Lemon juice-derived nitrogen-doped carbon quantum dots for highly sensitive and selective determination of ferrous ions and cell imaging

被引:6
|
作者
Zhang, Yue [1 ]
Li, Zhenjiang [2 ]
Sheng, Liying [1 ,2 ]
Meng, Alan [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Key Lab Opt Elect Sensing & Analyt Chem Life Sci, MOE,State Key Lab Base Ecochem Engn, Qingdao 266042, Shandong, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, Qingdao 266042, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescence probe; Nitrogen-doped carbon quantum dots; Fe2+detection; Low cytotoxicity; Bioimaging; FLUORESCENT-PROBES; FE2+; DIFFERENTIATION; ACID;
D O I
10.1016/j.colsurfa.2022.130580
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ferrous ion (Fe2+) plays an important role in a large number of chemical and biological processes in living organisms. So, the accurate and rapid determination of Fe2+ in environmental and biological systems is an important issue. In this paper, N-CDs with uniform particle size, outstanding water solubility, favorable stability, high quantum yield (QY, 58.66 %) and excellent photoluminescence performance were prepared by one-step hydrothermal method using biomass lemon and ethylene diamine. The N-CDs showed a bright blue fluorescence under UV light. This new type of N-CDs can be used to effectively detect Fe2+ with high selectivity and sensitivity. It displayed a fine linear relationship in the range of 2-625 & mu;\M with the LOD of 0.063 & mu;M under optimum conditions. The possible fluorescence quenching mechanism can be ascribed to the static quenching (SQ) and internal filtration effect (IFE) for Fe2+. More importantly, the optical imaging performance and cytotoxicity of N-CDs were also demonstrated. The results showed that N-CDs owned low cytotoxicity and glorious biocompatibility, and could be used as a biological imaging agent for labeling Hela cells. Therefore, this study possesses expansive application prospects in environmental monitoring and bioanalysis.
引用
收藏
页数:8
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