scholarly journals New Spectrophotometric Methods for Estimation of Diosmin in Pharmaceutical Formulations Using Batch and FIA Systems

2021 ◽  
pp. 3804-3815
Author(s):  
Mayasa Mansour Mohammed ◽  
Sadeem Subhi Abed
Keyword(s):  
Oxidative Coupling ◽  
Pharmaceutical Preparations ◽  
Coupling Reaction ◽  
Pharmaceutical Formulations ◽  
Assay Method ◽  
Batch Method ◽  
Spectrophotometric Methods ◽  
Oxidative Coupling Reaction ◽  
Relative Standard ◽  
Determination Range

A new attempt is made to determine diosmin (DIO) in its pure form and in dietary supplements by using spectrophotometric flow injection analysis (FIA) assay method conjugated with batch method. The analysis was achieved depending on the oxidative coupling reaction with N, N-dimethyl-p-phenylenediamine (DMPD) to form a green dye which is measured at wavelength of 677 nm. The tested methods were found to be economical, delicate, precise and sturdy. The validation variables of the batch and FIA methods gave linearity in the determination range of DIO (1-35) μg/mL and (5-120) μg/mL demonstrated calibration graphs with linearity coefficient  values of  r2 =0.9989 and r2 =0.9991, respectively. Limits of quantitation (LOQ) values were found to be (0.8463 and 1.022) μg/mL, while limits of detection (LOD) were (0.2539 and 0.3067) µg/mL for the two methods, respectively. The  precision for the developed methods denoted by relative standard deviation (RSD %), were 0.386 and 0.55 %, while the accuracy based on recovery values (Rec %) were 100.273 and 100.24, respectively. The relative error (RE %) was less than 1% for the batch method and (1.1%) for the FIA method. The values of these parameters were observed to fall within the specified accepted limits; therefore, the tested methods seem to be adequate for the analysis of DIO in pharmaceutical preparations.

scholarly journals Spectrophotometric Methods for the Assay of Pyrilamine Maleate Using Chromogenic Reagents

2010 ◽  
Vol 7 (4) ◽  
pp. 1507-1513 ◽  
Author(s):  
V. Annapurna ◽  
G. Jyothi ◽  
V. Nagalakshmi ◽  
B. B. V. Sailaja
Keyword(s):  
Charge Transfer ◽  
Oxidative Coupling ◽  
Coupling Reaction ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Method Of Least Squares ◽  
Spectrophotometric Methods ◽  
Oxidative Coupling Reaction ◽  
Charge Transfer Complexation

Simple, accurate and reproducible UV spectrophotometric methods were established for the assay of pyrilamine maleate (PYRA) based on the formation of oxidative coupling and precipitation, charge transfer complexation products. Method A includes the oxidative coupling reaction of PYRA with 3-methyl-2-benzathiazolinone hydrazone (MBTH) in presence of Ce(IV). The formation of oxidative coupling product with 4-amino phenazone (4-AP) in presence of K3Fe(CN)6is incorporated in method B. Precipitation/charge transfer complex formation of the PYRA with tannic acid (TA)/Metol-Cr(VI) in method C were proposed. The optical characteristics such as Beers law limits, molar absorptivity and Sandell’s sensitivity for the methods (A-C) are given. Regression analysis using the method of least squares was made to evaluate the slope (b), intercept (a) and correlation coefficient (r) and standard error of estimation (Se) for each system. Determination of pyrilamine in bulk form and in pharmaceutical formulations were also incorporated.

scholarly journals Spectrophotometric Determination of Bisacodyl in Pure and Pharmaceutical Preparation via Oxidative Coupling Organic Reaction

2017 ◽  
Vol 14 (1) ◽  
pp. 181-188
Author(s):  
Baghdad Science Journal
Keyword(s):  
Oxidative Coupling ◽  
Pharmaceutical Preparation ◽  
Pharmaceutical Preparations ◽  
Coupling Reaction ◽  
Molar Absorptivity ◽  
Water Soluble ◽  
Alkaline Media ◽  
Oxidative Coupling Reaction ◽  
Relative Standard ◽  
Limit Of Quantitation

A simple, accurate and sensitive spectrophotometric way is used to determine Bisacodyl in pure and pharmaceutical preparations. The proposed method depends on using 2,4-Dinitrophenylhydrazine as chromogenic reagent . The method was based on the oxidative coupling reaction of Bisacodyl with 2,4-Dinitrophenylhydrazine with Sodium periodate in the presence of sodium hydroxide as alkaline media to form red water soluble dye product , that has a maximum absorption at ?max 522nm . Beer ,s law is obeyed in the concentration of (2.00–20.00) ?g.ml -1 .The molar absorptivity is (6505) L.mol-1.cm-1,a sandall sensitivity of(0.0555) ?g.cm-2), correlation coefficient of (0.9970) , Limitof detection (LOD) (0.0312 ?g.ml-1), limit of Quantitation (LOQ) (0. 3125 ?g.ml-1) and the relative standard deviation of RSD% (1.6). The method gave a successful determination for Bisacodyl in pharmaceutical preparations and the value of recovery % was better than (100.16%)

