quantification using complex linearized equations (ORACLE) provides analytical solutions for bSSFP profiles. which instantaneously quantify , , proton density (PD), and . An aliasing correction formalism was derived to allow undersampling of bSSFP profiles. ORACLE was used to quantify , , PD, / , and based on fully sampled ( ) bSSFP profiles from numerical simulations and 3T MRI experiments in phantom and 10 healthy subjects' brains. Obtained values were compared with reference scans in the same scan session. Aliasing correction was validated in subsampled ( ) bSSFP profiles in numerical simulations and human brains. ORACLE quantifications agreed well with input values from simulations and phantom reference values (R2 = 0.99). In human brains, and quantifications when compared with reference methods showed coefficients of variation below 2.9% and 3.9%, biases of 182 and 16.6 ms, and mean white-matter values of 642 and 51 ms using ORACLE. The quantification differed less than 3 Hz between both methods. PD and maps had comparable histograms. The maps effectively identified cerebrospinal fluid. Aliasing correction removed aliasing-related quantification errors in undersampled bSSFP profiles, significantly reducing scan time. ORACLE enables simplified and rapid quantification of , , PD, and from phase-cycled bSSFP profiles, reducing acquisition time and eliminating biomarker maps' coregistration issues.

Capillary electrophoresis in parenteral nutrition control – validation of two analytical methods: Amino acids/glucose/glucose-1-phosphate and K/Na/Ca/Mg

ObjectivesProduction of parenteral nutrition bags (PNBs) involves many nutrients: complete control of the production process decreases the risk of error. This study aimed to develop and validate two analytical methods...

Analytical and clinical performance of eight Simoa® and Lumipulse® assays for automated measurement of plasma p-tau181 and p-tau217

BackgroundAmong the Alzheimer’s disease (AD) biomarkers measured in blood, phosphorylated forms of tau (p-tau) have been shown to exhibit a particularly high diagnostic potential. Here, we performed a comprehensive method comparison study, followed by evaluation of the diagnostic performance of eight recent plasma p-tau immunoassays targeting different tau phosphorylation sites, different tau fragments, and that are measured by two distinct platforms.MethodsWe enrolled a cohort of 40 patients with AD at the stage of dementia (AD-dem) characterized by positive CSF A + T + profile, and a control group of 40 cognitively healthy participants (Control), to conduct a comprehensive method comparison for three plasma p-tau181 and five plasma p-tau217 assays run on the Simoa® HD-X™ or Lumipulse® G600II/G1200 platforms. Design of the compared assays differed in regard to: (1) tau phosphorylation site targeted by the capture antibody (T181 or T217), and (2) epitope of the pan-tau detector antibody (N-terminal or mid-region). For each of the assays we determined precision and analytical sensitivity parameters and used Passing-Bablok regression and Bland-Altman plots for pairwise comparison of p-tau181 or p-tau217 assays. Subsequently, we evaluated the diagnostic accuracy of all the assays for discrimination between AD-dem and Control groups.ResultsWe found a strong, positive correlation between all the measurements. Fixed and/or proportional bias was observed for each of compared p-tau181 assay pairs or p-tau217 assay pairs. While both plasma p-tau181 and p-tau217 levels were significantly increased in AD-dem vs. Control groups as measured by all assays, higher median concentration AD-dem/Control fold change and AUC values were observed for p-tau217 (assays range: fold change 3.72–6.74, AUC 0.916–0.956) compared with p-tau181 (assays range 1.81–2.94, AUC 0.829–0.909), independently of the platform used. No significant differences were observed between diagnostic performance of p-tau181 assays or p-tau217 assays targeting tau N-terminus or mid-region.ConclusionsAlthough all plasma p-tau measurements enabled discrimination between clinical groups, p-tau217 assays showed the highest robustness, independently of the pan-tau detector antibody targeting N-terminal or mid-region, and independently of the platform used. Considering the observed method disagreement in measured absolute concentrations, we stress the need for development of certified reference material, harmonizing measurements across different platforms.

