Dissolution improvement of solid self-emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption material

Solidification of lipid formulations using adsorbents is a recent technique attracting great interest due to its favourable properties including flexibility in dose division, reduction of intra-subject and inter-subject variability, improvement in efficacy/safety profile and enhancement of physical/...

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Main Authors: Shazly Gamal, Mohsin Kazi
Format: Article
Language:English
Published: Sciendo 2015-03-01
Series:Acta Pharmaceutica
Subjects:
Online Access:https://doi.org/10.1515/acph-2015-0003
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author Shazly Gamal
Mohsin Kazi
author_facet Shazly Gamal
Mohsin Kazi
author_sort Shazly Gamal
collection DOAJ
description Solidification of lipid formulations using adsorbents is a recent technique attracting great interest due to its favourable properties including flexibility in dose division, reduction of intra-subject and inter-subject variability, improvement in efficacy/safety profile and enhancement of physical/ chemical stability. The current study aims to convert liquid self-emulsifying/nanoemulsifying drug delivery systems (SEDDS/SNEDDS) into solid SEDDS/SNEDDS and to assess how adsorption of the drug onto an inorganic high surface area material, NeusilinR grade US2 (NUS2), affects its in vitro dissolution performance. Lipid formulation classification systems (LFCS) Type III formulations were designed for the model anti-cholesterol drug fenofibrate. NUS2 was used to solidify the SEDDS/SNEDDS. Particle size and SEM analyses of solid SEDDS/SNEDDS powder were carried out to investigate the adsorption efficiency. In vitro dissolution studies were conducted to compare the developed formulations with the marketed product. The results of characterization studies showed that the use of 50 % (m/m) adsorbent resulted in superior flowability and kept the drug stable is amorphous state. Dissolution studies allow the conclusion that the formulation containing a surfactant of higher water solubility (particularly, Type IIIB SNEDDS) has comparably faster and higher release profiles than Type IIIA (SEDDS) and marketed product
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spelling doaj-art-ea72e7f979e14367a9b23e1a048a85d22025-02-02T09:55:40ZengSciendoActa Pharmaceutica1846-95582015-03-01651294210.1515/acph-2015-0003acph-2015-0003Dissolution improvement of solid self-emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption materialShazly Gamal0Mohsin Kazi1Department of Pharmaceutics College of Pharmacy King Saud University Riyadh, Saudi Arabia / Department of Industrial Pharmacy Faculty of Pharmacy Assiut University Assuit, EgyptDepartment of Pharmaceutics College of Pharmacy King Saud University Riyadh, Saudi ArabiaSolidification of lipid formulations using adsorbents is a recent technique attracting great interest due to its favourable properties including flexibility in dose division, reduction of intra-subject and inter-subject variability, improvement in efficacy/safety profile and enhancement of physical/ chemical stability. The current study aims to convert liquid self-emulsifying/nanoemulsifying drug delivery systems (SEDDS/SNEDDS) into solid SEDDS/SNEDDS and to assess how adsorption of the drug onto an inorganic high surface area material, NeusilinR grade US2 (NUS2), affects its in vitro dissolution performance. Lipid formulation classification systems (LFCS) Type III formulations were designed for the model anti-cholesterol drug fenofibrate. NUS2 was used to solidify the SEDDS/SNEDDS. Particle size and SEM analyses of solid SEDDS/SNEDDS powder were carried out to investigate the adsorption efficiency. In vitro dissolution studies were conducted to compare the developed formulations with the marketed product. The results of characterization studies showed that the use of 50 % (m/m) adsorbent resulted in superior flowability and kept the drug stable is amorphous state. Dissolution studies allow the conclusion that the formulation containing a surfactant of higher water solubility (particularly, Type IIIB SNEDDS) has comparably faster and higher release profiles than Type IIIA (SEDDS) and marketed producthttps://doi.org/10.1515/acph-2015-0003self-emulsifying/nanoemulsifying drug delivery systemsfenofibratein vitro dissolution testsolidification techniqueadsorption
spellingShingle Shazly Gamal
Mohsin Kazi
Dissolution improvement of solid self-emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption material
Acta Pharmaceutica
self-emulsifying/nanoemulsifying drug delivery systems
fenofibrate
in vitro dissolution test
solidification technique
adsorption
title Dissolution improvement of solid self-emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption material
title_full Dissolution improvement of solid self-emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption material
title_fullStr Dissolution improvement of solid self-emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption material
title_full_unstemmed Dissolution improvement of solid self-emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption material
title_short Dissolution improvement of solid self-emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption material
title_sort dissolution improvement of solid self emulsifying drug delivery systems of fenofi brate using an inorganic high surface adsorption material
topic self-emulsifying/nanoemulsifying drug delivery systems
fenofibrate
in vitro dissolution test
solidification technique
adsorption
url https://doi.org/10.1515/acph-2015-0003
work_keys_str_mv AT shazlygamal dissolutionimprovementofsolidselfemulsifyingdrugdeliverysystemsoffenofibrateusinganinorganichighsurfaceadsorptionmaterial
AT mohsinkazi dissolutionimprovementofsolidselfemulsifyingdrugdeliverysystemsoffenofibrateusinganinorganichighsurfaceadsorptionmaterial