Table 2.
Bioactive molecules content expressed as percentage (%, dry basis) found in affron® before and after in vitro digestion process at salivary, gastric, and duodenal steps.
Bioactive components | Initial sample | Digested sample | Bioaccessibility | ||
---|---|---|---|---|---|
Salivary | Gastric | Duodenal | |||
Safranal | 0.04 ± 0.01a | 0.03 ± 0.00a | 0.21 ± 0.01c | 0.08 ± 0.01b | 200.00 |
t-crocin-4 | 1.66 ± 0.04b | 1.11 ± 0.43b | 0.26 ± 0.03a | 0.20 ± 0.04a | 12.05 |
Total crocins | 3.63 ± 0.05b | 3.43 ± 0.12b | 1.87 ± 0.35a | 1.48 ± 0.22a | 40.77 |
Kaempferol diglucoside | 0.13 ± 0.01b,c | 0.14 ± 0.01c | 0.12 ± 0.01b | 0.09 ± 0.01a | 69.23 |
Picrocrocin | 3.21 ± 0.07c | 3.14 ± 0.11c | 2.07 ± 0.02a | 2.61 ± 0.05b | 81.31 |
Crocetin | 0.03 ± 0.01a | 0.02 ± 0.01a | 0.03 ± 0.01a | 0.02 ± 0.01a | 66.67 |
Data are represented as mean ± SD. Different letters within a column (a–c) indicate significant differences (p < 0.05) of the bioactive component of affron® in every step during the digestion process.