A Novel Platform Featuring Nanomagnetic Ligand Fishing Based on Fixed-Orientation Immobilized Magnetic Beads for Screening Potential Cyclooxygenase-2 Inhibitors from Panax notoginseng Leaves.

A novel screening platform based on an Fe3O4@C@PDA-Ni2+@COX-2 ligand fishing combination with high-performance liquid chromatography-mass spectrometry was first designed, synthesized, and employed to screen and identify COX-2 inhibitors from Panax notoginseng leaves. The obtained magnetic nanoparticles exhibit outstanding preconcentration ability that allows for controlling the enzyme orientation to avoid enzyme active site blocking, conformational changes, or denaturing during immobilization. The as-prepared Fe3O4@C@PDA-Ni2+@COX-2 composite was carefully characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared spectrometry (FT-IR), Xray powder diffraction (XRD), thermal gravimetric analyzer (TGA), vibrating sample magnetometer (VSM), and Zeta potential analysis. The analytical parameters influencing the magnetic solid-phase fishing efficiency were optimized by univariate and multivariate methods (Box-Behnken design) by testing a positive control and celecoxib with active and inactive COX-2. Under the optimized ligand fishing conditions, twelve potential COX-2 inhibitors were screened and characterized in Panax notoginseng leaves. The results indicate that the proposed method provides a simple, feasible, selective, and effective platform for the efficient screening and identification of active compounds from Chinese herbal medicine. It has guiding significance for the synthesis and development of novel anti-inflammatory drugs, and provides a reference for the efficient discovery of anti-inflammatory drugs or lead compounds from the complex system of Chinese herbal medicine.

Impact of Exercise on Physiological, Biochemical, and Analytical Parameters in Patients with Heart Failure with Reduced Ejection Fraction.

Heart failure with reduced ejection fraction (HFrEF) is a condition marked by diminished cardiac output and impaired oxygen delivery to tissues. Exercise, once avoided in HFrEF patients due to safety concerns, is now recognized as an important therapeutic intervention. Structured exercise improves various physiological, biochemical, and analytical parameters, including cardiac output, endothelial function, skeletal muscle performance, and autonomic regulation. Biochemically, exercise induces favorable changes in inflammatory markers, lipid profiles, glucose metabolism, and renal function. This paper reviews these changes, highlighting how exercise can be safely incorporated into HFrEF management. Further research is needed to tailor exercise interventions for individual patients to optimize outcomes.

Quantitative Analysis of Caffeine in Roasted Coffee: A Comparison of Brewing Methods

Coffee is one of the most widely consumed beverages in the world due to its sensory and health benefits. The caffeine content, a bioactive compound of coffee, depends on many factors, including the brewing method, which is the subject of ongoing scientific research. In addition, various methods are used in studies to determine the caffeine content. However, it is worth noting that there is considerable variation in the individual analytical parameters within these methods. The aim of this study was to update the data on the effects of different brewing methods on the caffeine content of the brew and to present the current state of knowledge on techniques for the determination of this compound. A literature review was conducted, taking into account the latest studies in this field. The results showed that the caffeine content (mg/100 mL) of the brew prepared with the Cold Brew method was 48.50–179.95, Espresso—50.40–965.60, French Press—52.00–123.90, AeroPress—56.35–120.92, and Moka—128.00–539.90. These methods were characterized by different brewing parameters (time, water temperature and pressure, ratio of coffee to water), which differentiated the caffeine content. In addition, some methods were characterized by a wide range of caffeine content, suggesting that even minor variations in brewing method parameters may affect the content of this ingredient. High-performance liquid chromatography (HPLC) was the predominant method used. The detector wavelengths, along with other parameters of the HPLC method, such as gradient profiles and column temperatures, can affect the precision and accuracy of the analysis, and these differences can modify analyte retention and detection, leading to discrepancies in results. These results point to the need for studies that consider various brewing methods and a wide range of coffee types, including roast and origin, to accurately determine the effects of these factors on caffeine content determined by one precise method.

Multimodal neural correlates of childhood psychopathology.

