Mesoporous structured MnSiO3@Fe3O4@C nanoparticles(NPs)were prepared via a facile and efficient strategy,with negligible cytotoxicity and minor side efforts.The as-prepared MnSiO3@Fe3O4@C NPs hold great potential in s...Mesoporous structured MnSiO3@Fe3O4@C nanoparticles(NPs)were prepared via a facile and efficient strategy,with negligible cytotoxicity and minor side efforts.The as-prepared MnSiO3@Fe3O4@C NPs hold great potential in serving as pH-responsive T1-T2^*dual-modal magnetic resonance(MR)imaging contrast agents.The released Mn^2+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.展开更多
In this study, we developed a highly sensitive dual-mode imaging system using gold nanoparticles （GNPs） conjugated to various fluorophores in solid phantoms. The system consists of fluorescence-lifetime imaging micr...In this study, we developed a highly sensitive dual-mode imaging system using gold nanoparticles （GNPs） conjugated to various fluorophores in solid phantoms. The system consists of fluorescence-lifetime imaging microscopy （FLIM） for surface imaging, diffusion reflection （DR） for deep-tissue imaging （up to 1 cm）, and metal-enhanced fluorescence （MEF）. We detected quenching in the fluorescent intensity （FI） for the conjugation of both gold nanospheres （GNS） and gold nanorods （GNRs） to Fluorescein, which has an excitation peak at a wavelength shorter than the surface plasmon resonance （SPR） of both types of GNPs. Enhanced FI was detected in conjugation to Rhodamine B （RhB） and Sulforhodamine B （SRB）, both with excitation peaks in the SPR regions of the GNPs. The enhanced FI was detected both in solution and in solid phantoms by the FLIM measurements. DR measurements detected the presence of GNRs within the solid phantoms by recording the dropped rates of light scattering in wavelengths corresponding to the absorption spectra of the GNRs. With the inclusion of MEF, this promising dual-mode imaging technique enables efficient and sensitive molecular and functional imaging.展开更多
基金supported by the National Natural Science Foundation of China(No.21571168)
文摘Mesoporous structured MnSiO3@Fe3O4@C nanoparticles(NPs)were prepared via a facile and efficient strategy,with negligible cytotoxicity and minor side efforts.The as-prepared MnSiO3@Fe3O4@C NPs hold great potential in serving as pH-responsive T1-T2^*dual-modal magnetic resonance(MR)imaging contrast agents.The released Mn^2+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.
文摘In this study, we developed a highly sensitive dual-mode imaging system using gold nanoparticles （GNPs） conjugated to various fluorophores in solid phantoms. The system consists of fluorescence-lifetime imaging microscopy （FLIM） for surface imaging, diffusion reflection （DR） for deep-tissue imaging （up to 1 cm）, and metal-enhanced fluorescence （MEF）. We detected quenching in the fluorescent intensity （FI） for the conjugation of both gold nanospheres （GNS） and gold nanorods （GNRs） to Fluorescein, which has an excitation peak at a wavelength shorter than the surface plasmon resonance （SPR） of both types of GNPs. Enhanced FI was detected in conjugation to Rhodamine B （RhB） and Sulforhodamine B （SRB）, both with excitation peaks in the SPR regions of the GNPs. The enhanced FI was detected both in solution and in solid phantoms by the FLIM measurements. DR measurements detected the presence of GNRs within the solid phantoms by recording the dropped rates of light scattering in wavelengths corresponding to the absorption spectra of the GNRs. With the inclusion of MEF, this promising dual-mode imaging technique enables efficient and sensitive molecular and functional imaging.
