2017
Hyaluronan polymeric micelles for topical drug delivery
ŠMEJKALOVÁ, Daniela; Kristina NEŠPOROVÁ; Tomáš MUTHNÝ; Martina HERMANNOVÁ; Eva ACHBERGEROVÁ et al.Základní údaje
Originální název
Hyaluronan polymeric micelles for topical drug delivery
Autoři
ŠMEJKALOVÁ, Daniela; Kristina NEŠPOROVÁ; Tomáš MUTHNÝ; Martina HERMANNOVÁ; Eva ACHBERGEROVÁ; Gloria HUERTA-ANGELES; Marek SVOBODA; Martin ČEPA; Veronika MACHALOVÁ; Dominika LUPTÁKOVÁ a Vladimír VELEBNÝ
Vydání
Carbohydrate Polymers, Oxford, ELSEVIER SCI LTD, 2017, 0144-8617
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30105 Physiology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 5.158
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14310/17:00108671
Organizační jednotka
Přírodovědecká fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Skin penetration; Polymeric micelle; Hyaluronan
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 11. 5. 2020 11:20, Mgr. Marie Novosadová Šípková, DiS.
Anotace
V originále
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.