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dc.contributor.authorShokri, J
dc.contributor.authorHasanzadeh, D
dc.contributor.authorGhanbarzadeh, S
dc.contributor.authorDizadji-Ilkhchi, M
dc.contributor.authorAdibkia, K
dc.date.accessioned2018-08-26T09:38:36Z
dc.date.available2018-08-26T09:38:36Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/58215
dc.description.abstractBackground: There is a serious concern about the topical and systemic absorption of organic ultraviolet filters in sunscreen formulations and subsequent phototoxic and photo allergic reactions. Ideally, a sunscreen should localize in the surface of stratum corneum and create a barrier against UV radiation, but not penetrate into the underlying viable tissues and systemic circulation. Purpose: The objective of the present study was to determine the effects of ?-cyclodextrin (?-CDX) complexation on the transdermal penetration of 3 commonly used sun blocking agents, Eusolex 4360 (avobenzone), Eusolex 9020 (Oxybenzone) and Eusolex 232 (Ensulizole). Methods: The complexation of the sunscreen agents with ?-CDX was performed by 3 methods and confirmed by differential scanning calorimetry (DSC). Sunscreens, and their physical mixtures and complexes with ?-CDX were introduced into a model cream base (o/w emulsion). To find out the influence of ?-CDX, sunscreen creams were applied to the rat skin in vitro in standard Franz diffusion cells and the amount of sunscreen permeated after 6 h was assessed by HPLC. Results: The skin penetration flux of the UV filters was significantly reduced (4-15 fold) by complexation with ?-CDX. Complexation also could prolong absorption lag time of sun blocking agents to more than 150 min. Conclusion: Considering the ability of ?-CDX complexation in the reduction of flux and enhancement ratio as well as prolongation of absorption lag time, this technique could be very helpful for reducing systemic absorption of the UV filters and subsequent toxicity and allergic reaction. © Georg Thieme Verlag KG Stuttgart · New York.
dc.language.isoEnglish
dc.relation.ispartofDrug Research
dc.subjectavobenzone
dc.subjectbeta cyclodextrin
dc.subjectensulizole
dc.subjecteusolex 9020
dc.subjectoxybenzone
dc.subjectunclassified drug
dc.subjectanimal experiment
dc.subjectarticle
dc.subjectcomplex formation
dc.subjectdifferential scanning calorimetry
dc.subjectdrug absorption
dc.subjectdrug distribution
dc.subjectdrug effect
dc.subjectdrug mixture
dc.subjectdrug potentiation
dc.subjecthigh performance liquid chromatography
dc.subjectin vitro study
dc.subjectlag
dc.subjectmale
dc.subjectnonhuman
dc.subjectrat
dc.subjectskin absorption
dc.subjectskin penetration
dc.subjectskin permeability
dc.subjecttime
dc.subjectultraviolet radiation
dc.subjectAnimals
dc.subjectBenzimidazoles
dc.subjectBenzophenones
dc.subjectbeta-Cyclodextrins
dc.subjectChemistry, Pharmaceutical
dc.subjectMale
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectSkin Absorption
dc.subjectSulfonic Acids
dc.subjectSunscreening Agents
dc.titleThe effect of beta-cyclodextrin on percutaneous absorption of commonly used Eusolex sunscreens
dc.typeArticle
dc.citation.volume63
dc.citation.issue11
dc.citation.spage591
dc.citation.epage596
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1055/s-0033-1349089


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