A study of the characteristics and in vitro permeation properties of CMC/ chitosan microparticles as a skin delivery system for vitamin E

Authors

  • Juliana Bucchi Alencastre Universidade de São Paulo; Departamento de Ciências Farmacêuticas
  • Maria Vitoria Lopes Badra Bentley Universidade de São Paulo; Departamento de Ciências Farmacêuticas
  • Fabiola Silva Garcia Universidade de São Paulo; Departamento de Ciências Farmacêuticas
  • Maria de Moragas Polígono Industrial San Vicente; IICognis Iberia (Primacare)
  • Joseph Luis Viladot Polígono Industrial San Vicente; IICognis Iberia (Primacare)
  • Juliana Maldonado Marchetti Universidade de São Paulo; Departamento de Ciências Farmacêuticas

DOI:

https://doi.org/10.1590/S1516-93322006000100007

Keywords:

Microparticles, Chitosan, Vitamin E, Skin permeation

Abstract

Carboxymethylcellulose (CMC)/chitosan microparticles containing vitamin E were prepared by a complex coacervation method and their potential use as a topical delivery system was evaluated. Morphology, particle size distribution, encapsulation yield, physical and chemical stability, in vitro release and permeation through skin were studied. The microparticles appeared to be spherical, with a homogeneous surface and were not aggregated. Mean diameters ranged from 2.7 to 7.6 µm and the encapsulation yield was 81%. Chemical stability studies indicated a protection of encapsulated vitamin E, of 8.1% for O/W and of 10.83% for W/O emulsions, following storage at 45 °C for 60 days. Forty-eight% of vitamin E, determined by HPLC, were released within 24 hours. In vitro permeation and retention studies showed a higher penetration rate of vitamin E in the free and encapsulated forms, from the W/O emulsion. The carriers studied seem to be promising systems for topical administration.

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Published

2006-03-01

Issue

Section

Original Papers

How to Cite

A study of the characteristics and in vitro permeation properties of CMC/ chitosan microparticles as a skin delivery system for vitamin E. (2006). Revista Brasileira De Ciências Farmacêuticas, 42(1), 69-76. https://doi.org/10.1590/S1516-93322006000100007