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Development and application of tumor-targeting magnetic nanoparticles FA-StNP@Fe2O3 for hyperthermia

  • Articles/Material Chemistry
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Chinese Science Bulletin

Abstract

Modified magnetic starch nanoparticles (FA-StNP@Fe2O3) were synthesized by conjugating folic acid (FA-PEG-NH2) onto the surface of magnetic starch nanoparticles (StNP@Fe2O3) prepared by reverse microemulsion method. The synthesized FA-StNP@Fe2O3 was investigated by transmission electron microscopy and zeta potential analysis. The average size of its well dispersed particles was 250 nm. The iron concentration of 2 mg/g was detected by phenanthroline method. Placing FA-StNP@Fe2O3 nanoparticles in the alternating magnetic field for 30 min resulted in an increase in the suspension temperature from ambient temperature (37°C) to a value between 42°C and 43°C. Co-cultured nanoparticles and Hela cell line or normal HUEC-12 cell line, and the biological effects at the cellular level were investigated in the alternating magnetic field using MTT assay, Hochest-PI double staining and flow cytometry analysis. Experimental results showed that FA-StNP@Fe2O3 within acertain concentration range has no obvious effect on cell proliferation. When treated in the magnetic field, apoptosis rate on Hela induced by FA-StNP@Fe2O3 was 13.4%. Prussian blue staining analysis confirmed that the nanoparticles modified with folic acid had improved ability in tumor cell-targeting, and therefore, potential applications in biomedical and magnetocaloric areas. It is expected be applied in tumor targeting therapy in the near future.

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Correspondence to Dan Li or XuanMing Liu.

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Supported by the Key Program for Science and Technology of Hunan Province (Grant No. 03NKY1001) and Key Construction Program of the National “985” Project.

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Zheng, Y., Tong, C., Wang, B. et al. Development and application of tumor-targeting magnetic nanoparticles FA-StNP@Fe2O3 for hyperthermia. Chin. Sci. Bull. 54, 2998–3004 (2009). https://doi.org/10.1007/s11434-009-0422-x

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  • DOI: https://doi.org/10.1007/s11434-009-0422-x

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