Abstract
This paper presents a sandwich enzyme-linked immunosorbent assay (ELISA) that allows the determination of traces of sesame in food. Chicken anti-sesame antibodies, used as coating antibodies, and rabbit anti-sesame antibodies, used as secondary antibodies, were prepared by immunization with a protein extract of white, peeled sesame. The ELISA did not show any cross-reactivity with 19 food ingredients commonly found in sesame-containing foodstuffs such as seeds, nuts, and cereals. In whole grain bread, crisp toast, and snacks, the limit of detection (S/N = 3) was 0.5, 0.5, and 0.3 ?g sesame protein/g, and the limit of quantification (S/N = 10) was 0.6, 0.8, and 1.4 ?g sesame protein/g, respectively. The analysis of blank food matrices (whole grain bread, white bread, crisp toast, and snacks) spiked with sesame protein at four spike levels generally resulted in mean recoveries from 72% to 145%. In the case of spiking blank food matrices with sesame seeds, the ELISA proved to be more accurate for whole wheat cookies than for whole wheat bread.
| Original language | English |
|---|---|
| Pages (from-to) | 1735-1745 |
| Number of pages | 11 |
| Journal | Analytical and Bioanalytical Chemistry |
| Volume | 398 |
| DOIs | |
| Publication status | Published - 2010 |
Austrian Fields of Science 2012
- 104002 Analytical chemistry
- 104009 Food chemistry