| Literature DB >> 24334269 |
Haijing Meng1, Ke Xu1, Yanyun Xu1, Ping Luo1, Fang Du1, Jin Huang2, Wei Lu1, Jiahui Yu3, Shiyuan Liu4, Ben Muir5.
Abstract
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.Entities:
Keywords: Artesunate; Controllable release; Nanocapsules; Passive targeting; mPEGylation
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Year: 2013 PMID: 24334269 DOI: 10.1016/j.colsurfb.2013.11.039
Source DB: PubMed Journal: Colloids Surf B Biointerfaces ISSN: 0927-7765 Impact factor: 5.268