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Development of Spectrofluorimetric and HPLC Methods for In vitro Analysis of Repaglinide

Spectrofluorimetric and high-performance liquid chromatography methods for estimation of repaglinide were developed. These methods were validated for estimation of repaglinide in tablets as well as in receptor fluid obtained during in vitro permeation studies. Repaglinide was observed to exhibit emi...

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Detalles Bibliográficos
Autores principales: Kaushal, N., Jain, S., Tiwary, A. K.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2929787/
https://www.ncbi.nlm.nih.gov/pubmed/20838532
http://dx.doi.org/10.4103/0250-474X.65029
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author Kaushal, N.
Jain, S.
Tiwary, A. K.
author_facet Kaushal, N.
Jain, S.
Tiwary, A. K.
author_sort Kaushal, N.
collection PubMed
description Spectrofluorimetric and high-performance liquid chromatography methods for estimation of repaglinide were developed. These methods were validated for estimation of repaglinide in tablets as well as in receptor fluid obtained during in vitro permeation studies. Repaglinide was observed to exhibit emission and excitation wavelengths, respectively, at 379 nm and 282 nm with linearity in the concentration range of 5-80 µg/ml. High-performance liquid chromatography analysis of repaglinide yielded retention time of 6.14 min with linearity ranging from 0.1-1.2 µg/ml concentration. Spectrofluorimetric analysis of repaglinide in tablets yielded results comparable to high performance liquid chromatography.
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spelling pubmed-29297872010-09-13 Development of Spectrofluorimetric and HPLC Methods for In vitro Analysis of Repaglinide Kaushal, N. Jain, S. Tiwary, A. K. Indian J Pharm Sci Short Communications Spectrofluorimetric and high-performance liquid chromatography methods for estimation of repaglinide were developed. These methods were validated for estimation of repaglinide in tablets as well as in receptor fluid obtained during in vitro permeation studies. Repaglinide was observed to exhibit emission and excitation wavelengths, respectively, at 379 nm and 282 nm with linearity in the concentration range of 5-80 µg/ml. High-performance liquid chromatography analysis of repaglinide yielded retention time of 6.14 min with linearity ranging from 0.1-1.2 µg/ml concentration. Spectrofluorimetric analysis of repaglinide in tablets yielded results comparable to high performance liquid chromatography. Medknow Publications 2010 /pmc/articles/PMC2929787/ /pubmed/20838532 http://dx.doi.org/10.4103/0250-474X.65029 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 Communications
Kaushal, N.
Jain, S.
Tiwary, A. K.
Development of Spectrofluorimetric and HPLC Methods for In vitro Analysis of Repaglinide
title Development of Spectrofluorimetric and HPLC Methods for In vitro Analysis of Repaglinide
title_full Development of Spectrofluorimetric and HPLC Methods for In vitro Analysis of Repaglinide
title_fullStr Development of Spectrofluorimetric and HPLC Methods for In vitro Analysis of Repaglinide
title_full_unstemmed Development of Spectrofluorimetric and HPLC Methods for In vitro Analysis of Repaglinide
title_short Development of Spectrofluorimetric and HPLC Methods for In vitro Analysis of Repaglinide
title_sort development of spectrofluorimetric and hplc methods for in vitro analysis of repaglinide
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2929787/
https://www.ncbi.nlm.nih.gov/pubmed/20838532
http://dx.doi.org/10.4103/0250-474X.65029
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