| Authors | حسین داستیار,سید مهدی قریشی,میلاد غنی |
| Journal | Polycyclic Aromatic Compounds |
| Page number | 2001 |
| Volume number | 43 |
| IF | 2.4 |
| Paper Type | Full Paper |
| Published At | 2023-02-20 |
| Journal Grade | Scientific - research |
| Journal Type | Electronic |
| Journal Country | Iran, Islamic Republic Of |
| Journal Index | SCOPUS ,JCR |
Abstract
A shaker-assisted liquid–liquid microextraction followed by solidification of
floating organic droplet and the final back-extraction method (SALLMESFOD-BE) was introduced for the simultaneous quantification of benzoic
acid (BA) and sorbic acid (SA) (as the model analytes) in different kinds of
food products. The presented method used partial least squares calibration
and UV–Vis detection. Then, the organic solvent was solidified and collected from the solution. Finally, the extracted analytes were backextracted into an alkaline solution and analyzed by UV–Vis. Under the optimized condition, the calibration graph was linear in the range of 1–200 ng
mL1 and 1–250 ng mL1 (R2 > 0.995) for BA and SA, respectively. The limits of detection (LODs) of 0.5 ng mL1 and 0.6 ng mL1 were determined
for BA and SA, respectively. The inter-day relative standard deviations
(RSDs) were in the range of 2.9–3.1% and 2.6–2.8% for BA and SA, respectively. The intra-day RSDs were also in the range of 2.6–2.9% and 2.4–2.7%,
respectively. The calculated enrichment factor (EF) and percent enrichment
recovery (ER%) were within the range of 16.4–16.6 and 98–99 for BA and
SA, respectively. The method was used for the determination of selected
model analytes in real samples, and satisfactory results were obtained.
Since very simple instruments were used, this method is affordable, efficient and convenient for extraction and simultaneous determination of BA
and SA in real samples