Abstract
Phytosterols are lipophilic compounds found in plants with structural similarity to mammalian cholesterol. They cannot be endogenously produced by mammals and therefore always originate from diet. There has been increased interest in dietary phytosterols over the last few decades due to their association with a variety of beneficial health effects including low-density lipoprotein cholesterol lowering, anti-inflammatory and anti-cancerous effects. They are proposed as potential moderators for diseases associated with the central nervous system where cholesterol homeostasis is found to be imperative (multiple sclerosis, dementia, etc.) due to their ability to reach the brain. Here we utilised an enzyme-assisted derivatization for sterol analysis (EADSA) in combination with a liquid chromatography tandem mass spectrometry (LC-MSn) to characterise phytosterol content in human serum. As little as 100 fg of plant sterol was injected on a reversed phase LC column. The method allows semi-quantitative measurements of phytosterols and their derivatives simultaneously with measurement of cholesterol metabolites. The identification of phytosterols in human serum was based on comparison of their LC retention times and MS2, MS3 spectra with a library of authentic standards. Campesterol was found at 12.00±2.68 ng/mL, β-sitosterol at 8.50±2.65 ng/mL and fucosterol was at lowest concentration at 1.50±0.84 ng/mL (n=6, healthy individuals). This analytical methodology could be applied to the analysis of other biological fluids and tissues.
Supplementary materials
Title
Phytosterols in human serum as measured using a liquid chromatography tandem mass spectrometry
Description
Supplementary materials describes method validation including LOD and LOQ, SPE cartridges method validation, Table summarising identified phytosterols and other sterols.
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