NEW SPECTROPHOTOMETRIC METHODS FOR THE QUANTITATIVE ESTIMATION OF ELETRIPTAN IN DRUG FORMULATION

INDIAN DRUGS ◽  
2014 ◽  
Vol 51 (01) ◽  
pp. 18-26
Author(s):  
N Usha Rani ◽  
◽  
R. Sreenivasa Rao ◽  
K. Saraswathi
Keyword(s):  
Oxidative Coupling ◽  
Quantitative Estimation ◽  
Coupling Reaction ◽  
Pharmaceutical Formulations ◽  
Drug Formulation ◽  
Reagent Blank ◽  
Colored Complex ◽  
Spectrophotometric Methods ◽  
Oxidative Coupling Reaction ◽  
Bulk Drug

Five simple, accurate, sensitive and economical UV spectrophotometric methods has been developed and subsequently validated for the determination of eletriptan in bulk and pharmaceutical formulations. The methods were based on the formulation of colored complex of eletriptan with different reagents. Absorbance of the formed color complex is measured against the reagent blank at the wavelength of maximum absorbance. In this paper, five spectrophotometric methods were proposed. Method A is based on the formation of oxidative coupling reaction involving the use of iron (III) – MBTH (3-methyl-2-benzo thiazolinone hydrazone hydrochloride). The resulting green colored chromogen complex absorbs at λmax = 520 nm. Reaction of eletriptan with ferric chloride and K3 [Fe (CN)6 ] to form a green colored species having absorption maxima at λmax =790 nm is used in Method B. Method C is based on the reaction eletriptan with FeCl3 and 1,10 phenanthroline to form a blood red colored chromogen, exhibiting absorption at λmax = 620 nm. Formation of oxidative coupling of drug with brucine in the presence of sodium meta periodate to form a purple red colored species is used in Method D which exhibits absorption maxima at λmax = 520 nm. Method E is based on the formation of complex with acidic dye WF BBL having absorption maxima at λmax = 610 nm. All these methods have different linearity ranges. Statistical analysis proves that the proposed methods are reproducible and selective for the estimation of eletriptan in bulk drug and in its tablet dosage form.

scholarly journals Spectrophotometric Determination of Azithromycin using Oxidative Coupling Reaction

2020 ◽  
Vol 10 (03) ◽  
pp. 389-394
Author(s):  
Maadh T. Abdulrahman ◽  
Ihab M. Rashid ◽  
Nashwan H. Ali
Keyword(s):  
Oxidative Coupling ◽  
Limit Of Detection ◽  
Pharmaceutical Preparations ◽  
Coupling Reaction ◽  
Sensitivity Index ◽  
Oxidative Coupling Reaction ◽  
Relative Standard ◽  
Sensitivity And Selectivity ◽  
Colored Product ◽  
The Stability

For determining the azithromycin (AZT) in medicinal and pure formulas, a simple spectrophotometric technique was developed. An approach suggested is dependent on an AZT’s oxidative coupling reaction by sodium period (SPI) and 4-amino antipyrine (AAP) producing a pink colored compound with optimum absorption of 480 nm. Different experimental parameters are extensively researched and mastered, which affects the stability of a colored product formed, then developed. The law of the Beer is obeyed over its concentration range 3 to 44 ppm, whereas the limit of detection and quantification is 0.1908 and 0.5726 ppm, respectively, for a connection factor (r) = 0.9998. Also calculated are the molar absorption of 8.23 × 103 L/mol.cm, and the sensitivity index for Sandell is 7 × 10-5 mg/cm2. A method’s accuracy and precision are tested by also determining a relative standard deviation (RSD) less than 0.645 percent, and 100.189 percent average recovery. Practically possible external interferences about a calculation for AZT are checked in drug tablets. The results demonstrated that the procedure for determining AZT was successful in its application in pharmaceutical preparations. Comparing the literature survey that shows good sensitivity and selectivity, the reliability of the proposed method is chalked in.

scholarly journals Indirect spectrophotometric Indirect spectrophotometric determination of chlordiazepoxide in pharmaceutical formulations via oxidative coupling reaction with phenothiazine

