Title: | An Improved Assay Method For The Estimation Of Ticagrelor Hydrochloride By Reverse Phase Liquid Chromatography |
Authors: | Ambasana, M.A. Kapuriya, N.P. Mangtani, K.M. Ladva, K.D. |
Keywords: | Ticagrelor HCl; Antiplatelet agent; HPLC; Validation Ticagrelor HCl; Antiplatelet agent; HPLC; Validation |
Issue Date: | 1-May-2016 |
Publisher: | International Journal Of Pharmaceutical Sciences And Research |
Citation: | Ambasana, M. A., Kapuriya, N. P., Mangtani, K. M., & Ladva, K. D. (2016). An improved assay method for the estimation of ticagrelor hydrochloride by reverse phase liquid chromatography,International Journal Of Pharmaceutical Sciences And Research7(5)2009-2014. |
Abstract: | The current investigation was carried out to develop and validate a fairly simple, accurate, precise, reproducible and robust RP-HPLC method for the estimation of Ticagrelor Hydrochloride. The separation was achieved using Agilent Infinity 1220, Infinity Fast-LC (Pressure limit up to 600 bars) with auto sampler and PDA detector. The Chromatographic analysis was performed on ZORBAX Eclipse Plus 300SB C18 (250 x 4.6mm, 5.0 micron, PN 880995-902) column. Mobile phase consist of (A) Acetonitrile: (B) 20mM Potassium dihydrogen ortho phosphate buffer (40:60 v/v) at a flow rate of 1.0 ml/min. The method showed linear in the mentioned concentrations having line equation y = 22.848x + 1.3214 with correlation coefficient R2 of 0.9995. The recovery values for Ticagrelor ranged from 99.63% to 100.34%. The % RSD was 0.49% and 0.54%, respectively for intraday and interday precision. The limit of detection and limit of quantification were 0.05μg/mL and 0.20μg/mL respectively. Newly developed method was statistically validated for accuracy, precision, linearity and solution stability; hence it is directly applicable for the estimation of Ticagrelor up to trace level in routine analysis. The current investigation was carried out to develop and validate a fairly simple, accurate, precise, reproducible and robust RP-HPLC method for the estimation of Ticagrelor Hydrochloride. The separation was achieved using Agilent Infinity 1220, Infinity Fast-LC (Pressure limit up to 600 bars) with auto sampler and PDA detector. The Chromatographic analysis was performed on ZORBAX Eclipse Plus 300SB C18 (250 x 4.6mm, 5.0 micron, PN 880995-902) column. Mobile phase consist of (A) Acetonitrile: (B) 20mM Potassium dihydrogen ortho phosphate buffer (40:60 v/v) at a flow rate of 1.0 ml/min. The method showed linear in the mentioned concentrations having line equation y = 22.848x + 1.3214 with correlation coefficient R2 of 0.9995. The recovery values for Ticagrelor ranged from 99.63% to 100.34%. The % RSD was 0.49% and 0.54%, respectively for intraday and interday precision. The limit of detection and limit of quantification were 0.05μg/mL and 0.20μg/mL respectively. Newly developed method was statistically validated for accuracy, precision, linearity and solution stability; hence it is directly applicable for the estimation of Ticagrelor up to trace level in routine analysis. |
URI: | https://ijpsr.com/bft-article/an-improved-assay-method-for-the-estimation-of-ticagrelor-hydrochloride-by-reverse-phase-liquid-chromatography/ http://10.9.150.37:8080/dspace//handle/atmiyauni/677 |
ISSN: | 0975-8232 |
Appears in Collections: | 01. Journal Articles |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
22-Vol.-7-Issue-5-May-2016-IJPSR-RA-6131.pdf | 375 kB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.