Neuroprotective ferulic acid (FA)-glycol chitosan (GC) nanoparticles for functional restoration of traumatically injured spinal cord

被引:102
作者
Wu, Wei [1 ]
Lee, Seung-Young [2 ]
Wu, Xiangbing [3 ,4 ]
Tyler, Jacqueline Y. [2 ]
Wang, He [2 ]
Ouyang, Zheng [2 ]
Park, Kinam [2 ]
Xu, Xiao-Ming [1 ,3 ,4 ]
Cheng, Ji-Xin [2 ,5 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Dept Neurobiol, Shanghai 200030, Peoples R China
[2] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
[3] Indiana Univ Sch Med, Spinal Cord & Brain Injury Res Grp, Stark Neurosci Res Inst, Dept Neurol Surg,Goldman & Campbell Brain & Spine, Indianapolis, IN 46202 USA
[4] Indiana Univ Sch Med, Dept Anat & Cell Biol, Indianapolis, IN 46202 USA
[5] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
Spinal cord injury; Neuroprotective polymer; Ferulic acid; Glycol chitosan; Functional restoration; Anti-excitotoxicity; RECEPTOR EXPRESSION; INDUCED APOPTOSIS; LOCAL-DELIVERY; METHYLPREDNISOLONE; RECOVERY; REPAIR; NEURONS; POLYMER;
D O I
10.1016/j.biomaterials.2013.11.074
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
An urgent unmet need exists for early-stage treatment of spinal cord injury (SCI). Currently methylprednisolone is the only therapeutic agent used in clinics, for which the efficacy is controversial and the side effect is well-known. We demonstrated functional restoration of injured spinal cord by self-assembled nanoparticles composed of ferulic acid modified glycol chitosan (FA-GC). Chitosan and ferulic acid are strong neuroprotective agents but their systemic delivery is difficult. Our data has shown a prolonged circulation time of the FA-GC nanoparticles allowing for effective delivery of both chitosan and ferulic acid to the injured site. Furthermore, the nanoparticles were found both in the gray matter and white matter. The in vitro tests demonstrated that nanoparticles protected primary neurons from glutamate-induced excitotoxicity. Using a spinal cord contusion injury model, significant recovery in locomotor function was observed in rats that were intravenously administered nanoparticles at 2 h post injury, as compared to non-improvement by methylprednisolone administration. Histological analysis revealed that FA-GC treatment significantly preserved axons and myelin and also reduced cavity volume, astrogliosis, and inflammatory response at the lesion site. No obvious adverse effects of nanoparticles to other organs were found. The restorative effect of FA-GC presents a promising potential for treating human SCIs. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2355 / 2364
页数:10
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