scholarly journals Novel Eco-Friendly Synthesis of Biosilver Nanoparticles as a Colorimetric Probe for Highly Selective Detection of Fe (III) Ions in Aqueous Solution

2021 ◽  
Vol 2021 ◽  
pp. 1-17
Author(s):  
Nguyen Le Nhat Trang ◽  
Van-Tuan Hoang ◽  
Ngo Xuan Dinh ◽  
Le Thi Tam ◽  
Van Phan Le ◽  
...  
Keyword(s):  
Limit Of Detection ◽  
Spherical Shape ◽  
Electrochemical Process ◽  
Metallic Silver ◽  
Face Centered Cubic ◽  
Experimental Conditions ◽  
Detection Mechanism ◽  
Lake Water Sample ◽  
Vis Spectroscopy

In this work, an eco-friendly approach for the synthesis of biogenic silver nanoparticles (bio-AgNPs) using botanical extracts in combination with an electrochemical process was carried out. We employed three types of plant extracts, including green tea leaf (GTE), grapefruit peel (GP), and mangosteen peel (MP) extracts to successfully synthesize the bio-AgNPs and optimized the experimental conditions aiming to get the highest synthetic yield. The formation of bio-AgNPs was monitored by UV-Vis spectroscopy via a surface plasmon resonance (SPR) band at about 420–430 nm. Transmission electron microscope (TEM) showed their spherical shape with the size range within 23–55 nm. While X-ray diffraction (XRD) analysis described in detail the crystalline structure of the bio-AgNPs with a face-centered cubic crystal lattice of metallic silver. The chemical bonding and elemental compositions of the bio-AgNPs were determined by Fourier Transform Infrared (FTIR) spectroscopy, in which organic compounds in the natural extracts not only acted as effective reductants but also capping agents for the fabricated bio-AgNPs. The prepared bio-AgNPs exhibited high stability and excellent dispersion for about four months. Based on the linear relationship between obtained SPR band intensity of bio-AgNP GTE in the presence of Fe (III) and concentration of Fe (III) ions, our bio-AgNP GTE can be used to develop a highly selective colorimetric sensor for the determination of Fe (III) ions within a linear range from 1 to 25 μM. According to that, the limit of detection (LOD) was recorded at approximately 0.532 μM, and the quantitative limit (LOQ) was calculated to be 1.77 μM. A detection mechanism was proposed through redox reactions between bio-AgNP GTE and Fe (III) ions. More interestingly, this method was successfully applied for the determination of Fe (III) ions in a lake water sample with percentage recovery of 107-150% and high reproducibility ( RSD = 1.49 % ).

scholarly journals Determination of cobalt in water samples by atomic absorption spectrometry after pre-concentration with a simple ionic liquid-based dispersive liquid-liquid micro-extraction methodology

2010 ◽  
Vol 8 (3) ◽  
pp. 617-625 ◽  
Author(s):  
Hossein Abdolmohammad-Zadeh ◽  
Elnaz Ebrahimzadeh
Keyword(s):  
Ionic Liquid ◽  
Atomic Absorption Spectrometry ◽  
Atomic Absorption ◽  
Water Samples ◽  
Limit Of Detection ◽  
Absorption Spectrometry ◽  
Experimental Conditions ◽  
Flame Atomic Absorption ◽  
Relative Standard

AbstractA rapid dispersive liquid-liquid micro-extraction (DLLME) methodology based on the application of 1-hexylpyridinium hexafluorophosphate [C6py][PF6] ionic liquid (IL) as an extractant solvent was applied for the pre-concentration of trace levels of cobalt prior to determination by flame atomic absorption spectrometry (FAAS). 1-Phenyl-3-methyl-4-benzoyl-5-pyrazolone (PMBP) was employed as a chelator forming a Co-PMBP complex to extract cobalt ions from aqueous solution into the fine droplets of [C6py][PF6]. Some effective factors that influence the micro-extraction efficiency include the pH, the PMBP concentration, the amount of ionic liquid, the ionic strength, the temperature and the centrifugation time which were investigated and optimized. In the optimum experimental conditions, the limit of detection (3s) and the enrichment factor were 0.70 µg L−1 and 60, respectively. The relative standard deviation (RSD) for six replicate determinations of 50 µg L−1 Co was 2.36%. The calibration graph using the pre-concentration system was linear at levels 2–166 µg L−1 with a correlation coefficient of 0.9982. The applicability of the proposed method was evaluated by the determination of trace amounts of cobalt in several water samples.

