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RPLC Determination of Tinidazole and Diloxanide Furoate in Tablets

A simple reverse phase liquid chromatographic method has been developed and subsequently validated for simultaneous determination of tinidazole and diloxanide furoate. The separation was carried out using a mobile phase consisting of acetonitrile, methanol and 0.2 M potassium dihydrogen phosphate (p...

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Detalles Bibliográficos
Autores principales: Pai, P. N. S, Rao, G. K., Srinivas, B., Puranik, S.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038301/
https://www.ncbi.nlm.nih.gov/pubmed/21394273
http://dx.doi.org/10.4103/0250-474X.45415
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author Pai, P. N. S
Rao, G. K.
Srinivas, B.
Puranik, S.
author_facet Pai, P. N. S
Rao, G. K.
Srinivas, B.
Puranik, S.
author_sort Pai, P. N. S
collection PubMed
description A simple reverse phase liquid chromatographic method has been developed and subsequently validated for simultaneous determination of tinidazole and diloxanide furoate. The separation was carried out using a mobile phase consisting of acetonitrile, methanol and 0.2 M potassium dihydrogen phosphate (pH 5) in the ratio 2:3:2.The column used was SS Wakosil-II C-18 with a flow rate of 1 ml/min and UV detection at 282 nm. The described method was linear over a concentration range of 10-70 μg/ml and 10-90 μg/ml for the assay of diloxanide furoate and tinidazole, respectively. The mean recovery was found to be 100-101% for tinidazole and 97-103% for diloxanide furoate when determined at three different levels.
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spelling pubmed-30383012011-03-10 RPLC Determination of Tinidazole and Diloxanide Furoate in Tablets Pai, P. N. S Rao, G. K. Srinivas, B. Puranik, S. Indian J Pharm Sci Short Communication A simple reverse phase liquid chromatographic method has been developed and subsequently validated for simultaneous determination of tinidazole and diloxanide furoate. The separation was carried out using a mobile phase consisting of acetonitrile, methanol and 0.2 M potassium dihydrogen phosphate (pH 5) in the ratio 2:3:2.The column used was SS Wakosil-II C-18 with a flow rate of 1 ml/min and UV detection at 282 nm. The described method was linear over a concentration range of 10-70 μg/ml and 10-90 μg/ml for the assay of diloxanide furoate and tinidazole, respectively. The mean recovery was found to be 100-101% for tinidazole and 97-103% for diloxanide furoate when determined at three different levels. Medknow Publications 2008 /pmc/articles/PMC3038301/ /pubmed/21394273 http://dx.doi.org/10.4103/0250-474X.45415 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Pai, P. N. S
Rao, G. K.
Srinivas, B.
Puranik, S.
RPLC Determination of Tinidazole and Diloxanide Furoate in Tablets
title RPLC Determination of Tinidazole and Diloxanide Furoate in Tablets
title_full RPLC Determination of Tinidazole and Diloxanide Furoate in Tablets
title_fullStr RPLC Determination of Tinidazole and Diloxanide Furoate in Tablets
title_full_unstemmed RPLC Determination of Tinidazole and Diloxanide Furoate in Tablets
title_short RPLC Determination of Tinidazole and Diloxanide Furoate in Tablets
title_sort rplc determination of tinidazole and diloxanide furoate in tablets
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038301/
https://www.ncbi.nlm.nih.gov/pubmed/21394273
http://dx.doi.org/10.4103/0250-474X.45415
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