4.8 Article

In vivo dual-targeted chemotherapy of drug resistant cancer by rationally designed nanocarrier

Journal

BIOMATERIALS
Volume 75, Issue -, Pages 71-81

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2015.09.030

Keywords

Nanoparticle; Yolk-shell structure; Combined target effect; In vivo distribution; Drug resistant cancer

Funding

  1. National Natural Science Foundation of China [21571155]
  2. Fundamental Research Funds for the Central Universities [2012XZZX005]

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Multidrug resistance is one of major obstacles to the effective cancer chemotherapy. To address this issue, we developed the effective circumvention of multidrug resistance in cancer cells by a yolk-shell Fe3O4@MgSiO3 nanoplatform with the polymerpoly(ethylene glycol) and folic acid modifications can achieve active targeted delivery of anti-cancer drug by using combined magnetic and ligand targeting. The direct intracellular drug delivery of doxorubicin by nanocarrier was much more effectively than free DOX for multidrug resistant Hep-G2/MDR cancer cells. Besides the excellent biocompatibility, high drug loading efficiency, dual-targeting delivery, and controlled releasing behavior, in vivo experiments demonstrate that this nanocarrier can specifically deliver and concentrate doxorubicin hydrochloride in tumor sites to overcome drug resistance. It follows an alternative strategy for effective chemotherapy against drug resistant cancers by using rationally designed nanomaterial. (C) 2015 Elsevier Ltd. All rights reserved.

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