Ultrasound-Enhanced Generation of Reactive Oxygen Species for MRI-Guided Tumor Therapy by the Fe@Fe 3 O 4 -Based Peroxidase-Mimicking Nanozyme.
Ming ChenGuang DengYu HeXiaoling LiWei LiuWu WangZhiguo ZhouHong YangShi-Ping YangPublished in: ACS applied bio materials (2020)
Reactive oxygen species (ROS)-based tumor therapy is still challenging due to limited ROS-generating efficacy. Herein, we constructed heparin-conjugated Fe@Fe 3 O 4 NPs (Fe@Fe 3 O 4 @heparin, denoted as MNPs) as a peroxidase-mimicking nanozyme to generate ROS for tumor therapy through the combination of the ultrasound-stimulated Fenton reaction and the increased concentration of H 2 O 2 by β-lapachone (La) in a tumor. La was first intraperitoneally injected into mice and induced to generate a considerable quantity of H 2 O 2 through a specific tumor reaction, which was catalyzed by MNPs to produce highly hydroxyl radicals (•OH). Furthermore, the therapy efficacy for malignant tumors could significantly be enhanced by an ultrasonic stimulation. With the help of the increased amount of H 2 O 2 generated by La in the tumor and the enhanced peroxidase-mimicking activity of MNPs by ultrasound, MNPs manifest good therapeutic performance in a 4T1 xenograft model, which provides a strategy for enhanced nanozyme-mediated tumor therapy.
Keyphrases
- reactive oxygen species
- magnetic resonance imaging
- hydrogen peroxide
- dna damage
- cell death
- computed tomography
- type diabetes
- oxidative stress
- wastewater treatment
- insulin resistance
- nitric oxide
- magnetic resonance
- cell therapy
- ionic liquid
- diabetic rats
- high glucose
- replacement therapy
- wild type
- drug induced
- contrast enhanced ultrasound
- electron transfer