scholarly journals Construction of a Highly Selective Membrane Sensor for the Determination of Cobalt (II) Ions

Chemosensors ◽  
2021 ◽  
Vol 9 (5) ◽  
pp. 86
Author(s):  
Sabry Khalil ◽  
Mohamed El-Sharnouby
Keyword(s):  
Detection Limit ◽  
Metal Ions ◽  
Ph Effect ◽  
Pharmaceutical Formulations ◽  
Selectivity Coefficient ◽  
Selective Electrode ◽  
Cobalt Ions ◽  
Membrane Sensor ◽  
Selective Membrane

A highly Co (II) liquid ion-selective electrode depending on the reaction of cobalt ions with the reagent 2-(5-Bromo-2-pyridylazo)-5-[N-n-propyl-N-(3-sulfopropyl) amino] aniline is successfully fabricated. The characteristic slope (56.66 mV), the linear range response from 3.4 × 10−8 to 2.4 × 10−2 molar, the detection limit (2.7 × 10−8) molar, the selectivity coefficient toward some metal ions, the time of response (10 s), lifetime (seven months), the pH effect on the sensor potential and the basic analytical parameters were studied. The sensor was used to estimate the concentration of cobalt ions in food products and pharmaceutical formulations. The obtained results of the developed sensor were statistically analyzed and compared with those of other different reported electrodes.

scholarly journals Potentiometric Determination of Prednisolone in Pharmaceutical Formulations

2021 ◽  
Vol 7 (3) ◽  
pp. 742-748
Author(s):  
A. Zaki Gehan ◽  
M.E. Hassouna Mohammed
Keyword(s):  
Detection Limit ◽  
Linear Response ◽  
Pharmaceutical Formulations ◽  
Fast Response ◽  
Indicator Electrode ◽  
Selective Electrode ◽  
Sodium Tetraphenyl Borate ◽  
Tetraphenyl Borate ◽  
Borate Solution

In this present work, a prednisolone ion selective electrode (PRED-ISE) has been developed. The electrode shows linear response towards prednisolone in the range 3.0×10−6 – 8.6×10−3 M with a detection limit of 2.5×10−6. PRED-ISE was used as an indicator electrode for the potentiometric titration of different concentrations of standard prednisolone against standardized sodium tetraphenyl borate solution and in tablets. The electrode manifests advantages of low resistance, fast response and, most importantly, good selective relativity to a variety of other cations.

scholarly journals Cobalt(II) ion-selective electrode with solid contact

2008 ◽  
Vol 6 (4) ◽  
pp. 607-612 ◽  
Author(s):  
Cecylia Wardak
Keyword(s):  
Detection Limit ◽  
Response Time ◽  
Potentiometric Titration ◽  
Indicator Electrode ◽  
Solid Contact ◽  
Selective Electrode ◽  
Cobalt Ions ◽  
Real Samples ◽  
Nernstian Slope

AbstractA new all plastic sensor for Co2+ ions based on 2-amino-5 (hydroxynaphtyloazo-1′)-1,3,4 thiadiazole (ATIDAN) as ionophore was prepared. The electrode exhibits a low detection limit of 1.5 × 10−6 mol L−1 and almost theoretical Nernstian slope in the activity range 4.0 × 10−6–1 × 10−1 mol L−1 of cobalt ions. The response time of the sensor is less than 10 s and it can be used over a period of 6 months without any measurable divergence in potential. The proposed sensor shows a fairly good selectivity for Co(II) over other metal ions. The electrode was successfully applied for determination of Co2+ in real samples and as an indicator electrode in potentiometric titration of Co2+ ions with EDTA.

scholarly journals A rapid cadmium determination based on ion selective membrane potentiometric sensor by bis (salicylaldehydo)ethylenediimine as carrier

2021 ◽  
Vol 4 (02) ◽  
pp. 25-33
Author(s):  
Mahdiyeh Ghazizadeh ◽  
Hamideh Asadollahzadeh
Keyword(s):  
Detection Limit ◽  
The Other ◽  
Aqueous Samples ◽  
Selective Electrode ◽  
Cadmium Determination ◽  
Cadmium Ions ◽  
Liquid Samples ◽  
Selective Membrane ◽  
Ph Range

