scholarly journals Spectrophotometric Determination of Gemifloxacin Mesylate in Pharmaceutical Formulations Through Ion-Pair Complex Formation

2008 ◽  
Vol 5 (3) ◽  
pp. 515-520 ◽  
Author(s):  
Marothu Vamsi Krishna ◽  
Dannana Gowri Sankar
Keyword(s):  
Methylene Blue ◽  
Acidic Medium ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Ion Pair ◽  
Basic Medium ◽  
Spectrophotometric Methods ◽  
Relative Standard ◽  
Safranin O

Four simple and sensitive ion-pairing spectrophotometric methods have been described for the assay of gemifloxacin mesylate (GFX) either in pure form or in pharmaceutical formulations. The developed methods involve formation of colored chloroform extractable ion-pair complexes of the drug with safranin O (SFN O) and methylene blue (MB) in basic medium; Napthol blue 12BR (NB 12BR) and azocaramine G (AG) in acidic medium. The extracted complexes showed absorbance maxima at 525, 650, 620 and 540 nm for SFN O, MB, NB 12BR and AG, respectively.Beer's law is obeyed in the concentration ranges 3-15, 4-20, 2-10 and 2-10 μg/mL with molar absorptivity of 2.81 × 104, 2.20 x 104, 4.02 × 104and 4.15 × 104L mole−1cm−1and relative standard deviation of 0.077, 0.104, 0.080 and 0.103% for SFN O, MB, NB 12BR and AG, respectively. These methods have been successfully applied for the assay of drug in pharmaceutical formulations. No interference was observed from common pharmaceutical adjuvants. Results of analysis were validated statistically and through recovery studies.

scholarly journals Extractive Spectrophotometric Determination of Nortriptyline Hydrochloride Using Sudan II, IV and Black B

2001 ◽  
Vol 69 (2) ◽  
pp. 151-160
Author(s):  
A. Amin ◽  
H. Saleh
Keyword(s):  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Ion Pair ◽  
Calibration Graph ◽  
Official Method ◽  
Spectrophotometric Methods ◽  
Sudan Black B ◽  
Relative Standard ◽  
Nortriptyline Hydrochloride

A simple spectrophotometric methods has been developed for the determination of nortriptyline hydrochloride in pure and in pharmaceutical formulations based on the formation of ion-pair complexes with sudun II (SII), sudan (IV) (SIV) and sudan black B (SBB). The selectivity of the method was improved through extraction with chloroform. The optimum conditions for complete extracted colour development were assessed. The absorbance measurements were made at 534, 596 and 649 nm for SII, SIV and SBB complexes, respectively. The calibration graph was linear in the ranges 0.5- 280. 0.5- 37.5 and 0.5 – 31.0 μg ml−1 of the drug usiny the same reagents, respectively. The precision of the procedure was checked by calculating the relative standard deviation of ten replicate determinations on 15 μg ml−1 of nortriptyline HCI and was found to be 1.7, 1.3 and 1.55% using SII, SIV, and SBB complexes, respectively. The molar absorptivity and Sandell sensitivity for each ion-pair were calculated. The proposed methods were successfully applied to the deterniination of pure nortriptyline HCI and in pharmaceutical formulations, and the results demonstrated that the method is equally accurate, precise and reproducible as the official method.

scholarly journals Validated Extractive Spectrophotometric Method for Determination of Domperidone in Pharmaceutical Formulations

2015 ◽  
Vol 17 (1) ◽  
pp. 25-31
Author(s):  
Jasmin Shah ◽  
M Rasul Jan ◽  
Muhammad Tariq Shah
Keyword(s):  
Acidic Medium ◽  
Pharmaceutical Formulations ◽  
Pharmaceutical Journal ◽  
Bromothymol Blue ◽  
Hplc Method ◽  
Ion Pair ◽  
Bromophenol Blue ◽  
Spectrophotometric Methods ◽  
New Methods

Simple, precise and sensitive extractive spectrophotometric methods have been developed for the determination of domperidone in pharmaceutical formulations. The new methods involve the formation of colored extractable ion pair complexes of the drug with bromothymol blue (BTB) and bromophenol blue (BPB) in acidic medium. The effects of various parameters like pH, reagent concentration and shaking time were studied. The extracted complexes of domperidone showed maximum absorbance at 410 nm with BTB and at 415 nm with BPB dye. The stiochiometry of the reaction between domperidone, BTB and BPB was found to be 1: 4. Domperidone was found to obey Beer’s law in the concentration ranges of 0.6-35 ?g/ml, 1-30 ?g/ml with BTB and BPB, respectively. The method has been applied successfully for the determination of domperidone in commercial tablets and suspension samples. The results obtained by the proposed methods were validated statistically and compared with the official HPLC method. DOI: http://dx.doi.org/10.3329/bpj.v17i1.22310 Bangladesh Pharmaceutical Journal 17(1): 25-31, 2014

