Author(s): Sudhanshu I Chauhan, Pankaj D. Savani, Hasumati Raj, Sagar Patel

Email(s): sudhanshuchauhan32@yahoo.com

DOI: 10.5958/2231-5675.2016.00009.0   

Address: Sudhanshu I Chauhan1, 2*, Pankaj D. Savani1, Hasumati Raj1, Sagar Patel1
1Department of Quality Assurance, Shree Dhanvantary Pharmacy College, Kim, Surat, Gujarat, India.
2Research Scholar 2015, Gujarat Technological University, Gujarat, India.
*Corresponding Author

Published In:   Volume - 6,      Issue - 1,     Year - 2016


ABSTRACT:
Candesartan Cilexetil is classified as an AT1 Angiotensin II receptor antagonist as a Antihypertensive agent. There are widely used in treatment of diseases like hypertension, heart failure, myocardial infarction and diabetic nephropathy. The clinical and pharmaceutical analysis of this drug requires effective analytical procedures for quality control and Pharmcodynamic and pharmacokinetic studies as well as stability study. There are many article examines published analytical methods reported so far in the literature for the determination of Candesartan Cilexetil in biological samples and pharmaceutical formulations. These article comprise reviews of analytical methods like Spectrophotometric methods, Chromatographic method including HPLC, HPTLC.


Cite this article:
Sudhanshu I Chauhan, Pankaj D. Savani, Hasumati Raj, Sagar Patel. Candesartan Cilexetil: A Review of Spectroscopic and Chromatographic Method. Asian J. Pharm. Ana. 6(1): January- March, 2016; Page 53-58. doi: 10.5958/2231-5675.2016.00009.0


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DOI: 10.5958/2231–5675 

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