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首页> 外文期刊>Food Analytical Methods >Determination of Aflatoxins M1, M2, B1, B2, G1, and G2 and Ochratoxin A in UHT and Powdered Milk by Modified QuEChERS Method and Ultra-High-Performance Liquid Chromatography Tandem Mass Spectrometry
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Determination of Aflatoxins M1, M2, B1, B2, G1, and G2 and Ochratoxin A in UHT and Powdered Milk by Modified QuEChERS Method and Ultra-High-Performance Liquid Chromatography Tandem Mass Spectrometry

机译:改进的QuEChERS方法和超高效液相色谱串联质谱法测定超高温灭菌和奶粉中的黄曲霉毒素M1,M2,B1,B2,G1和G2和ch曲毒素A

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摘要

A suitable method for routine analysis of aflatoxins M1, M2, B1, B2, G1, and G2 and ochratoxin A in milk by modified Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) sample treatment method and ultra-high-performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) was developed and validated. Satisfactory recoveries ranging from 72 to 121 %, with relative standard deviation lower than 17 % were obtained for the target compounds. The limits of quantification for aflatoxin M1 were 0.017 and 0.25 μg kg−1 for ultra-high-temperature (UHT) milk and powdered milk, respectively. The validated method was successfully applied to the determination of mycotoxins in milk samples from local supermarkets in Rio de Janeiro, Brazil. Ochratoxin A and aflatoxins B1, B2, G1, and G2 were not detected in the analyzed samples. Aflatoxin M1 was found in 53 (74 %) of the powdered milk samples analyzed at concentration levels ranging from 0.08 to 1.19 μg kg−1. In UHT milk, aflatoxin M1 was found in 11 (69 %) of the analyzed samples at concentration levels ranging from 0.005 to 0.042 μg kg−1. The concentrations found for aflatoxin M1 in milk samples were lower than the maximum permitted level according to Brazilian regulation. Aflatoxin M2 was detected in 17 (24 %) of the powdered milk samples (>0.08 μg kg−1) and in 3 (18 %) of the UHT milk samples (>0.009 μg kg−1). The present study is the first report showing the incidence of aflatoxin M2 in milk in Brazil.
机译:通过改进的快速,简便,廉价,有效,坚固耐用和安全的(QuEChERS)样品处理方法和超高纯度样品,对牛奶中的黄曲霉毒素M1,M2,B1,B2,G1,G2和曲霉毒素A进行常规分析的合适方法开发并验证了高效液相色谱串联质谱(UHPLC-MS / MS)。目标化合物的回收率从72%到121%不等,相对标准偏差低于17%。黄曲霉毒素M1的超高温(UHT)奶粉和奶粉定量限分别为0.017和0.25μgkg-1。经过验证的方法已成功应用于巴西里约热内卢当地超市的牛奶样品中霉菌毒素的测定。在分析的样品中未检出曲霉毒素A和黄曲霉毒素B1,B2,G1和G2。在分析的53份奶粉样品中发现了黄曲霉毒素M1(74%),浓度范围为0.08至1.19μgkg-1。在超高温灭菌牛奶中,在11个样品中(69%)发现了黄曲霉毒素M1,浓度范围为0.005至0.042μgkg-1。根据巴西法规,牛奶样品中黄曲霉毒素M1的浓度低于最大允许水平。在17份(24%)奶粉样品(> 0.08μgkg-1)和3份(18%)UHT牛奶样品(> 0.009μgkg-1)中检测到黄曲霉毒素M2。本研究是第一个报告,显示了巴西牛奶中黄曲霉毒素M2的发生率。

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