Novel synthesis of a dual fluorimetric sensor for the simultaneous analysis of levodopa and pyridoxine

Anal Bioanal Chem. 2021 Jan;413(2):377-387. doi: 10.1007/s00216-020-03005-9. Epub 2020 Oct 27.

Abstract

Herein, a fluorimetric sensor was fabricated based on molecularly imprinted polymers (MIPs) with two types of carbon dots as fluorophores. The MIPs produced had similar excitation wavelengths (400 nm) and different emission wavelengths (445 and 545 nm). They were used for the simultaneous analysis of levodopa and pyridoxine. First, two types of carbon dots, i.e. nitrogen-doped carbon dots (NCDs) with a quantum yield of 43%, and carbon dots from o-phenylenediamine (O-CDs) with a quantum yield of 17%, were prepared using the hydrothermal method. Their surfaces were then covered with MIPs through the reverse microemulsion method. Finally, a mixture of powdered NCD@MIP and O-CD@MIP nanocomposites was used for the simultaneous fluorescence measurement of levodopa and pyridoxine. Under optimal conditions using response surface methodology and Design-Expert software, a linear dynamic range of 38 to 369 nM and 53 to 457 nM, and detection limits of 13 nM and 25 nM were obtained for levodopa and pyridoxine, respectively. The capability of the proposed fluorimetric sensor was investigated in human blood serum and urine samples. Graphical Abstract Schematic representation of nitrogen-doped carbon dots (NCDs), carbon dots from o-phenylenediamine (O-CDs), NCDs coated with imprinted polymers (NCD@MIPs), and O-CDs coated with imprinted polymers (O-CD@MIPs) in the presence and absence of levodopa and pyridoxine.

Keywords: Carbon dots; Fluorescence sensor; Levodopa; Molecularly imprinted polymers; Pyridoxine; Simultaneous analysis.

MeSH terms

  • Calibration
  • Carbon / chemistry
  • Chemistry Techniques, Analytical
  • Emulsions
  • Fluorescent Dyes
  • Fluorometry / methods*
  • Humans
  • Levodopa / blood*
  • Levodopa / urine*
  • Light
  • Limit of Detection
  • Microscopy, Electron, Transmission
  • Molecular Imprinting / methods
  • Nanocomposites
  • Phenylenediamines / analysis
  • Polymers / chemical synthesis
  • Pyridoxine / blood*
  • Pyridoxine / urine*
  • Quantum Dots
  • Scattering, Radiation
  • Spectrometry, Fluorescence
  • X-Ray Diffraction

Substances

  • Emulsions
  • Fluorescent Dyes
  • Phenylenediamines
  • Polymers
  • Levodopa
  • Carbon
  • 1,2-diaminobenzene
  • Pyridoxine