Please use this identifier to cite or link to this item: http://hdl.handle.net/1/737
Title: Development and Validation of Method for the Estimation of Telmisartan as Active Pharmaceutical Ingredient in Tablet Dosage form and Prepared Spherical Agglomerates by RP-HPLC
Authors: Shaina, Sharma
Varinder, Soni
Sandeep, Rahar
Nitish, Bhatia
Keywords: RP HPLC
Method Development
Telmisartan
tablet
Spherical agglomerates
Validation
Issue Date: 7-May-2016
Publisher: Chitkara University Publications
Abstract: The Present work was designed to develop and validate an accurate, precise and rapid method for the estimation of Telmisartan as Active Pharmaceutical Ingredient (API) as well as in tablet dosage form and prepared spherical agglomerates by RP-HPLC. The developed method was found to be simple, accurate, precise and sensitive. The separation was achieved on an Isocratic High Pressure Liquid Chromatography (HPLC) (Thermo Scientific) using pumps Jasco PU 2080 Plus, UV detector, column oven (Jasco), and a Reverse Phase C-18 (phenyl) Column (25 cm x 4.6 mm) i.d., particle size 5 μm. The HPLC system was run with flow rate: 0.8 ml/min Injection Volume: 10μl and run time: 10 min, Detector temp: 40 oC. The method was validated for specificity, precision, linearity, and accuracy, robustness, LOD and LOQ parameters. The recovery range was within the range of 99.0–102.0% and the method could be successfully applied for the routine analysis of the drug substance as well as the spherical agglomerates prepared by crystallo coagglomeration technique.
URI: http://dspace.chitkara.edu.in/xmlui/handle/1/737
http://hdl.handle.net/1/737
ISSN: Print 2321-2217
Online 2321-2225
Appears in Collections:JPTRM Volume 4 Number 1 (May - 2016)

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