Pilot continuous centrifugal liquid-liquid extraction of extra virgin olive oil biophenols and gram-scale recovery of pure oleocanthal, oleacein, MFOA, MFLA and hydroxytyrosol

• Published in: Separation and purification technology 2021-01, Vol.255, p.117692, Article 117692
• Main Authors: Angelis, Apostolis, Michailidis, Dimitris, Antoniadi, Lemonia, Stathopoulos, Panagiotis, Tsantila, Vasiliki, Nuzillard, Jean-Marc, Renault, Jean-Hugues, Skaltsounis, Leandros A.
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Annular centrifugal extractor; Centrifugal partition chromatography; Chemical engineering; Chemical Sciences; Continuous liquid-liquid extraction; Extra virgin olive oil; Food engineering; Life Sciences; Oleacein; Oleocanthal
• ISSN: 1383-5866; 1873-3794
• DOI: 10.1016/j.seppur.2020.117692

[Display omitted] •Pioneering pilot scale Annular Centrifugal Extraction performed on olive oil.•Considerable amounts of high-value biophenols were obtained.•Centrifugal Partition Chromatography fractionation of olive oil.•Isolation of oleocanthal, oleacein, MFOA, MFLA and hydroxytyrosol in gram scale.•New minor compounds of olive oil were isolated. This study provides an efficient pilot-scale liquid-liquid extraction process for the recovery of total phenolic fraction (TPF) from extra virgin olive oil (EVOO) and the further purification of the major TPF constituents (oleocanthal, oleacein, monoaldehydic form of oleuropein aglycone, monoaldehydic form of ligstroside aglycone and hydroxytyrosol) using successively centrifugal partition chromatography and reversed phase high performance liquid chromatography. Special attention was paid for the selection of the appropriate raw material, which should be rich in the targeted high-value compounds. For the extraction of the selected EVOOs, a green technique based on liquid-liquid partitioning using the biphasic system n-Hept/EVOO/EtOH/H2O 3:2:3:2 v/v was carried out, first on pioneering laboratory-scale annular centrifugal extractor (ACE) and then on pilot device. 240 L from three different EVOOs (3x80 L of each EVOO) were extracted yielding 285 g of TPF in approximately 2 h. The second step of this procedure was the purification of the target compounds. A preparative centrifugal partition chromatography (CPC) process was firstly applied for the initial TPF fractionation using a step gradient elution-extrusion method with a series of 4 biphasic systems composed of n-Hept/EtOAc/EtOH/H2O in ratios 4:1:3:2, 3:2:3:2, 2:3:3:2 and 1:4:3:2 (v/v/v/v). Preparative reversed phase high performance liquid chromatography (prep-RP-HPLC) was then carried out to polish the target compounds from the enriched CPC fractions resulting in purity higher than 97%. In parallel, the above purification analysis led to the isolation of four minor TPF constituents of which three are new natural products (EDA lactone, (1R, 8E)-1-ethoxy-ligstroside aglycon and (1S, 8E)-1-ethoxy-ligstroside aglycon) and one ((9E, 11E)-13-oxotrideca-9,11-diencoic acid) is described for the first time as EVOO constituent.