Infant formula and adult nutritionals. Determination of β-carotene, lycopene and lutein by reversed-phase ultra-high performance liquid chromatography (RP-UHPLC)
This document specifies a method for the quantitative determination of ?-carotene and lycopene in infant formula and adult nutritionals in solid (i.e. powders) or liquid (i.e. ready-to-feed liquids and liquid concentrates) forms using reversed-phase ultra-high performance liquid chromatography (RP-UHPLC) and UV-visible detection. The application range runs from 1 ?g/100 g to 1 500 ?g/100 g for lycopene and from 1 ?g/100 g to 2 250 ?g/100 g for ?-carotene. Based on the single-laboratory validation, the limit of detection (LOD) was 0,1 ?g/100 g and the limit of quantification (LOQ) was 0,3 ?g/100 g for each carotenoid.
The method does not apply to materials that contain measurable levels of ?-apo-8?-carotenal. The reproducibility data meets the requirements given in References [8] and [10].
Annex C specifies the determination of lutein. The reproducibility data does not meet the requirements given in Reference [9].
| SDO | BSI: British Standards Institution |
| Document Number | ISO 23443 |
| Publication Date | July 6, 2020 |
| Language | en - English |
| Page Count | 42 |
| Revision Level | |
| Supercedes | |
| Committee | AW/34 |