Author(s): Ware Agasti L., Pekamwar S. S.

Email(s): agastiware@gmail.com

DOI: 10.52711/2231-5675.2021.00015   

Address: Ware Agasti L.1,2*, Pekamwar S. S.3
1Jawaharlal Nehru Technological University, Hyderabad.
2Sanjivani College of Pharmaceutical Education and Research, Kopargaon.
3Swami Ramanand Tirth Marathwada University, Nanded.
*Corresponding Author

Published In:   Volume - 11,      Issue - 2,     Year - 2021


ABSTRACT:
The accurate, precise, sensitive and economical spectrophotometric bioanalytical method was developed and validated for estimation of candesartan in plasma. The UV method was also employed for estimation of candesartan in bulk drug and in dosage form. The absorption maximum found for candesartan was 245nm. The correlation coefficient was found to be 0.999. The mean recovery for candesartan was found to be 99.92%. The developed method was validated according to ICH guidelines and values of accuracy, precision and other statistical analysis were found to be in good accordance with the prescribed values. Thus the proposed method was successfully applied for estimation of candesartan in plasma and for routine industrial work.


Cite this article:
Ware Agasti L., Pekamwar S. S. Development and Validation of Bioanalytical UV-Spectrophotometric Method for Determination of Candesartan and Development and Validation of UV-Spectrophotometric Method for Determination of Candesartan in Bulk Drug and Formulation. Asian Journal of Pharmaceutical Analysis. 2021; 11(2):79-3. doi: 10.52711/2231-5675.2021.00015

Cite(Electronic):
Ware Agasti L., Pekamwar S. S. Development and Validation of Bioanalytical UV-Spectrophotometric Method for Determination of Candesartan and Development and Validation of UV-Spectrophotometric Method for Determination of Candesartan in Bulk Drug and Formulation. Asian Journal of Pharmaceutical Analysis. 2021; 11(2):79-3. doi: 10.52711/2231-5675.2021.00015   Available on: https://ajpaonline.com/AbstractView.aspx?PID=2021-11-2-5


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