School of Materials Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 500712, South Korea.
School of Materials Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 500712, South Korea; Fire Protection Laboratory, Chemistry Division, National Institute of Standards, 136, Giza 12211, Egypt.
J Colloid Interface Sci. 2017 Jul 15;498:364-377. doi: 10.1016/j.jcis.2017.03.057. Epub 2017 Mar 16.
A straightforward and facile method for the exfoliation of graphene sheets using poly(vinylpyrrolidone) nanoparticles of an average size of 42nm was developed and their dual role as pH-sensitive drug carrier and anti-cancer agent was evaluated. The cytotoxic impact of the exfoliated nanosheets (GRP-PVP-NP) was examined on various cells (HCT-116, HeLa, SCC-9, NIH-3T3 and HEK-293cells) by a series of assays. Their cytotoxic nature was attributed to affecting the mitochondrial enzyme activity, proliferation capability, and the formation of tight junctions in cancer cells. The endocytosis was found to be internalization mechanism for the cellular uptake of nanosheets. The generation of reactive oxygen species and elicitation of caspase-3 activity which was undoubtedly associated with triggering of oxidative stress speculated to be the dominant cause of the cytotoxic pattern of nanosheets against cancer cells. Additionally, the results also showed the role of the nanosheets as a pH-sensitive drug carrier through drug loading by supramolecular interaction. The efficient release of doxorubicin was seen at low pH and in an environment with a low oxygen concentration, thus under conditions mimicking the typical tumor microenvironment. Therefore, these findings provide the first evidence for a dual function of exfoliated graphene sheets and also elucidate the cytotoxic mechanism responsible for the cancer cell death.
开发了一种使用平均粒径为 42nm 的聚(N-乙烯基吡咯烷酮)纳米粒子直接且易于剥离石墨烯片的方法,并评估了其作为 pH 敏感药物载体和抗癌剂的双重作用。通过一系列测定,研究了剥离纳米片(GRP-PVP-NP)对各种细胞(HCT-116、HeLa、SCC-9、NIH-3T3 和 HEK-293 细胞)的细胞毒性影响。它们的细胞毒性性质归因于影响线粒体酶活性、增殖能力以及癌细胞中紧密连接的形成。发现内吞作用是纳米片被细胞摄取的内化机制。活性氧的产生和半胱天冬酶-3 活性的诱导,这无疑与引发氧化应激有关,推测这是纳米片对癌细胞产生细胞毒性作用的主要原因。此外,研究结果还表明纳米片作为通过超分子相互作用进行药物负载的 pH 敏感药物载体的作用。在低 pH 和低氧浓度的环境中可以看到阿霉素的有效释放,因此在模拟典型肿瘤微环境的条件下。因此,这些发现为剥离石墨烯片的双重功能提供了第一个证据,并阐明了导致癌细胞死亡的细胞毒性机制。