Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8012388 | Materials Letters | 2018 | 10 Pages |
Abstract
Methoxy poly(ethylene glycol)-poly(ε-caprolactone) (MePEG-PCL) nanoparticles (NPs) were fabricated using an emulsion solvent evaporation technique, aiming at improving the limited clinical application of Saikosaponin-a (SSa) due to its poor water solubility and hemolysis. The mean diameter of SSa loaded MePEG-PCL NPs (MePEG-PCL@SSa) were determined to be 97.02â¯Â±â¯1.17â¯nm. The results of 1H NMR confirmed the core-shell structure of NPs. In vitro release of SSa from MePEG-PCL@SSa NPs was a sustained manner with no apparent initial drug burst. The hemolysis and cytotoxicity of MePEG-PCL@SSa were investigated with Red Blood Cells (RBC) and bEnd.3 cells, respectively. The results displayed that hemolysis reduced greatly (3.26â¯Â±â¯0.17% at high NPs concentration), and the cytotoxicity was not seriously observed. Our findings provided a promising method to develop a SSa formulation for the potential clinical application.
Related Topics
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Materials Science
Nanotechnology
Authors
Mi Zhou, Wei Xie, Yu Hong, Ning Deng, Yezhao Wang, Yabin Zhu,