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Chiral Graphene Quantum Dots Enhanced Drug Loading into Small Extracellular Vesicles.
Zhang, Youwen; Kim, Gaeun; Zhu, Yini; Wang, Ceming; Zhu, Runyao; Lu, Xin; Chang, Hsueh-Chia; Wang, Yichun.
Affiliation
  • Zhang Y; Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States.
  • Kim G; Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States.
  • Zhu Y; Department of Biological Sciences, University of Notre Dame, Notre Dame, Indiana 46556, United States.
  • Wang C; Integrated Biomedical Sciences Graduate Program, University of Notre Dame, Notre Dame, Indiana 46556, United States.
  • Zhu R; Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States.
  • Lu X; Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States.
  • Chang HC; Department of Biological Sciences, University of Notre Dame, Notre Dame, Indiana 46556, United States.
  • Wang Y; Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States.
ACS Nano ; 17(11): 10191-10205, 2023 06 13.
Article in En | MEDLINE | ID: mdl-37127891
ABSTRACT
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 π-π 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quantum Dots / Extracellular Vesicles / Graphite Language: En Journal: ACS Nano Year: 2023 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quantum Dots / Extracellular Vesicles / Graphite Language: En Journal: ACS Nano Year: 2023 Document type: Article Affiliation country: Estados Unidos