Development of phyllanthin containing microcapsules and their improved biological activity towards skin cells and Staphylococcus aureus

Chitosan based microcapsule which encapsulated with phyllanthin was developed by simple coacervation. The composition and surface morphology of phyllanthin containing microcapsules were analyzed by Fourier Transform Infrared spectroscopy and Scanning Electron Microscopy, respectively. The release of...

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Published in:Bioorganic & medicinal chemistry letters Vol. 22; no. 1; pp. 468 - 471
Main Authors: Lam, Pik-Ling, Gambari, Roberto, Yip, Joanne, Yuen, Marcus Chun-Wah, Lam, Kim-Hung, Wong, Raymond Siu-Ming, Wang, Xiao-Wen, Tang, Johnny Cheuk-On, Kok, Stanton Hon-Lung, Chui, Chung-Hin
Format: Journal Article
Language:English
Published: Amsterdam Elsevier Ltd 01-01-2012
Elsevier
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Summary:Chitosan based microcapsule which encapsulated with phyllanthin was developed by simple coacervation. The composition and surface morphology of phyllanthin containing microcapsules were analyzed by Fourier Transform Infrared spectroscopy and Scanning Electron Microscopy, respectively. The release of phyllanthin from the microcapsules was found to be more than 60% after 120h. In vitro biological assays demonstrated that these phyllanthin containing microcapsules showed a stronger anti-oxidation potential on both human fibroblasts and keratinocytes as well as a better growth inhibitory activity towards Staphylococcus aureus. Chitosan based microcapsule which encapsulated with phyllanthin was developed by simple coacervation. The composition and surface morphology of phyllanthin containing microcapsules were analyzed by Fourier Transform Infrared spectroscopy and Scanning Electron Microscopy, respectively. The release of phyllanthin from the microcapsules was found to be more than 60% after 120h. In vitro biological assays demonstrated that these phyllanthin containing microcapsules showed a stronger anti-oxidation potential on both human fibroblasts and keratinocytes as well as a better growth inhibitory activity towards Staphylococcus aureus.
Bibliography:http://dx.doi.org/10.1016/j.bmcl.2011.10.097
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ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2011.10.097