Guijarro-Díez Miguel, Nozal Leonor, Marina María Luisa, Crego Antonio Luis
Department of Analytical Chemistry, Physical Chemistry and Chemical Engineering, University of Alcalá, Ctra. Madrid-Barcelona Km. 33,600, 28871, Alcalá de Henares, Madrid, Spain.
Anal Bioanal Chem. 2015 Sep;407(23):7197-213. doi: 10.1007/s00216-015-8882-0. Epub 2015 Jul 23.
An untargeted metabolomic approach using liquid chromatography coupled to electrospray ionization time-of-flight mass spectrometry was developed in this work to identify novel markers for saffron authenticity which is an important matter related to consumer protection, quality assurance, active properties, and also economical impact (saffron is the most expensive spice). Metabolic fingerprinting of authentic and suspicious saffron samples from different geographical origin was obtained and analyzed. Different extracting protocols and chromatographic methodologies were evaluated to obtain the most adequate extracting and separation conditions. Using an ethanol/water mixture at pH 9.0 and an elution gradient with a fused core C18 column enabled obtaining the highest number of significant components between authentic and adulterated saffron. By using multivariate statistical analysis, predictive classification models for authenticity and geographical origin were obtained. Moreover, 84 and 29 significant metabolites were detected as candidates for markers of authenticity and geographical origin, respectively, from which only 34 metabolites were tentatively identified as authenticity markers of saffron, but none related to its geographical origin. Six characteristic compounds of saffron (kaempferol 3-O-glucoside, kaempferol 3-O-sophoroside, kaempferol 3,7-O-diglucoside, kaempferol 3,7,4'-O-triglucoside, kaempferol 3-O-sophoroside-7-O-glucoside, and geranyl-O-glucoside) were confirmed by comparing experimental MS/MS fragmentation patterns with those provided in scientific literature being proposed as novel markers of authenticity. Graphical Abstract Metabolomic fingerprinting of saffron.
本研究开发了一种非靶向代谢组学方法,该方法采用液相色谱与电喷雾电离飞行时间质谱联用技术,以鉴定藏红花真伪的新型标志物。这是一个与消费者保护、质量保证、活性特性以及经济影响(藏红花是最昂贵的香料)相关的重要问题。对来自不同地理来源的正宗和可疑藏红花样品进行了代谢指纹图谱分析。评估了不同的提取方案和色谱方法,以获得最适宜的提取和分离条件。使用pH 9.0的乙醇/水混合物以及带有熔融核C18柱的洗脱梯度,能够在正宗藏红花和掺假藏红花之间获得数量最多的显著成分。通过多元统计分析,获得了关于真伪和地理来源的预测分类模型。此外,分别检测到84种和29种显著代谢物作为真伪和地理来源标志物的候选物,其中仅34种代谢物被初步鉴定为藏红花的真伪标志物,但无一与地理来源相关。通过将实验性MS/MS裂解模式与科学文献中提供的模式进行比较,确认了藏红花的六种特征化合物(山奈酚3 - O - 葡萄糖苷、山奈酚3 - O - 槐糖苷、山奈酚3,7 - O - 二葡萄糖苷、山奈酚3,7,4'- O - 三葡萄糖苷、山奈酚3 - O - 槐糖苷 - 7 - O - 葡萄糖苷和香叶基 - O - 葡萄糖苷),并将其提议作为新型真伪标志物。图形摘要 藏红花的代谢组学指纹图谱。