An ion selective potentiometric electrode (IPE) was prepared based on salen material (bis(salicylaldehydo)ethylenediimine) as a suitable carrier for determination of cadmium ions. An acceptable response for cadmium ions obtained over a linear range 8 × 10−7 to 1.0 × 10−2 M with a slope of 29.8 ± 0.8 mV per decade of activity and a detection limit of 3.2 × 10−7 M for Cd (II) ions in water and liquid samples. It has a response time less than 10 s and can be used for at least 2.5 months without any measurable divergence in potential.  The ion selective electrode can be used based on potential and potential changes in the pH range 3.5 to 6.5, so, the cadmium determination was obtained at independent pH. Moreover, the selectivity of proposed method in presence of interference ions was studied. The results showed that the other cations do not interfere significantly in response electrode at optimized pH. This electrode was successfully used for the determination of cadmium ions in aqueous samples. The validation was obtained based on ICP analyzer and certified reference material in water samples (CRM, NIST).

scholarly journals Polyvinyl Chloride Modified Carbon Paste Electrodes for Sensitive Determination of Levofloxacin Drug in Serum, Urine, and Pharmaceutical Formulations

Sensors ◽  
2021 ◽  
Vol 21 (9) ◽  
pp. 3150
Author(s):  
Fatehy M. Abdel-Haleem ◽  
Sonia Mahmoud ◽  
Nour Eldin T. Abdel-Ghani ◽  
Rasha Mohamed El Nashar ◽  
Mikhael Bechelany ◽  
...  
Keyword(s):  
Bacterial Infections ◽  
Pharmaceutical Preparation ◽  
Pharmaceutical Formulations ◽  
Selectivity Coefficient ◽  
Pvc Membrane ◽  
Carbon Paste ◽  
Serum Samples ◽  
Carbon Paste Electrodes ◽  
Antibiotic Drug

Levofloxacin (LF) is a medically important antibiotic drug that is used to treat a variety of bacterial infections. In this study, three highly sensitive and selective carbon paste electrodes (CPEs) were fabricated for potentiometric determination of the LF drug: (i) CPEs filled with carbon paste (referred to as CPE); (ii) CPE coated (drop-casted) with ion-selective PVC membrane (referred to as C-CPE); (iii) CPE filled with carbon paste modified with a plasticizer (PVC/cyclohexanone) (referenced as P-CPE). The CPE was formulated from graphite (Gr, 44.0%) and reduced graphene oxide (rGO, 3.0%) as the carbon source, tricresyl phosphate (TCP, 47.0%) as the plasticizer; sodium tetrakis[3,5-bis(trifluoromethyl)phenyl] borate (St-TFPMB, 1.0%) as the ion exchanger; and levofloxacinium-tetraphenylborate (LF-TPB, 5.0%) as the lipophilic ion pair. It showed a sub-Nernstian slope of 49.3 mV decade−1 within the LF concentration range 1.0 × 10−2 M to 1.0 × 10−5 M, with a detection limit of 1.0 × 10−5 M. The PVC coated electrode (C-CPE) showed improved sensitivity (in terms of slope, equal to 50.2 mV decade−1) compared to CPEs. After the incorporation of PVC paste on the modified CPE (P-CPE), the sensitivity increased at 53.5 mV decade−1, indicating such improvement. The selectivity coefficient (log KLF2+,Fe+3pot.) against different interfering species (Na+, K+, NH4+, Ca2+, Al3+, Fe3+, Glycine, Glucose, Maltose, Lactose) were significantly improved by one to three orders of magnitudes in the case of C-CPE and P-CPE, compared to CPEs. The modification with the PVC membrane coating significantly improved the response time and solubility of the LF-TPB within the electrode matrix and increased the lifetime. The constructed sensors were successfully applied for LF determination in pharmaceutical preparation (Levoxin® 500 mg), spiked urine, and serum samples with high accuracy and precision.

