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Effects of polyethylene glycols on intestinal efflux pump expression and activity in Caco-2 cells BJPS
Hodaei,Darya; Baradaran,Behzad; Valizadeh,Hadi; Zakeri-Milani,Parvin.
The 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%...
Tipo: Info:eu-repo/semantics/article Palavras-chave: P-glycoprotein/activity; P-glycoprotein/expression; Caco-2; Rhodamine-123; Excipients; Drugs/bioavailability; Polyethylene glycol/effects.
Ano: 2015 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502015000300745
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Solubility and dissolution enhancement of flurbiprofen by solid dispersion using hydrophilic carriers BJPS
Daravath,Bhaskar; Naveen,Chella; Vemula,Sateesh Kumar; Tadikonda,Rama Rao.
ABSTRACT The intent of the current work is to study the effect of polyethylene glycol 8000 and polyethylene glycol 10000 as hydrophilic carriers on dissolution behaviour of flurbiprofen. In the present study, solvent evaporation method was used to prepare flurbiprofen solid dispersions and evaluated for physico-chemical properties, drug-carrier compatibility studies and dissolution behaviour of drug. Solubility studies showed more solubility in higher pH values and formulations SD4 and SD8 were selected to prepare the fast dissolving tablets. FTIR and DSC study showed no interaction and drug was dispersed molecularly in hydrophilic carrier. XRD studies revealed that there was change in the crystallinity of the drug. The results of In vitro studies showed...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Polyethylene glycol/effects; Flurbiprofen/solubility; Flurbiprofen/dissolution rate; Drug-carrier compatibility/study; Dissolution efficiency.
Ano: 2017 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502017000400625
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