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Biomass-derived carbon dots as a sensitive and selective dual detection platform for fluoroquinolones and tetracyclines
被引:43
作者:
Korah, Binila K.
[1
]
Chacko, Anu Rose
[1
]
Mathew, Sneha
[1
]
John, Bony K.
[1
]
Abraham, Thomas
[1
,2
]
Mathew, Beena
[1
]
机构:
[1] Mahatma Gandhi Univ, Sch Chem Sci, Priyadarsini Hills PO, Kottayam 686560, Kerala, India
[2] Catholicate Coll, Dept Chem, Pathanamthitta 689645, Kerala, India
关键词:
Carbon dot;
Curcuma amada;
Fluorescence;
Electrochemical analysis;
Tetracyclines;
Fluoroquinolones;
RATIOMETRIC FLUORESCENT-PROBE;
MICROWAVE-ASSISTED SYNTHESIS;
RESONANCE ENERGY-TRANSFER;
ONE-STEP SYNTHESIS;
ELECTROCHEMICAL APTASENSOR;
ULTRASENSITIVE DETECTION;
SENSING PLATFORM;
HUMAN URINE;
NANODOTS;
SENSOR;
D O I:
10.1007/s00216-022-04119-y
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
A novel carbon dot (CD) was synthesized through the facile and simple hydrothermal method from Curcuma amada, as the precursor for the first time. These CDs with an average diameter of 4.6 nm display blue fluorescence, with excitation/emission maxima at 360/445 nm and a quantum yield of 14.1%. It exhibited high stability under different conditions and was characterized using various techniques. These CDs can be employed as a dual-sensing platform to detect tetracyclines and fluoroquinolones, two antibiotic classes. Even though antibiotics are regarded as an inevitable commodity, overuse and improper management of discarded antibiotics pose a severe threat to the environment. Herein, we developed a dual-sensing, biocompatible sensor with high selectivity and sensitivity to detect antibiotics. CD was employed as a fluorescence probe and detected tetracycline and fluoroquinolone antibiotic through inner filter effect-based fluorescence quenching and hydrogen bonding-based enhancement process, respectively. The linear range was 0-16 mu M and the detection limit was 33 nM for tetracycline and 2 nM for fluoroquinolone antibiotic. As an electrochemical probe, CD selectively detected tetracycline with a lower detection limit of 0.5 nM over a linear range of 0-16 mu M. Using both methods, a real sample analysis of the developed sensor exhibited accurate reliability and precision.
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页码:4935 / 4951
页数:17
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