Storage stability and skin permeation of vitamin C liposomes improved by pectin coating

Colloids Surf B Biointerfaces. 2014 May 1:117:330-7. doi: 10.1016/j.colsurfb.2014.02.036. Epub 2014 Mar 2.

Abstract

A transdermal drug delivery system was prepared by high methoxyl pectin (HMP) or low methoxyl pectin (LMP) coated vitamin C liposomes. HMP coated vitamin C liposomes (HMP-L) and LMP coated vitamin C liposomes (LMP-L) exhibited an increase in average diameter (from 66.9 nm to 117.3 nm and 129.6 nm, respectively), a decrease in zeta potential (from -2.3 mV to -23.9 mV and -35.5 mV, respectively), and a similar entrapment efficiency (48.3-50.1%). Morphology and FTIR analysis confirmed that pectin was successfully coated on the surface of vitamin C liposomes mainly through the hydrogen bonding interactions. Besides, HMP-L and LMP-L exhibited an obvious improvement in storage stability, with lower aggregation, oxidation of lipid and leakage ratio of vitamin C from liposomes, and LMP-L showed better physicochemical stability than HMP-L. Moreover, skin permeation of vitamin C was improved 1.7-fold for HMP-L and 2.1-fold for LMP-L after 24 h, respectively, compared with vitamin C nanoliposomes. Therefore, this study suggested that pectin coated liposomes, especially the LMP-L, could be a promising transdermal drug delivery system with better storage stability and skin permeation.

Keywords: Liposomes; Pectin; Skin permeation; Storage stability; Vitamin C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ascorbic Acid / pharmacology*
  • Coated Materials, Biocompatible / pharmacology*
  • Drug Stability
  • Liposomes
  • Male
  • Mice, Inbred BALB C
  • Microscopy, Atomic Force
  • Particle Size
  • Pectins / pharmacology*
  • Skin Absorption / drug effects*
  • Spectroscopy, Fourier Transform Infrared
  • Static Electricity

Substances

  • Coated Materials, Biocompatible
  • Liposomes
  • Pectins
  • Ascorbic Acid