ISSN

0974-4150 (Online)
0974-4169 (Print)


Author(s): Rajan V. Rele, Prathamesh P. Tiwatane

Email(s): drvinraj@gmail.com

DOI: 10.52711/0974-4150.2025.00049   

Address: Rajan V. Rele*, Prathamesh P. Tiwatane
Central Research Laboratory, D.G. Ruparel College, Matunga, Mumbai 400016.
*Corresponding Author

Published In:   Volume - 18,      Issue - 5,     Year - 2025


ABSTRACT:
Simple sensitive and accurate extractive spectrophotometric methods have developed for the estimation of Candesartan cilexetil in pharmaceutical dosage form. The methods are based on the formation of coloured complexes by the drug with reagents like bromophenol blue, solochrome dark blue and bromocresol green in acidic medium. The ion associated complexes were formed and quantitatively extracted under the experimental condition in chloroform. The absorbance values were measured at 420 nm, 495 nm and 430 nm respectively. The proposed methods were validated statistically. Recoveries of methods were carried out by standard addition methods. The linearity was found to be 1-10 µg/ml, 1 -12µg/ml, 1-16 µg/ ml for methods 1, 2 and 3 respectively. The low values of standard deviation and percentage RSD indicate high precision of methods. Hence these methods are useful for routine estimation of Candesartan cilexetil in tablets.


Cite this article:
Rajan V. Rele, Prathamesh P. Tiwatane. Estimation of Candesartan Cilexetil by Extractive Colorimetric Methods in Bulk and Pharmaceutical Dosage Form. Asian Journal of Research in Chemistry. 2025; 18(5):324-6. doi: 10.52711/0974-4150.2025.00049

Cite(Electronic):
Rajan V. Rele, Prathamesh P. Tiwatane. Estimation of Candesartan Cilexetil by Extractive Colorimetric Methods in Bulk and Pharmaceutical Dosage Form. Asian Journal of Research in Chemistry. 2025; 18(5):324-6. doi: 10.52711/0974-4150.2025.00049   Available on: https://ajrconline.org/AbstractView.aspx?PID=2025-18-5-4


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3.    Anjan Paudel, Ameeduzzafar, Farhan Jalees Ahmad, Mohd Qumbar, Chetan Dhal, Asgar Ali. Stress degradation studies on candesartan cilexetil bulk drug and development of validated method by UV spectrophotometry in marketed tablet. World Journal of Pharmaceutical Science. 2014; 3(3): 3975-3986.
4.    Kalyani G., Vaishnav Y, Deshmukh S.V, Sahu R.  Stability Indicating Method Development and Validation of Candesartan in Bulk and Pharmaceutical Dosage Form by Derivative Spectrophotometric Method (First Order). International Journal of Pharmamedix India. 2013; 1(2): 222-232.
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12.    Manisha P Puranik, Sailesh J Wadher, Ashish L Kosarkar, Pramod G Yeole. Method Development and Validation of Candesartan cilexetil by RP-HPLC. International Journal of Research in Pharmaceutical and Biomedical Sciences. 2014; 3(3): 1227-1230.
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