首页> 外文期刊>Journal of nanoparticle research: An interdisciplinary forum for nanoscale science and technology >Dual functions of polyvinyl alcohol (PVA): Fabricating particles and electrospinning nanofibers applied in controlled drug release
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Dual functions of polyvinyl alcohol (PVA): Fabricating particles and electrospinning nanofibers applied in controlled drug release

机译:Dual functions of polyvinyl alcohol (PVA): Fabricating particles and electrospinning nanofibers applied in controlled drug release

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The fabrication of submicron size microsphere from 8-Phe-4 poly(ester amide) (PEA) using polyvinyl alcohol (PVA) as the emulsion was reported. The biodegradable microspheres were prepared by an oil-in-water emulsion/solvent evaporation technique, and PVA was used as the emulsion. Furthermore, the emulsion PVA was electrospun into nanofibrous mats, and 8-Phe-4 PEA microspheres were entrapped in the resultant mats. The dual functions of PVA to fabricate ideal nanofibrous mats which can entrap microspheres in them and to obtain 8-Phe-4 microspheres as emulsion in their potential application were demonstrated. The anti-cancer drug doxorubicin (DOX) was encapsulated in the 8-Phe-4 amino acid-based PEA microspheres and the entrapment efficiency is almost 100 . At the same time, the DOX can be controlled released in PBS solution and in α-chymotrypsin solution. The cytotoxicity of PVA, PVA mats-entrapped 8-Phe-4 microspheres and PVA mats-entrapped DOX-loaded 8-Phe-4 microspheres, was investigated. Hela cells were used to test the cytotoxicity of the DOX that released from the PVA mats-entrapped DOX-loaded 8-Phe-4 microspheres for 2 days, and the cell viability is below 30 when the 8-Phe-4 microspheres concentration is 1 mg/mL. It demonstrated that the PVA mats-entrapped DOX-loaded 8-Phe-4 microspheres have a potential biomedical application. Graphical Abstract: The table of contents: DOX-loaded microspheres can be encapsulated in the PVA fibers by electrospinning and the DOX can be controlled released from the PVA fibers-entrapped microspheres. MTT assay indicated that the more than 70 Hela cells were killed by the DOX released from DOX-loaded microspheres encapsulated in the PVA after 48 h. Figure not available: see fulltext.

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