期刊
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 413, 期 2, 页码 377-387出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00216-020-03005-9
关键词
Carbon dots; Levodopa; Pyridoxine; Fluorescence sensor; Molecularly imprinted polymers; Simultaneous analysis
A fluorimetric sensor based on MIPs and two types of carbon dots as fluorophores was successfully engineered for the simultaneous analysis of levodopa and pyridoxine. The sensor showed a linear dynamic range, low detection limits, and was capable of analyzing human blood serum and urine samples.
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.
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