## Abstract The adulteration of bovine milk fat with foreign fat can be detected by the analysis of its triacylglycerol (TAG) composition in combination with TAG formulae to calculate __S__‐values. With genuine milk fats these __S__‐values must not exceed certain limits already laid down in German
HPLC-APCI analysis of triacylglycerols in milk fat from different sources
✍ Scribed by Daniela Gastaldi; Claudio Medana; Valeria Giancotti; Riccardo Aigotti; Federica Dal Bello; Claudio Baiocchi
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 456 KB
- Volume
- 113
- Category
- Article
- ISSN
- 1438-7697
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Triacylglycerols (TAG) from milk‐fat from different sources (cow, goat and human milks) were characterised using non‐aqueous reversed phase high‐performance liquid chromatography–atmospheric‐pressure chemical ionisation, coupled to MS/MS (RP HPLC‐APCI MS/MS). The fatty‐acid content of all samples was also established by methyl transesterification and GC‐MS analysis. Optimisation of the HPLC gradient, combined with APCI tandem MS, enables TAGs complex mixtures to be analysed without prior separation. More than 160 different glycerides were identified; between 50 and 70 compounds were identified in the chromatograms of each sample. This method also enabled the principal TAG regioisomers to be recognized. The study focused on the investigation of the structure of TAGs containing very‐long‐chain PUFA, namely all cis‐ 4,7,10,13,16,19‐ DHA (DHA, C~22:6, n‐3~) and all cis‐5,8,11,14,17‐eicosapentaenoic acid (EPA, C~20:5, n‐3~), both in human and in n‐3‐enriched cow's milks. Ten TAGs containing DHA were identified in human milk and only one in milk from cows fed an n‐3 enriched diet.
📜 SIMILAR VOLUMES
Crude lipid extracts from di †erent tissues were analysed by 31P NMR spectroscopy in a mixture of triethylamine, dimethylformamide and guanidinium chloride. Higher dispersion of the 31P NMR signals and better reproducibility of the chemical shifts were achieved with respect to the spectra acquired i
## Abstract A validated liquid chromatography method was first developed to evaluate the quality of crude and processed Radix Scrophulariae extracts through establishing chromatographic fingerprint and simultaneous determination of five bioactive compounds, namely 5‐hydroxymethylfurfural (5‐HMF), a