4.8 Article

A biodegradable MnSiO3@Fe3O4 nanoplatform for dual-mode magnetic resonance imaging guided combinatorial cancer therapy

期刊

BIOMATERIALS
卷 194, 期 -, 页码 151-160

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2018.12.004

关键词

Microenvironment-responsive; Degradable; Combinatorial therapy; Magnetic resonance imaging; Nanotheranostics

资金

  1. Youth Innovation Promotion Association of Chinese Academy of Sciences [2015385]
  2. Science and Technology Major Project of Anhui Province, China [17030701051]
  3. Natural Science Foundation of Anhui Province, China [1808085MB38]
  4. National Natural Science Foundation of China [21407151, 31870969, 81801039]
  5. Anhui Science and Technology Plan Project [1604a0802082, 1401045013]
  6. Anhui Province Funds for Distinguished Young Scientists [1508085J08]
  7. Key Projects of the Outstanding Young Talents in Colleges and Universities [gxyqZD2016058]
  8. Gaofeng Clinical Medicine Grant Support from Shanghai Jiao Tong University School of Medicine [shkw2017]

向作者/读者索取更多资源

In this work, a tumor microenvironment (TME)-responsive biodegradable MnSiO3@Fe3O4 nanoplatform for dual-mode magnetic resonance imaging (MRI)-guided combinatorial cancer therapy was constructed. Fe3O4 nanoparticles decorated on the surface of MnSiO3 could effectively obstruct the pores of MnSiO3 and reduce the leakage of anticancer drugs under physiological conditions. The structure of the nanoplatform was broken under the weakly acidic and high-concentration glutathione conditions in the TME, resulting in the separation of the Fe3O4 nanoparticles from the nanoplatform and rapid drug release. In addition, the exfoliated Fe3O4 and released Mn2+ can help reduce the interference between their T-1 and T-2 contrast abilities, resulting in dual-mode MRI contrast enhancement. Furthermore, during the exfoliation process of the Fe3O4 nanocrystals, the catalytic activity of the Fe3O4 nanocrystals toward a Fenton-like reaction within cancer cells could be improved because of the increase in specific surface area, which led to the generation of highly toxic hydroxyl radicals and induced HeLa cell apoptosis. The nanoplatform also displayed excellent T-1-T-2 dual-mode MRI contrast enhancement and anticancer activity in vivo with reduced systemic toxicity. Thus, this multifunctional nanoplatform could be a potential nanotheranostic for dual-mode MRI-guided combinatorial cancer therapy.

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