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Polyethyleneimine-coated Iron Oxide Nanoparticles as a Vehicle for the Delivery of Small Interfering RNA to Macrophages In Vitro and In Vivo
Published on: February 5, 2019
Nano-therapeutics targeting the macrophage-based microenvironment in the treatment of atherosclerosis
Yingjie Xu1, Yuan Zhang2, Wanpeng Yu3
1Qingdao Stomatological Hospital Affiliated to Qingdao University, Qingdao University, Qingdao, China.
Insights
Novel nanotherapeutics target macrophages to combat atherosclerosis (AS), a chronic inflammatory disease. These strategies reduce plaque burden and inflammation, offering promising new treatments for cardiovascular disease.
Area of Science:
- Cardiovascular Research
- Nanomedicine
- Immunology
Background:
- Atherosclerosis (AS) is a chronic inflammatory arterial disease, a primary cause of cardiovascular diseases.
- Macrophages are key regulators of inflammation in AS, influencing plaque stability and the immune microenvironment.
Purpose of the Study:
- To review nanotherapeutic strategies for treating AS by targeting macrophages.
- To explore novel nanosystems enhancing drug delivery and efficacy in AS lesions.
Main Methods:
- Reviewing nanocarrier design, including ligand modification and biomimetic approaches.
- Analyzing macrophage-targeted nanotherapeutics regulating apoptosis, autophagy, and efferocytosis.
- Examining intelligent nanoparticles responsive to the inflammatory microenvironment.
Main Results:
- Nanosystems can enhance drug accumulation and bioavailability at AS lesion sites.
- Macrophage-targeted therapies synergistically reduce plaque burden and inflammation.
- Responsive nanoparticles can selectively eliminate inflammatory elements within plaques.
Conclusions:
- Macrophage-targeted nanotherapeutics represent a promising strategy for AS treatment.
- Biomimetic and intelligent nanosystems offer advanced approaches to combat AS progression.
- These nanomedicine strategies hold significant potential for clinical application in cardiovascular disease management.
Abstract:
Atherosclerosis (AS) is a chronic inflammatory disease that primarily affects large and medium-sized arteries and serves as the major pathological basis for cardiovascular diseases such as coronary heart disease. During the progression of AS, macrophages play a crucial role in promoting inflammatory regulation. Sustained local inflammatory responses are triggered by the accumulation of macrophages in arterial walls, which either promote or inhibit the development of AS by modulating inflammatory progression, plaque stability, and the surrounding immune microenvironment. Therefore, therapeutic strategies targeting macrophages and eliminating pro-inflammatory features in the plaque microenvironment hold promise as novel approaches to slow the progression of AS. With the deepening understanding of the mechanisms underlying AS, numerous innovative nanotherapeutic systems for its diagnosis and treatment have been developed. Here, we review strategies for designing novel nanosystems to treat AS, including modifying targeting ligands and utilizing biomimetic nanoparticles to enhance drug accumulation in target lesions and improve bioavailability. Macrophage-targeted nanotherapeutic approaches aim to reduce plaque burden and inflammation by regulating macrophage apoptosis, autophagy, and inducing efferocytosis synergistically. Concurrently, the development of intelligent responsive nanoparticles based on the inflammatory microenvironment enables targeted elimination of inflammatory characteristics within plaque microenvironments. These strategies demonstrate significant potential for application in AS treatment.
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