Abstract:The present work reports the development and application of a new carbon paste electrode modified with graphene and nanodiamond for the determination of nimesulide in biological and environmental samples. The morphology and electrochemical properties of the carbon nanostructures were characterized by scanning electron microscopy, cyclic voltammetry and electrochemical impedance spectroscopy. The application of the proposed electrochemical sensor led to a significant improvement in the analytical signal and nim… Show more
“…The limit of detection (LOD) and limit of quantification (LOQ) for H 2 O 2 oxidation by CV were 5.0 and 16.6 nM, respectively, whereas they were 4.0 and 13.3 nM for its reduction, respectively. The LOD and LOQ values were calculated using equations (3.6) and (3.7).LOD=true03σmandLOQ=true010σmwhere σ is the blank standard deviation and m is the linear's slope [16].…”
Section: Resultsmentioning
confidence: 99%
“…After the CPE modification with p1,5-DAN, there is a small decrease of ΔE p ∼0. 16 V with E 0 of 0.124 V (figure 2c), whereas the ΔE p decreased to approximately 0.099 V with E 0 of 0.25 V after the deposition of palladium nanoparticles (PdNPs), as shown in figure 2d [48]. ΔE p is inversely proportional to the electron transfer rate [49].…”
Section: Determination Of the Electroactive Surface Areamentioning
confidence: 95%
“…The limit of detection (LOD) and limit of quantification (LOQ) for H 2 O 2 oxidation by CV were 5.0 and 16.6 nM, respectively, whereas they were 4.0 and 13.3 nM for its reduction, respectively. The LOD and LOQ values were calculated using equations (3.6) where s is the blank standard deviation and m is the linear's slope [16]. These results suggest that the PdNPs/p1,5-DAN/CPE can effectively mediate electron transfer between the electrode and H 2 O 2 , showing clear catalytic activity toward electrochemical redox determination.…”
Section: Behaviour Of Square Wave Voltammetry 'Swv'mentioning
In this work, palladium nanoparticles (PdNPs)/p1,5-DAN/ carbon paste electrode (CPE) and p1,5-DAN/CPE sensors have been developed for determination of hydrogen peroxide. Both sensors showed a highly sensitive and selective electrochemical behaviour, which were derived from a large specific area of poly 1,5 DAN and super excellent electroconductibility of PdNPs. PdNPs/p1,5-DAN/CPE exhibited excellent performance over p1,5-DAN/CPE. Thus, it was used for detecting hydrogen peroxide (H
2
O
2
) with linear ranges of 0.1 to 250 µM and 0.2 to 300 µM as well as detection limits (
S/N = 3
) of 1.0 and 5.0 nM for square wave voltammetry (SWV) and cyclic voltammetry (C.V) techniques, respectively. The modified CPE has good reproducibility, adequate catalytic activity, simple synthesis and stability of peak response during H
2
O
2
oxidation on long run that exceeds many probes. Both reproducibility and stability for H
2
O
2
detection are attributable to the PdNPs immobilized on the surface of p1,5-DAN/CPE. The modified CPE was used for determining H
2
O
2
in real specimens with good stability, sensitivity, and reproducibility.
