101. Effects of surface modification of As 2 O 3 -loaded PLGA nanoparticles on its anti-liver cancer ability: An in vitro and in vivo study
- Author
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Juan You, Caifeng Yan, Xiaoli Song, and Hongxia Shao
- Subjects
inorganic chemicals ,education ,Nanoparticle ,macromolecular substances ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,chemistry.chemical_compound ,Colloid and Surface Chemistry ,In vivo ,PEG ratio ,Physical and Theoretical Chemistry ,health care economics and organizations ,Chemistry ,technology, industry, and agriculture ,Surfaces and Interfaces ,General Medicine ,021001 nanoscience & nanotechnology ,In vitro ,0104 chemical sciences ,PLGA ,Covalent bond ,Drug delivery ,Surface modification ,0210 nano-technology ,Biotechnology ,Nuclear chemistry - Abstract
As2O3-loaded nanoparticles (NPs) based on poly (lactic-co-glycolic acid) (PLGA) were prepared by double emulsion-solvent evaporation method. Then Lactose acid (LA) and/or PEG were modified onto the NPs by chemical covalent coupling through -NH2 and -COOH. The FTIR results showed that LA and PEG could be successfully modified onto the surface of the NPs. All the As2O3-loaded PLGA NPs (As2O3@PLGA NPs) presented suitable physical stability, favorable size, and spherical shape. The in vitro release rate of As2O3 from the NPs depended on the surface of the NPs. As expected, the As2O3@PLGA-PEG/LA NPs showed a moderate release rate, the highest anticancer effects and cellular internalization against SMMC-7721 cell line. The PLGA-PEG/LA NPs could represent an effective nano-size delivery system of As2O3 for treatment of liver cancer.
- Published
- 2018