Enhancement of the Skin-Protective Activities of Centella asiatica L. Urban by a Nano-encapsulation Process

Aqueous extracts of Centella asiatica L. Urban were encapsulated by an edible biopolymer, gelatin, which has no effect on their cosmetic activities. The nanoparticles were w/o-type spherical liposomes that had an average diameter of 115.0nm. The encapsulation efficiency was estimated to be approxima...

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Veröffentlicht in:Journal of biotechnology 2012-01, Vol.157 (1), p.100-106
Hauptverfasser: Kwon, Min Chul, Choi, Woon Yong, Seo, Yong Chang, Kim, Ji Seon, Yoon, Chang Soon, Lim, Hye Won, Kim, Hack Soo, Ahn, Ju hee, Lee, Hyeon Yong
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Sprache:eng
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Zusammenfassung:Aqueous extracts of Centella asiatica L. Urban were encapsulated by an edible biopolymer, gelatin, which has no effect on their cosmetic activities. The nanoparticles were w/o-type spherical liposomes that had an average diameter of 115.0nm. The encapsulation efficiency was estimated to be approximately 67%, which was relatively high for these aqueous extracts. The nanoparticles showed lower cytotoxicity (10%) in human skin fibroblast cells than the unencapsulated crude extract (15%) at 1.0mg/ml, this was possibly because a smaller amount of the extract was present in the nanoparticles. The nanoparticles efficiently reduced the expression of matrix metalloproteinase (MMP)-1 in UV-irradiated cells from 136.1% to 77.6% (UV-irradiated control) and inhibited hyaluronidase expression (>60%) at a concentration of 0.5mg/ml, which was higher than the levels produced by the unencapsulated crude extracts. The nanoparticles had a very high flux through mouse skin and also remained at relatively large concentrations in the derma when compared to the unencapsulated crude extracts. These results clearly indicate that the skin-protective activities of C. asiatica were significantly improved through the nano-encapsulation process. These findings also imply that a crude extract can be used and have the same efficacy as purified compounds, which should reduce the purification process and production costs.
ISSN:0168-1656
1873-4863
DOI:10.1016/j.jbiotec.2011.08.025