Platelet-Mimicking Therapeutic System for Noninvasive Mitigation of the Progression of Atherosclerotic Plaques.
Yi MaYuxuan MaMengqiu GaoZhihao HanWen JiangYueqing GuYi LiuPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2021)
Atherosclerotic plaque is the primary cause of cardiovascular disorders and remains a therapeutic hurdle for the early intervention of atherosclerosis. Traditional clinical strategies are often limited by surgery-related complications or unsatisfactory effects of long-term drug administration. Inspired by the plaque-binding ability of platelets, a biomimic photodynamic therapeutic system is designed to mitigate the progression of atherosclerotic plaques. This system is composed of photosensitizer-loaded upconversion nanoparticle cores entrapped in the platelet membrane. The platelet membrane coating facilitates specific targeting of the therapeutic system to macrophage-derived foam cells, the hallmark, and main component of early stage atherosclerotic plaques, which is firmly confirmed by in vivo fluorescent and single-photon emission computed tomography/computed tomography (SPECT/CT) radionuclide imaging. Importantly, in vivo phototherapy guided by SPECT/CT imaging alleviates plaque progression. Further immunofluorescence analysis reveals foam cell apoptosis and ameliorated inflammation. This biomimic system, which combines plaque-binding with radionuclide imaging guidance, is a novel, noninvasive, and potent strategy to mitigate the progression of atherosclerotic plaque.
Keyphrases
- computed tomography
- coronary artery disease
- dual energy
- high resolution
- positron emission tomography
- early stage
- image quality
- contrast enhanced
- photodynamic therapy
- magnetic resonance imaging
- cancer therapy
- randomized controlled trial
- oxidative stress
- induced apoptosis
- minimally invasive
- drug administration
- cell proliferation
- type diabetes
- radiation therapy
- mouse model
- climate change
- quantum dots
- magnetic resonance
- squamous cell carcinoma
- signaling pathway
- percutaneous coronary intervention
- dna binding
- single molecule
- wound healing