Fe3O4/Au/porous Au nanohybrid for efficient delivery of doxorubicin as a model drug

被引:3
|
作者
Hakimian, Fatemeh [1 ]
Haghiralsadat, Bibi Fatemeh [2 ]
Hadian-Ghazvini, Samaneh [1 ]
Azizi, Marzieh [1 ]
Ghourchian, Hedayatollah [1 ]
机构
[1] Univ Tehran, Inst Biochem & Biophys, Lab Bioanal, Tehran, Iran
[2] Shahid Sadoughi Univ Med Sci, Yazd Reprod Sci Inst, Med Nanotechnol & Tissue Engn Res Ctr, Yazd, Iran
关键词
Doxorubicin; Fe3O4/Au/porous Au nanohybrids; Drug delivery; MCF-7; cells; IRON-OXIDE NANOPARTICLES; MAGNETIC NANOPARTICLES; FE3O4; NANOPARTICLES; GOLD NANOPARTICLES; ENHANCEMENT; STABILITY; SYSTEMS;
D O I
10.1007/s00604-023-05685-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Fe3O4/Au/porous Au nanohybrids being bi-functional nanoparticles with magnetic properties and high porosity, were synthesized and used for drug delivery. To achieve this purpose, after Fe3O4 nanoparticles synthesis, a gold layer coats them to increase their stability. Then, to improve the loading capacity of Fe3O4/Au nanoparticles, a shell of porous gold was synthesized on the Fe3O4/Au surface by creating an Ag-Au nanohybrid layer on Fe3O4/Au and dissolving the metallic silver atoms in HNO3 (0.01 M). The DLS results show that the synthesized nanohybrid has an average size of 68.0 +/- 7.7 nm and a zeta potential of - 28.1 +/- 0.2 mV. Finally, doxorubicin (DOX), as a pharmaceutical agent, was loaded onto the Fe3O4/Au/porous Au nanohybrids. The prepared nano-drug enhanced the therapeutic efficacy of DOX on MCF-7 cancer cells compared to the free DOX. These results confirmed a 1.5 times improvement in the antitumor activity of DOX-loaded Fe3O4/Au/porous Au nanohybrids.
引用
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页数:9
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