Improved Neuroprotective Effects of Gallic Acid-Loaded Chitosan Nanoparticles Against Ischemic Stroke

被引:53
作者
Zhao, Yongmei [1 ]
Li, Duolu [1 ]
Zhu, Zhenfeng [1 ]
Sun, Ya [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Pharm, Zhengzhou 45000000, Peoples R China
关键词
ischemic stroke; gallic acid; nanoparticle; pharmacokinetics; pharmacodynamics; CEREBRAL-ARTERY OCCLUSION; MITOCHONDRIAL DYSFUNCTIONS; INJURY; ISCHEMIA/REPERFUSION; BIOAVAILABILITY; INFLAMMATION; EXTRACT; DAMAGE; RATS;
D O I
10.1089/rej.2019.2230
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Ischemic stroke is a typical cerebrovascular illness with high morbidity and mortality worldwide. Nevertheless, strategies for the prevention and treatment of cerebral ischemia/reperfusion injury (CIRI) are limited. Gallic acid (GA) is a plant polyphenol that has been used against CIRI. However, the pharmacokinetic (PK) properties of GA, such as its low absorption, poor bioavailability, and quick elimination, have negative effects on its application. To strengthen its effectiveness, a delivery system of GA-loaded o-carboxymethyl chitosan nanoparticles (GA-NPs) was synthesized in our study. In PKs study, GA-NPs apparently increases the area under the curve of plasma concentration-time and prolonged half-life of GA. Then, we measured thein vitroandin vivoeffects of the GA-NPs in the oxygen glucose deprivation model and the middle cerebral artery occlusion model. The results from our pharmacodynamic studies, including assessment of neurological deficit, cerebral infarction, levels of inflammation, and oxidative stress, showed that GA-NPs possess better neuroprotection compared with GA. In conclusion, GA-NPs may be used as an efficacious delivery vehicle for GA in the treatment of CIRI.
引用
收藏
页码:284 / 292
页数:9
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