Method Development and Validation for the Simulataneous Estimation of Amlodipine and Telmisartan in Pharamaceutical Dosage form by HPLC

Yahia Adam, Hassan Adam (2019) Method Development and Validation for the Simulataneous Estimation of Amlodipine and Telmisartan in Pharamaceutical Dosage form by HPLC. Masters thesis, Annai JKK Sampoorani Ammal College of Pharmacy, Komarapalayam.

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Abstract

The developed chromatographic method or the simultaneous determination of amlodipine and telmisartan in dosage form is simple, reliable, sensitive and less time consuming. This method advantage is dose not require complicated mobile phase and it is simple method. This can be used or routine and quality control analysis of amlodipine and telmisartan in bulk and pharmaceutical dosage form. The present work shows a validated, sensitive and selected method for the determination of amlodipine and telmisartan in pharmaceutical dosage form. Accuracy and precision are major parameters of control of the all validation procedures are within the acceptable limits. This developed method has a valuable data for the validation of amlodipine and telmisartan combination method in bulk and pharmaceutical dosage form.

Item Type: Thesis (Masters)
Additional Information: 261730702
Uncontrolled Keywords: Method, Development, Validation, Simulataneous, Estimation, Amlodipine,Telmisartan, Pharamaceutical Dosage, HPLC.
Subjects: PHARMACY > Pharmaceutical Analysis
Depositing User: Thavamani K
Date Deposited: 23 Mar 2022 12:02
Last Modified: 23 Mar 2022 12:02
URI: http://repository-tnmgrmu.ac.in/id/eprint/19087

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