Cargando…
A Validated HPLC Method for Zanamivir and its Application to In vitro Permeability Study in Caco-2 Culture Model
A simple HPLC method was developed and validated for the quantification of zanamivir in permeability studies using Caco-2 cell culture model. Chromatographic resolution was achieved using 98% (v/v) ultrapure water and 2% (v/v) acetonitrile as mobile phase with flow rate of 0.5 ml/min on a BDS Hypers...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425069/ https://www.ncbi.nlm.nih.gov/pubmed/22923870 http://dx.doi.org/10.4103/0250-474X.99015 |
_version_ | 1782241318480642048 |
---|---|
author | Boonyapiwat, B. Sarisuta, N. Ma, Y. Steventon, G. B. |
author_facet | Boonyapiwat, B. Sarisuta, N. Ma, Y. Steventon, G. B. |
author_sort | Boonyapiwat, B. |
collection | PubMed |
description | A simple HPLC method was developed and validated for the quantification of zanamivir in permeability studies using Caco-2 cell culture model. Chromatographic resolution was achieved using 98% (v/v) ultrapure water and 2% (v/v) acetonitrile as mobile phase with flow rate of 0.5 ml/min on a BDS Hypersil Cyano column (length 250 mm; internal diameter 4.6 mm; particle size 5 μm) and UV detection at 230 nm. The method was linear for the quantification of zanamivir at concentration ranging from 0.1-10 μg/ml with coefficient of determination greater than 0.999. The recovery of zanamivir was in the range of 99.76-105.08%. The relative standard deviations of the within-day precision and between-day precision were lower than 10.32 and 14.33%, respectively. The permeability of zanamivir was independent of the transport direction and zanamivir concentrations, indicating a passive transport of zanamivir across Caco-2 cells. With the absence of Ca(2+) in transport medium, the permeability values of zanamivir increased 56.21 and 57.20 fold in the directions of apical to basolateral and basolateral to apical, respectively. On the basis of these results, zanamivir was found to be predominantly transported across Caco-2 monolayers via the passive paracellular pathway. |
format | Online Article Text |
id | pubmed-3425069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-34250692012-08-24 A Validated HPLC Method for Zanamivir and its Application to In vitro Permeability Study in Caco-2 Culture Model Boonyapiwat, B. Sarisuta, N. Ma, Y. Steventon, G. B. Indian J Pharm Sci Research Paper A simple HPLC method was developed and validated for the quantification of zanamivir in permeability studies using Caco-2 cell culture model. Chromatographic resolution was achieved using 98% (v/v) ultrapure water and 2% (v/v) acetonitrile as mobile phase with flow rate of 0.5 ml/min on a BDS Hypersil Cyano column (length 250 mm; internal diameter 4.6 mm; particle size 5 μm) and UV detection at 230 nm. The method was linear for the quantification of zanamivir at concentration ranging from 0.1-10 μg/ml with coefficient of determination greater than 0.999. The recovery of zanamivir was in the range of 99.76-105.08%. The relative standard deviations of the within-day precision and between-day precision were lower than 10.32 and 14.33%, respectively. The permeability of zanamivir was independent of the transport direction and zanamivir concentrations, indicating a passive transport of zanamivir across Caco-2 cells. With the absence of Ca(2+) in transport medium, the permeability values of zanamivir increased 56.21 and 57.20 fold in the directions of apical to basolateral and basolateral to apical, respectively. On the basis of these results, zanamivir was found to be predominantly transported across Caco-2 monolayers via the passive paracellular pathway. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3425069/ /pubmed/22923870 http://dx.doi.org/10.4103/0250-474X.99015 Text en Copyright: © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Boonyapiwat, B. Sarisuta, N. Ma, Y. Steventon, G. B. A Validated HPLC Method for Zanamivir and its Application to In vitro Permeability Study in Caco-2 Culture Model |
title | A Validated HPLC Method for Zanamivir and its Application to In vitro Permeability Study in Caco-2 Culture Model |
title_full | A Validated HPLC Method for Zanamivir and its Application to In vitro Permeability Study in Caco-2 Culture Model |
title_fullStr | A Validated HPLC Method for Zanamivir and its Application to In vitro Permeability Study in Caco-2 Culture Model |
title_full_unstemmed | A Validated HPLC Method for Zanamivir and its Application to In vitro Permeability Study in Caco-2 Culture Model |
title_short | A Validated HPLC Method for Zanamivir and its Application to In vitro Permeability Study in Caco-2 Culture Model |
title_sort | validated hplc method for zanamivir and its application to in vitro permeability study in caco-2 culture model |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425069/ https://www.ncbi.nlm.nih.gov/pubmed/22923870 http://dx.doi.org/10.4103/0250-474X.99015 |
work_keys_str_mv | AT boonyapiwatb avalidatedhplcmethodforzanamiviranditsapplicationtoinvitropermeabilitystudyincaco2culturemodel AT sarisutan avalidatedhplcmethodforzanamiviranditsapplicationtoinvitropermeabilitystudyincaco2culturemodel AT may avalidatedhplcmethodforzanamiviranditsapplicationtoinvitropermeabilitystudyincaco2culturemodel AT steventongb avalidatedhplcmethodforzanamiviranditsapplicationtoinvitropermeabilitystudyincaco2culturemodel AT boonyapiwatb validatedhplcmethodforzanamiviranditsapplicationtoinvitropermeabilitystudyincaco2culturemodel AT sarisutan validatedhplcmethodforzanamiviranditsapplicationtoinvitropermeabilitystudyincaco2culturemodel AT may validatedhplcmethodforzanamiviranditsapplicationtoinvitropermeabilitystudyincaco2culturemodel AT steventongb validatedhplcmethodforzanamiviranditsapplicationtoinvitropermeabilitystudyincaco2culturemodel |