Abstract

In this study, a rapid and efficient method has been used for the extraction and determination of morin and quercetin in fruit juice samples based on air-assisted liquid-liquid microextraction based on solidification of floating organic droplet and HPLC-UV. The effects of 7 important parameters on the extraction recovery were examined and were optimized by Plackett-Burman design and Central Composite design. According to the Plackett-Burman design results, ionic strength of the sample solutions, the aspiration/dispersion cycles, and the rate and time of centrifuge did not show significant effects on the extraction of morin and quercetin. The optimized conditions of extraction were as follows; the volume of the extraction solvent of 83.6 µL, pH of 4.34 for the sample, and 1-undecanol as extraction solvent. Under these conditions, the linear calibration curve was in the ranges of 1-1000 ng/mL and 0.5-1000 ng/mL for morin and quercetin, respectively, with the determination coefficient values above 0.99. The limit of detection of morin and quercetin was 0.3 and 0.2 ng/mL, respectively. The extraction recoveries for 10 ng/mL of morin and quercetin were 98.9% and 96.5%, respectively; while, relative standard deviations (n = 3) were lower than 3.2%.

Highlights

  • Flavonoids are an important group of natural polyphenolic compounds, which are the essential plant metabolites with antioxidant activity.[1]

  • enrichment factor (EF) is calculated according to the ratio of the final concentrations of analyte in the floating phase (Co) to its initial concentration in an aqueous sample (Caq)

  • The selection of an appropriate extraction solvent is crucial in the optimization of the AALLME-SFO process

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Summary

Introduction

Flavonoids are an important group of natural polyphenolic compounds, which are the essential plant metabolites with antioxidant activity.[1] Morin (MR) and quercetin (QR) are isomeric antioxidant flavonols widely distributed in fruits and vegetables.[2] Studies have shown that MR has numerous pharmacological activities such as coronary artery disease prevention, inhibition of proliferation of tumors, antioxidant, anticancer, anti-inflammatory, as well as free radicals scavenging activity.[3] It has been published that QR has several biological properties in the inhibition of human diseases, such as cancer, ulcer, diabetes, cataract, and allergies.[4] Based on these activities, many investigations have been undertaken to determine QR and MR in recent decades. Several techniques including high-performance liquid chromatography (HPLC),[5,6,7] thin-layer chromatography (TLC),[8] gas chromatography (GC),[9] micellar electrokinetic chromatography (MEKC),[10] capillary electrophoresis (CE),[11] and electrochemical methods[12] have been employed for the determination of MR and/or QR in various samples

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