体内
大麻酚
药理学
医学
免疫系统
药代动力学
生物利用度
药物输送
巨噬细胞
体外
化学
免疫学
材料科学
生物
纳米技术
生物化学
大麻
精神科
生物技术
作者
Qi Li,Chunqing Wang,Jinglu Hu,Wencheng Jiao,Ziyan Tang,Xingshuang Song,Yanping Wu,Jing Dai,Peng Gao,Lina Du,Yiguang Jin
标识
DOI:10.1016/j.ijpharm.2023.122872
摘要
Post-traumatic stress disorder (PTSD), which normally follows psychological trauma, has been increasingly studied as a brain disease. However, the blood-brain barrier (BBB) prevents conventional drugs for PTSD from entering the brain. Our previous studies proved the effectiveness of cannabidiol (CBD) against PTSD, but low water solubility, low brain targeting efficiency and poor bioavailability restricted its applications. Here, a bionic delivery system, camouflage CBD-loaded macrophage-membrane nanovesicles (CMNVs), was constructed via co-extrusion of CBD with macrophage membranes, which had inflammatory and immune escape properties. In vitro anti-inflammatory, cellular uptake and pharmacokinetic experiments respectively verified the anti-inflammatory, inflammatory targeting and immune escape properties of CMNVs. Brain targeting and excellent anti-PTSD effects of CMNVs had been validated in vivo by imaging and pharmacodynamics studies. In our study, the potential of ultrasound to open BBBs and improve the brain-targeted delivery of CBD was evaluated. In conclusion, this cell membrane bionic delivery system assisted with ultrasound had good therapeutic effect against PTSD mice, which is expected to help convey CBD to inflammatory areas within the brain and alleviate the symptoms of PTSD.
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