Complex structural and functional changes occurring in typical and atypical development necessitate multidimensional approaches to better understand the risk of developing psychopathology. Here, we simultaneously examined structural and functional brain network patterns in relation to dimensions of psychopathology in the Adolescent Brain Cognitive Development dataset. Several components were identified, recapitulating the psychopathology hierarchy, with the general psychopathology (p) factor explaining most covariance with multimodal imaging features, while the internalizing, externalizing, and neurodevelopmental dimensions were each associated with distinct morphological and functional connectivity signatures. Connectivity signatures associated with the p factor and neurodevelopmental dimensions followed the sensory-to-transmodal axis of cortical organization, which is related to the emergence of complex cognition and risk for psychopathology. Results were consistent in two separate data subsamples and robust to variations in analytical parameters. Although model parameters yielded statistically significant brain-behavior associations in unseen data, generalizability of the model was rather limited for all three latent components (r change from within- to out-of-sample statistics: LC1within=0.36, LC1out=0.03; LC2within=0.34, LC2out=0.05; LC3within=0.35, LC3out=0.07). Our findings help in better understanding biological mechanisms underpinning dimensions of psychopathology, and could provide brain-based vulnerability markers.

Catalytic effect of the in-situ rhodium(III) complexes in surfactant medium on the auto-oxidation of 1,2-hydroxyphenylthiourea: A theoretical and experimental study for rhodium(III) sensing

1,2-hydroxyphenylthiourea(HPTU) undergoes auto-oxidation to form an yellow colored dimer. The process of auto-oxidation is enhanced by the presence of trace quantities of transition metal ions and transition metal complexes that act as catalysts. In the current study, catalytic potential of rhodium(III) complexes on the auto-oxidation of 1,2-hydroxyphenylthiourea(HPTU) was studied theoretically using quantum mechanical calculations and experiments were carried out using photometry and fluorometry. DFT studies inferred that [Rh(Py)6]Cl3 showed a better catalytic activity in the dimerization of HPTU. Theoretical studies were subsequently validated through experiments using photometric methods and the range of detection was determined to be 6 ng/mL–100 ng/mL. The detection limit was observed to be 2 ng/mL. Analytical parameters such as pH, reagent concentration, metal ion concentration, appropriate activators and surfactants were established.

High-performance full-etched fiber-to-chip grating couplers at 3.7-micron wavelength on silicon

Mid-infrared (MIR) silicon photonics have attracted great interest for potential applications in on-chip spectroscopy, free-space communication, and remote imaging. Currently, the high-performance and fabrication-friendly fiber-to-chip grating couplers operating at 3–4 μm wavelength band are still desired urgently. Here, we propose an efficient method for designing a 2D subwavelength grating coupler. The few analytical fitting parameters defining the subwavelength grating periods and fill factors in two dimensions enable a high design degree of freedom and a low search space dimension, resulting in high figure-of-merit and fast convergence simultaneously. The developed 3.7 μm grating coupler showcases record-high coupling efficiency both theoretically (−2.2 dB) and experimentally (−4.4 dB) among the 3–4 μm MIR counterparts. This study provides an effective method for designing fiber-to-chip grating couplers, by which the MIR grating couplers with high performance and fabrication ease are developed, thus paving the way for developing high-performance silicon photonic integrated circuits operating in the MIR wavelength band.

An antibody-free bio-layer interferometry biosensor for immunoglobulin G1 detection in human serum by using molecularly imprinted polynorepinephrine.

Bio-Layer Interferometry (BLI) has emerged as a versatile technique in affinity-based biosensing, analogous to Surface Plasmon Resonance. BLI enables real-time, label-free detection, and quantification of biomolecular interactions between an immobilized receptor and an analyte in solution. The BLI sensor comprises an optical fiber with an internal reference layer at the end and an external biocompatible layer where biological receptors are immobilized and exposed to the solution. We report the first BLI bioassay using a mimetic receptor based on molecularly imprinted polynorepinephrine (MIPNE) for detecting immunoglobulin G isotype 1 in whole, untreated, human serum. Using BLI fiber optics with different chemical linkers, we compared the analytical performance, with a focus on selectivity against other Ig classes and across the four IgG isotypes. The bioassay displayed the ability to detect IgG1 with excellent analytical parameters both in buffer condition (LOD=0.54±0.01μgmL-1, LOQ=2.09±0.02μgmL-1, avRSD=5.3%) and in whole serum (%RE=0.3%, avRSD=3%). These findings highlight the potential of integrating PNE-based molecular imprinting technology with BLI platforms for diverse analytical and diagnostic applications.

