Mitochondria-Targeted Natural Antioxidant Nanosystem for Diabetic Vascular Calcification Therapy.
Jinjin LiTianyu LanQianqian GuoChuang ZhangXin LuXiaoxia HuXiangchun ShenYanyan ZhangPublished in: Biomacromolecules (2024)
The development of nanotherapy targeting mitochondria to alleviate oxidative stress is a critical therapeutic strategy for vascular calcification (VC) in diabetes. In this study, we engineered mitochondria-targeted nanodrugs (T4O@TPP/PEG-PLGA) utilizing terpinen-4-ol (T4O) as a natural antioxidant and mitochondrial protector, PEG-PLGA as the nanocarrier, and triphenylphosphine (TPP) as the mitochondrial targeting ligand. In vitro assessments demonstrated enhanced cellular uptake of T4O@TPP/PEG-PLGA, with effective mitochondrial targeting. This nanodrug successfully reduced oxidative stress induced by high glucose levels in vascular smooth muscle cells. In vivo studies showed prolonged retention of the nanomaterials in the thoracic aorta for up to 24 h. Importantly, experiments in diabetic VC models underscored the potent antioxidant properties of T4O@TPP/PEG-PLGA, as evidenced by its ability to mitigate VC and restore mitochondrial morphology. These results suggest that these nanodrugs could be a promising strategy for managing diabetic VC.
Keyphrases
- oxidative stress
- drug delivery
- cancer therapy
- type diabetes
- drug release
- diabetic rats
- vascular smooth muscle cells
- ischemia reperfusion injury
- dna damage
- high glucose
- induced apoptosis
- cell death
- wound healing
- endothelial cells
- chronic kidney disease
- reactive oxygen species
- anti inflammatory
- angiotensin ii
- spinal cord
- aortic valve
- heat shock
- stem cells
- bone marrow
- skeletal muscle
- bone regeneration
- spinal cord injury
- coronary artery