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Nanocapsules based on mPEGylated artesunate prodrug and its cytotoxicity

  • Haijing Meng
  • , Ke Xu
  • , Yanyun Xu
  • , Ping Luo
  • , Fang Du
  • , Jin Huang
  • , Wei Lu
  • , Jiahui Yu*
  • , Shiyuan Liu
  • , Ben Muir
  • *此作品的通讯作者
  • East China Normal University
  • Wuhan University of Technology
  • Changzheng Hospital
  • CSIRO

科研成果: 期刊稿件文章同行评审

摘要

mPEGylated artesunate prodrug was synthesized via esterification between poly(ethylene glycol) monomethyl ether (mPEG) and artesunate (ART). The product was inclined to form nanocapsules in aqueous media due to its amphiphilic nature. These nanocapsules showed narrow size distribution, with an average particle size of 88.7. nm measured by dynamic laser scattering (DLS). Their vesical morphology was further confirmed by transmission electron microscopy (TEM). We found that the release of ART from the nanocapsules was controllable, which was contributed to the easily hydrolyzed property of the ester bond. In addition, the cytotoxicity of the prodrug against L1210 and MCF7 cell lines showed an essential decrease compared with the free ART. These results present a new strategy in designing anti-tumor ART nanocapsules for targeting tumor cells.

源语言英语
页(从-至)164-169
页数6
期刊Colloids and Surfaces B: Biointerfaces
115
DOI
出版状态已出版 - 1 3月 2014

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