Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical Formulation

A rapid and sensitive RP-HPLC method with UV detection (262 nm) for routine analysis of adefovir dipivoxil in bulk and in pharmaceutical formulation was developed. Chromatography was performed with mobile phase containing a mixture of acetonitrile and phosphate buffer (50:50, v/v) with flow rate 1.0...

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Main Authors: Zaheer Ahmed, B. Gopinath, A. Sathish Kumar Shetty, B. K. Sridhar
Format: Article
Language:English
Published: Hindawi Limited 2009-01-01
Series:E-Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2009/157868
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author Zaheer Ahmed
B. Gopinath
A. Sathish Kumar Shetty
B. K. Sridhar
author_facet Zaheer Ahmed
B. Gopinath
A. Sathish Kumar Shetty
B. K. Sridhar
author_sort Zaheer Ahmed
collection DOAJ
description A rapid and sensitive RP-HPLC method with UV detection (262 nm) for routine analysis of adefovir dipivoxil in bulk and in pharmaceutical formulation was developed. Chromatography was performed with mobile phase containing a mixture of acetonitrile and phosphate buffer (50:50, v/v) with flow rate 1.0 mL min-l. In the range of 5.0-100 µg/mL, the linearity of adefovir dipivoxil shows a correlation co-efficient of 0.9999. The proposed method was validated by determining sensitivity accuracy, precision, robustness stability, specificity, selectivity and system suitability parameters.
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spelling doaj.art-ffc2633646d5433ea35f026506fd16502022-12-22T03:58:48ZengHindawi LimitedE-Journal of Chemistry0973-49452090-98102009-01-016246947410.1155/2009/157868Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical FormulationZaheer Ahmed0B. Gopinath1A. Sathish Kumar Shetty2B. K. Sridhar3Department of Pharmaceutical Analysis, National College of Pharmacy, Shimoga-577201, (K.S.), IndiaDepartment of Pharmaceutical Analysis, National College of Pharmacy, Shimoga-577201, (K.S.), IndiaDepartment of Pharmaceutical Analysis, National College of Pharmacy, Shimoga-577201, (K.S.), IndiaDepartment of Pharmaceutical Analysis, National College of Pharmacy, Shimoga-577201, (K.S.), IndiaA rapid and sensitive RP-HPLC method with UV detection (262 nm) for routine analysis of adefovir dipivoxil in bulk and in pharmaceutical formulation was developed. Chromatography was performed with mobile phase containing a mixture of acetonitrile and phosphate buffer (50:50, v/v) with flow rate 1.0 mL min-l. In the range of 5.0-100 µg/mL, the linearity of adefovir dipivoxil shows a correlation co-efficient of 0.9999. The proposed method was validated by determining sensitivity accuracy, precision, robustness stability, specificity, selectivity and system suitability parameters.http://dx.doi.org/10.1155/2009/157868
spellingShingle Zaheer Ahmed
B. Gopinath
A. Sathish Kumar Shetty
B. K. Sridhar
Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical Formulation
E-Journal of Chemistry
title Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical Formulation
title_full Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical Formulation
title_fullStr Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical Formulation
title_full_unstemmed Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical Formulation
title_short Development and Validation of RP-HPLC Method for the Determination of Adefovir Dipivoxil in Bulk and in Pharmaceutical Formulation
title_sort development and validation of rp hplc method for the determination of adefovir dipivoxil in bulk and in pharmaceutical formulation
url http://dx.doi.org/10.1155/2009/157868
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