Formulation and characterization of self emulsifing pellets of carvedilol

The purpose of present study was aimed at developing self emulsifying drug delivery system in liquid and then in pellet form that would result in improved solubility, dissolution and permeability of the poorly water soluble drug carvedilol. Pellets were prepared using extrusion-spheronization techni...

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Main Authors: Vikas Bhandari, Amelia Avachat
Format: Article
Language:English
Published: Universidade de São Paulo 2015-09-01
Series:Brazilian Journal of Pharmaceutical Sciences
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502015000300663&lng=en&tlng=en
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spelling doaj-99306875d59d4d2fa1373ddd3e575cdb2020-11-24T22:16:42ZengUniversidade de São PauloBrazilian Journal of Pharmaceutical Sciences2175-97902015-09-0151366367110.1590/S1984-82502015000300018S1984-82502015000300663Formulation and characterization of self emulsifing pellets of carvedilolVikas BhandariAmelia AvachatThe purpose of present study was aimed at developing self emulsifying drug delivery system in liquid and then in pellet form that would result in improved solubility, dissolution and permeability of the poorly water soluble drug carvedilol. Pellets were prepared using extrusion-spheronization technique incorporating liquid SEDDS (carvedilol, capmul MCM EP, cremophore EL, tween 20, propylene glycol), adsorbents ( and crospovidone), microcrystalline cellulose and binder (povidone K-30). Ternary phase diagram was constructed to identify different oil-surfactant-cosurfactant mixtures according to the proportion of each point in it. The optimal CAR-SEDDS pellets showed a quicker redispersion with a droplet size of the reconstituted microemulsion being 160.47 nm, which was almost unchanged after solidification. SEM analysis confirmed good spherical appearance of solid pellets; DSC and XRD analysis confirmed that there was no crystalline carvedilol in the pellets. Pellets were then capable of transferring lipophilic compounds into the aqueous phase and significantly enhancing its release with respect to pure drug.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502015000300663&lng=en&tlng=enFármacos/sistema líquido de liberação auto emulsificantePéletes/auto emulsificante/preparaçãoPéletes/auto emulsificante/sistema líquido de liberaçãoCarvedilol/farmacocinética
collection DOAJ
language English
format Article
sources DOAJ
author Vikas Bhandari
Amelia Avachat
spellingShingle Vikas Bhandari
Amelia Avachat
Formulation and characterization of self emulsifing pellets of carvedilol
Brazilian Journal of Pharmaceutical Sciences
Fármacos/sistema líquido de liberação auto emulsificante
Péletes/auto emulsificante/preparação
Péletes/auto emulsificante/sistema líquido de liberação
Carvedilol/farmacocinética
author_facet Vikas Bhandari
Amelia Avachat
author_sort Vikas Bhandari
title Formulation and characterization of self emulsifing pellets of carvedilol
title_short Formulation and characterization of self emulsifing pellets of carvedilol
title_full Formulation and characterization of self emulsifing pellets of carvedilol
title_fullStr Formulation and characterization of self emulsifing pellets of carvedilol
title_full_unstemmed Formulation and characterization of self emulsifing pellets of carvedilol
title_sort formulation and characterization of self emulsifing pellets of carvedilol
publisher Universidade de São Paulo
series Brazilian Journal of Pharmaceutical Sciences
issn 2175-9790
publishDate 2015-09-01
description The purpose of present study was aimed at developing self emulsifying drug delivery system in liquid and then in pellet form that would result in improved solubility, dissolution and permeability of the poorly water soluble drug carvedilol. Pellets were prepared using extrusion-spheronization technique incorporating liquid SEDDS (carvedilol, capmul MCM EP, cremophore EL, tween 20, propylene glycol), adsorbents ( and crospovidone), microcrystalline cellulose and binder (povidone K-30). Ternary phase diagram was constructed to identify different oil-surfactant-cosurfactant mixtures according to the proportion of each point in it. The optimal CAR-SEDDS pellets showed a quicker redispersion with a droplet size of the reconstituted microemulsion being 160.47 nm, which was almost unchanged after solidification. SEM analysis confirmed good spherical appearance of solid pellets; DSC and XRD analysis confirmed that there was no crystalline carvedilol in the pellets. Pellets were then capable of transferring lipophilic compounds into the aqueous phase and significantly enhancing its release with respect to pure drug.
topic Fármacos/sistema líquido de liberação auto emulsificante
Péletes/auto emulsificante/preparação
Péletes/auto emulsificante/sistema líquido de liberação
Carvedilol/farmacocinética
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502015000300663&lng=en&tlng=en
work_keys_str_mv AT vikasbhandari formulationandcharacterizationofselfemulsifingpelletsofcarvedilol
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