2018 ◽  
pp. 7-14
Author(s):  
Hind Hadi ◽  
Mariam Jamal
Keyword(s):  
Oxidative Coupling ◽  
Coupling Reaction ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Dosage Forms ◽  
Calibration Plot ◽  
Pharmaceutical Dosage Forms ◽  
Oxidative Coupling Reaction ◽  
Formed Product

Abstract A sensitive, precise and reliable indirect spectrophotometric method for the determination of chlordiazepoxide (CDE) in pure and pharmaceutical dosage forms is described. The method is based on oxidative coupling reaction between amino group resulting from acidic decomposition of CDE with phenothiazine in the presence of sodium periodate to produce an intense green soluble dye that is stable and shows a maximum absorption at 602 nm. The calibration plot indicates that Beer’s law is obeyed over the concentration range of 0.1?50 µg/mL, with a molar absorptivity of 1×104 L/mol cm and correlation coefficient of 0.9994.All the conditions that affecting on the stability and sensitivity of the formed product were studied and optimized and the suggested method was effectively applied for the determination of CDE in commercial dosage forms.

Spectrophotometric Determination of Chlorpromazine Hydrochloride Using 4-Nitroanilline by Oxidative Coupling Reaction

2019 ◽  
Vol 16 (1(Suppl.)) ◽  
pp. 0194
Author(s):  
Al-rashidy Et al.
Keyword(s):  
Oxidative Coupling ◽  
Analytical Data ◽  
Reaction Medium ◽  
Coupling Reaction ◽  
Suggested Method ◽  
Sensitivity Index ◽  
Chlorpromazine Hydrochloride ◽  
Oxidative Coupling Reaction ◽  
Relative Standard

A simple, rapid spectrophotometric method has been established for the determination of chlorpromazine hydrochloride (CPZ) in its pure form and in a tablet formulations. The  suggested  method  is  based  on  the  oxidative coupling  reaction  with4-nitroainlline using KIO3 in acidic solution to produce a violet colored product with maximum absorption at λ=526 nm.The  analytical data  obtained  throughout  this  study  could  be  summarid  as  follows:  1ml of 1M HCl (pH=2.2), 1 ml  of  4-nitroanilline (1x10-2M), and 1.5ml  of (1x10-2)KIO3 per 25 ml reaction medium. The order of additions, coupling reaction time, and temperature in addition to the type of solvent were studied. The Beer′s law is obeyed over the concentration range of(5–40) µg ml-1, but the detection limit and quantification limit are 0.34 besides 1.03 µg ml-1 respectively. The correlation coefficient (r) for the calibration graph was found to be 0.9980, molar absorptivity of 10. 25 × 103 L.mol -1.cm-1, and Sandell′s sensitivity index of 0.03467 µg.cm-2. The precision and accuracy of the method were tested by calculating the percentage of relative standard deviation (RSD%) (<1.831%) and the average recovery percent (99.22%) average error percent Erel%(0.558). Direct and standard addition procedures were applied to both standards and specimens of pharmaceutical and the results indicate that the suggested method was successfully applied for the determination of CPZ.

scholarly journals A novel sensitive colorimetric determination of catecholamine drug in dosage form via oxidative coupling reaction with MBTH and potassium ferricyanide

2021 ◽  
Vol 5 (1) ◽  
pp. 51-58
Author(s):  
Safwan Ashour
Keyword(s):  
Oxidative Coupling ◽  
Colorimetric Method ◽  
Standard Free Energy ◽  
Coupling Reaction ◽  
Pharmaceutical Formulations ◽  
Molar Absorptivity ◽  
Potassium Ferricyanide ◽  
Colorimetric Determination ◽  
Oxidative Coupling Reaction

A new and direct colorimetric method has been established for the determination of catecholamine (methyldopa, MD) in both pure form and in pharmaceutical formulations. The method is based on the oxidative coupling reaction of MD with 3-methyl-2-benzothiazolinone hydrazone hydrochloride monohydrate (MBTH) and potassium ferricyanide at pH 10.4 in aqueous medium to form an orange product that has a maximum absorption at 460 nm. Beer's law plot showed good correlation in the concentration range of 1.0−56.0 µg mL-1, with detection limit of 0.31 µg mL-1. Molar absorptivity for the above method was found to be 6.56×103 L mol-1 cm-1. All the measurements were carried out at 25 ± 1.0 °C, the formation constant (logKf) value of colored species is 9.48 and the standard free energy (DG‡) is − 54.09 KJ mol-1. This method was applied successfully to determination of MD in tablets and the results were compared with the USP method. Common excipients used as additives in tablets do not interfere in the proposed method. The method is accurate, precise and highly reproducible, while being simple, cheap and less time consuming and hence can be suitably applied for routine analysis of MD in bulk and dosage forms.

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