scholarly journals Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent

2018 ◽  
Vol 33 (2) ◽  
pp. 47
Author(s):  
Orlando Fatibello-Filho ◽  
Heberth Juliano Vieira
Keyword(s):  
Standard Deviation ◽  
Detection Limit ◽  
Flow Injection ◽  
Pharmaceutical Formulations ◽  
Injection Method ◽  
Indirect Determination ◽  
Analytical Curve ◽  
Relative Standard ◽  
Injection Procedure

A spectrophotometric flow injection method for the determination of paracetamol in pharmaceutical formulations is proposed. The procedure was based on the oxidation of paracetamol by sodium hypochloride and the determination of the excess of this oxidant using o-tolidine dichloride as chromogenic reagent at 430 nm. The analytical curve was linear in the paracetamol concentration range from 8.50 x 10-6 to 2.51 x 10-4 mol L-1 with a detection limit of 5.0 x 10-6 mol L-1. The relative standard deviation was smaller than 1.2% for 1.20 x 10-4 mol L-1 paracetamol solution (n = 10). The results obtained for paracetamol in pharmaceutical formulations using the proposed flow injection method and those obtained using a USP Pharmacopoeia method are in agreement at the 95% confidence level.

scholarly journals Spectrophotometric determination of nicradipine and isradipine in pharmaceutical formulations

2009 ◽  
Vol 15 (2) ◽  
pp. 69-76 ◽  
Author(s):  
S.M. Al-Ghannam ◽  
A.M. Al-Olyan
Keyword(s):  
Standard Deviation ◽  
Detection Limit ◽  
Reaction Pathway ◽  
Pharmaceutical Preparations ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Zinc Powder ◽  
Conditional Stability ◽  
Conditional Stability Constant

A sensitive spectrophotometric method was developed for the determination of some 1,4-dihydropyridine compounds namely, nicardipine and isradipine either in pure form or in pharmaceutical preparations. The method is based on the reduction of nicardipine and isradipine with zinc powder and calcium chloride followed by further reduction with sodium pentacyanoaminoferrate (II) to give violet and red products having the absorbance maximum at 546 and 539 nm with nicardipine and isradipine, respectively. Beer's law was obeyed over the concentration range 8.0-180 ?g/ml with the detection limit of 1.67 ?g/ml for nicardipine and 8.0-110 ?g/ml with the detection limit of 1.748 ?g/ml for isradipine. The analytical parameters and their effects on the reported methods were investigated. The molar absorptivity, quantization limit, standard deviation of intercept (Sa), standard deviation of slope (Sb) and standard deviation of the residuals (Sy/x) were calculated. The composition of the result compounds were found 1:1 for nicardipine and 1:2 for isradipine by Job's method and the conditional stability constant (Kf) and the free energy changes (?G) were calculated for compounds formed. The proposed method was applied successfully for the determination of nicardipine and isradipine in their dosage forms. The results obtained were in good agreement with those obtained using the reference or official methods. A proposal of the reaction pathway was presented.

scholarly journals A novel online coupling of ion selective electrode with the flow injection system for the determination of vitamin B1

2016 ◽  
Vol 13 (2) ◽  
pp. 458-469
Author(s):  
Baghdad Science Journal
Keyword(s):  
Flow Injection ◽  
Dynamic Range ◽  
Limit Of Detection ◽  
Vitamin B1 ◽  
Pharmaceutical Formulations ◽  
Ion Selective Electrode ◽  
Injection System ◽  
Selective Electrode ◽  
Flow Injection System

