| Literature DB >> 30606527 |
Aline Marquez Cardoso1, Edilene Gadelha de Oliveira1, Karine Coradini1, Franciele Aline Bruinsmann1, Tanira Aguirre2, Ricardo Lorenzoni1, Raquel Cristiane Silva Barcelos3, Karine Roversi3, Domenika Rubert Rossato3, Adriana Raffin Pohlmann4, Sílvia Stanisçuaski Guterres1, Marilise Escobar Burger3, Ruy Carlos Ruver Beck5.
Abstract
Although phenytoin is an antiepileptic drug used in the oral treatment of epilepsy, its off-label use as a cutaneous healing agent has been studied in recent years due to the frequent reports of gingival hyperplasia after oral administration. However, the cutaneous topical application of phenytoin should prevent percutaneous skin permeation. Therefore, the aim of this study was to evaluate the in vitro skin permeation/retention and in vivo effects of nanocapsules and nanoemulsions loaded with phenytoin and formulated as chitosan hydrogels on the healing process of cutaneous wounds in rats. The hydrogels had adequate pH values (4.9-5.6) for skin application, drug content of 0.025% (w/w), and non-Newtonian pseudoplastic rheological behaviour. Hydrogels containing nanocapsules and nanoemulsions enabled improved controlled release of phenytoin and adhesion to skin, compared with hydrogels containing non-encapsulated phenytoin. In vitro skin permeation studies showed that phenytoin permeation to the receptor compartment, and consequently the risk of systemic absorption, may be reduced by nanoencapsulation without any change in the in vivo performance of phenytoin in the wound healing process in rats.Entities:
Keywords: Hydrogels; Nanocapsules; Nanoemulsions; Phenytoin; Skin permeation; Wound healing
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Year: 2018 PMID: 30606527 DOI: 10.1016/j.msec.2018.11.013
Source DB: PubMed Journal: Mater Sci Eng C Mater Biol Appl ISSN: 0928-4931 Impact factor: 7.328