4.7 Article

NIR-emitting carbon dots for discriminative imaging and photo-inactivation of pathogenic bacteria

期刊

CHEMICAL ENGINEERING JOURNAL
卷 450, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.137384

关键词

NIR-emitting carbon dots; Discriminative imaging; Fluorescence imaging-guided photodynamic-inactivating bacteria

资金

  1. National Science Foundation of China [21878039, 21925802, 22090010]
  2. National Key Research and Development Plan [2018AAA0100301]
  3. NSFC-Liaoning United Fund [U1908202]

向作者/读者索取更多资源

By synthesizing real near-infrared emitting carbon dots Cy7-CDs, the rapid identification of bacterial species and monitoring of bacterial viability can be achieved, which holds great potential for the diagnosis and treatment of infectious diseases.
The rapid identification of pathogens and their viability are important for the effective diagnosis and treatment of infectious diseases. In this study, real near-infrared (NIR)-emitting carbon dots (Cy7-CDs, lambda(max) = 710 nm) were synthesized using a solvothermal reaction method, in which the optical properties of cyanine dye were partially retained, and the water solubility and fluorescence quantum yield were greatly improved. The abundant functional groups on the surface of Cy7-CDs facilitated their interactions with biomolecules within the bacteria. Cy7-CDs quickly integrated into cell wall of G(+) bacteria with obvious fluorescence or outer membrane of G- bacteria with no fluorescence. As a result, Cy7-CDs can not only be used to identify bacterial species (G(+) or G(-) bacteria), but can also be used to quickly and efficiently monitor bacterial viability using fluorescence imaging. Furthermore, within 15 min, 97.7% Escherichia coli (G(-)) and 95.8% Methicillin-resistant Staphylococcus aureus (G(+)) were killed rapidly by Cy7-CDs, due to its powerful ability to produce singlet oxygen (O-1(2)) under single light irradiation (650 nm). Therefore, the Cy7-CDs strategy has the potential to be used for diagnosis and treatment of bacterial disease integration.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据