A simple, fast, selective of a new flow injection analysis method coupled with potentiometric detection was used to determine vitamin B1 in pharmaceutical formulations via the prepared new selective membranes. Two electrodes were constructed for the determination of vitamin B1 based on the ion-pair vitamin B1-phosphotungestic acid (B1-PTA) in a poly (vinyl chloride) supported with a plasticized di-butyl phthalate (DBPH) and di-butyl phosphate (DBP). Applications of these ion selective electrodes for the determination of vitamin B1 in the pharmaceutical preparations for batch and flow injection systems were described. The ion selective membrane exhibited a near-Nernstian slope values 56.88 and 58.53 mV / decade, with the linear dynamic range of vitamin B1 was 5 x 10-5- 1 x 10-2 and 1 x 10-4-1 x 10-2 mol.L-1, in batch and FIA, respectively. The limit of detection was 3.5 x 10-5 and 9.5 x 10-5 mol.L-1, with the percentage linearity 98.85 and 95.22 in batch and FIA, respectively. The suggested ion selective electrode has been utilized perfection in the determination of vitamin B1 in pharmaceutical formulations using batch and flow injection system, respectively.

scholarly journals Preparation, Characterization, and Analytical Application of Ramipril Membrane-Based Ion-Selective Electrode

2009 ◽  
Vol 2009 ◽  
pp. 1-7 ◽  
Author(s):  
Hassan Arida ◽  
Mona Ahmed ◽  
Abdallah Ali
Keyword(s):  
Pharmaceutical Formulations ◽  
Ion Pair ◽  
Pvc Membrane ◽  
Ion Selective Electrodes ◽  
Selective Electrode ◽  
Response Sensitivity ◽  
Direct Potentiometry ◽  
Plasticized Pvc ◽  
Electrochemical Evaluation

The fabrication and electrochemical evaluation of two PVC membrane-based Ion-Selective electrodes responsive for ramipril drug have been proposed. The sensitive membranes were prepared using ramipril-phosphomolibdate and ramipril-tetraphenylborate ion-pair complexes as electroactive sensing materials in plasticized PVC support. The electrodes based on these materials provide near-Nernestian response (sensitivity of53±0.5–54±0.5 mV/concentration decade) covering the concentration range of1.0×10-2–1.0×10-5 molL−1with a detection limit of3.0×10-6–4.0×10-6 molL−1. The suggested electrodes have been successfully used in the determination of ramipril drug in some pharmaceutical formulations using direct potentiometry with average recovery of >96% and mean standard deviation of <3% (n=5).

Dysprosium(III) Ion-Selective Electrochemical Sensor Based on 6-Hydrazino-1,5-diphenyl-6,7-dihydropyrazolo[3,4-d]pyrimidine-4(5H)-imine

2007 ◽  
Vol 72 (9) ◽  
pp. 1189-1206 ◽  
Author(s):  
Hassan Ali Zamani ◽  
Mohammad Reza Ganjali ◽  
Nasim Seifi
Keyword(s):  
Heavy Metal Ions ◽  
Alkaline Earth ◽  
Fast Response ◽  
Sensor Response ◽  
Indicator Electrode ◽  
Selective Electrode ◽  
Membrane Sensor ◽  
Sensing Material ◽  
Ph Range

A Dy(III) ion-selective electrode based on 6-hydrazino-1,5-diphenyl-6,7-dihydropyrazolo[3,4-d]pyrimidine-4(5H)-imine (HDDPI) as an excellent sensing material was developed. The sensor exhibits a Nernstian behavior (a slope of 19.6 ± 0.3 mV per decade) over a wide concentration range (from 1.0 × 10-1 to 8.0 × 10-7 M Dy) with a detection limit of 4.2 × 10-7 M. The sensor response is independent of pH of the solution in the pH range 3.5-8.3. The sensor possesses the advantages of short conditioning time, fast response time (<10 s) and in particular, good selectivity and sensitivity to the dysprosium ion in the presence of a variety of cations, including alkali, alkaline earth, transition and heavy metal ions. The sensor also showed a great enhancement in selectivity coefficients for dysprosium ions, in comparison with the formerly mentioned dysprosium sensors. The electrode can be used for at least 10 weeks without any considerable divergence in the potentials. The proposed electrode was successfully used as an indicator electrode in potentiometric titration of Dy(III) ions with EDTA. The membrane sensor was also used in the determination of concentration of F- ions in some mouth washing solutions and in the Dy3+ recovery from solution.

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