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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. |