Spectrophotometric Determination of Aspirin in Pure Form and Pharmaceutical Formulations using Oxidation-reduction reaction

A simple, sensitive and accurate spectrophotometric method of determination of aspirin in pure form and pharmaceutical formulation. The method is based on the formation of Prussian blue (PB) complex. The reaction between the acidic hydrolysis product of the aspirin with the mixture of FeCl3 and pota...

Full description

Saved in:
Bibliographic Details
Main Authors: Ayad M.R. Raauf (Author), Huda Mohammed (Author), Ali Wathiq Alwan Ajil (Author)
Format: Book
Published: College of Pharmacy / Mustansiriyah University, 2010-12-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_22b5e5e9e343437d9d7e57dd1c1e84f8
042 |a dc 
100 1 0 |a Ayad M.R. Raauf  |e author 
700 1 0 |a Huda Mohammed  |e author 
700 1 0 |a Ali Wathiq Alwan Ajil  |e author 
245 0 0 |a Spectrophotometric Determination of Aspirin in Pure Form and Pharmaceutical Formulations using Oxidation-reduction reaction 
260 |b College of Pharmacy / Mustansiriyah University,   |c 2010-12-01T00:00:00Z. 
500 |a 10.32947/ajps.v8i2.349 
500 |a 1815-0993 
500 |a 2959-183X 
520 |a A simple, sensitive and accurate spectrophotometric method of determination of aspirin in pure form and pharmaceutical formulation. The method is based on the formation of Prussian blue (PB) complex. The reaction between the acidic hydrolysis product of the aspirin with the mixture of FeCl3 and potassium hexacyanoferrate (ΙΙΙ) was evaluated for the spectrophotometric determination of the aspirin. The maximum absorbance of the colored complex occurred at λ=765nm. Reaction conditions have been optimized to obtain PB complex of high sensitivity and longer stability. Under optimum conditions the absorbance of the PB complex where found to increase linearly with increase in concentration of the aspirin, which corroborated with correlation coefficient value. The concentration ranges are 0.5-7μg mL-1 with detection limit 0,2267μg mL-1 and relative standard deviation 0,025%. The proposed method was successfully applied to determine of the selected aspirin in pure form and pharmaceutical formulations with good precision and accuracy compared to standard method as revealed by t- and F- values and the results obtained agree well with the labeled contents. 
546 |a EN 
690 |a Aspirin, spectrophotometric, oxidation-reduction reaction 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Al-Mustansiriyah Journal of Pharmaceutical Sciences, Vol 8, Iss 2 (2010) 
787 0 |n https://ajps.uomustansiriyah.edu.iq/index.php/AJPS/article/view/349 
787 0 |n https://doaj.org/toc/1815-0993 
787 0 |n https://doaj.org/toc/2959-183X 
856 4 1 |u https://doaj.org/article/22b5e5e9e343437d9d7e57dd1c1e84f8  |z Connect to this object online.