荧光
检出限
生物相容性
化学
荧光寿命成像显微镜
纳米探针
分析化学(期刊)
纳米技术
纳米颗粒
材料科学
色谱法
光学
物理
有机化学
作者
Yu-Qi Liang,Xiaoyi Wu,Jiayu Zeng,Yanni Wu,Jia‐Ping Lai,Hui Sun
标识
DOI:10.1007/s00216-022-03908-9
摘要
The novel dual-emission carbon dots (DECDs) for highly selective and sensitive recognition of chlortetracycline (CTC) and cell imaging were synthesized successfully by one-step synthesis. The obtained DECDs possessed two fluorescence peaks (345 nm and 450 nm) and showed specific response to CTC, resulting in a decrease in fluorescence intensity at 345 nm, a blue shift, and an increase in fluorescence intensity at 450 nm. The obtained DECDs exhibited highly selective response to CTC and not to its analogues, such as tetracycline, doxycycline, and oxytetracycline. Thus, an excellent ratiometric probe for the detection of CTC was fabricated successfully and used for the detection of CTC in real samples with the detection limit (LOD) of 16.45 nM. More importantly, the DECDs were used for quantitative detection of CTC in living cells, which demonstrated excellent biocompatibility and broad prospects in biomedicine application. Finally, the excellent selectivity of DECDs toward CTC was attributed to the FRET mechanism and the formation of complexes.
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