| Literature DB >> 32937179 |
Zhong Chen1, Wenhua Li1, Liwang Shi1, Lei Jiang1, Minghui Li1, Changmei Zhang2, Haisheng Peng3.
Abstract
Diabetic nephropathy (DN) is a frequent and severe microvascular complication associated with oxidative stress of diabetes mellitus. A novel astaxanthin-based natural antioxidant nanosystem, namely AST-GLU-LIP, with preferential renal uptake and bioavailability were prepared and applied for treatment of diabetic nephropathy in rats. Our results of kidney-targeted evaluation showed that glucose-PEG600-DSPE ligand modified AST liposomes could be specifically transported by overexpressed GLUT1 on the membrane of glomerular mesangial cells and achieved excellent kidney-targeted drug delivery. In addition, the results of pharmacodynamics and therapeutics in DN rats demonstrated that AST-GLU-LIP could improve the bioavailability and antioxidant capacity of AST to scavenge redundant ROS induced by oxidative stress. AST-GLU-LIP could also significantly improve the renal pathological morphology to protect the kidney as a therapeutic drug for diabetic nephropathy.Entities:
Keywords: Astaxanthin; Diabetic nephropathy; GLUT1; Kidney-targeted; Liposome; Oxidative stress
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Year: 2020 PMID: 32937179 DOI: 10.1016/j.ejpb.2020.09.005
Source DB: PubMed Journal: Eur J Pharm Biopharm ISSN: 0939-6411 Impact factor: 5.571