Multifunctional Fe3O4@SiO2-CDs magnetic fluorescent nanoparticles as effective carrier of gambogic acid for inhibiting VX2 tumor cells
This paper reports a dual-functional platform that can be used for synergistic therapy, including drug release and magnetic targeting. The platform is realized through an amide reaction between high-fluorescence carbon quantum dots (CD) prepared by microwave method and amino-functional Fe3O4@SiO2 wi...
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Veröffentlicht in: | Journal of molecular liquids 2021-04, Vol.327, p.114783, Article 114783 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This paper reports a dual-functional platform that can be used for synergistic therapy, including drug release and magnetic targeting. The platform is realized through an amide reaction between high-fluorescence carbon quantum dots (CD) prepared by microwave method and amino-functional Fe3O4@SiO2 with high saturation magnetic strength and a core-shell structure to obtain multifunctional magnetic fluorescent nanocomposite particles Fe3O4@SiO2-CDs. The structure, drug release behavior, cytotoxicity, fluorescence and distribution in vivo of Fe3O4@SiO2-CDs nanoparticles were studied. The results show that the Fe3O4@SiO2-CDs with a dynamic diameter of about 155.0 nm and a magnetic saturation intensity of 31.2 emu/g has a higher loading of gambogic acid (GA), and is more conducive to drug release in an environment of pH = 5.7. In addition, Fe3O4@SiO2-CDs has low cytotoxicity and can enter VX2 cells. However, GA-loaded Fe3O4@SiO2-CDs has an inhibitory effect on VX2 cells, and the cell survival rate is less than 20% at a concentration of 100 μg/mL. Magnetic targeting experiments show that bifunctional magnetic nanoparticles have an outstanding magnetic targeting effect on tumors.
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•Highly magnetized and core-shell structured Fe3O4@SiO2-CDs was synthesized.•Fe3O4@SiO2-CDs has a pH dependency on the releasing of GA.•Fe3O4@SiO2-CDs (GA) loaded with GA had an inhibitory effect on VX2 cells.•Dual-functional nanoparticles have strong magnetic targeting capacity on tumors. |
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ISSN: | 0167-7322 1873-3166 |
DOI: | 10.1016/j.molliq.2020.114783 |