| Literature DB >> 26456292 |
Hanna Wosicka-Frąckowiak1, Krzysztof Cal2, Justyna Stefanowska3, Eliza Główka1, Magdalena Nowacka4, Wiktoria Struck-Lewicka5, Biljana Govedarica6, Monika Pasikowska7, Renata Dębowska7, Teofil Jesionowski4, Stane Srčič6, Michał Jan Markuszewski5.
Abstract
Particulate drug carriers e.g. nanoparticles (NPs) have been shown to penetrate and accumulate preferentially in skin hair follicles creating high local concentration of a drug. In order to develop such a follicle targeting system we obtained and characterized solid lipid nanoparticles (SLN) loaded with roxithromycin (ROX). The mean particle size (172±2 nm), polydisperisty index (0.237±0.007), zeta potential (-31.68±3.10 mV) and incorporation efficiency (82.1±3.0%) were measured. The long term stability of ROX-loaded SLN suspensions was proved up to 26 weeks. In vitro drug release study was performed using apparatus 4 dialysis adapters. Skin irritation test conducted using the EpiDerm™ tissue model demonstrated no irritation potential for ROX-loaded SLN. Ex vivo human skin penetration studies, employing rhodamine B hexyl ester perchlorate (RBHE) as a fluorescent dye to label the particles, revealed fluorescence deep in the skin, specifically around the hair follicles up to over 1mm depth. The comparison of fluorescence intensities after application of RBHE solution and RBHE-labelled ROX-loaded SLN was done. Then cyanoacrylate follicular biopsies were obtained in vivo and analyzed for ROX content, proving the possibility of penetration to human pilosebaceous units and delivering ROX by using SLN with the size below 200 nm.Entities:
Keywords: Differential stripping; Ex vivo skin penetration; Hair follicles; In vivo skin penetration; Lipid nanoparticles; Roxithromycin
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Year: 2015 PMID: 26456292 DOI: 10.1016/j.ijpharm.2015.09.068
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875