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Combining hard and soft magnetism into a single core-shell nanoparticle to achieve both hyperthermia and image contrast.


ABSTRACT: A biocompatible core/shell structured magnetic nanoparticles (MNPs) was developed to mediate simultaneous cancer therapy and imaging.A 22-nm MNP was first synthesized via magnetically coupling hard (FePt) and soft (Fe3O4) materials to produce high relative energy transfer. Colloidal stability of the FePt@Fe3O4 MNPs was achieved through surface modification with silane-polyethylene glycol (PEG). Intravenous administration of PEG-MNPs into tumor-bearing mice resulted in a sustained particle accumulation in the tumor region, and the tumor burden of treated mice was a third that of the mice in control groups 2 weeks after a local hyperthermia treatment. In vivo magnetic resonance imaging exhibited enhanced T2 contrast in the tumor region.This work has demonstrated the feasibility of cancer theranostics with PEG-MNPs.

SUBMITTER: Yang Q 

PROVIDER: S-EPMC4702516 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Combining hard and soft magnetism into a single core-shell nanoparticle to achieve both hyperthermia and image contrast.

Yang Qiuhong Q   Gong Maogang M   Cai Shuang S   Zhang Ti T   Douglas Justin T JT   Chikan Viktor V   Davies Neal M NM   Lee Phil P   Choi In-Young IY   Ren Shenqiang S   Forrest M Laird ML  

Therapeutic delivery 20151008 10


<h4>Background</h4>A biocompatible core/shell structured magnetic nanoparticles (MNPs) was developed to mediate simultaneous cancer therapy and imaging.<h4>Methods & results</h4>A 22-nm MNP was first synthesized via magnetically coupling hard (FePt) and soft (Fe3O4) materials to produce high relative energy transfer. Colloidal stability of the FePt@Fe3O4 MNPs was achieved through surface modification with silane-polyethylene glycol (PEG). Intravenous administration of PEG-MNPs into tumor-bearing  ...[more]

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