Numerical Modelling of Complex Modulus Tests on Asphalt Concrete using the 2D Discrete Element Method

The VENoL analytical model was developed to reproduce the nonlinear viscoelastic behaviour of asphalt concrete in dynamic analysis. In this paper, it is integrated as a contact law in a 2D model using the Discrete Element Method. The asphalt concrete is modelled on a macroscopic scale. The VENoL model is applied in the numerical code without any recalibration of its analytical parameters. Particular attention is paid to modelling variations in the Poisson's ratio as a function of test conditions. This integration is checked by comparing the results of the numerical model with those extracted from the literature for complex modulus tests in direct tension-compression. Despite the use of a macroscopic scale, it appears that the model can reproduce porosity effects through the mechanisms of DEM. Using the same set of parameters, two-point bending tests are also conducted to ensure their compliance in the characterisation of bituminous mixes.

Intradialytic Parenteral Nutrition in Patients on Hemodialysis: A Multicenter Retrospective Study.

To evaluate the effectiveness and safety of intradialytic parenteral nutrition (IDPN) on different nutritional outcomes. This was a retrospective analysis for a "routinely collected data bank" in a multicenter cohort, conducted on consecutive malnourished or at-risk of malnutrition patients with chronic kidney disease on hemodialysis who underwent IDPN with a three-in-one parenteral nutrition formula for a period ≥ 2 weeks. The primary endpoint was the mean change in the malnutrition inflammation score (MIS) score between baseline and the last follow-up visit on IDPN. Fifty-six patients were included. The mean age was 72.4 ± 12.0 years, and 24 (42.9%) were women. In the overall study sample, MIS significantly decreased from 16.4 (95%CI: 15.3-17.65) at baseline to 14.3 (95%CI: 12.8-15.8) at the last follow-up visit on IDPN (p = 0.0019). Fifteen (26.8%) patients achieved a MIS reduction ≥ 5 points after IDPN. As compared to baseline, IDPN significantly reduced the proportion of patients with protein-energy wasting (PEW) (89.3% versus 66.1%, respectively, p = 0.0023). Regarding analytical parameters, serum albumin (p = 0.0003) and total proteins (p = 0.0024) significantly increased after IDPN administration. Throughout the study's follow-up period, 45 (80.4%) patients reported experiencing some type of adverse event. IDPN was associated with a significant improvement in the nutritional profile. Notably, our research found that the administration of IDPN over a duration > 3 months significantly improved the nutritional status of patients evaluated by the MIS test.

First Experience of Late Pruning on Kékfrankos Grapevine (Vitis vinifera L.) in Eger Wine Region (Hungary)

Traditional winter pruning in dormancy (BBCH-00) as control (C) and three late pruning treatments, LP1 (wool stage—BBCH-05), LP2 (two leaves folded—BBCH-12), and LP3 (four leaves folded—BBCH-14), were applied on Kékfrankos grapevines. The evolution of the phenological growth stages, grape juice, wine analytical parameters, and phenolic composition were evaluated. The quantitative aspects of the grape berry, bunch, yield, and cane were also assessed. Our goal was to reach a decrease in sugar content and an increase in acidity. Delaying or postponing the phenological phases to bring technological and phenolic ripening closer together was also one of our objectives. These were accomplished, but the negative aspects of late pruning, which resulted in a reduction in the diameter and weight of the canes, should also be taken into account. We also found that, the later the late pruning, the more the yield was reduced. By postponing pruning, the phenological phases were also extended.

Bibliometric analysis of olaparib and pancreatic cancer from 2009 to 2022: A global perspective.

