2019
DOI: 10.1039/c9ra08477k
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Carbon quantum dots as a fluorophore for “inner filter effect” detection of metronidazole in pharmaceutical preparations

Abstract: CDs were prepared using Houttuynia cordata via hydrothermal process, the absorption band of MNZ can well overlap the excitation bands of CDs, a simple, rapid approach for detection of MNZ was established on the basis of IFE.

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Cited by 27 publications
(15 citation statements)
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References 54 publications
(66 reference statements)
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“…It has been previously reported by Devi et al that the JM complex (TNT-NH 2 ) shows the absorption in wavelength ranging from 400 to 550 nm [4,30]. Therefore, the possible spectral overlap between the fluorescence emission spectrum of the IRMOF-3 particles and the absorption spectrum of the JM complex is expected to result in this energy transfer, i.e., IFE [4,30,31].…”
Section: Selectivity and Interference Studymentioning
confidence: 93%
“…It has been previously reported by Devi et al that the JM complex (TNT-NH 2 ) shows the absorption in wavelength ranging from 400 to 550 nm [4,30]. Therefore, the possible spectral overlap between the fluorescence emission spectrum of the IRMOF-3 particles and the absorption spectrum of the JM complex is expected to result in this energy transfer, i.e., IFE [4,30,31].…”
Section: Selectivity and Interference Studymentioning
confidence: 93%
“…It is noteworthy that the uorescent probe of this method uses natural biomass as carbon source and adopts one-step hydrothermal method, which is simpler and more environmentally friendly. FCNs Hydrothermal method gardenia 0.8 -225 0.28 [31] CDs Solvent hot method H. cordata 3.3-240 0.12 [32] Cu/NCQDs Hydrothermal method frangipani 0-350 0.28 work…”
Section: Analysis and Test Of Actual Samplesmentioning
confidence: 99%
“… Analyte Method Matrix Linearity range LOD Refs. MNZ Extractional spectrophotometry Pure and dosage forms 2.50–22.50 µg/mL 5.33 × 10 −2 µg/mL 9 UV-spectrophotometry Pure and dosage forms 2.0–16.0 µg/mL 12 RP-HPLC Pure and dosage forms 0.10–0.30 mg/mL 22 Flow injection analysis Pure and dosage forms 2.0–20.0 mg/L 0.7 mg/L 29 Capillary electrophoresis Porcine muscle samples 5.00–300.0 µg/kg 0.5 µg/kg 32 Spectrofluorimetry (N-CDs were synthesized by a microwave-assisted method) Real milk samples 0.5–22.0 µM 0.22 µM 15 Spectrofluorimetry (CDs were synthesized by a hydrothermal technique) Pure and dosage forms 3.3 × 10 −6 —2.4 × 10 −4 M 1.2 × 10 −7 M 18 ONZ Extractional spectrophotometry Pure and dosage forms 7.50–35.0 µg/mL 5.01 × 10 –2 µg/mL 9 Spectrophotometry Pure and dosage forms …”
Section: Introductionmentioning
confidence: 99%
“…Several methods for analysis of MNZ, TNZ and/or ONZ in bulk and dosage forms, as-well-as-biological-fluids, have been published. These methods include-spectrophotometry [9][10][11][12][13][14] , spectrofluorimetry [15][16][17][18][19] , HPLC [20][21][22] , electrochemistry [23][24][25][26][27] , non-aqueous titration 28 , flow injection analysis 29 , capillary electrophoresis [30][31][32] , and gas chromatography 33 .…”
mentioning
confidence: 99%