Cholesterol (Blood lipid) lowering potential of Rosuvastatin chitosan nanoparticles for atherosclerosis: Preclinical study in rabbit model
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Updated: Dec 4, 2025

The Rabbit Model of Accelerated Atherosclerosis: A Methodological Perspective of the Iliac Artery Balloon Injury
Published on: October 3, 2017
Lin Chen1, Caihong Wang1, Yuanchu Wu1
1Department of Cardiology, Affiliated Wujiang Hospital of Nantong University, Suzhou, Jiangsu, China 215200.
Abstract:
Atherosclerosis is the condition of narrowing of arteries due to plaque buildup on the artery walls. Aortic valve calcification (AVC) is one of the reasons of atherosclerosis which leads to narrowing at the opening of the aortic valve which is commonly referred as Aortic valve stenosis (AS). The Rosuvastatin-chitosan (ROS-chitosan) nanoparticles were prepared using ionotropic gelation method. Nanoparticulate formulation was optimized by 3 factor, 2 level full factorial design to find the effect of independent variables on particle size and percentage encapsulation efficiency. Particle size, encapsulation efficiency, scanning electron microscopy, in vitro drug release of nanoparticles was determined. The adult male rabbit of 4-5 months old were chosen for the study. Hypercholesterolemia was induced in experimental animals by administering diet with Cholesterol and Cholic acid (1.25 % and 0.5% respectively.) Blood lipid profile, interleukin 6 levels and histopathological study was performed. Rosuvastatin was found to be significantly effective in lowering the blood lipid levels. It helps to attenuate atherosclerosis as well as calcification of various valve tissues in experimental animals.
Insights
Rosuvastatin-chitosan nanoparticles effectively reduced atherosclerosis and aortic valve calcification in rabbits. This study highlights their potential in managing arterial plaque buildup and valve stenosis.
Area of Science:
- Cardiovascular Science
- Nanomedicine
- Pharmacology
Background:
- Atherosclerosis involves arterial narrowing due to plaque buildup.
- Aortic valve calcification (AVC) contributes to atherosclerosis, leading to aortic valve stenosis (AS).
- Developing effective nanoparticle drug delivery systems is crucial for managing cardiovascular diseases.
Purpose of the Study:
- To prepare and optimize Rosuvastatin-chitosan (ROS-chitosan) nanoparticles.
- To evaluate the efficacy of ROS-chitosan nanoparticles in an experimental atherosclerosis and AVC model.
- To assess the impact of nanoparticles on lipid profiles and inflammatory markers.
Main Methods:
- ROS-chitosan nanoparticles were synthesized using ionotropic gelation and optimized via a full factorial design.
- Nanoparticle characteristics (particle size, encapsulation efficiency, morphology, drug release) were analyzed.
- Hypercholesterolemia and atherosclerosis were induced in rabbits using a specific diet.
- Blood lipid profiles, interleukin-6 levels, and histopathology of valve tissues were examined.
Main Results:
- The ROS-chitosan nanoparticle formulation was successfully optimized.
- Rosuvastatin demonstrated significant reduction in blood lipid levels in experimental animals.
- Histopathological studies indicated attenuation of atherosclerosis and calcification in valve tissues.
- Interleukin-6 levels were also modulated, suggesting an anti-inflammatory effect.
Conclusions:
- ROS-chitosan nanoparticles are a promising formulation for treating atherosclerosis and associated aortic valve calcification.
- Rosuvastatin delivered via nanoparticles effectively manages hyperlipidemia and reduces arterial plaque and valve calcification.
- This approach offers a potential therapeutic strategy for preventing or treating aortic valve stenosis and atherosclerosis progression.
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