Why the study?
Do simvastatin nanocarriers reduce blood lipids and increase smooth muscle cell apoptosis compared to standard simvastatin in a hyperlipidemia rat model?
Do simvastatin nanocarriers reduce blood lipids and increase smooth muscle cell apoptosis compared to standard simvastatin in a hyperlipidemia rat model?
Simvastatin nanocarriers may offer an improved delivery mechanism for reducing blood lipids and delaying atherosclerosis in a preclinical model.
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Simvastatin-NLCs feasible in hyperlipidemic rats; leaves open translation to human lower-limb atherosclerosis therapy.
This article prepared a simvastatin-NLCs for the treatment of arteriosclerotic occlusive disease of lower limbs. Taking the size distribution, polydispersity coefficient, encapsulation efficiency and drug loading of simvastatin-NLCs as evaluation indicators, various prescription factors of simvastatin-NLCs were investigated. The in vitro release behavior and stability of simvastatin-NLCs were also investigated. A hyperlipidemia rat model was established using high-fat diets. SD rats fed ordinary diet were set as normal control groups. 20 rats, 20 in the simvastatin group and 20 in the simvastatin nanocarrier group. After 5 weeks of drug intervention, the rats were sacrificed and the aorta was taken to determine the smooth muscle cell apoptosis rate. Studies have shown that simvastatin nanocarriers can more effectively reduce blood lipids in hyperlipidemia rats, increase the rate of smooth muscle cell apoptosis in hyperlipidemia rats, and delay the onset of atherosclerosis.
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Wu et al. (2020) studied this question.
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