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Description
  • A nanofibrous membrane carrier for nearly water insoluble drug diosmin was formulated. The aim of this study was to evaluate the drug release and dissolution properties in an aqueous buffer of pH 7.8, and to compare the suitability of the drug carrier with the available drug forms and screen diosmin absorption extent. The membranes were produced from HPC/PVA/PEO-drug water solutions and then evaluated by SEM and DSC measurements. The results showed that diosmin was incorporated within the nanofibers in an amorphous state, and/or as a solid dispersion. The results of in vitro release experiments excerpt a very fast release of the drug, followed by the formation of an over saturated solution and partial precipitation of the drug (a %22spring%22 effect). The enormous increases in dissolution of the drug from a nanofibrous carrier, compared to a micronized and crystalline form, was achieved. The in vivo bioavailability study carried out on rats showed higher initial drug plasma levels and higher AUC values after administration of the nanofibrous drug formulation, compared to the micronized form. The results of the study demonstrated that the improvement of the diosmin in vitro dissolution also brought the enhanced in vivo absorption extent of the drug.
  • A nanofibrous membrane carrier for nearly water insoluble drug diosmin was formulated. The aim of this study was to evaluate the drug release and dissolution properties in an aqueous buffer of pH 7.8, and to compare the suitability of the drug carrier with the available drug forms and screen diosmin absorption extent. The membranes were produced from HPC/PVA/PEO-drug water solutions and then evaluated by SEM and DSC measurements. The results showed that diosmin was incorporated within the nanofibers in an amorphous state, and/or as a solid dispersion. The results of in vitro release experiments excerpt a very fast release of the drug, followed by the formation of an over saturated solution and partial precipitation of the drug (a %22spring%22 effect). The enormous increases in dissolution of the drug from a nanofibrous carrier, compared to a micronized and crystalline form, was achieved. The in vivo bioavailability study carried out on rats showed higher initial drug plasma levels and higher AUC values after administration of the nanofibrous drug formulation, compared to the micronized form. The results of the study demonstrated that the improvement of the diosmin in vitro dissolution also brought the enhanced in vivo absorption extent of the drug. (en)
Title
  • Electrospinning of diosmin from aqueous solutions for improved dissolution and oral absorption
  • Electrospinning of diosmin from aqueous solutions for improved dissolution and oral absorption (en)
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  • Electrospinning of diosmin from aqueous solutions for improved dissolution and oral absorption
  • Electrospinning of diosmin from aqueous solutions for improved dissolution and oral absorption (en)
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  • RIV/00216208:11160/14:10282246!RIV15-MSM-11160___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • I, S
http://linked.open...iv/cisloPeriodika
  • 1-2
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 14231
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11160/14:10282246
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Oral bioavailability; Solubility; Nanofibre; Diosmin; Electrospinning (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • NL - Nizozemsko
http://linked.open...ontrolniKodProRIV
  • [2C5FC95133CE]
http://linked.open...i/riv/nazevZdroje
  • International Journal of Pharmaceutics
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 473
http://linked.open...iv/tvurceVysledku
  • Doležal, Pavel
  • Berka, Pavel
  • Lázníček, Milan
  • Stránská, Denisa
  • Vrbata, Petr
http://linked.open...ain/vavai/riv/wos
  • 000342656800045
issn
  • 0378-5173
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.ijpharm.2014.07.017
http://localhost/t...ganizacniJednotka
  • 11160
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