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通过协同光催化和物理切割增强钛酸钠/石墨烯量子点自支撑膜的抗菌活性

Enhanced Antibacterial Activity of Sodium Titanate/Graphene Quantum Dot Self-Supporting Membranes via Synergistic Photocatalysis and Physical Cutting.

作者信息

Shen Shuling, Wang Ji, Li Yaru, Liu Xinjuan, Tang Zhihong, Xiu Huixin, Li Jing, Zhou Guanglei

机构信息

School of Materials and Chemistry, University of Shanghai for Science and Technology, Shanghai 200093, China.

Academy of Forensic Science, Shanghai 200063, China.

出版信息

Materials (Basel). 2025 Apr 17;18(8):1844. doi: 10.3390/ma18081844.

Abstract

Graphene quantum dots (GQDs) show significant promise as antibacterial agents, but their application is hindered by several limitations, including potential cytotoxicity at high concentrations, as well as concerns regarding aggregation and reusability. In this study, sodium titanate (NTO) ultralong nanotubes were utilized as both a photocatalyst and support for GQDs. The NTO/GQDs heterojunction was formed by embedding GQDs nanoplates onto the walls of NTO nanotubes. This integration significantly improved the visible light absorption and enhanced the separation and transfer of electron-hole pairs, leading to an efficient photocatalytic antibacterial process. The NTO/GQD-8 self-supporting membrane composed of these ultralong nanotubes demonstrated outstanding antibacterial efficiency (99.99%) against and exhibited remarkable cycling stability. Radical scavenging experiments revealed that ∙OH and e were the primary reactive species driving the photocatalytic antibacterial process. Notably, NTO and NTO/GQDs-8 exhibited distinct antibacterial outcomes. After photocatalytic treatment with NTO/GQDs-8, cells were completely fragmented, with no intact cell structures remaining due to the synergy effect of GQDs' physical cutting during photocatalytic treatment.

摘要

石墨烯量子点(GQDs)作为抗菌剂显示出巨大的潜力,但其应用受到若干限制,包括高浓度时的潜在细胞毒性,以及对聚集和可重复使用性的担忧。在本研究中,钛酸钠(NTO)超长纳米管既用作光催化剂,又作为GQDs的载体。通过将GQDs纳米片嵌入NTO纳米管壁上形成NTO/GQDs异质结。这种整合显著提高了可见光吸收,并增强了电子-空穴对的分离和转移,从而实现了高效的光催化抗菌过程。由这些超长纳米管组成的NTO/GQD-8自支撑膜对 表现出出色的抗菌效率(99.99%),并具有显著的循环稳定性。自由基清除实验表明,∙OH和e是驱动光催化抗菌过程的主要活性物种。值得注意的是,NTO和NTO/GQDs-8表现出不同的抗菌结果。在用NTO/GQDs-8进行光催化处理后, 细胞完全破碎,由于光催化处理过程中GQDs的物理切割协同作用,没有完整的细胞结构残留。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9233/12028856/846babdb0ef2/materials-18-01844-g001.jpg

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