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Ozcan, Ipek; Azizoglu, Erkan; Senyigit, Taner; Ozyazici, Mine; Ozer, Ozgen
<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd"> <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/11931</identifier> <creators> <creator> <creatorName>Ozcan, Ipek</creatorName> <givenName>Ipek</givenName> <familyName>Ozcan</familyName> <affiliation>Ege Univ, Fac Pharm, Dept Pharmaceut Technol, TR-35100 Izmir, Turkey</affiliation> </creator> <creator> <creatorName>Azizoglu, Erkan</creatorName> <givenName>Erkan</givenName> <familyName>Azizoglu</familyName> <affiliation>Ege Univ, Fac Pharm, Dept Pharmaceut Technol, TR-35100 Izmir, Turkey</affiliation> </creator> <creator> <creatorName>Senyigit, Taner</creatorName> <givenName>Taner</givenName> <familyName>Senyigit</familyName> <affiliation>Ege Univ, Fac Pharm, Dept Pharmaceut Technol, TR-35100 Izmir, Turkey</affiliation> </creator> <creator> <creatorName>Ozyazici, Mine</creatorName> <givenName>Mine</givenName> <familyName>Ozyazici</familyName> <affiliation>Ege Univ, Fac Pharm, Dept Pharmaceut Technol, TR-35100 Izmir, Turkey</affiliation> </creator> <creator> <creatorName>Ozer, Ozgen</creatorName> <givenName>Ozgen</givenName> <familyName>Ozer</familyName> <affiliation>Ege Univ, Fac Pharm, Dept Pharmaceut Technol, TR-35100 Izmir, Turkey</affiliation> </creator> </creators> <titles> <title>Enhanced Dermal Delivery Of Diflucortolone Valerate Using Lecithin/Chitosan Nanoparticles: In-Vitro And In-Vivo Evaluations</title> </titles> <publisher>Aperta</publisher> <publicationYear>2013</publicationYear> <dates> <date dateType="Issued">2013-01-01</date> </dates> <resourceType resourceTypeGeneral="Text">Journal article</resourceType> <alternateIdentifiers> <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/11931</alternateIdentifier> </alternateIdentifiers> <relatedIdentifiers> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.2147/IJN.S40519</relatedIdentifier> </relatedIdentifiers> <rightsList> <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights> <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights> </rightsList> <descriptions> <description descriptionType="Abstract">The objective of this study was to prepare a suitable formulation for dermal delivery of diflucortolone valerate (DFV) that would maintain the localization in skin layers without any penetration and to optimize efficiency of DFV. Drug-loaded lecithin/chitosan nanoparticles with high entrapment efficiency (86.8%), were successfully prepared by ionic interaction technique. Sustained release of DFV was achieved without any initial burst release. Nanoparticles were also incorporated into chitosan gel at different ratios for preparing a more suitable formulation for topical drug delivery with adequate viscosity. In ex-vivo permeation studies, nanoparticles increased the accumulation of DFV especially in the stratum corneum + epidermis of rat skin without any significant permeation. Retention of DFV from nanoparticle in chitosan gel formulation (0.01%) was twofold higher than commercial cream, although it contained ten times less DFV. Nanoparticles in gel formulations produced significantly higher edema inhibition in rats compared with commercial cream in in-vivo studies. Skin blanching assay using a chromameter showed vasoconstriction similar to that of the commercial product. There were no barrier function changes upon application of nanoparticles. In-vitro and in-vivo results demonstrated that lecithin/chitosan nanoparticles in chitosan gel may be a promising carrier for dermal delivery of DFV in various skin disorders.</description> </descriptions> </resource>
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