Mesoporous MnSiO3@Fe3O4@C Nanoparticle as pH-responsive T1-T2* Dual-modal Magnetic Resonance Imaging Contrast Agent for Tumor Diagnosis
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Graphical Abstract
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Abstract
Mesoporous structured MnSiO3@Fe3O4@C nanoparticles (NPs) were prepared via a facile and efficient strategy, with negligible cytotoxicity and minor side efforts. The asprepared MnSiO3@Fe3O4@C NPs hold great potential in serving as pH-responsive T1-T2* dual-modal magnetic resonance (MR) imaging contrast agents. The released Mn2+ shortened T1 relaxation time, meanwhile the superparamagnetic Fe3O4 enhanced T2 contrast imaging. The release rate of Mn ions reaches 31.66% under the condition of pH=5.0, which is similar to tumor microenvironment and organelles. Cytotoxicity assays show that MnSiO3@Fe3O4@C NPs have minor toxicity, even at high concentrations. After intravenous injection of MnSiO3@Fe3O4@C NPs, a rapid contrast enhancement in tumors was achieved with a significant enhancement of 132% after 24 h of the administration. Moreover, a significant decreasement of 53.8% was witnessed in T2 MR imaging signal. It demonstrated that MnSiO3@Fe3O4@C NPs can act as both positive and negative MR imaging contrast agents. Besides, owing to the pH-responsive degradation of mesoporous MnSiO3, MnSiO3@Fe3O4@C NPs can also be used as potential drug systems for cancer theranostics.
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