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建立并验证了一种用液相色谱-质谱法测定水果中吗啉残留的标准方法。

Development and validation of a standardized method for the determination of morpholine residues in fruit commodities by liquid chromatography-mass spectrometry.

机构信息

Department of Environmental Toxicology, University of California at Davis , One Shields Avenue, Davis, California 95616, United States.

出版信息

J Agric Food Chem. 2014 Apr 30;62(17):3697-701. doi: 10.1021/jf500734b. Epub 2014 Feb 26.

Abstract

An analytical method was developed for the determination of morpholine on apples and citrus. The method utilized acidified methanol extraction, centrifugation, and determination by hydrophilic interaction liquid chromatography with electrospray ionization and tandem mass spectrometry (HILIC-ESI-MS/MS). Validation of the method occurred at the Pacific Agricultural Laboratory (PAL, Portland, OR, USA) and the Trace Analytical Laboratory (TAL, UC Davis, CA, USA). Method validation recoveries from control apple, orange, lemon, and grapefruit samples ranged from 84 to 120% over three levels of fortification (0.01, 0.04, and 0.2 μg/g). The limit of quantitation (LOQ) for all commodities was 0.01 μg/g, and the calculated method detection limit (MDL) ranged from 0.0010 to 0.0040 μg/g.

摘要

建立了苹果和柑橘中吗啉的分析方法。该方法采用酸化甲醇提取、离心、亲水相互作用液相色谱-电喷雾串联质谱(HILIC-ESI-MS/MS)测定。方法验证在太平洋农业实验室(PAL,波特兰,OR,美国)和痕量分析实验室(TAL,加州大学戴维斯分校,CA,美国)进行。在 0.01、0.04 和 0.2μg/g 三个加标水平下,从对照苹果、橙子、柠檬和葡萄柚样品中获得的方法回收率为 84%至 120%。所有商品的定量限(LOQ)均为 0.01μg/g,计算出的方法检测限(MDL)范围为 0.0010 至 0.0040μg/g。

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