4.8 Article

High-Performance Worm-like Mn-Zn Ferrite Theranostic Nanoagents and the Application on Tumor Theranostics

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 11, 期 33, 页码 29536-29548

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b08948

关键词

Mn-Zn ferrite; nanocarriers; nanotechnology for diagnosis and treatment; shape effects; tumor theranostics

资金

  1. National Key Research and Development Program of China [2017YFA0205502]
  2. National Natural Science Foundation of China [81473160]
  3. National New Drug Innovation Program of China [2017ZX09309024]
  4. Basic Research Program of Jiangsu Province (Natural Science Foundation) [BK20151422]
  5. Fundamental Research Funds for the Central Universities [2242018K3DN30]
  6. Qing Lan Project
  7. Collaborative Innovation Center of Suzhou Nano Science and Technology

向作者/读者索取更多资源

Previous reports from our team revealed the significant potential advantage of Mn-Zn ferrite nanoparticles (NPs) in magnetic resonance imaging (MRI), whereas anisotropic NPs reportedly increased the blood circulation time of nanocarriers. Thus, anisotropic Mn-Zn ferrite displayed a huge potential in cancer synchronous diagnosis and treatment, that is, enhanced MRI observation was performed simultaneously when drug-targeted delivery therapy was applied to the tumor. Here, we developed three shaped Mn-Zn ferrite (Mn0.63Zn0.37Fe2O4) MNPs used as cancer theranostic nanoagents and compared the effect of the three shaped MNPs on cancer theranostics. Compared to the monodisperse sphere MNPs (S-MNPs-PPR) and clustering MNPs (C-MNPs-PPR), worm-like Mn-Zn ferrite MNPs (W-MNPs-PPR) achieved better results in T-2-weighted MM and achieved more sustained drug release than S-MNPs-PPR and more complete drug release than C-MNPs-PPR in vitro. Additionally, polyethylene glycol (PEG) coating and RGD modification encouraged the three shaped MNPs to evade the recruitment of macrophages more easily and to target the integrin-enriched endothelial cells instead. Meanwhile, W-MNPs-PPR coupled with Paclitaxel (PTX) exhibited more delivery of PTX in the integrin-enriched cells than the other two shaped MNPs, and the content of PTX was far more than that of the wild-type Taxol control group. What is more, in vivo results demonstrated that PTX-coated W-MNPs-PPR not only gained good dual-mode imaging in the tumor (MRI and fluorescence images) but also achieved longer blood circulation time and more PTX-targeted delivery to the tumor, as well as more efficiency in tumor cell killing, which make the simultaneous diagnosis and treatment of tumors to be conducted. Therefore, our works further revealed the importance of the NP shape on its functionality and ultimately provided an alternative and efficient worm-like theranostic nanoagent for tumor theranostics.

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