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采用高效液相色谱-混合三重四极杆-线性离子阱质谱联用技术(LC-QqQLIT-MS/MS)提高咖啡中赭曲霉毒素A分析的灵敏度。

Improved sensitivity of ochratoxin A analysis in coffee using high-performance liquid chromatography with hybrid triple quadrupole-linear ion trap mass spectrometry (LC-QqQLIT-MS/MS).

作者信息

Kokina Aija, Pugajeva Iveta, Bartkevics Vadims

机构信息

a Institute of Food Safety , Animal Health and Environment 'BIOR' , Riga , Latvia.

b Faculty of Chemistry , University of Latvia , Riga , Latvia.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2016;33(4):693-702. doi: 10.1080/19440049.2016.1152138. Epub 2016 Mar 2.

Abstract

A novel and sensitive method utilising high-performance liquid chromatography coupled to triple quadrupole-linear ion trap mass spectrometry (LC-QqQLIT-MS/MS) was developed in order to analyse the content of ochratoxin A (OTA) in coffee samples. The introduction of the triple-stage MS scanning mode (MS(3)) has been shown to increase greatly sensitivity and selectivity by eliminating the high chromatographic baseline caused by interference of complex coffee matrices. The analysis included the sample preparation procedure involving extraction of OTA using a methanol-water mixture and clean-up by immunoaffinity columns and detection using the MS(3) scanning mode of LC-QqQLIT-MS/MS. The proposed method offered a good linear correlation (r(2) > 0.998), excellent precision (RSD < 2.9%) and recovery (94%). The limit of quantification (LOQ) for coffee beans and espresso beverages was 0.010 and 0.003 µg kg(-1), respectively. The developed procedure was compared with traditional methods employing liquid chromatography coupled to fluorescent and tandem quadrupole detectors in conjunction with QuEChERS and solid-phase extraction. The proposed method was successfully applied to the determination of OTA in 15 samples of coffee beans and in 15 samples of espresso coffee beverages obtained from the Latvian market. OTA was found in 10 samples of coffee beans and in two samples of espresso in the ranges of 0.018-1.80 µg kg(-1) and 0.020-0.440 µg l(-1), respectively. No samples exceeded the maximum permitted level of OTA in the European Union (5.0 µg kg(-1)).

摘要

为了分析咖啡样品中赭曲霉毒素A(OTA)的含量,开发了一种新颖且灵敏的方法,该方法利用高效液相色谱与三重四极杆-线性离子阱质谱联用(LC-QqQLIT-MS/MS)。通过消除复杂咖啡基质干扰导致的高色谱基线,三级质谱扫描模式(MS(3))的引入已被证明能大大提高灵敏度和选择性。分析包括样品制备过程,该过程涉及使用甲醇-水混合物萃取OTA、通过免疫亲和柱净化以及使用LC-QqQLIT-MS/MS的MS(3)扫描模式进行检测。所提出的方法具有良好的线性相关性(r(2) > 0.998)、出色的精密度(RSD < 2.9%)和回收率(94%)。咖啡豆和浓缩咖啡饮料的定量限(LOQ)分别为0.010和0.003 µg kg(-1)。将所开发的方法与采用液相色谱与荧光和串联四极杆检测器联用并结合QuEChERS和固相萃取的传统方法进行了比较。所提出的方法成功应用于测定从拉脱维亚市场获得的15个咖啡豆样品和15个浓缩咖啡饮料样品中的OTA。在10个咖啡豆样品和2个浓缩咖啡样品中分别检测到OTA,其含量范围分别为0.018 - 1.80 µg kg(-1)和0.020 - 0.440 µg l(-1)。没有样品超过欧盟规定的OTA最大允许限量(5.0 µg kg(-1))。

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