A Comparison between High-Performance Countercurrent Chromatography and Fast-Centrifugal Partition Chromatography for a One-Step Isolation of Flavonoids from Peanut Hulls Supported by a Conductor like Screening Model for Real Solvents.
Mats KieneSvenja BlumGerold JerzPeter WinterhalterPublished in: Molecules (Basel, Switzerland) (2023)
Peanut hulls ( Arachis hypogaea , Leguminosae ), which are a side stream of global peanut processing, are rich in bioactive flavonoids such as luteolin, eriodictyol, and 5,7-dihydroxychromone. This study aimed to isolate these flavonoid derivatives by liquid-liquid chromatography with as few steps as possible. To this end, luteolin, eriodictyol and 5,7-dihydroxychromone were isolated from peanut hulls using two different techniques, high-performance countercurrent chromatography (HPCCC) and fast-centrifugal partition chromatography (FCPC). The suitability of the biphasic solvent system composed of n -hexane/ethyl acetate/methanol/water (1.0/1.0/1.0/1.5; v / v / v / v ) was determined by the Conductor like Screening Model for Real Solvents ( COSMO-RS ), which allowed the partition ratio K D -values of the three main flavonoids to be calculated. After a one-step HPCCC separation of ~1000 mg of an ethanolic peanut hull extract, 15 mg of luteolin and 8 mg of eriodictyol were isolated with purities over 96%. Furthermore, 3 mg of 5,7-dihydroxychromone could be isolated after purification by semi-preparative reversed-phase liquid chromatography (semi-prep. HPLC) in purity of over 99%. The compounds were identified by electrospray ionization mass spectrometry (ESI-MS) and nuclear magnetic resonance spectroscopy (NMR).
Keyphrases
- liquid chromatography
- mass spectrometry
- tandem mass spectrometry
- high resolution mass spectrometry
- ionic liquid
- high performance liquid chromatography
- simultaneous determination
- high resolution
- high speed
- gas chromatography
- ms ms
- solid phase extraction
- capillary electrophoresis
- magnetic resonance
- oxidative stress
- multiple sclerosis
- anti inflammatory
- structure activity relationship