Folic acid-functionalized graphene oxide nanosheets via plasma etching as a platform to combine NIR anticancer phototherapy and targeted drug delivery

被引:65
|
作者
Mauro, Nicold [1 ,2 ]
Scialabba, Cinzia [1 ]
Agnello, Simonpietro [3 ]
Cavallaro, Gennara [1 ]
Giammona, Gaetano [1 ,4 ]
机构
[1] Univ Palermo, Dept Sci & Tecnol Biol Chim & Farmaceut STEBICEF, Lab Biocompatible Polymers, Via Archirafi 32, I-90123 Palermo, Italy
[2] Fdn Umberto Veronesi, Piazza Velasca 5, I-20122 Milan, Italy
[3] Univ Palermo, Dept Fis & Chim Emilio Segre, Via Archirafi 36, I-90123 Palermo, Italy
[4] Italian Natl Res Council, Inst Biophys, Via Ugo La Malfa 153, I-90146 Palermo, Italy
关键词
Graphene oxide; Breast cancer; Doxorubicin; Folic acid; Phototherapy; CANCER-CELLS; DOXORUBICIN; NANOPARTICLES; NANOMEDICINE; ABLATION; SYSTEM; AGENTS;
D O I
10.1016/j.msec.2019.110201
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
PEGylated graphene oxide (GO) has shown potential as NIR converting agent to produce local heat useful in breast cancer therapy, since its suitable photothermal conversion, high stability in physiological fluids, biocompatibility and huge specific surface. GO is an appealing nanomaterial for potential clinical applications combining drug delivery and photothermal therapy in a single nano-device capable of specifically targeting breast cancer cells. However, native GO sheets have large dimensions (0.5-5 mu m) such that tumor accumulation after a systemic administration is usually precluded. Herein, we report a step-by-step synthesis of folic acid-functionalized PEGylated GO, henceforth named GO-PEG-Fol, with small size and narrow size distribution (similar to 30 +/- 5 nm), and the ability of efficiently converting NIR light into heat. GO-PEG-Fol consists of a nano-GO sheet, obtained by fragmentation of GO by means of non-equilibrium plasma etching, fully functionalized with folic acid-terminated PEG(2000) chains through amidic coupling and azide-alkyne click cycloaddition, which we showed as active targeting agents to selectively recognize breast cancer cells such as MCF7 and MDA-MB-231. The GO-PEG-Fol incorporated a high amount of doxorubicin hydrochloride (Doxo) (> 33%) and behaves as NIR-light-activated heater capable of triggering sudden Doxo delivery inside cancer cells and localized hyperthermia, thus provoking efficient breast cancer death. The cytotoxic effect was found to be selective for breast cancer cells, being the IC50 up to 12 times lower than that observed for healthy fibroblasts. This work established plasma etching as a cost-effective strategy to get functionalized nano-GO with a smart combination of properties such as small size, good photothermal efficiency and targeted cytotoxic effect, which make it a promising candidate as photothermal agent for the treatment of breast cancer.
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页数:14
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