Chemiluminescence determination of dopamine using N, P-graphene quantum dots after preconcentration on magnetic oxidized nanocellulose modified with graphene quantum dots.
Roya AfsharipourShayessteh DadfarniaAli Mohammad Haji ShabaniPublished in: Mikrochimica acta (2022)
A novel sorbent consisting of magnetic oxidized nanocelluloses modified with graphene quantum dots was prepared and used for the separation and preconcentration of dopamine. The eluted dopamine from the sorbent was determined by a designed chemiluminescence system containing luminol, H 2 O 2 , Fe 3+ , and graphene quantum dots doped with nitrogen and phosphorus. Graphene quantum dots cause an increase in the intensity of the chemiluminescence system of luminol-H 2 O 2 , but the presence of Fe 3+ ions in this system decreases its intensity because of the sorption of the Fe 3+ ions on the surface of P, N-graphene quantum dots. However, the addition of dopamine resulted in the retrieval of P, N-graphene quantum dots, as well as the chemiluminescence intensity, due to the formation of its complex with Fe 3+ . The sorbent made of magnetic oxidized nanocelluloses modified with graphene quantum dots was characterized by various analytical techniques, and the effective parameters on the extraction of dopamine were investigated and optimized. Under the optimized conditions, the method displayed good linearity in the concentration range 0.25-17.5 µg L -1 for dopamine (R 2 = 0.9918) with a limit of detection of 0.054 µg L -1 . The intra- and inter-day relative standard deviations at a 10.0 µg L -1 concentration level of dopamine (n = 6) were 2.6 and 4.1%, respectively. This method was successfully applied to the extraction and determination of dopamine in human serum and urine samples.
Keyphrases
- quantum dots
- molecularly imprinted
- sensitive detection
- solid phase extraction
- energy transfer
- uric acid
- room temperature
- carbon nanotubes
- walled carbon nanotubes
- liquid chromatography
- prefrontal cortex
- metal organic framework
- loop mediated isothermal amplification
- metabolic syndrome
- mass spectrometry
- tandem mass spectrometry
- ionic liquid
- low density lipoprotein
- gas chromatography
- aqueous solution
- heavy metals