scholarly journals Cerimetric determination of simvastatin in pharmaceuticals based on redox and complex formation reactions

2018 ◽  
Vol 33 (2) ◽  
pp. 21
Author(s):  
Kanakapura Basavaiah ◽  
Okram Zenita Devi
Keyword(s):  
Limit Of Detection ◽  
Reference Method ◽  
Standard Addition ◽  
Molar Absorptivity ◽  
Experimental Conditions ◽  
Spectrophotometric Methods ◽  
Fixed Quantity ◽  
Bulk Drug ◽  
Student’S T

Two sensitive spectrophotometric methods are described for the determination of simvastatin (SMT) in bulk drug and in tablets. The methods are based on the oxidation of SMT by a measured excess of cerium (IV) in acid medium followed by determination of unreacted oxidant by two different reaction schemes. In one procedure (method A), the residual cerium (IV) is reacted with a fixed concentration of ferroin and the increase in absorbance is measured at 510 nm. The second approach (method B) involves thereduction of the unreacted cerium (IV) with a fixed quantity of iron (II), and the resulting iron (III) is complexed with thiocyanate and the absorbance measured at 470 nm. In both methods, the amount of cerium (IV) reacted corresponds to SMT concentration. The experimental conditions for both methods were optimized. In method A, the absorbance is found to increase linearly with SMT concentration (r = 0.9995) whereas in method B, the same decreased (r = -0.9943). The systems obey Beer’s law for 0.6-7.5 and 0.5-5.0 μg mL-1 for method A and method B, respectively. The calculated molar absorptivity values are 2.7 X 104 and 1.06 X 105 Lmol-1 cm-1, respectively; and the corresponding sandel sensitivity values are 0.0153 and 0.0039μg cm-2, respectively. The limit of detection (LOD) and quantification (LOQ) are reported for both methods. Intra-day and inter-day precision, and accuracy of the methods were established as per the current ICH guidelines. The methods were successfully applied to the determination of SMT in tablets and the results were statistically compared with those of the reference method by applying the Student’s t-test and F-test. No interference was observed from the common excipients added to tablets. The accuracy and validity of the methods were further ascertained by performing recovery experiments via standard addition procedure.

scholarly journals Use of Dispersive Liquid-Liquid Microextraction and UV-Vis Spectrophotometry for the Determination of Cadmium in Water Samples

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
J. Pérez-Outeiral ◽  
E. Millán ◽  
R. Garcia-Arrona
Keyword(s):  
Water Samples ◽  
Limit Of Detection ◽  
Experimental Conditions ◽  
Cadmium Determination ◽  
A Value ◽  
Relative Standard ◽  
Potential Applicability ◽  
Dispersive Liquid Liquid Microextraction ◽  
Liquid Microextraction

A simple and inexpensive method for cadmium determination in water using dispersive liquid-liquid microextraction and ultraviolet-visible spectrophotometry was developed. In order to obtain the best experimental conditions, experimental design was applied. Calibration was made in the range of 10–100 μg/L, obtaining good linearity (R2 = 0.9947). The obtained limit of detection based on calibration curve was 8.5 μg/L. Intra- and interday repeatability were checked at two levels, obtaining relative standard deviation values from 9.0 to 13.3%. The enrichment factor had a value of 73. Metal interferences were also checked and tolerable limits were evaluated. Finally, the method was applied to cadmium determination in real spiked water samples. Therefore, the method showed potential applicability for cadmium determination in highly contaminated liquid samples.

