纳米复合材料
石墨烯
材料科学
细胞凋亡
锌
细胞毒性
细胞培养
光热治疗
细胞毒性T细胞
纳米技术
程序性细胞死亡
胶质瘤
生物物理学
癌症研究
化学
体外
生物
生物化学
冶金
遗传学
作者
Bárbara L. Jovito,Leonardo G. Paterno,Maria J. A. Sales,Marcos A. Gross,Luciano Paulino Silva,P De Souza,Sônia Nair Báo
标识
DOI:10.1021/acsabm.0c01369
摘要
Glioblastoma is considered the most aggressive and prevalent type of glioma. Resistance mechanisms, side effects, and the blood–brain barrier are factors that make its treatment difficult, requiring the development of alternative therapeutic strategies. Herein, we propose a nanocomposite composed of carboxylated graphene oxide nanosheets decorated with zinc oxide nanoparticles and post-functionalized with Pluronic (GOC-ZnO-P) for chemotherapy against U87MG and U138MG human glioblastoma cell lines. The GOC-ZnO-P formulation is fairly stable in the physiological medium (DMEM-FBS) and demonstrates selectivity toward tumor cell lines, even though it is less cytotoxic than free ZnO. Whereas the photothermal activity of the nanocomposite has a negligible cytotoxic effect, images obtained by scanning and transmission electron microscopies reveal that it induces changes in adhesion points and roughness of the tumor cell membrane, and it is uptaken through vesicles and capable of accumulating in the nucleus, a process that can induce cell death by apoptosis, as verified by flow cytometry. In summary, the GOC phase serves as an inert platform for transporting ZnO, which maintains its selectivity for tumor cells and does not interfere with the mechanisms for inducing apoptotic pathways. Therefore, the GOC-ZnO-P nanocomposite offers a strategy for glioblastoma treatment.
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