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dc.contributor.authorHodaei, D
dc.contributor.authorBaradaran, B
dc.contributor.authorValizadeh, H
dc.contributor.authorZakeri-Milani, P
dc.date.accessioned2018-08-26T07:42:38Z
dc.date.available2018-08-26T07:42:38Z
dc.date.issued2015
dc.identifier10.1590/S1984-82502015000300026
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47848
dc.description.abstractThe present study was planned to investigate the influence of polyethylene glycols (PEGs) on the activity and expression of P-glycoprotein (P-gp). Sub-toxic concentrations of PEGs in Caco-2 cells were determined using the MTT test assay. Then the measurement of Rhodamine-123 (Rho-123) uptake, a P-gp fluorescence substrate, in Caco-2 cells confronting PEG 400 (1% and 2% w/v), PEG 4000 (2% and 4% w/v), PEG 6000 (2% and 4% w/v), PEG 10000 (2% and 4% w/v), PEG 15000 (1% and 2% w/v), and PEG 35000 (2% and 4% w/v) overnight was taken to elucidate whether non-toxic concentrations of PEGs are able to impact P-gp activity. Furthermore, western blotting was carried out to investigate P-gp protein expression. The results showed that PEG 400 at concentrations of 1% (w/v) and 2% (w/v) and PEG 6000 at the concentration of 4% (w/v) are notably capable of blocking P-gp. Based on the obtained results it is concluded that the mentioned excipients could be used to obstruct P-gp efflux transporter in order to increase the bioavailability of co-administered substrate drug.
dc.language.isoEnglish
dc.relation.ispartofBRAZILIAN JOURNAL OF PHARMACEUTICAL SCIENCES
dc.relation.ispartof18th Pharmaceutical Congress of Sao Paulo held together with the 10th International Seminar of Pharmaceutical Sciences and Expofar
dc.subjectP-glycoprotein/activity
dc.subjectP-glycoprotein/expression
dc.subjectCaco-2
dc.subjectRhodamine-123
dc.subjectExcipients
dc.subjectDrugs/bioavailability
dc.subjectPolyethylene glycol/effects
dc.titleEffects of polyethylene glycols on intestinal efflux pump expression and activity in Caco-2 cells
dc.typeArticle; Proceedings Paper
dc.citation.volume51
dc.citation.issue3
dc.citation.spage745
dc.citation.epage753
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1590/S1984-82502015000300026


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