scholarly journals Sensitive Determination of Terazosin in Pharmaceutical Formulations and Biological Samples by Ionic-Liquid Microextraction Prior to Spectrofluorimetry

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Mohsen Zeeb ◽  
Mahdi Sadeghi
Keyword(s):  
Ionic Liquid ◽  
Ionic Strength ◽  
Biological Samples ◽  
Limit Of Detection ◽  
Pharmaceutical Formulations ◽  
Experimental Conditions ◽  
Relative Standard ◽  
Common Ion ◽  
Liquid Microextraction

An efficient and environmentally friendly sample preparation method based on the application of hydrophobic 1-Hexylpyridinium hexafluorophosphate [Hpy][PF6] ionic liquid (IL) as a microextraction solvent was proposed to preconcentrate terazosin. The performance of the microextraction method was improved by introducing a common ion of pyridinium IL into the sample solution. Due to the presence of the common ion, the solubility of IL significantly decreased. As a result, the phase separation successfully occurred even at high ionic strength, and the volume of the settled IL-phase was not influenced by variations in the ionic strength (up to 30% w/v). After preconcentration step, the enriched phase was introduced to the spectrofluorimeter for the determination of terazosin. The obtained results revealed that this system did not suffer from the limitations of that in conventional ionic-liquid microextraction. Under optimum experimental conditions, the proposed method provided a limit of detection (LOD) of 0.027 μg L−1and a relative standard deviation (R.S.D.) of 2.4%. The present method was successfully applied to terazosin determination in actual pharmaceutical formulations and biological samples. Considering the large variety of ionic liquids, the proposed microextraction method earns many merits, and will present a wide application in the future.

scholarly journals Development of a new analytical spectroscopic methodology based on the competitive aggregation in a dye–surfactant–drug system: Application to the determination of gemfibrozil

2008 ◽  
Vol 22 (4) ◽  
pp. 309-317 ◽  
Author(s):  
Mohammad Amjadi ◽  
Jamshid L. Manzoori ◽  
Leila Farzampour
Keyword(s):  
Limit Of Detection ◽  
Pharmaceutical Preparations ◽  
Calibration Graph ◽  
Experimental Conditions ◽  
Analytical Methodology ◽  
Surfactant Aggregates ◽  
Didodecyldimethylammonium Bromide ◽  
The Difference ◽  
Absorption Features

A new analytical methodology based on the competitive aggregation in a dye–surfactant–drug system is developed for the determination of gemfibrozil. Eriochrome Blue Black R (EBBR) and Didodecyldimethylammonium bromide (DDABr) were the dye and surfactant used, respectively. In the proposed method, the anions of the dye bind to the cationic surfactant molecules to form dye–surfactant aggregates, which are monitored from changes in UV-Vis absorption features of the dye. In the ternary EBBR–DDABr–drug mixtures, the drug competes with the dye to interact with the surfactant, which results in a decrease in dye–surfactant aggregates formation. This, again, causes a change in absorption properties of the dye. The measurement parameter is the difference between the absorption of the dye in the presence and absence of the drug. In the appropriate experimental conditions the absorbance differences are directly proportional to the drug concentration. The influence of several experimental variables such as pH, concentrations of buffer, EBBR and DDABr on the measurement parameter were studied. Under the optimum conditions, the calibration graph was linear up to 6.0 μg ml−1with the correlation coefficient of 0.998. The limit of detection and quantification were found to be 0.044 and 0.15 μg ml−1, respectively. The method was validated and applied to the determination of gemfibrozil in pharmaceutical preparations.

scholarly journals Application of Derivative Spectrophotometry to Simultaneous Determination of Indomethacin and 5-Methoxy-2-methyl-3-indoleacetic Acid in Metindol Injections

2004 ◽  
Vol 87 (3) ◽  
pp. 592-595 ◽  
Author(s):  
Mariusz Stolarczyk ◽  
Jan Krzek ◽  
Włodzimierz Rzeszutko
Keyword(s):  
Simultaneous Determination ◽  
Indoleacetic Acid ◽  
Limit Of Detection ◽  
Accurate Method ◽  
Derivative Spectrophotometry ◽  
Experimental Conditions

