Title: Multifunctional GQDs-Concanavalin A@Fe3O4 nanocomposites for cancer cells detection and targeted drug delivery
Authors: Chowdhury, Ankan Dutta
Ganganboina, Akhilesh Babu
Tsai, Yuan-chung
Chiu, Hsin-cheng
Doong, Ruey-an
環境工程研究所
Institute of Environmental Engineering
Keywords: Cancerous cells;Multifunctional nanocomposites;Electrochemical detection;Biosensing;Doxorubicin
Issue Date: 16-Oct-2018
Abstract: Multifunctional nanocomposites containing intrinsic property for serving as the sensing elements as well as targeted nanoconjugates are highly preferred in various therapeutic applications. In this work, nanocomposites of graphene quantum dots (GQDs) and Fe3O4 with conjugation of lectin protein, concanavalin A, to form GQD-ConA@ Fe3O4 nanocomposites are developed for both detection of cancer cell and release of drugs to HeLa cells. The GQD-ConA@ Fe3O4 nanocomposites deposited on Pt electrode can detect cancerous HeLa cells over normal endothelial cells with a dynamic linear range of 5 x 10(2) to 1 x 10(5) cells mL(-1) with a detection limit of 273 cell mL(-1). The GQD-ConA@ Fe3O4 also can serve as nanocarriers for loading and delivering doxorubicin (Dox). The in vitro cell images show that the Dox concentration in HeLa cells is enhanced more than double in the presence of external magnetic field due to the incorporation of Fe3O4 in the nanocarrier. The cytotoxicity assay indicates that the susceptibility of cancerous HeLa cells to Dox is 13% higher than that of normal cells, confirming the selective role of ConA in nanocarriers. Results clearly indicate the GQD-ConA@ Fe3O4 nanocomposites as a promising material for cancer cell detection and targeted Dox release toward HeLa cells which can serve as the multifunctional platform for novel cancer cell diagnostic and therapeutic applications. (C) 2018 Elsevier B.V. All rights reserved.
URI: http://dx.doi.org/10.1016/j.aca.2018.04.029
http://hdl.handle.net/11536/145070
ISSN: 0003-2670
DOI: 10.1016/j.aca.2018.04.029
Journal: ANALYTICA CHIMICA ACTA
Volume: 1027
Begin Page: 109
End Page: 120
Appears in Collections:Articles