In Vitro Drug Delivery through the Blood-Brain Barrier Using Cold Atmospheric Plasma

被引:1
|
作者
Alam, Md Jahangir [1 ]
Sadiq, Abubakar Hamza [2 ]
Kristof, Jaroslav [3 ]
Rimi, Sadia Afrin [2 ]
Hasan, Mahedi [2 ]
Tomoki, Yamano [4 ]
Shimizu, Kazuo [1 ,2 ,3 ,4 ]
机构
[1] Shizuoka Univ, Grad Sch Med Photon, Hamamatsu 4328561, Japan
[2] Shizuoka Univ, Grad Sch Sci & Technol, Hamamatsu 4328561, Japan
[3] Shizuoka Univ, Org Innovat & Social Collaborat, Shizuoka 4328561, Japan
[4] Shizuoka Univ, Grad Sch Integrated Sci & Technol, Hamamatsu 4328561, Japan
来源
MACROMOL | 2024年 / 4卷 / 03期
关键词
drug delivery; cold atmospheric plasma; blood-brain barrier; TIGHT JUNCTIONS; FOCUSED ULTRASOUND; NITRIC-OXIDE; PERMEABILITY; DYSFUNCTION;
D O I
10.3390/macromol4030036
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This study explores the potential of cold atmospheric plasma (CAP) to facilitate the delivery of large-molecule drugs to the brain. The blood-brain barrier (BBB) restricts the passage of most drugs, hindering treatment for neurological disorders. CAP generates reactive oxygen and nitrogen species (RONS) that may disrupt the BBB's tight junctions, potentially increasing drug permeability. An in vitro BBB model and an immortalized cell line (bEND.3) were used in this experiment. Fluorescein isothiocyanate dextran (FD-4), a model drug, was added to the cells to determine drug permeability. Custom microplasma was used to produce reactive oxygen species (ROS). Trans-endothelial electrical resistance (TEER) measurements assessed the integrity of the BBB after the CAP treatment. A decrease in TEER was observed in the CAP-treated group compared to the controls, suggesting increased permeability. Additionally, fluorescence intensity measurements from the basal side of the trans-well plate indicated higher drug passage in the CAP-treated group. Moreover, the higher presence of ROS in the plasma-treated cells confirmed the potential of CAP in drug delivery. These findings suggest that CAP may be a promising approach for enhancing brain drug delivery.
引用
收藏
页码:597 / 609
页数:13
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