摘要
Core@shell,magnetic nanoprticles (core@shell MNPs) are attracting widespread attention due to their enhancement properties for potential applications in hyperthermia treatment, magnetic resonance imaging (MRI), diagnostics, and so forth. Herein,we developed a facile thertrial decomposition method for controllable synthesis of a superparamagnetic, monodispersed core@shell structure (Co@Mn = CoFe2O4.@MnFe2O4) with uniform size distribution (sigma < 5%, d(c) 15 nm). The CoFe2O4 core could enhance. magnetic anisotropy, and the MnFe2O4 shell could improve the magnetization value. The CO@Mn MNPs were transferred into aqueous solution with an amphiphilic polymer (labeled 2% TAMRA) and fiinctionolized with PEG(2k), and target molecules (folic acid, FA) to fabricate multifunctional PMA(TAMRA)-Co@Mn-PEG(2k)-FA nanoprobes. The obtained PMA(TAMRA)-Co@Mn-PEG(2k)-FA nanoprobes" exhibit good biocompatibility,, high T-2 relaxation values, and long-term fluorescence stability,(at least 6 months). Our results 'demonstrate that the synthesized PMA(TAMRA)Co@Mn-PEG(2k)-FA nanoprobes can effectively enhance the targeted MRI and fluorescent labeling in vitro and in vivo. The research outcomes will contribute to the rational design of new nanoprobes and ptovide a promising pathway, to promote core@shell nanoprobes for further clinical contrast MRI and photodynamic therapy in the near future.