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Hyaluronan polymeric micelles for topical drug delivery

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dc.title Hyaluronan polymeric micelles for topical drug delivery en
dc.contributor.author Šmejkalová, Daniela
dc.contributor.author Muthný, Tomáš
dc.contributor.author Nešporová, Kristina
dc.contributor.author Hermannová, Martina
dc.contributor.author Achbergerová, Eva
dc.contributor.author Huerta-Angeles, Gloria
dc.contributor.author Svoboda, Marek
dc.contributor.author Čepa, Martin
dc.contributor.author Machalová, Veronika
dc.contributor.author Luptáková, Dominika
dc.contributor.author Velebný, Vladimír
dc.relation.ispartof Carbohydrate Polymers
dc.identifier.issn 0144-8617 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2017
utb.relation.volume 156
dc.citation.spage 86
dc.citation.epage 96
dc.type article
dc.language.iso en
dc.publisher Pergamon Elsevier Science Ltd.
dc.identifier.doi 10.1016/j.carbpol.2016.09.013
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0144861716310670
dc.subject Hyaluronan en
dc.subject Polymeric micelle en
dc.subject Skin penetration en
dc.description.abstract Nanosized materials offer promising strategy for topical drug delivery due to their enhancing effect on drug percutaneous transport across the stratum corneum barrier. In this work, polymeric micelles made from hydrophobized hyaluronic acid (HA) were probed for skin delivery. Compared to non-polymeric micelle solutions containing similar drug amount, in vitro skin penetration analysis indicated 3 times larger deposition of drug in the epidermis and 6 times larger drug deposition in the dermis after 5 h of topical treatment in Franz diffusion cells. The drug deposition was further increased with prolonged time of topical treatment. Laser confocal microscopy revealed the accumulation of both, the HA forming the vehicle and the payload, in the epidermis and dermis. Although fluorescent labeling of the HA would suggest co-transport of the HA and the drug, loading FRET pair dyes in the micellar core clearly demonstrated gradual micelle disruption with increasing skin depth. Transcellular penetration was the predominant pathway for the loaded drug. The HA polymeric micelles also demonstrated increased bioactivity of loaded compound in vitro and in vivo. In addition, the loaded micelles were found to be stable in cream formulations and thus they have great potential for topical applications for cosmetic and pharmaceutical purposes. © 2016 en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1006625
utb.identifier.obdid 43877127
utb.identifier.scopus 2-s2.0-84986286533
utb.identifier.wok 000388110900011
utb.identifier.coden CAPOD
utb.source j-scopus
dc.date.accessioned 2016-10-25T12:37:59Z
dc.date.available 2016-10-25T12:37:59Z
dc.description.sponsorship Internal Funding Agency of the Tomas Bata University in Zlin [IGA/FT/2016/001]
utb.contributor.internalauthor Achbergerová, Eva
utb.fulltext.affiliation Daniela Smejkalová a, Tomáš Muthný a , Kristina Nešporová a,b,∗ , Martina Hermannová a , Eva Achbergerová a,c, Gloria Huerta-Angeles a , Marek Svoboda a,d , Martin Čepa a , Veronika Machalová a , Dominika Luptáková e,f , Vladimír Velebný a Contipro a.s., Dolní Dobrouč, Czech Republic b Institute of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech Republic c Faculty of Technology, Department of Chemistry, Tomas Bata University in Zlín, Zlín, Czech Republic d Department of Biological and Biochemical Sciences, Faculty of Chemical-Technology, University of Pardubice, Pardubice, Czech Republic e Institute of Microbiology of the CAS, v.v.i., Prague, Czech Republic f Department of Pharmacology, Jessenius Faculty of Medicine, Comenius University Bratislava, BioMed Martin, Slovakia ∗ Corresponding author at: Dolní Dobrouč 401, Dolni Dobrouč, Czech Republic. E-mail address: kristina.nesporova@contipro.com (K. Nešporová).
utb.fulltext.dates Received 8 August 2016 Received in revised form 30 August 2016 Accepted 4 September 2016 Available online 5 September 2016
utb.fulltext.sponsorship The authors are thankful to Miroslava Brunclikova from Academy of Science (Institute of Macromolecular Chemistry, Prague) for Golden Gate-ATR analysis. This work was supported by the Internal Funding Agency of the Tomas Bata University in Zlín under Grant IGA/FT/2016/001.
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