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UV-Enhanced Cytotoxicity of CdTe Quantum Dots in PANC-1 Cells Depend on Their Size Distribution and Surface Modification

机译:紫外线增强CNC量子点在PANC-1细胞中的细胞毒性取决于其大小分布和表面修饰

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The cytotoxicity of quantum dots (QDs) under normal conditions has received more and more attention, but their cytotoxicity under light illumination has not been fully investigated. In this study, different sized CdTe QDs coated with mercaptopropionic acid (MPA) and N-acetylcysteine (NAC) were employed to investigate the influences of size distribution and surface modification on their UV-enhanced cytotoxicity and mechanism. The results indicated that different sized MPA-CdTe QDs exhibited distinct cytotoxicity under UV illumination and the smaller-sized QDs presented more obviously damages to cells than the larger-sized QDs. Comparing with MPA-CdTe QDs, NAC-CdTe QDs had better cellular metabolizability and lower cytotoxicity. The generation of reactive oxygen species (ROS) were also investigated. The results revealed that ROS in cells containing MPA-CdTe QD_(538) were about 1.7 times of NAC-CdTe QD_(538) under UV illumination. ROS might play an important role in the UV-enhanced cytotoxicity of QDs. By selecting appropriate surface modifications and particle sizes, the cytotoxicity of QDs under UV illumination could be controlled.
机译:量子点(QDs)在正常条件下的细胞毒性已受到越来越多的关注,但是在光照下其量子点的细胞毒性尚未得到充分研究。在这项研究中,采用巯基丙酸(MPA)和N-乙酰半胱氨酸(NAC)包覆的不同尺寸的CdTe量子点来研究尺寸分布和表面改性对其紫外线增强细胞毒性和机理的影响。结果表明,不同大小的MPA-CdTe量子点在紫外线照射下表现出明显的细胞毒性,而较小的量子点比较大的量子点对细胞的损伤更为明显。与MPA-CdTe QD相比,NAC-CdTe QD具有更好的细胞代谢能力和更低的细胞毒性。还研究了活性氧(ROS)的产生。结果表明,在紫外线照射下,含有MPA-CdTe QD_(538)的细胞中的ROS约为NAC-CdTe QD_(538)的1.7倍。 ROS可能在量子点的紫外线增强的细胞毒性中起重要作用。通过选择适当的表面修饰和粒径,可以控制QD在紫外线照射下的细胞毒性。

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