4.6 Article

Gallic acid-affinity molecularly imprinted polymer adsorbent for capture of cis-diol containing Luteolin prior to determination by high performance liquid chromatography

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1637, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.chroma.2020.461829

Keywords

Luteolin; Gallic acid-affinity; Molecularly imprinted polymer; Adsorbent; Herbal medicines

Funding

  1. Key Projects of Natural Science Foundation of Heilongjiang Province of China [ZD2018001]
  2. University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province [UNPYSCT-2018179]

Ask authors/readers for more resources

A gallic acid-affinity molecularly imprinted polymer (G-MIP) was successfully used for the selective identification and capture of luteolin in herbal medicine samples. The method showed high adsorption capacity and superior recoveries, making it a potential platform for the determination of luteolin in complex matrices.
A gallic acid-affinity molecularly imprinted polymer (G-MIP) was first used as an adsorbent for selective identification and capture of luteolin (LTL) in herbal medicine samples. The G-MIP was prepared by using LTL as the template, gallic acid (GA) as the functional monomer, ethylene glycol dimethacrylate (EGDMA) as the crosslinking agent, and 2,2 1 -azobis(2-methylpropionitrie) (AIBN) as the initiator. The properties of G-MIP were characterized by FT-IR, transmission electron microscope, scanning electron microscope, dynamic light scattering, specific surface area, and X-ray photoelectron spectrum. The adsorption conditions were optimized, and the adsorption equilibrium model and adsorption kinetics model of the adsorbent were investigated under the best experimental conditions. The saturated adsorption capacity is 1.24 mg g(-1), which is not only higher than the adsorption capacity of 4-carboxyphenylboronic acid-affinity MIP adsorbent but also superior to those of many reported adsorbents for enriching of LTL. The LTL was quantified by HPLC. The linear range is 0.05-100 mg L-1, the detection limit is 0.020 mg L-1. This method was successfully applied in the selective recognition of LTL in herbal medicines with recoveries of 93.9-114.2%, and the relative standards deviations (RSDs) are 0.4-5.6%. Thus, this work provides a potential possibility and practical platform for the determination of LTL in complex matrices. (C) 2020 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available