A fluorometric aptamer based assay for cytochrome C using fluorescent graphitic carbon nitride nanosheets

被引:69
|
作者
Salehnia, Foad [1 ]
Hosseini, Morteza [2 ]
Ganjali, Mohammad Reza [1 ,3 ]
机构
[1] Univ Tehran, Fac Chem, Ctr Excellence Electrochem, Tehran, Iran
[2] Univ Tehran, Fac New Sci & Technol, Dept Life Sci Engn, Tehran, Iran
[3] Univ Tehran Med Sci, Biosensor Res Ctr, Endocrinol & Metab Mol & Cellular Res Inst, Tehran, Iran
关键词
2D material; G-C3N4; nano-sheets; Melamine; Pyrolysis; Quenching; Off-on assay; X-ray diffraction; Scanning electron microscopy; Transmission electron microscopy; PHASE C3N4 NANOSHEETS; CELLS; MITOCHONDRIA; QUANTITATION; RESPIRATION; APOPTOSIS; RELEASE; SWITCH; DEATH; IONS;
D O I
10.1007/s00604-017-2130-6
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method is introduced for the fluorometric turn-on detection of cytochrome C (cyt c) by using a specific aptamer and nanosheets composed of fluorescent graphitic carbon nitride (g-C3N4) nanosheets. Bulk g-C3N4 was obtained by pyrolysis of melamine at 550 A degrees C. The nanosheets were characterized by scanning electron microscopy and X-ray diffraction. The material was then subjected to protonation and exfoliation to obtain blue fluorescent g-C3N4 nano-sheets. The adsorption of aptamers on the surface of the g-C3N4 nanosheets leads to quenching of its fluorescence (measured at excitation/emission wavelengths of 320/450 nm), but fluorescence is restored on addition of cyt c. Response is linear in the 16 to 140 nM cyt c concentration window, and the detection limit is as low as 2.6 nM. The assay is simple, inexpensive, and can be easily performed. It is selective for cyt c over a number of interfering species. The method was successfully applied to the determination of cyt c in spiked human serum samples.
引用
收藏
页码:2157 / 2163
页数:7
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