Kobra Moteabbed; Jafar Burromandpiroze; Vahid Zare-Shahabadi; Soheil Sayyahi
Abstract
In this study, we used a prepared from chitosan-capped AuNPs for the determination of trace amount acetaminophen drug in various matrices such human fluids by kinetic spectrophotometric method. The calibration curve was linear in the range of (0.05 to 10.0 µg L−1). The standard deviation ...
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In this study, we used a prepared from chitosan-capped AuNPs for the determination of trace amount acetaminophen drug in various matrices such human fluids by kinetic spectrophotometric method. The calibration curve was linear in the range of (0.05 to 10.0 µg L−1). The standard deviation of (1.9%), and detection limit of the method (0.05 µg L−1 in time 6 min, 325 nm) were obtained for Sensor level response chitosan-capped AuNPs with (95%) confidence evaluated. Observed outcomes confirmed the suitability recovery, and a very low detection limit for measuring the acetaminophen drug. The method introduced to measure acetaminophen drug in real samples such as urine, and blood can be used for other drugs, and hospital samples.
Ghobad Mansori; Mohammad_Bagher - Gholivand; Zarrin - Es'haghi
Abstract
For the first time, an analytical methodology based ondifferential pulse voltammetry (DPV) at a glassy carbon electrode (GCE) assisted by two multivariate calibration (MVC) models including back propagation-artificial neural network (BP-ANN), non-linear class, and partial least squares-1 (PLS-1), classical ...
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For the first time, an analytical methodology based ondifferential pulse voltammetry (DPV) at a glassy carbon electrode (GCE) assisted by two multivariate calibration (MVC) models including back propagation-artificial neural network (BP-ANN), non-linear class, and partial least squares-1 (PLS-1), classical class, thatthey have been constructed on the basis of non-bilinear first order differential pulse voltammetry (DPV) data,was developed and validated for the simultaneous determination of Ascorbic acid, Uric acid, Acetaminophen, and Noradrenalinto identify which approach offers the best predictions.The baselines of the DPV signals were corrected by asymmetric least square spline regression (AsLSSR) algorithm. Before applying the PLS-1,lack of bi-linearity was tackled by potential shift correction using correlation optimised warping (COW) algorithm. The multivariate calibration (MVC) model was developed as a quaternary calibration modelin a blank human serum sample (drug-free) provided by a healthy volunteer to regard the presence of a strong matrix effect which may be caused by the possible interferents present in the serum, and it was validated and tested with two independent sets of analytes mixtures in the blank and actual human serum samples, respectively.According to the obtained results, the PLS-1 was recommended for simultaneous determination of AA, UA, AC, and NA in both blank and actual human serum samples .
Afroozeh Arabi; Alireza Mohadesi; Mohammad Ali Karimi; Mehdi Ranjbar
Abstract
In this study, a new Zeolite Al/Na (ZAN) was synthesized and characterized and then a new modified Carbon Paste Electrode with ZAN was made to determine Acetaminophen. Electrochemical studies using Linear Sweep Voltammetry and differential pulse voltammetry were used to determine electrochemical Acetaminophen ...
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In this study, a new Zeolite Al/Na (ZAN) was synthesized and characterized and then a new modified Carbon Paste Electrode with ZAN was made to determine Acetaminophen. Electrochemical studies using Linear Sweep Voltammetry and differential pulse voltammetry were used to determine electrochemical Acetaminophen . In the presence of Acetaminophen , modified electrode with ZAN shows a specific anodic peak at ~ 0.59 volts which is the result of using electrocatalytic oxidation of Acetaminophen . The determination limit of this method to measure Acetaminophen was 5.8 µM, the relative standard deviation for 7 repeated measurements was 1.1 % and linear range of the calibration to measure Acetaminophen was 10 up to 115 µM . for the characterization of ZAN nanostructures we used SEM (Scanning Electron Microscopy), DLS (Dynamic Light Scattering) and FT-IR (Fourier-Transform Infrared spectroscopy).
Arash Mohammadinejad; Mahmoud Ebrahimi; Ali Morsali; Zarrin Es’haghi; Hamed Chegini; Abdolhossein Ebrahimitalab
Volume 3, Issue 1 , March 2016, , Pages 27-37
Abstract
In this work, a carbon paste electrode modified with multiwall carbon nanotubes (MWCNTPE) was used for the sensitive voltammetric determination of acetaminophen (AC) in biological and pharmaceutical samples. The electrochemical behavior of acetaminophen was investigated employing cyclic voltammetry. ...
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In this work, a carbon paste electrode modified with multiwall carbon nanotubes (MWCNTPE) was used for the sensitive voltammetric determination of acetaminophen (AC) in biological and pharmaceutical samples. The electrochemical behavior of acetaminophen was investigated employing cyclic voltammetry. It was revealed that the standard electrode potential of half reaction for AC(O), H+/AC(R) was 0.898 V. under the optimized experimental conditions, the oxidation peak current for acetaminophen was found to vary linearly with concentration range of 0.12 to 99 µM with detection limit of 0.06 µM using differential pulse voltammetry. DFT-B3LYP/6-31G (d,p) and HF/6-31G (d,p) calculations were performed for deoxidized acetaminophen (AC(R)) and its oxidized form (AC(O)). The calculated standard electrode potentials are relatively in agreement with experimental data. This electrode was employed for determination of acetaminophen in hospital waste water, hair, blood and pharmaceutical samples considering its high sensitivity, low detection limit, good reproducibility and its non-existent interference at trace levels in clinical and quality control laboratories.
