A Multifunctional Graphene Oxide Platform for Targeting Cancer

被引:19
作者
Bugarova, Nikola [1 ]
Spitalsky, Zdenko [1 ]
Micusik, Matej [1 ]
Bodik, Michal [2 ]
Siffalovic, Peter [2 ]
Koneracka, Martina [3 ]
Zavisova, Vlasta [3 ]
Kubovcikova, Martina [3 ]
Kajanova, Ivana [4 ]
Zat'ovicova, Miriam [4 ]
Pastorekova, Silvia [4 ]
Slouf, Miroslav [5 ]
Majkova, Eva [2 ]
Omastova, Maria [1 ]
机构
[1] SAS, Polymer Inst, Dubravska Cesta 9, Bratislava 84541, Slovakia
[2] SAS, Inst Phys, Dubravska Cesta 9, Bratislava 84511, Slovakia
[3] SAS, Inst Expt Phys, Watsonova 47, Kosice 04001, Slovakia
[4] SAS, Biomed Res Ctr, Inst Virol, Dubravska Cesta 9, Bratislava 84511, Slovakia
[5] Inst Macromol Chem AS CR, Heyrovskeho 2, Prague 16206 6, Czech Republic
关键词
graphene oxide; magnetic nanoparticles; monoclonal antibodies; tumor targeting; CARBONIC-ANHYDRASE-IX; FE3O4; NANOPARTICLES; DRUG-DELIVERY; BIODISTRIBUTION; COMPOSITES; ROADMAP; MICE;
D O I
10.3390/cancers11060753
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diagnosis of oncological diseases remains at the forefront of current medical research. Carbonic Anhydrase IX (CA IX) is a cell surface hypoxia-inducible enzyme functionally involved in adaptation to acidosis that is expressed in aggressive tumors; hence, it can be used as a tumor biomarker. Herein, we propose a nanoscale graphene oxide (GO) platform functionalized with magnetic nanoparticles and a monoclonal antibody specific to the CA IX marker. The GO platforms were prepared by a modified Hummers and Offeman method from exfoliated graphite after several centrifugation and ultrasonication cycles. The magnetic nanoparticles were prepared by a chemical precipitation method and subsequently modified. Basic characterization of GO, such as the degree of oxidation, nanoparticle size and exfoliation, were determined by physical and chemical analysis, including X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), and atomic force microscopy (AFM). In addition, the size and properties of the poly-L-lysine-modified magnetic nanoparticles were characterized. The antibody specific to CA IX was linked via an amidic bond to the poly-L-lysine modified magnetic nanoparticles, which were conjugated to GO platform again via an amidic bond. The prepared GO-based platform with magnetic nanoparticles combined with a biosensing antibody element was used for a hypoxic cancer cell targeting study based on immunofluorescence.
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页数:19
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