Validated Spectrophotometric Determination of Rizatriptan Benzoate in Pharmaceutical Formulations using Alizarin Derivatives

2019 ◽  
Vol 10 (01) ◽  
Author(s):  
El Sheikh R ◽  
Hassan W. S. ◽  
Gouda A. A. ◽  
Al OwairdhiA. ◽  
Al Hassani K K H
Keyword(s):  
Standard Addition ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Optimum Conditions ◽  
Reaction Conditions ◽  
Alizarin Red ◽  
Rizatriptan Benzoate ◽  
Spectrophotometric Methods ◽  
Relative Standard

Two simple, sensitive, accurate, precise and economical spectrophotometric methods have been developed and validated for the determination of rizatriptan benzoate (RZT) in pure form and pharmaceutical formulations. These methods were based on the formation of charge transfer complex between RZT as n-electron donor and alizarin red S (ARS) or quinalizarin (Quinz) as π-acceptor in methanol to form highly colored chromogens which showed an absorption maximum at 532 and 574 nm using ARS and Quinz, respectively. The optimization of the reaction conditions such as the type of solvent, reagent concentration and reaction time were investigated. Under the optimum conditions, Beer’s law is obeyed in the concentration ranges 1.0-16 and 2.0-20 g mL-1 using ARS and Quinz, respectively with good correlation coefficient (r2 ≥ 0.9996) and with a relative standard deviation (RSD% ≤ 1.16). The molar absorptivity, Sandell sensitivity, detection and quantification limits were also calculated. The methods were successfully applied to the determination of RZT in its pharmaceutical formulations and the validity assesses by applying the standard addition technique. Results obtained by the proposed methods for the pure RZT and commercial tablets agreed well with those obtained by the reported method.

scholarly journals Spectrophotometric Determination of Pipazethate Hydrochloride in Pure Form and in Pharmaceutical Formulations

2007 ◽  
Vol 90 (3) ◽  
pp. 686-692 ◽  
Author(s):  
Ragaa El-Shiekh ◽  
Alaa S Amin ◽  
Faten Zahran ◽  
Ayman A Gouda
Keyword(s):  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Pure Form ◽  
Acetate Buffer Solution ◽  
Buffer Solution ◽  
Accurate Analysis ◽  
Spectrophotometric Methods ◽  
Relative Standard ◽  
Optimum Ph

Abstract Three simple, sensitive, and reproducible spectrophotometric methods (AC) for the determination of pipazethate hydrochloride (PiCl) in pure form and in pharmaceutical formulations are described. The first and second methods, A and B, are based on the oxidation of the drug by Fe3+ in the presence of o-phenanthroline (o-phen) or bipyridyl (bipy). The formation of tris-complex upon reactions with Fe3+-o-phen and/or Fe3+-bipy mixture in an acetate buffer solution of the optimum pH values was demonstrated at 510 and 522 nm, respectively, with o-phen and bipy. The third method, C, is based on the reduction of Fe(III) by PiCl in acid medium and subsequent interaction of Fe(II) with ferricyanide to form Prussian blue, which exhibits an absorption maximum at 750 nm. The concentration ranges are from 0.5 to 8, 2 to 16, and 3 to 15 g/mL for Methods AC, respectively. For more accurate analysis, Ringbom optimum concentration ranges were calculated. The molar absorptivity, Sandell sensitivity, and detection and quantitation limits were calculated. The developed methods were successfully applied to the determination of PiCl in bulk and pharmaceutical formulations without any interference from common excipients. The relative standard deviations were 0.83% with recoveries of 98.9101.15%.

scholarly journals Synthesis of a new organic probe 4-(4 acetamidophenylazo) pyrogallol for spectrophotometric determination of Bi(III) and Al(III) in pharmaceutical samples

2021 ◽  
Vol 40 (1) ◽  
pp. 108-126
Author(s):  
Jumana W. Ammar ◽  
Zainab A. Khan ◽  
Marwa N. Ghazi ◽  
Naser A. Naser
Keyword(s):  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Scanning Calorimetry ◽  
Spectrophotometric Methods ◽  
Modern Development ◽  
Relative Standard ◽  
Visible Spectra ◽  
Ft Ir ◽  
Linear Solvation Energy

