| Literature DB >> 25129696 |
Xiaojuan Wang1, Xing Sun2, Jun Lao2, Hua He2, Tiantian Cheng2, Mingqing Wang2, Shengjie Wang2, Fang Huang3.
Abstract
This study demonstrates that ligand-modified graphene quantum dots (GQDs) facilitate the simultaneous operation of multiple tasks without the need for external dyes. These tasks include selective cell labeling, targeted drug delivery, and real-time monitoring of cellular uptake. Folic acid (FA)-conjugated GQDs are synthesized and utilized to load the antitumor drug doxorubicin (DOX). The fabricated nanoassembly can unambiguously discriminate cancer cells from normal cells and efficiently deliver the drug to targeted cells. The inherent stable fluorescence of GQDs enables real-time monitoring of the cellular uptake of the DOX-GQD-FA nanoassembly and the consequent release of drugs. The nanoassembly is specifically internalized rapidly by HeLa cells via receptor-mediated endocytosis, whereas DOX release and accumulation are prolonged. In vitro toxicity data suggest that the DOX-GQD-FA nanoassembly can target HeLa cells differentially and efficiently while exhibiting significantly reduced cytotoxicity to non-target cells.Entities:
Keywords: Confocal microscopy; Drug delivery; Fluorescence; Graphene quantum dots; Selective cytotoxicity
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Year: 2014 PMID: 25129696 DOI: 10.1016/j.colsurfb.2014.07.043
Source DB: PubMed Journal: Colloids Surf B Biointerfaces ISSN: 0927-7765 Impact factor: 5.268