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UHPLC-ESI-MS/MS for the Quantification of Eight Major Cingerols and Shogaols in Ginger Products: Effects of Ionization Polarity and Mobile Phase Modifier on the Sensitivity

机译:UHPLC-ESI-MS / MS对生姜产品中的八种主要香精油和松香油进行定量:电离极性和流动相修饰剂对灵敏度的影响

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We developed and validated an improved ultra high performance liquid chromatography (UHPLC)- electrospray ionization (ESI)-tandem mass spectrometry (MS/MS) method for the fast separation and quantification of 8 major gingerols and shogaols (4-, 6-, 8-, 10-, and 12-gingerols, and 6-, 8-, and 10-shogaols) in gingerol products. The ionization polarity and mobile phase modifier greatly affected the mass ion profiles and sensitivity of the analytes. A mobile phase modifier of 0.05 mM ammonium formate dramatically decreased the sodium adduct ions and greatly increased the protonated ions of the gingerols and shogaols. Positive ion UHPLC-MS/MS with the ammonium formate in mobile phase showed greatly higher (4.5- to 15.7-fold) sensitivities than negative ion UHPLC. The positive ion UHPLC-MS/MS method showed excellent linearities (r2 > 0.999), low limits of detection (LOD = 2.5 to 8.2 pg), high accuracy and precision, and no considerable matrix effect. Baseline separation of the 8 target compounds was achieved in 1 min by the UHPLC with a short C18 core-shell column. The method was successfully applied to analyze the compounds in fresh and dried powdered gingers, and dietary supplements. The total contents of the major compounds in the fresh gingers, dried powdered gingers, and dietary supplements were in the range of 1114 to 1478, 4380 to 11324, and 2915 to 29998 mg/kg, respectively. There was about 10-fold variation of the content in the dietary supplements with the commercial brands. This represents the 1st report on the ionization polarity and mobile phase modifier on the sensitivity of gingerols and shogaols in LC-mass spectrometry. Furthermore, the established method provided great improvement in chromatographic separation of the target gingerols.
机译:我们开发并验证了一种改进的超高效液相色谱(UHPLC)-电喷雾电离(ESI)-串联质谱(MS / MS)方法,用于快速分离和定量8种主要的生姜酚和生姜酚(4-,6-,8姜醇产品中的-,10-和12-姜醇以及6-,8和10-shogaols。电离极性和流动相改性剂极大地影响了质量离子分布和分析物的灵敏度。 0.05 mM甲酸铵的流动相改性剂显着降低了姜醇和shogaols的钠加合离子,并大大增加了质子化离子。流动相中带有甲酸铵的正离子UHPLC-MS / MS显示的灵敏度比负离子UHPLC高得多(4.5到15.7倍)。阳离子UHPLC-MS / MS方法具有出色的线性(r2> 0.999),低检测限(LOD = 2.5至8.2 pg),高精度和高精度,并且没有明显的基质效应。用短C18核壳色谱柱通过UHPLC在1分钟内完成了8种目标化合物的基线分离。该方法已成功地用于分析生姜和干姜粉以及膳食补充剂中的化合物。新鲜生姜,干姜粉和膳食补充剂中主要化合物的总含量分别为1114至1478、4380至11324和2915至29998 mg / kg。商业品牌的膳食补充剂中的含量变化约10倍。这是有关LC-质谱法中姜黄酚和小松酚的敏感性的第一份有关电离极性和流动相改性剂的报告。此外,所建立的方法在目标姜醇的色谱分离方面提供了很大的改进。

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