Please use this identifier to cite or link to this item: https://doi.org/10.1016/S1570-0232(02)00911-X
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dc.titleDetermination of thalidomide in transport buffer for Caco-2 cell monolayers by high-performance liquid chromatography with ultraviolet detection
dc.contributor.authorZhou, S.
dc.contributor.authorLi, Y.
dc.contributor.authorKestell, P.
dc.contributor.authorPaxton, J.W.
dc.date.accessioned2014-10-29T01:51:01Z
dc.date.available2014-10-29T01:51:01Z
dc.date.issued2003-02-25
dc.identifier.citationZhou, S., Li, Y., Kestell, P., Paxton, J.W. (2003-02-25). Determination of thalidomide in transport buffer for Caco-2 cell monolayers by high-performance liquid chromatography with ultraviolet detection. Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences 785 (1) : 165-173. ScholarBank@NUS Repository. https://doi.org/10.1016/S1570-0232(02)00911-X
dc.identifier.issn15700232
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/105807
dc.description.abstractWe report simple validated HPLC methods for the determination of thalidomide in the transport buffer for the human colonic cell line (Caco-2) cell monolayers. An aliquot of 50 μl of the mixture was injected onto a Spherex C18 column (150×4.6 mm; 5 μm) at a flow-rate of 0.5 ml/min of mobile phase consisting of acetonitrile-10 mM ammonium acetate buffer (24:76, v/v, pH 5.5), and thalidomide was detected by ultraviolet detector at a wavelength of 220 nm. Calibration curves for thalidomide were constructed at the concentration range of 0.025-1.0 and 1.0-50 μM in transport buffer. The validated methods were used to determine the transport of thalidomide by Caco-2 monolayers. The transport across the monolayers from the apical (A) to basolateral (B) side was similar to that from B to A side. The apparent permeability coefficient (Papp) values of thalidomide at 10-300 μM from the A to B and from B to A side was 2-6×10-5 cm/s, with a marked decrease in Papp values from A to B side at increased thalidomide concentration. The A to B transport appears to be dependent on temperature and sodium ion. Sodium azide, 2,4-dinitrophenol (both ATP inhibitors), 5-fluorouracil, cytidine and glutamic acid significantly inhibited the transport of thalidomide. These results indicate that the transport of thalidomide by Caco-2 monolayers was rapid, which might involve an energy-dependent mechanism. © Elsevier Science B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S1570-0232(02)00911-X
dc.sourceScopus
dc.subjectCaco-2 cell monolayers
dc.subjectThalidomide
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.doi10.1016/S1570-0232(02)00911-X
dc.description.sourcetitleJournal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences
dc.description.volume785
dc.description.issue1
dc.description.page165-173
dc.description.codenJCBAA
dc.identifier.isiut000180592700016
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