Determining MOSH and MOAH with High Sensitivity in Vegetable Oil─A New, Reliable, and Comparable Approach Using Online LC-GC-FID─Evaluation of Method Precision Data.
Christopher AlbertHans-Ulrich HumpfLudger BrühlPublished in: Journal of agricultural and food chemistry (2022)
A method for the analysis of saturated mineral oil hydrocarbons (MOSH) and aromatic mineral oil hydrocarbons (MOAH) has been developed to improve interlaboratory precisions especially for amounts below 10 mg/kg. This approach was adopted as the standard method DGF C-VI 22 (20) of the German Society of Fat Sciences. Therefore, this method was evaluated on different edible oils containing a variety of interfering biogenic substances. The precision data were determined in an interlaboratory trial with an international group of 14 laboratories from Germany, Austria, and Italy. Good reproducible relative standard deviations for total MOSH (12.5-20.7%) and total MOAH (12.4-39.5%) as well as HorRat values ranging between 1.1 and 2.3 for total MOSH and between 0.9 and 2.6 for total MOAH have been achieved. As some matrices showed residual interferences in the MOAH fraction, these substances were further analyzed by online high-performance liquid chromatography-comprehensive two dimensional gas chromatography with time of flight mass detection.
Keyphrases
- gas chromatography
- tandem mass spectrometry
- high performance liquid chromatography
- mass spectrometry
- solid phase extraction
- simultaneous determination
- fatty acid
- liquid chromatography
- social media
- health information
- high resolution mass spectrometry
- big data
- randomized controlled trial
- study protocol
- adipose tissue
- healthcare
- gas chromatography mass spectrometry
- phase ii
- high resolution
- open label
- amino acid
- sensitive detection
- label free