Curcumin Equipped Nanozyme-Like Metal-Organic Framework Platform for the Targeted Atherosclerosis Treatment with Lipid Regulation and Enhanced Magnetic Resonance Imaging Capability.
Fanzhen LvHuaqiang FangLi HuangQingqing WangShuangyuan CaoWenpeng ZhaoZhibin ZhouWeimin ZhouXiaolei WangPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Atherosclerotic cardiovascular disease (ASCVD) has become the leading cause of death worldwide, and early diagnosis and treatment of atherosclerosis (AS) are crucial for reducing the occurrence of acute cardiovascular events. However, early diagnosis of AS is challenging, and oral anti-AS drugs suffer from limitations like imprecise targeting and low bioavailability. To overcome the aforementioned shortcomings, Cur/MOF@DS is developed, a nanoplatform integrating diagnosis and treatment by loading curcumin (Cur) into metal-organic frameworks with nanozymes and magnetic resonance imaging (MRI) properties. In addition, the surface-modification of dextran sulfate (DS) enables PCN-222(Mn) effectively target scavenger receptor class A in macrophages or foam cells within the plaque region. This nanoplatform employs mechanisms that effectively scavenge excessive reactive oxygen species in the plaque microenvironment, promote macrophage autophagy and regulate macrophage polarization to realize lipid regulation. In vivo and in vitro experiments confirm that this nanoplatform has outstanding MRI performance and anti-AS effects, which may provide a new option for early diagnosis and treatment of AS.
Keyphrases
- metal organic framework
- magnetic resonance imaging
- cardiovascular disease
- cardiovascular events
- cancer therapy
- contrast enhanced
- coronary artery disease
- photodynamic therapy
- drug delivery
- reactive oxygen species
- diffusion weighted imaging
- computed tomography
- induced apoptosis
- drug release
- endoplasmic reticulum stress
- cell death
- magnetic resonance
- cell cycle arrest
- stem cells
- cardiovascular risk factors
- type diabetes
- fatty acid
- oxidative stress
- risk assessment
- signaling pathway
- adipose tissue
- liver failure
- drug induced
- single cell
- aortic dissection
- metabolic syndrome
- smoking cessation
- weight gain
- binding protein