Genetic screening for breast cancer gene 1 (BRCA)1/2 mutations can inform breast/ovarian/pancreatic cancer patients of suitable therapeutic interventions. Four to seven percent of pancreatic cancer patients have germline BRCA mutations. BRCA genes aid in DNA repair, especially homologous recombination, which impacts genomic stability and cancer cell growth. BRCA1 regulates the cell cycle, ubiquitination, and chromatin remodeling, whereas BRCA2 stimulates the immune response. They predict the efficacy of platinum chemotherapy or polymerase (PARP) inhibitors such as olaparib. To determine the trends and future directions in the use of olaparib for pancreatic cancer treatment. To evaluate the trends in how olaparib works in pancreatic cancer, we performed a bibliometric analysis. One hundred and ninety-six related publications were accessed from the Web of Science Core Collection and were published between 2009 and 2022. The analytic parameters included publications, related citations, productive countries and institutes, influential authors, and keyword development. This study visualizes and discusses the current research, including the present global trends and future directions in olaparib and pancreatic cancer. Overall, this study sheds light on optimizing the use of olaparib in pancreatic cancer treatment, offering valuable guidance for researchers in this field. Our findings identified trends in olaparib and pancreatic cancer, with China and the USA leading and with global cooperation tightening. O'Reilly EM's team and Memorial Sloan-Kettering had the highest output. The Journal of Clinical Oncology was the most cited journal. More PARP inhibitors are emerging, and combination therapy is suggested for future therapeutic trends.

Synthesis, crystal structure and exploration of N,N'-(ethane-1,2-diyl)bis(4-acetylbenzenesulfonamide) (EDBABS) fabricated glassy carbon electrode as highly sensitive barium (Ba2+) sensor: An electrochemical approach

Environmental pollution spurred by dint of noxious chemicals and heavy metals has popped up as a pressing threat for present day community. In this study, we synthesized the N,N'-(ethane 1,2-diyl)bis(4-acetylbenzene-1-sulfonamide) (EDBABS) and N,N'-(cyclohexane-1,2-diyl)bis(4-acetylbenzenesulfonamide) (CDBABS) as bidentate chelating agents with the intention to detect the heavy metal cations in water systems. Conventional spectroscopic techniques such as UV–Vis spectroscopy, Fourier transform-infra red (FT-IR) spectroscopy, 1H-NMR and 13C-NMR in addition to single crystal X-ray diffraction studies were performed to expound structural characterization data of these newly synthesized non-reported bidentate chelating agents. After Characterization, a novel electrochemical current – potential (I-V) approach based on their modified GCEs was applied to detect the toxic cations in water systems. For this purpose, Keithley electrometer was employed as a constant voltage source. On the trail of fabricating an efficient as well as selective electrochemical sensor, for the detection of heavy metal cations in phosphate buffer system of pH = 7.0, EDBABS and CDBABS coupled with nafion as adhesive conducting binder were coated separately onto the Glassy Carbon Electrodes (GCEs). It was delineated that newly designed EDBABS/Nafion/GCE induced a high current response for Ba2+ cations in the presence of other interfering heavy metal cations (Y3+, Sn2+, Sb3+, Mn2+, Hg2+, Cr3+, As3+ and Ag+) than CDBABS/Nafion/GCE and found to be selective and sensitive towards Ba2+ cations, predominantly contributing towards environmental pollution. In order to optimize this newly designed EDBABS/Nafion/GCE as selective electrochemical Ba2+ cationic sensor, different analytical parameters such as sensitivity, limit of detection (LOD) at S/N of 3, limit of quantification (LOQ), and linear dynamic range (LDR) turned out to be satisfactory towards Ba2+ cations. The calibration curve emerged to be linear with a broad concentration range of Ba2+cations from 0.1 nM to 0.01 M and sensitivity was estimated as 3.481 × 10−3µAµM−1cm−2 in addition to (r2) as 0.9834, limit of detection (LOD) as 0.027 nM (at S/N = 3) and limit of quantification (LOQ) as 0.091 nM. Within the realm of extensive environmental protection and public health care field, this work inducts a reliable and effective way for the fabrication of sensitive as well as selective cationic electrochemical sensors based on chelating agents which can be launched as an advanced approach for quick probing of heavy metal cations in water systems, reliably and effectively.