微泡
外体
体内
脾脏
腹腔注射
药物输送
分布(数学)
药理学
脂肪组织
医学
小RNA
化学
免疫学
生物
内科学
生物化学
基因
生物技术
数学分析
有机化学
数学
作者
Xueying Zhou,Zhelong Li,Wenqi Sun,Guodong Yang,Changyang Xing,Lijun Yuan
出处
期刊:Current Drug Delivery
[Bentham Science]
日期:2020-01-23
卷期号:17 (3): 186-194
被引量:27
标识
DOI:10.2174/1567201817666200122163251
摘要
Background: Exosomes are cell-derived nanovesicles that play vital roles in intercellular communication. Recently, exosomes are recognized as promising drug delivery vehicles. Up till now, how the in vivo distribution of exosomes is affected by different administration routes has not been fully understood. Methods: In the present study, in vivo distribution of exosomes following intravenous and intraperitoneal injection approaches was systemically analyzed by tracking the fluorescence-labeled exosomes and qPCR analysis of C. elegans specific miRNA abundance delivered by exosomes in different organs. Results: The results showed that exosomes administered through tail vein were mostly taken up by the liver, spleen and lungs while exosomes injected intraperitoneally were more dispersedly distributed. Besides the liver, spleen, and lungs, intraperitoneal injection effectively delivered exosomes into the visceral adipose tissue, making it a promising strategy for obesity therapy. Moreover, the results from fluorescence tracking and qPCR were slightly different, which could be explained by systemic errors. Conclusion: Together, our study reveals that different administration routes cause a significant differential in vivo distribution of exosomes, suggesting that optimization of the delivery route is prerequisite to obtain rational delivery efficiency in detailed organs.
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