Stability-indicating methods for quantitative determination of zidovudine and stavudine in capsules

Zidovudine (AZT) and stavudine (D4T) are nucleoside reverse transcriptase inhibitors extensively used in human immunodeficiency virus (HIV) infected patients. In order to evaluate the quality of these drugs, two stability indicating HPLC methods were developed. The validated methods were applied in quantitative determination of AZT, D4T and their induced degradation products in capsule preparations. The stability studies were conducted at controlled temperature and relative humidity conditions based on the International Conference on Harmonization stability studies protocol for Zone IV areas. Easy sample preparation and low-cost make these methods especially useful for quality control and stability studies of AZT and D4T in drug products.

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Main Authors: Santoro,Maria Inês R. M., Taborianski,Andréia M., Singh,Anil Kumar, Kedor-Hackmann,Erika R. M.
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2006
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422006000200012
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spelling oai:scielo:S0100-404220060002000122006-04-03Stability-indicating methods for quantitative determination of zidovudine and stavudine in capsulesSantoro,Maria Inês R. M.Taborianski,Andréia M.Singh,Anil KumarKedor-Hackmann,Erika R. M. liquid chromatography antiviral drugs stability studies Zidovudine (AZT) and stavudine (D4T) are nucleoside reverse transcriptase inhibitors extensively used in human immunodeficiency virus (HIV) infected patients. In order to evaluate the quality of these drugs, two stability indicating HPLC methods were developed. The validated methods were applied in quantitative determination of AZT, D4T and their induced degradation products in capsule preparations. The stability studies were conducted at controlled temperature and relative humidity conditions based on the International Conference on Harmonization stability studies protocol for Zone IV areas. Easy sample preparation and low-cost make these methods especially useful for quality control and stability studies of AZT and D4T in drug products.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaQuímica Nova v.29 n.2 20062006-04-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422006000200012en10.1590/S0100-40422006000200012
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country Brasil
countrycode BR
component Revista
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region America del Sur
libraryname SciELO
language English
format Digital
author Santoro,Maria Inês R. M.
Taborianski,Andréia M.
Singh,Anil Kumar
Kedor-Hackmann,Erika R. M.
spellingShingle Santoro,Maria Inês R. M.
Taborianski,Andréia M.
Singh,Anil Kumar
Kedor-Hackmann,Erika R. M.
Stability-indicating methods for quantitative determination of zidovudine and stavudine in capsules
author_facet Santoro,Maria Inês R. M.
Taborianski,Andréia M.
Singh,Anil Kumar
Kedor-Hackmann,Erika R. M.
author_sort Santoro,Maria Inês R. M.
title Stability-indicating methods for quantitative determination of zidovudine and stavudine in capsules
title_short Stability-indicating methods for quantitative determination of zidovudine and stavudine in capsules
title_full Stability-indicating methods for quantitative determination of zidovudine and stavudine in capsules
title_fullStr Stability-indicating methods for quantitative determination of zidovudine and stavudine in capsules
title_full_unstemmed Stability-indicating methods for quantitative determination of zidovudine and stavudine in capsules
title_sort stability-indicating methods for quantitative determination of zidovudine and stavudine in capsules
description Zidovudine (AZT) and stavudine (D4T) are nucleoside reverse transcriptase inhibitors extensively used in human immunodeficiency virus (HIV) infected patients. In order to evaluate the quality of these drugs, two stability indicating HPLC methods were developed. The validated methods were applied in quantitative determination of AZT, D4T and their induced degradation products in capsule preparations. The stability studies were conducted at controlled temperature and relative humidity conditions based on the International Conference on Harmonization stability studies protocol for Zone IV areas. Easy sample preparation and low-cost make these methods especially useful for quality control and stability studies of AZT and D4T in drug products.
publisher Sociedade Brasileira de Química
publishDate 2006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422006000200012
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