Abstract Derivative spectrophotometry was employed to develop a rapid and accurate method for simultaneous determination of indomethacin and 5-methoxy-2-methyl-3-indoleacetic acid as its possible impurity in Metindol injections. At the selected wavelengths, 233.04 and 284.65 nm, no interference between the components determined was observed. Under the established experimental conditions, recoveries of the particular components were from 96.14 to 98.17%. Linearity was maintained over a broad range of concentrations, from 11.88 × 10−3 to 35.64 × 10−3 mg/mL for indomethacin and 0.4 to 1.2 mg/mL for 5-methoxy-2-methyl-3-indoleacetic acid. The limit of detection was found to be 6.0 × 10−3 mg/mL for indomethacin and 0.04 × 10−3 mg/mL for 5-methoxy-2-methyl-3-indoleacetic acid. The limits of quantitation were found to be 10.0 × 10−3 mg/mL and 0.20 × 10−3 mg/mL, respectively.

scholarly journals Spectrofluorimetric determination of amlodipine in human plasma without derivatization

2012 ◽  
Vol 48 (4) ◽  
pp. 719-725 ◽  
Author(s):  
Yucel Kadioglu ◽  
Murat Ozturk
Keyword(s):  
Channel Blocker ◽  
Limit Of Detection ◽  
Plasma Samples ◽  
Experimental Conditions ◽  
Spectrofluorimetric Method ◽  
Relative Standard ◽  
Limit Of Quantitation ◽  
Spectrofluorimetric Determination ◽  
Better Than

A rapid and sensitive spectrofluorimetric method was developed for the determination of amlodipine (AD), a calcium channel blocker, in the plasma. The type of solvent, the wavelength range, and the range of AD concentration were selected to optimize the experimental conditions. The calibration curves were linear (r² >0.997) in the concentration range of 0.1-12.5 ppm of AD. The limit of quantitation and limit of detection values for the method for plasma samples were 0.1 ppm and 0.07 ppm, respectively. The precision calculated as the relative standard deviation was less than 3.5%, and the accuracy (relative error) was better than 5.5% (n=6). The method developed in this study can be directly and easily applied for the determination of AD in the plasma without derivatization in plasma.

scholarly journals Analytical application of the reaction system disulphonated hydroquinone-hydrogen peroxide for the kinetic spectrophotometric determination of iron traces in acidic media

2019 ◽  
Vol 73 (6) ◽  
pp. 387-396
Author(s):  
Snezana Tosic ◽  
Snezana Mitic ◽  
Aleksandra Pavlovic ◽  
Emilija Pecev-Marinkovic ◽  
Danijela Kostic ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Limit Of Detection ◽  
Reaction System ◽  
Absorption Spectrometry ◽  
Acidic Media ◽  
Experimental Conditions ◽  
Method Effects ◽  
Kinetic Spectrophotometric ◽  
White Radish

A simple, rapid, sensitive and selective kinetic spectrophotometric method for determination of Fe(III) traces was elaborated in this paper. It is based on the catalytic effect of Fe(III) ions on oxidation of potassium salt of disulphonated hydroquinone (K2S2Hy) by hydrogen peroxide in acidic media, at a constant ionic strength. At the working temperature of 20?C and the wavelength of 450.0 nm, optimal conditions for determination of iron were found so that iron (III) can be determined by the proposed method in the concentration range of 1.87 to 18.7 ng cm-3. Corresponding RSD values were determined to be in the range 4.22 to 10.33 %. The limit of detection (LOD) calculated in two ways was found to be 1.07 ng cm-3 i.e. 1.11 ng cm-3 Fe(III). In order to assess the selectivity of the method effects of different ions on the reaction rate were also determined. It was found that presence of oxalates and citrates in the w/w ratio to Fe(III) 1:1 under selected experimental conditions interferes with determination of iron. Then the method was applied for determination of Fe(III) traces in white radish juice. The results agreed well with those obtained by atomic absorption spectrometry.

