Drug Design and Discovery Group, College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.
Laboratory for the Analysis of Medicines, Department of Pharmacy, CIRM, University of Liège, 4000 Liege, Belgium.
Molecules. 2021 Mar 5;26(5):1402. doi: 10.3390/molecules26051402.
Phytosterols and tocopherols are commonly used in food and pharmaceutical industries for their health benefits. Current analysis methods rely on conventional liquid chromatography, using an analytical column, which can be tedious and time consuming. However, simple, and fast analytical methods can facilitate their qualitative and quantitative analysis. In this study, a fast chromatography-tandem mass spectrometric (FC-MS/MS) method was developed and validated for the quantitative analysis of phytosterols and tocopherols. Omitting chromatography by employing flow injection analysis-mass spectrometry (FIA-MS) failed in the quantification of target analytes due to analyte-to-analyte interferences from phytosterols. These interferences arise from their ambiguous MS fingerprints that would lead to false identification and inaccurate quantification. Therefore, a C18 guard column with a 1.9 µm particle size was employed for FC-MS/MS under isocratic elution using acetonitrile/methanol (99:1 /) at a flow rate of 600 µL/min. Analyte-to-analyte interferences were identified and eliminated. The false peaks could then be easily identified due to chromatographic separation. In addition, two internal standards were evaluated, namely cholestanol and deuterated cholesterol. Both internal standards contributed to the observed analyte-to-analyte interferences; however, adequate shift in the retention time for deuterated cholesterol eliminated its interferences and allowed for an accurate quantification. The method is fast (1.3 min) compared to published methods and can distinguish false peaks observed in FIA-MS. Seven analytes were quantified simultaneously, namely brassicasterol, campesterol, stigmasterol, β-sitosterol, α-tocopherol, δ-tocopherol, and γ-tocopherol. The method was successfully applied in the quantitative analysis of phytosterols and tocopherols present in the unsaponifiable matter of canola oil deodorizer distillate (CODD). β-sitosterol and γ-tocopherol were the most abundant phytosterols and tocopherols, respectively.
植物甾醇和生育酚常用于食品和制药行业,因为它们具有健康益处。目前的分析方法依赖于常规的液相色谱法,使用分析柱,这可能很繁琐和耗时。然而,简单、快速的分析方法可以促进它们的定性和定量分析。在这项研究中,开发并验证了一种快速色谱-串联质谱(FC-MS/MS)方法,用于植物甾醇和生育酚的定量分析。由于植物甾醇之间的分析物相互干扰,省略色谱法采用流动注射分析-质谱法(FIA-MS)进行定量分析会失败。这些干扰源于它们模糊的 MS 指纹,会导致错误的鉴定和不准确的定量。因此,在等度洗脱条件下,采用粒径为 1.9 µm 的 C18 保护柱和流速为 600 µL/min 的乙腈/甲醇(99:1 /),进行 FC-MS/MS。鉴定并消除了分析物相互干扰。由于色谱分离,可以轻松识别假峰。此外,还评估了两种内标物,即胆甾醇和氘代胆固醇。这两种内标物都对观察到的分析物相互干扰有贡献;然而,氘代胆固醇的保留时间有足够的偏移,消除了其干扰,实现了准确的定量。与已发表的方法相比,该方法速度较快(1.3 分钟),可以区分 FIA-MS 中观察到的假峰。同时定量了 7 种分析物,分别为菜油甾醇、谷甾醇、豆甾醇、β-谷甾醇、α-生育酚、δ-生育酚和γ-生育酚。该方法成功应用于菜油脱臭馏出物不皂化物中植物甾醇和生育酚的定量分析。β-谷甾醇和γ-生育酚分别是最丰富的植物甾醇和生育酚。