کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4982709 | 1454243 | 2018 | 8 صفحه PDF | دانلود رایگان |
- The nano-sized PLA-PEG particles were efficiently prepared by using coaxial tri-capillary electrospray-template removal method.
- Caveolae-mediated endocytosis was one of endocytosis pathways in A549 cells for PLA-PEG nanoparticles.
- Clathrin mediated endocytosis was not involved in the endocytosis process.
- The endocytosed PLA-PEG nanoparticles enriched in the head of A549 cells.
- A small amount of PLA-PEG nanoparticles was transported into lysosome after 24Â h incubation.
The nano-sized poly(lactic acid)-poly(ethylene glycol) (PLA-PEG) particles with core-shell structure were efficiently prepared by using coaxial tri-capillary electrospray-template removal method. The cellular uptake mechanism, intracellular distribution and exocytosis in A549 cell model of electrosprayed PLA-PEG nanoparticles were systemically studied. The drug release behavior of electrosprayed PLA-PEG nanoparticles were also investigated. Our results showed that PLA-PEG nanoparticles can be endocytosed quickly by A549 cells. The cellular uptake of PLA-PEG nanoparticles was an energy dependent endocytosis process. Caveolae-mediated endocytosis was only one of endocytosis pathways in A549 cells for PLA-PEG nanoparticles, while clathrin mediated endocytosis was not involved in the endocytosis process. The endocytosed PLA-PEG nanoparticles enriched in the head of A549 cells and only a small amount of them was transported into lysosome after 24Â h incubation. These findings provided insights into the application of electrosprayed PLA-PEG nanoparticles in nano drug delivery field.
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Journal: Colloids and Surfaces B: Biointerfaces - Volume 161, 1 January 2018, Pages 10-17