“…The limit of detection (LOD) and limit of quantification (LOQ) for H 2 O 2 oxidation by CV were 5.0 and 16.6 nM, respectively, whereas they were 4.0 and 13.3 nM for its reduction, respectively. The LOD and LOQ values were calculated using equations (3.6) and (3.7).LOD=true03σmandLOQ=true010σmwhere σ is the blank standard deviation and m is the linear's slope [16].…”
Section: Resultsmentioning
confidence: 99%
“…After the CPE modification with p1,5-DAN, there is a small decrease of ΔE p ∼0. 16 V with E 0 of 0.124 V (figure 2c), whereas the ΔE p decreased to approximately 0.099 V with E 0 of 0.25 V after the deposition of palladium nanoparticles (PdNPs), as shown in figure 2d [48]. ΔE p is inversely proportional to the electron transfer rate [49].…”
Section: Determination Of the Electroactive Surface Areamentioning
confidence: 95%
“…The limit of detection (LOD) and limit of quantification (LOQ) for H 2 O 2 oxidation by CV were 5.0 and 16.6 nM, respectively, whereas they were 4.0 and 13.3 nM for its reduction, respectively. The LOD and LOQ values were calculated using equations (3.6) where s is the blank standard deviation and m is the linear's slope [16]. These results suggest that the PdNPs/p1,5-DAN/CPE can effectively mediate electron transfer between the electrode and H 2 O 2 , showing clear catalytic activity toward electrochemical redox determination.…”
Section: Behaviour Of Square Wave Voltammetry 'Swv'mentioning
In this work, palladium nanoparticles (PdNPs)/p1,5-DAN/ carbon paste electrode (CPE) and p1,5-DAN/CPE sensors have been developed for determination of hydrogen peroxide. Both sensors showed a highly sensitive and selective electrochemical behaviour, which were derived from a large specific area of poly 1,5 DAN and super excellent electroconductibility of PdNPs. PdNPs/p1,5-DAN/CPE exhibited excellent performance over p1,5-DAN/CPE. Thus, it was used for detecting hydrogen peroxide (H
2
O
2
) with linear ranges of 0.1 to 250 µM and 0.2 to 300 µM as well as detection limits (
S/N = 3
) of 1.0 and 5.0 nM for square wave voltammetry (SWV) and cyclic voltammetry (C.V) techniques, respectively. The modified CPE has good reproducibility, adequate catalytic activity, simple synthesis and stability of peak response during H
2
O
2
oxidation on long run that exceeds many probes. Both reproducibility and stability for H
2
O
2
detection are attributable to the PdNPs immobilized on the surface of p1,5-DAN/CPE. The modified CPE was used for determining H
2
O
2
in real specimens with good stability, sensitivity, and reproducibility.
“…Considering its widespread use and the risks it poses to humans and the environment, it is necessary to develop increasingly sensitive, practical and low-cost analytical methods for the determination and/or monitoring of TMP in environmental and biological samples. In this sense, electrochemical sensors stand out for their chemical and physical characteristics, in addition to the possibility of modification, which in turn can further increase their sensitivity and/or selectivity [8][9][10].…”
This work proposes a simple, fast and low-cost voltammetric method for the determination of trimethoprim at low concentrations in an analytical and real matrix (river water sample, bovine serum and synthetic urine). For this, a glassy carbon electrode was modified with Printex(6L) carbon and gold nanoparticles in a chitosan film crosslinked with epichlorohydrin. After that, the electrochemical measurement system contained a solution of phosphate buffer at pH 4.0 with commands for the square wave voltammetry technique. The results achieved showed a limit of detection equal to 12.4 nmol L−1 and a linear concentration range from 0.20 to 6.0 μmol L−1. The sensor selectivity was tested in the presence of various electroactive molecules, and the results showed that the detection of TMP in the presence of possible interferents was not masked. In addition, the applicability of the AuNPs–Printex(6L)–CTS:EPH/GCE sensor was also verified in synthetic samples of urine, bovine serum and river water through standard addition and recovery tests. Finally, the results of this analytical proposal portray a simple, fast and efficient method for the detection of TMP in different matrices.
“…In recent decades, carbon-based materials have garnered significant attention due to their structural and morphological properties [ 13 , 14 , 15 ]. Those materials have active centers that generate faradaic and reversible oxidation and reduction reactions originating from interactions between an ionic solution and carbon [ 16 ].…”
Nifedipine, a widely utilized medication, plays a crucial role in managing blood pressure in humans. Due to its global prevalence and extensive usage, close monitoring is necessary to address this widespread concern effectively. Therefore, the development of an electrochemical sensor based on a glassy carbon electrode modified with carbon nanofibers and gold nanoparticles in a Nafion® film was performed, resulting in an active electrode surface for oxidation of the nifedipine molecule. This was applied, together with a voltammetric methodology, for the analysis of nifedipine in biological and environmental samples, presenting a linear concentration range from 0.020 to 2.5 × 10−6 µmol L−1 with a limit of detection 2.8 nmol L−1. In addition, it presented a good recovery analysis in the complexity of the samples, a low deviation in the presence of interfering potentials, and good repeatability between measurements.
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