鼻腔给药
中枢神经系统
药物输送
体内
离体
亲脂性
纳米颗粒
脑脊液
药理学
医学
磁共振成像
纳米医学
纳米技术
神经科学
化学
生物医学工程
材料科学
病理
生物
立体化学
内科学
生物技术
放射科
作者
Dandan Kou,Yun Gao,Cang Li,Dandan Zhou,Kuan Lu,Ning Wang,Ruru Zhang,Zhe Yang,Yi Zhou,Lei Chen,Jianxian Ge,Jianfeng Zeng,Mingyuan Gao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-03-30
卷期号:23 (11): 5381-5390
被引量:9
标识
DOI:10.1021/acs.nanolett.2c05056
摘要
Intranasal administration was previously proposed for delivering drugs for central nervous system (CNS) diseases. However, the delivery and elimination pathways, which are very imperative to know for exploring the therapeutic applications of any given CNS drugs, remain far from clear. Because lipophilicity has a high priority in the design of CNS drugs, the as-prepared CNS drugs tend to form aggregates. Therefore, a PEGylated Fe3O4 nanoparticle labeled with a fluorescent dye was prepared as a model drug and studied to elucidate the delivery pathways of intranasally administered nanodrugs. Through magnetic resonance imaging, the distribution of the nanoparticles was investigated in vivo. Through ex vivo fluorescence imaging and microscopy studies, more precise distribution of the nanoparticles across the entire brain was disclosed. Moreover, the elimination of the nanoparticles from cerebrospinal fluid was carefully studied. The temporal dose levels of intranasally delivered nanodrugs in different parts of the brain were also investigated.
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