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用于藏红花中多种掺假物多目标快速检测的DART-三重四极杆质谱法

DART-Triple Quadrupole Mass Spectrometry Method for Multi-Target and Fast Detection of Adulterants in Saffron.

作者信息

Monaci Linda, Luparelli Anna, Schirinzi William Matteo, Quintieri Laura, Verdu Alexandre

机构信息

Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies, National Research Council (IBIOM-CNR), Via G. Amendola, 122/O, 70126 Bari, Italy.

Institute of Sciences of Food Production, National Research Council (ISPA-CNR), Via G. Amendola, 122/O, 70126 Bari, Italy.

出版信息

Metabolites. 2025 May 28;15(6):357. doi: 10.3390/metabo15060357.

Abstract

Saffron is a high-cost spice due to the specific conditions for optimal growth and because of being harvested by hand. The massive income from commercializing saffron substituted with other plant parts or low-cost spices makes this spice the main target of fraudsters. : Different methods have been developed for detecting saffron adulteration. Most of them are time consuming and complex, and in some types of analysis, the whole untargeted dataset is combined with advanced chemometric tools to differentiate authentic from non-authentic saffron. The official method, combining UV-vis spectroscopy and LC to determine the colour strength and the crocin content, is unable to detect saffron adulterants (safflower, marigold, or turmeric) added at a level lower than 20% (/). As a result, innovative approaches based on rapid, high-throughput methods for the identification of adulterated saffron samples are urgently demanded to counteract food frauds. : This paper describes, for the first time, the development of a method combining Direct Analysis in Real Time (DART) with the triple quadrupole MS EVOQ based on the detection of specific MS/MS transitions, promoting a rapid, robust and chromatography-free method capable of monitoring safflower and turmeric adulteration in saffron. : The method proved to reach low LODs, allowing the determination of tiny amounts of turmeric and safflower powder in saffron as low as 3% and 5%, respectively, speeding up the whole analytical workflow and enabling us to perform 20 analyses in 10 min. Finally, the greenness of the method was also assessed according to the 0.88 score achieved by submitting it to the greenness calculator AGREE. : Given its speed, simplicity, and robustness, this method stands out as a strong candidate for routine implementation in testing laboratories as a rapid screening tool to detect saffron adulteration with safflower or turmeric.

摘要

藏红花是一种高成本香料,因为其生长需要特定的最佳条件,且需人工采摘。用其他植物部分或低成本香料替代藏红花进行商业化所带来的巨额收入,使得这种香料成为欺诈者的主要目标。:人们已经开发出不同的方法来检测藏红花掺假。其中大多数方法耗时且复杂,在某些类型的分析中,整个非靶向数据集会与先进的化学计量工具相结合,以区分正宗藏红花和非正宗藏红花。官方方法是结合紫外可见光谱法和液相色谱法来测定色强度和藏花素含量,但无法检测添加量低于20%(/)的藏红花掺假物(红花、万寿菊或姜黄)。因此,迫切需要基于快速、高通量方法来识别掺假藏红花样品的创新方法,以应对食品欺诈。:本文首次描述了一种将实时直接分析(DART)与基于特定二级质谱/质谱跃迁检测的三重四极杆质谱EVOQ相结合的方法,该方法促进了一种快速、稳健且无需色谱的方法的发展,能够监测藏红花中红花和姜黄的掺假情况。:该方法被证明具有低检测限,能够分别测定藏红花中低至3%和5%的微量姜黄和红花粉末,加快了整个分析流程,使我们能够在10分钟内完成20次分析。最后,根据将该方法提交给绿色度计算器AGREE所获得的0.88分,对该方法的绿色度进行了评估。:鉴于其速度、简便性和稳健性,该方法作为一种快速筛查工具,用于检测藏红花中红花或姜黄掺假,是测试实验室常规实施的有力候选方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1705/12195507/858ea3aab451/metabolites-15-00357-g001.jpg

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