Multifunctional tunable ZnFe 2 O 4 @MnFe 2 O 4 nanoparticles for dual-mode MRI and combined magnetic hyperthermia with radiotherapy treatment.
Ilia D ShabalkinAleksei S KomlevSergey A TsymbalOleg I BurmistrovVladimir I ZverevPavel V KrivoshapkinPublished in: Journal of materials chemistry. B (2023)
With the increase in non-communicable diseases, cancer is becoming one of the most lethal ailments of the coming decades. Significant progress has been made in the development of NPs that combine diagnostic and therapeutic properties in a single system. Multimodal NPs that sequentially perform MRI diagnostics with increased contrast and then act as synergistic agents for magnetic hyperthermia and radiotherapy can be considered as next-generation anticancer drugs. Thus, we propose a systematic study of composite theranostic ZnFe 2 O 4 @MnFe 2 O 4 NPs for the first time. Two types of magnetic NPs with MnFe 2 O 4 shell thicknesses of 0.5 (ZM0.5) and 1.7 nm (ZM3) were prepared via hydrothermal synthesis. Tuning the shell thickness was shown to influence the NP r 2 and r 1 relaxivities and allow T 1 - T 2 dual-mode contrast agents to be obtained. A radiotherapy study demonstrated a significant dose factor enhancement (about 40%) for both NP types. The specific absorption rate of ZM3 in a 100 Oe alternating magnetic field with a frequency of 75 kHz was found to be 8 W g -1 , which results in heating up to 42 °C within a few seconds. This work presents high-performance multifunctional NPs capable of combining different diagnostic and therapeutic methods for a full course of treatment using only one type of NP.
Keyphrases
- early stage
- contrast enhanced
- magnetic resonance imaging
- locally advanced
- magnetic resonance
- drug delivery
- radiation therapy
- molecularly imprinted
- cancer therapy
- oxide nanoparticles
- radiation induced
- photodynamic therapy
- computed tomography
- papillary thyroid
- mass spectrometry
- rectal cancer
- combination therapy
- metal organic framework
- fluorescence imaging
- lymph node metastasis
- drug induced
- walled carbon nanotubes