Abstract A modern development discusses the synthesis and validity of simple, sensitive, and versatile spectrophotometric methods for Bi(III) and Al(III) determination in pharmaceutical formulations have been conducted. In the present paper, 4-(4 acetamidophenylazo) pyrogallol has been synthesized as a new organic compound, 4-APAP, by coupling pyrogallol in a regulated pH medium with diazotized p-aminoacetanilide. 4-APAP was identified by methods of FT-IR, 1H-NMR, 13C-NMR, and thermal analysis (thermogravimetry and differential scanning calorimetry). Solvatochromic activity was also studied in solvents with different polarities. The Kamlet and Taft linear solvation energy relationship was used to correlate shifts in UV-Visible spectra of 4-APAP with Kamlet-Taft parameters (α, β, and π*). The optimum assay conditions showed linearity from 0.3–13 to 0.5–11 μg·mL−1 for Bi(III) and Al(III), respectively. Molar absorptivity values were 3.365 × 104 and 0.356 × 104 L·mol−1·cm−1 for Bi(III) and Al(III), with similar Sandell's sensitivity measures of 0.006 and 0.008 μg·cm−2. Detection limits and quantification limits were 0.013 and 0.043 μg·mL−1 for Bi(III), respectively, and 0.018 and 0.059 μg·mL−1 for Al(III) with the relative standard deviation for determination of both metal ions using 4-APAP probe being <2.0%. The validity, accuracy, and efficiency of the approaches were demonstrated by the determination of Bi(III) and Al(III) in different formulations.

scholarly journals Extractive Spectrophotometric Methods for the Determination of Rosuvastatin Calcium in Pure Form and in Pharmaceutical Formulations by Using Safranin O and Methylene blue

2007 ◽  
Vol 4 (1) ◽  
pp. 46-49 ◽  
Author(s):  
Marothu Vamsi Krishna ◽  
Dannana Gowri Sankar
Keyword(s):  
Methylene Blue ◽  
Ion Association ◽  
Pharmaceutical Formulations ◽  
Pure Form ◽  
Reagent Blank ◽  
Spectrophotometric Methods ◽  
Chloroform Layer ◽  
Safranin O ◽  
Rosuvastatin Calcium

Two simple extractive Spectrophotometric methods are described for the determination of rosuvastatin calcium (RST) in pure form and in pharmaceutical formulations. These methods are based on the formation of ion association complexes of the RST with basic dyes safranin O (Method A) and methylene blue (Method B) in basic buffer of pH 9.8 followed by their extraction in chloroform. The absorbance of the chloroform layer for each method was measured at its appropriate λmaxagainst the reagent blank. These methods have been statistically evaluated and are found to be precise and accurate.

scholarly journals Condensation Methods for the Determination of Darunavir in Pure and Pharmaceutical Formulations

2020 ◽  
Vol 13 (4) ◽  
pp. 394-401
Author(s):  
M.L.N. Acharyulu ◽  
P.V.S.R. Mohana Rao ◽  
I. Siva Ramakoti
Keyword(s):  
Regression Analysis ◽  
Acidic Medium ◽  
Low Cost ◽  
Condensation Reaction ◽  
Reference Method ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Spectrophotometric Methods

Two visible spectrophotometric methods were developed Aand B for the determination of Darunavir in pure and pharmaceutical formulations. The methods are based on condensation reaction with PDAB (Method-A) and ONB (Method-B) in presence of acidic medium with the primaryamine group in DNV. The coloured products exhibit absorption λmax at 639 nm and 452nm for methods A and B respectively. Regression analysis of Beer-Lambert plots showed good correlation in the concentration ranges 10-60μg/ml, 50-300 μg/ml, correlation co-efficients are 0.9983, 0.9989;Sandell’s sensitivities are9.9833 x 10-3, 3.0456 x 10-2(1 mole cm-1); and molar absorptivity values are5.4857 x 104,1.7981x 104 (μg cm-2) for methods-Aand B respectively. The proposed methods are applied to commercial available formulations and the results are statistically compared with those obtained by the UV reference method and validated by recovery studies. The results are found satisfactory and reproducible. These methods are applied successfully for the estimation of the DNV in the presence of other ingredients that are usually present in formulations. These methods offer the advantages of rapidity, simplicity and sensitivity and low cost without the need for expensive instrumentation and reagents.

scholarly journals Sensitive Spectrophotometric Determination of Lamotrigine in Bulk Drug and Pharmaceutical Formulations using Bromocresol Green

