Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4982709 | Colloids and Surfaces B: Biointerfaces | 2018 | 8 Pages |
â¢The nano-sized PLA-PEG particles were efficiently prepared by using coaxial tri-capillary electrospray-template removal method.â¢Caveolae-mediated endocytosis was one of endocytosis pathways in A549 cells for PLA-PEG nanoparticles.â¢Clathrin mediated endocytosis was not involved in the endocytosis process.â¢The endocytosed PLA-PEG nanoparticles enriched in the head of A549 cells.â¢A small amount of PLA-PEG nanoparticles was transported into lysosome after 24 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.
Graphical abstractDownload high-res image (152KB)Download full-size image