scholarly journals Marine plant mediated green synthesis of silver nanoparticles using mangrove Rhizophora stylosa: Effect of variable process and their antibacterial activity

F1000Research ◽  
2021 ◽  
Vol 10 ◽  
pp. 768
Author(s):  
Nancy Willian ◽  
Syukri Syukri ◽  
Zulhadjri Zulhadjri ◽  
Syukri Arief
Keyword(s):  
Staphylococcus Aureus ◽  
Silver Nanoparticles ◽  
Antibacterial Activity ◽  
Leaf Extract ◽  
Nitrate Solution ◽  
Narrow Particle Size Distribution ◽  
Metallic Silver ◽  
Face Centered Cubic ◽  
Rhizophora Stylosa ◽  
Vis Spectroscopy

Background: Most natural plants used in the synthesis of silver nanoparticles are limited to marine plants. To carry out applications, colloidal silver nanoparticles (AgNps) should have appropriate properties such as homogeneous shapes, small and narrow particle size distribution, and long time stability. This study aims to determine the effects of a variable process of AgNps mediated mangrove Rhizophora stylosa (RS) leaf extract, and antibacterial activity.  Methods: Synthesis of AgNps was carried out by stirring silver nitrate solution with aqueous extract. The characterization of AgNps was carried out using UV-Vis spectrophotometry, X-ray diffraction (XRD), Dynamic Light Scattering (DLS) zetasizer and Transmission Electron Microscopy (TEM). Evaluation of antibacterial activity was carried out on Escherichia coli and Staphylococcus aureus. Reaction conditions such as the concentration of metal ions (0.001 M, 0.005 M, and 0.01 M), extracts (1%, 3%, and 5% v/v), and the reaction time on the size and stability of nanoparticles were also explored. Results: The UV-Vis spectroscopy showed an absorption of colloidal AgNps in a wavelength range of 403–443 nm.  TEM analysis showed that as-synthesized AgNps were spherical in shape with a size range of 5–87 nm. The use of 0.001 M and 0.005 M of Ag+ resulted in a smaller diameter than the synthesized AgNps, using 0.01 M Ag+, in the same extract concentration. The range of zeta potential was -24.9 mV to -27.7 mV. The as-synthesized AgNps were stable for more than one month. The XRD analysis showed four peaks, which were attributed to the face centered cubic crystal structure of metallic silver. The results of the silver nanoparticles synthesis showed good activity on Escherichia coli and Staphylococcus aureus, with an inhibition zone between 4.1–7.2 mm. Conclusions: The AgNps synthesized with RS leaf extract, which is a reducing agent, showed good potential as an antibacterial component.

scholarly journals A Sensitive Validated Spectrophotometric Method for the Determination of Flucloxacillin Sodium

2009 ◽  
Vol 6 (s1) ◽  
pp. S397-S405 ◽  
Author(s):  
R. Singh Gujral ◽  
S. Manirul Haque ◽  
P. Shanker
Keyword(s):  
Spectrophotometric Method ◽  
Limit Of Detection ◽  
Pharmaceutical Formulations ◽  
Complexation Reaction ◽  
Reagent Blank ◽  
Experimental Conditions ◽  
Charge Transfer Complexation ◽  
Sensitive Spectrophotometric Method

A simple and sensitive spectrophotometric method has been proposed for the determination of flucloxacillin sodium. The determination method is based on charge transfer complexation reaction of the drug with iodine in methanol-dichloromethane medium. The absorbance was measured at 362 nm against the reagent blank. Under optimized experimental conditions, Beer's law is obeyed in the concentration ranges 1-9 μg/mL for flucloxacillin. The method was validated for specificity, linearity, precision, accuracy. The degree of linearity of the calibration curves, the percent recoveries, limit of detection and quantitation for the spectrophotometric method were determined. No interferences could be observed from the additives commonly present in the pharmaceutical formulations. The method was successfully applied forin vitrodetermination of human urine samples with low RSD value. This is simple, specific, accurate and sensitive spectrophotometric method.

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