Protein templated Au-Pt nanoclusters-graphene nanoribbons as a high performance sensing layer for the electrochemical determination of diazinon

2018 ◽  
Vol 275 ◽  
pp. 180-189 ◽  
Author(s):  
Niyoosha Pajooheshpour ◽  
Mosayeb Rezaei ◽  
Ali Hajian ◽  
Abbas Afkhami ◽  
Mika Sillanpää ◽  
...  
2021 ◽  
Vol 45 (6) ◽  
pp. 3215-3223
Author(s):  
Selvarasu Maheshwaran ◽  
Ramachandran Balaji ◽  
Shen-Ming Chen ◽  
Ray Biswadeep ◽  
Vengudusamy Renganathan ◽  
...  

A high-performance electrochemical sensing platform based on CuS nano-globules is efficiently developed.


RSC Advances ◽  
2021 ◽  
Vol 11 (47) ◽  
pp. 29590-29597
Author(s):  
Chuanen Guo ◽  
Chengxiang Wang ◽  
Hongyan Sun ◽  
Dongmei Dai ◽  
Hongtao Gao

High-performance electrode modification materials play a crucial role in improving the sensitivity of sensor detection in electrochemical determination of heavy metals.


Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4115
Author(s):  
Severyn Salis ◽  
Nadia Spano ◽  
Marco Ciulu ◽  
Ignazio Floris ◽  
Maria I. Pilo ◽  
...  

5-(hydroxymethyl)furan-2-carbaldehyde, better known as hydroxymethylfurfural (HMF), is a well-known freshness parameter of honey: although mostly absent in fresh samples, its concentration tends to increase naturally with aging. However, high quantities of HMF are also found in fresh but adulterated samples or honey subjected to thermal or photochemical stresses. In addition, HMF deserves further consideration due to its potential toxic effects on human health. The processes at the origin of HMF formation in honey and in other foods, containing saccharides and proteins—mainly non-enzymatic browning reactions—can also produce other furanic compounds. Among others, 2-furaldehyde (2F) and 2-furoic acid (2FA) are the most abundant in honey, but also their isomers (i.e., 3-furaldehyde, 3F, and 3-furoic acid, 3FA) have been found in it, although in small quantities. A preliminary characterization of HMF, 2F, 2FA, 3F, and 3FA by cyclic voltammetry (CV) led to hypothesizing the possibility of a comprehensive quantitative determination of all these compounds using a simple and accurate square wave voltammetry (SWV) method. Therefore, a new parameter able to provide indications on quality of honey, named “Furanic Index” (FI), was proposed in this contribution, which is based on the simultaneous reduction of all analytes on an Hg electrode to ca. −1.50 V vs. Saturated Calomel Electrode (SCE). The proposed method, validated, and tested on 10 samples of honeys of different botanical origin and age, is fast and accurate, and, in the case of strawberry tree honey (Arbutus unedo), it highlighted the contribution to the FI of the homogentisic acid (HA), i.e., the chemical marker of the floral origin of this honey, which was quantitatively reduced in the working conditions. Excellent agreement between the SWV and Reverse-Phase High-Performance Liquid Chromatography (RP-HPLC) data was observed in all samples considered.


1983 ◽  
Vol 29 (12) ◽  
pp. 2031-2034 ◽  
Author(s):  
B Kågedal ◽  
A Pettersson

Abstract A phenylboronate affinity gel has been investigated for use in the prepurification of urine before "high-performance" liquid chromatography and electrochemical determination of 5-S-L-cysteinyl-L-dopa. At pH 5.6 this naturally occurring 5-S-cysteinyldopa was adsorbed on a phenylboronate column and was quantitatively eluted with trichloroacetate, pH 3.0. This pretreatment of urine before "high-performance" liquid chromatography produced satisfactory chromatographic separations, and the results were further improved when the purification procedure also included treatment on a cation exchanger. By using 5-S-D-cysteinyl-L-dopa--a diastereomer to 5-S-L-cysteinyl-L-dopa--as an internal standard, we have developed a practical routine method for the quantitative determination of urinary 5-S-L-cysteinyl-L-dopa. The precision (CV = 2.4%) and analytical recovery (96.9%, SD 5.3%) were satisfactory and the results obtained correlated well with a previously described method.


1999 ◽  
Vol 82 (5) ◽  
pp. 1077-1082 ◽  
Author(s):  
Juan A Squella ◽  
Anny E Iribarren ◽  
Juan C Sturm ◽  
Luis J Núñez-Vergara

Abstract Lacidipine is an antihypertensive drug that is oxidizable at the glassy carbon electrode. The voltammetric oxidation of lacidipine in aqueous-alcoholic solutions (70 + 30) produces a well-defined voltammetric peak when subjected to a differential pulse voltammetric experiment. This peak is due to oxidation of the dihydropyridine ring to a pyridine derivative. This voltammetric response result is irreversible, pH dependent, and diffusion controlled. The best resolution for the peak was obtained at pH 6 in Britton-Robinson buffer-ethanol (70 + 30). The peak potential at pH 6 was 800 mV against an Ag-AgCI reference electrode. A linear relationship between peak current and lacidipine concentration was obtained. For analytical purposes, a calibration curve for lacidipine that covered concentrations between 5 x 10-6 and 2 x 10-6 was used. Detection and quantitation limits were 3.52 x 10-6 and 3.78 x 10-6M, respectively. The repeatability of the measurement was 2%. On the basis of the voltammetric response, we also developed high-performance liquid chromatographic methods with electrochemical detection. For comparative purposes, we also developed a spectrophotometric method.


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