4.7 Article

Bicellar systems as a new colloidal delivery strategy for skin

Journal

COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 92, Issue -, Pages 322-326

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.colsurfb.2011.12.005

Keywords

Bicellar systems; In vitro percutaneous absorption; Diclofenac; Flufenamic acid; Dipalmitoyl-glycero-phosphatidylcholine; Dimyristoyl-glycero-phosphatidylcholine; Dihexanoyl-glycero-phosphatidylcholine; Cryo-transmission electron microscopy

Funding

  1. CICYT [CTQ 2010-16964]
  2. Generalitat de Catalunya [SGR 1212]
  3. European Social Fund (Programa Nacional de Potenciacion de Recursos Humanos del Plan Nacional de I+D+I)
  4. CSIC
  5. FSE

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The presented work evaluates the use of bicellar systems as new delivery vectors for controlled release of compounds through the skin. Two different active principles were introduced into the bicellar systems: diclofenac diethylamine (DDEA) and flufenamic acid (Ffa). Bicellar systems are discoidal aggregates formed by long and short alkyl chain phospholipids. Characterization of the bicellar systems by dynamic light scattering (DLS) and cryogenic transmission electron microscopy (Cryo-TEM) showed that particle size decreased when DDEA was encapsulated and increased when Ffa was included in the bicellar systems. Percutaneous absorption studies demonstrated a lower penetration of DDEA and Ffa through the skin when the drugs were included in the bicellar systems than when the drugs were applied in an aqueous solution (DDEA) and in an ethanolic solution (Ffa); the reduction in penetration was more pronounced with Ffa. These bicellar systems may have retardant effects on percutaneous absorption, which result in a promising strategy for future drug or cosmetic delivery applications. (C) 2011 Elsevier B.V. All rights reserved.

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