2018 ◽  
Vol 35 (1) ◽  
pp. 55
Author(s):  
N. Rajendraprasad ◽  
K. Basavaiah ◽  
K. B. Vinay
Keyword(s):  
Potassium Hydroxide ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Ion Pair ◽  
Bromocresol Green ◽  
Spectrophotometric Methods ◽  
Base Form ◽  
Bulk Drug ◽  
The Stability

Two new, simple, rapid and reproducible spectrophotometric methods have been developed for the determination of lamotrigine (LMT) both in pure form and in its tablets. The first method (method A) is based on the formation of a colored ion-pair complex (1:1 drug/dye) of LMT with bromocresol green (BCG) at pH 5.02±0.01 and extraction of the complex into dichloromethane followed by the measurement of the yellow ion-pair complex at 410 nm. In the second (method B), the drug-dye ion-pair complex was dissolved in ethanolic potassium hydroxide and the resulting base form of the dye was measured at 620 nm. Beer’s law was obeyed in the concentration range of 1.5-15 μg mL-1 and 0.5-5.0 μg mL-1 for method A and method B, respectively, and the  = corresponding molar absorptivity values are 1.6932 x 104 and 3.748 x 104L mol-1cm-1. The Sandell sensitivity values are 0.0151 and 0.0068 μg cm-2 for method A and method B, respectively. The stoichiometry of the ion-pair complex formed between the dug and dye (1:1) was determined by Job’s continuous variations method and the stability constant of the complex was also calculated. The proposed methods were applied successfully for the determination of drug in commercial tablets.

scholarly journals Spectrophotometric Determination of Carbamazepine in Pharmaceutical Formulations Based on its Reaction with a Brominating Agent

2019 ◽  
Vol 9 (2) ◽  
pp. 42-49
Author(s):  
Warda Rizgar ◽  
Diyar S. Ali
Keyword(s):  
Methylene Blue ◽  
Spectrophotometric Determination ◽  
General Procedure ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Pure Form ◽  
Great Precision ◽  
Spectrophotometric Methods ◽  
Precision And Accuracy

Two accurate spectrophotometric methods described for the estimation of carbamazepine (CBZ) in both pharmaceutical and pure form. These methodologies are attached to the bromination of CBZ by bromine formed in instantly from the bromate-bromide reaction. The general procedure includes the additional of a known amount of bromate-bromide reagent in an acidic mediocre to CBZ. After the reaction is integrated, the unreacted bromine was reacted with a steady amount of methylene blue, and the absorbance was measured at 665 nm (method A) or, cresol red could be used for the reaction and the absorbance moderated at 517 nm (method B). Beer’s law was submitted from 0.45 to 15.00 μg/mL CBZ with a molar absorptivity of 4.93 × 103 L/mol.cm for method A and from 0.50 to 12.00 μg/mL CBZ with a molar absorptivity of 1.37 × 104 L/mol.cm for method B. The proposed methods were effective for the determination of CBZ in tablets with great precision and accuracy.

Colorimetric Determination of Amoxicillin in Pure and some Pharmaceutical Formulations Via Reaction with Potassium Permanganate as Oxidant Reagent

2019 ◽  
Vol 10 (02) ◽  
Author(s):  
Abbas Shebeeb Al-kadumi ◽  
Sahar Rihan Fadhel ◽  
Mohammed Abdullah Ahmed ◽  
Luma Amer Musa
Keyword(s):  
Potassium Permanganate ◽  
Pharmaceutical Preparations ◽  
Pharmaceutical Formulations ◽  
Atomic Emission ◽  
Basic Medium ◽  
Photometric Method ◽  
Colorimetric Determination ◽  
Spectrophotometric Methods ◽  
Label Claim

We proposed two simple, rapid, and convenient spectrophotometric methods are described for the determination of Amoxicillin in bulk and its pharmaceutical preparations. They are based on the measurement of the flame atomic emission of potassium ion (in first method) and colorimetric determination of the green colored solution for manganite ion at 610 nm formed after reaction of Amoxicillin with potassium permanganate as oxidant agent (in the second method) in basic medium. The working conditions of the methods were investigated and optimized. Beer's law plot showed a good correlation in the concentration range of 5-45 μg/ml. The detection limits and relative standared deviations were (2.573, 2.814 μg/ml) (2.137, 2.498) for the flame emission photometric method and (1.844, 2.016 μg/ml) (1.645,1.932) for colorimetric methods for capsules and suspensions respectively. The methods were successfully applied to the determination of Amoxicillin in capsules and suspensions, and the obtained results were in good agreement with the label claim. No interference was observed from the commonly encountered additives and expectancies.

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