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A New NO-Releasing Nanoformulation for the Treatment of Pulmonary Arterial Hypertension
被引:0
作者:
Nura A. Mohamed
Blerina Ahmetaj-Shala
Lucie Duluc
Louise S. Mackenzie
Nicholas S. Kirkby
Daniel M. Reed
Paul D. Lickiss
Robert P. Davies
Gemma R. Freeman
Beata Wojciak-Stothard
Adrian H. Chester
Ibrahim M. El-Sherbiny
Jane A. Mitchell
Magdi H. Yacoub
机构:
[1] Imperial College,Department of Cardiothoracic Pharmacology, National Heart and Lung Institute
[2] Imperial College,Heart Science Centre
[3] Qatar Foundation Research and Development Division,Department of Experimental Medicine and Toxicology, Hammersmith Campus
[4] Imperial College London,School of Life and Medical Sciences
[5] University of Hertfordshire,Synthesis Section, Department of Chemistry
[6] Imperial College London,undefined
[7] Center for Materials Science,undefined
来源:
Journal of Cardiovascular Translational Research
|
2016年
/
9卷
关键词:
Pulmonary arterial hypertension;
Nanomedicine;
Nanoparticles;
Nitric oxide;
NO-releasing nanoparticles;
Endothelial cells;
Pulmonary artery vascular smooth muscle cells;
Pulmonary artery;
Aorta;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Pulmonary arterial hypertension (PAH) is a chronic and progressive disease which continues to carry an unacceptably high mortality and morbidity. The nitric oxide (NO) pathway has been implicated in the pathophysiology and progression of the disease. Its extremely short half-life and systemic effects have hampered the clinical use of NO in PAH. In an attempt to circumvent these major limitations, we have developed a new NO-nanomedicine formulation. The formulation was based on hydrogel-like polymeric composite NO-releasing nanoparticles (NO-RP). The kinetics of NO release from the NO-RP showed a peak at about 120 min followed by a sustained release for over 8 h. The NO-RP did not affect the viability or inflammation responses of endothelial cells. The NO-RP produced concentration-dependent relaxations of pulmonary arteries in mice with PAH induced by hypoxia. In conclusion, NO-RP drugs could considerably enhance the therapeutic potential of NO therapy for PAH.
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页码:162 / 164
页数:2
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