Chiral Graphene Quantum Dots Enhanced Drug Loading into Small Extracellular Vesicles

被引:27
|
作者
Zhang, Youwen [1 ]
Kim, Gaeun [1 ]
Zhu, Yini [2 ,3 ]
Wang, Ceming [1 ]
Zhu, Runyao [1 ]
Lu, Xin [2 ]
Chang, Hsueh-Chia [1 ]
Wang, Yichun [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Dept Biol Sci, Notre Dame, IN 46556 USA
[3] Univ Notre Dame, Integrated Biomed Sci Grad Program, Notre Dame, IN 46556 USA
基金
美国国家科学基金会;
关键词
chirality; extracellular vesicles; graphene quantum dots; chemotherapy; siRNA; drug delivery; CHROMATIN EFFECTOR PYGO2; EXOSOMES; DELIVERY; CHEMISTRY; LIPIDS; SIRNA;
D O I
10.1021/acsnano.3c00305
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As nanoscale extracellular vesicles secreted by cells, small extracellular vesicles (sEVs) have enormous potential as safe and effective vehicles to deliver drugs into lesion locations. Despite promising advances with sEV-based drug delivery systems, there are still challenges to drug loading into sEVs, which hinder the clinical applications of sEVs. Herein, we report an exogenous drug -agnostic chiral graphene quantum dots (GQDs) sEV-loading platform, based on chirality matching with the sEV lipid bilayer. Both hydrophobic and hydrophilic chemical and biological drugs can be functionalized or adsorbed onto GQDs by pi-pi stacking and van der Waals interactions. By tuning the ligands and GQD size to optimize its chirality, we demonstrate drug loading efficiency of 66.3% and 64.1% for doxorubicin and siRNA, which is significantly higher than other reported sEV loading techniques.
引用
收藏
页码:10191 / 10205
页数:15
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