Diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery system

Solid lipid nanoparticles (SLNs) are promising delivery carriers that have been utilized for formulation and delivery of various drugs. For topical administration, they are usually incorporated into gel or cream to increase their residence time, which is time-consuming process and could affect their...

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Main Authors: Fatma S. Abdel-Salam, Seham A. Elkheshen, Azza A. Mahmoud, Hussein O. Ammar
Format: Article
Language:English
Published: Faculty of Pharmacy, Cairo University 2016-06-01
Series:Bulletin of Faculty of Pharmacy Cairo University
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1110093115000472
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author Fatma S. Abdel-Salam
Seham A. Elkheshen
Azza A. Mahmoud
Hussein O. Ammar
author_facet Fatma S. Abdel-Salam
Seham A. Elkheshen
Azza A. Mahmoud
Hussein O. Ammar
author_sort Fatma S. Abdel-Salam
collection DOAJ
description Solid lipid nanoparticles (SLNs) are promising delivery carriers that have been utilized for formulation and delivery of various drugs. For topical administration, they are usually incorporated into gel or cream to increase their residence time, which is time-consuming process and could affect their stability and characteristics. Preparation of solid lipid nanoparticles based semisolid formulations could have potential pharmaceutical applications. The aim of this study was to formulate the corticosteroidal drug, diflucortolone valerate (DFV) into topical semisolid SLN formulations using a rapid cheap one-step process. SLN formulations were developed using a high-shear homogenization combined with sonication, using different types of solid lipids (e.g., Geleol®, Precirol® ATO5, Tristearin® and Compritol® 888ATO) and Poloxamer® 407 as a surfactant. Selection of the lipids and using high lipid concentration were the key elements to get semisolid formulation immediately after sonication without incorporating the nanoparticles into a gel or a cream base. DFV SLN formulations possessed average particle size ranging from 203.71 ± 5.61 to 1421.00 ± 16.32 nm with a narrow size distribution and possessed shear thinning behavior. Incorporation of lipid based surfactants (Labrasol® or Labrafil®) was found to significantly increase DFV encapsulation efficiency (up to 45.79 ± 4.40%). Semisolid DFV-loaded SLN with high drug encapsulation efficiency and acceptable rheological behavior for topical preparation could be prepared in a one-step process.
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spelling doaj.art-31b4f953b2a941c4b461f78b3fc0557b2023-01-02T10:44:06ZengFaculty of Pharmacy, Cairo UniversityBulletin of Faculty of Pharmacy Cairo University1110-09312016-06-015411710.1016/j.bfopcu.2015.11.002Diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery systemFatma S. Abdel-Salam0Seham A. Elkheshen1Azza A. Mahmoud2Hussein O. Ammar3Egyptian Patent Office, Academy of Research and Technology, Cairo, EgyptDepartment of Pharmaceutics, Faculty of Pharmacy, Cairo University, Cairo, EgyptDepartment of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt, Cairo, EgyptDepartment of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt, Cairo, EgyptSolid lipid nanoparticles (SLNs) are promising delivery carriers that have been utilized for formulation and delivery of various drugs. For topical administration, they are usually incorporated into gel or cream to increase their residence time, which is time-consuming process and could affect their stability and characteristics. Preparation of solid lipid nanoparticles based semisolid formulations could have potential pharmaceutical applications. The aim of this study was to formulate the corticosteroidal drug, diflucortolone valerate (DFV) into topical semisolid SLN formulations using a rapid cheap one-step process. SLN formulations were developed using a high-shear homogenization combined with sonication, using different types of solid lipids (e.g., Geleol®, Precirol® ATO5, Tristearin® and Compritol® 888ATO) and Poloxamer® 407 as a surfactant. Selection of the lipids and using high lipid concentration were the key elements to get semisolid formulation immediately after sonication without incorporating the nanoparticles into a gel or a cream base. DFV SLN formulations possessed average particle size ranging from 203.71 ± 5.61 to 1421.00 ± 16.32 nm with a narrow size distribution and possessed shear thinning behavior. Incorporation of lipid based surfactants (Labrasol® or Labrafil®) was found to significantly increase DFV encapsulation efficiency (up to 45.79 ± 4.40%). Semisolid DFV-loaded SLN with high drug encapsulation efficiency and acceptable rheological behavior for topical preparation could be prepared in a one-step process.http://www.sciencedirect.com/science/article/pii/S1110093115000472TopicalHigh shear homogenizationCorticosteroidDiflucortolone valerateSolid lipid nanoparticles
spellingShingle Fatma S. Abdel-Salam
Seham A. Elkheshen
Azza A. Mahmoud
Hussein O. Ammar
Diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery system
Bulletin of Faculty of Pharmacy Cairo University
Topical
High shear homogenization
Corticosteroid
Diflucortolone valerate
Solid lipid nanoparticles
title Diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery system
title_full Diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery system
title_fullStr Diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery system
title_full_unstemmed Diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery system
title_short Diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery system
title_sort diflucortolone valerate loaded solid lipid nanoparticles as a semisolid topical delivery system
topic Topical
High shear homogenization
Corticosteroid
Diflucortolone valerate
Solid lipid nanoparticles
url http://www.sciencedirect.com/science/article/pii/S1110093115000472
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AT azzaamahmoud diflucortolonevalerateloadedsolidlipidnanoparticlesasasemisolidtopicaldeliverysystem
AT husseinoammar diflucortolonevalerateloadedsolidlipidnanoparticlesasasemisolidtopicaldeliverysystem