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Fluorescent sensing of colloidal CePO4:Tb nanorods for rapid, ultrasensitive and selective detection of vitamin C
被引:57
作者:
Di, Weihua
[1
,2
]
Shirahata, Naoto
[2
,3
]
Zeng, Haibo
[4
]
Sakka, Yoshio
[1
,2
]
机构:
[1] Natl Inst Mat Sci, World Premier Int Res Ctr Initiat Mat Nanoarchitr, Tsukuba, Ibaraki 3050047, Japan
[2] NIMS, Fine Particle Proc Grp, Nano Ceram Ctr, Tsukuba, Ibaraki 3050047, Japan
[3] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
[4] Chinese Acad Sci, Key Lab Mat Phys, Anhui Key Lab Nanomats & Nanotechnol, Inst Solid State Phys, Hefei 230031, Peoples R China
关键词:
ASCORBIC-ACID;
ENERGY-TRANSFER;
QUANTUM-DOTS;
3D XPS;
NANOPARTICLES;
LUMINESCENCE;
BIOSENSOR;
ASSAY;
WATER;
FRET;
D O I:
10.1088/0957-4484/21/36/365501
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Vitamin C is an essential biological molecule for living organisms. The detection of vitamin C is always required due to its wide use in chemical, biological and pharmaceutical engineering. Here, we established a novel sensing system for rapid, ultrasensitive and highly selective detection of vitamin C based on a 'turn-on' fluorescent method. The turn-on fluorescent sensing system was built up of a colloidal CePO4: Tb nanocrystalline solution with its fluorescence quenched by KMnO4. The addition of vitamin C leads to a linear increase of fluorescence. The sensing principle of nanocrystalline CePO4: Tb is based on a redox reaction via simply modulating the surface chemistry of nanocrystals. Our present sensing system for vitamin C exhibits a rapid response rate of less than 2 min, and highly selective and ultrasensitive detection with a detection limit of 108 nM, which is two orders of magnitude lower than that acquired by previously reported methods. The repeated reversibility of fluorescence quenching/recovery with time revealed a high reproducibility and long-term stability of our sensing materials. Furthermore, our developed sensing material overcomes the disadvantages such as complex surface modification/immobilization and serious biotoxicity compared to quantum-dot-based fluorescent sensing systems.
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