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Storage stability and skin permeation of vitamin C liposomes improved by pectin coating
- Zhou, Wei, Liu, Wei, Zou, Liqiang, Liu, Weilin, Liu, Chengmei, Liang, Ruihong, Chen, Jun
- Colloids and Surfaces B: Biointerfaces 2014 v.117 pp. 330-337
- Fourier transform infrared spectroscopy, ascorbic acid, coatings, colloids, drug delivery systems, hydrogen bonding, lipid peroxidation, pectins, storage quality, zeta potential
- 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 66.9nm to 117.3nm and 129.6nm, respectively), a decrease in zeta potential (from −2.3mV to −23.9mV and −35.5mV, 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 24h, 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.