Multifunctional nanoplatforms capable of integrating therapy and imaging functions are of significant interest for cancer research. In this work, we report the synthesis of bovine serum albumin (BSA)-functionalized manganese ferrite nanoassemblies (MnFe 2 O 4 @BSA NAs) as a multifunctional platform for chemo-photodynamic therapy and magnetic functionality. Ethylenediamine-modified MnFe 2 O 4 nanoassemblies were first prepared via a thermal decomposition route and subsequently conjugated with BSA to improve aqueous stability, biocompatibility, and drug-loading capability. The resulting nanoassemblies exhibited well-defined morphology (50–60 nm), good colloidal stability, and superparamagnetic behavior that was confirmed by Fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, zeta-potential, DLS and magnetic measurements. The anticancer drug doxorubicin hydrochloride (DOX) and the photosensitizer Rose Bengal (RB) were successfully loaded into MnFe 2 O 4 @BSA NAs, showing high loading efficiency and pH-responsive DOX release. Under visible-light irradiation, RB-loaded MnFe 2 O 4 @BSA NAs generated reactive oxygen species (ROS) through combined photodynamic and photo-Fenton-like processes. In vitro studies using MCF-7 breast cancer cells demonstrated that the combined RB-DOX-loaded MnFe 2 O 4 @BSA NAs exhibited enhanced cytotoxicity under light irradiation compared to individual chemotherapy or photodynamic therapy, indicating a synergistic chemo-photodynamic effect. Moreover, MnFe 2 O 4 @BSA NAs showed good heating efficacy under an AC magnetic field and significant signal reduction on the T 2 -weighted phantom image with transverse relaxivity ( r 2 ) of 123.7 mM −1 s −1 . Overall, this study presents MnFe 2 O 4 @BSA NAs as a multifunctional in-vitro platform integrating drug delivery, photodynamic activity, magnetic heating, and MRI contrast properties, providing a foundation for future image-guided and in vivo therapeutic investigations.
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Gupta et al. (2026) studied this question.
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