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气相色谱-质谱联用快速测定果汁和药物中吗啉的方法开发

Development of a Method for Rapid Determination of Morpholine in Juices and Drugs by Gas Chromatography-Mass Spectrometry.

作者信息

Cao Mengsi, Zhang Pingping, Feng Yanru, Zhang Huayin, Zhu Huaijiao, Lian Kaoqi, Kang Weijun

机构信息

School of Public Health, Hebei Medical University, Shijiazhuang 050017, China.

Department of Reproductive Genetic Family, Hebei General Hospital, Shijiazhuang 050017, China.

出版信息

J Anal Methods Chem. 2018 Apr 26;2018:9670481. doi: 10.1155/2018/9670481. eCollection 2018.

Abstract

A reliable derivatization method has been developed to detect and quantify morpholine in apple juices and ibuprofen with gas chromatography-mass spectrometry. Morpholine can react with sodium nitrite under acidic condition to produce stable and volatile N-nitrosomorpholine derivative. In this experiment, various factors affecting the derivatization and extraction process were optimized, including volume and concentration of hydrochloric acid, quantity of sodium nitrite, derivatization temperature, derivatization time, extraction reagents, and extraction time. The derivative was extracted with dichloromethane and determined by gas chromatography-mass spectrometry. The linearity range of morpholine was 10-500 g·L with good correlation, and limits of detection (LOD) and limits of quantification (LOQ) were 7.3 g·L and 24.4 g·L, respectively. Low, medium, and high concentrations of morpholine were added in apple juices and ibuprofen samples to evaluate standard recovery rate and relative standard deviation. The spiked recovery rate ranged from 94.3% to 109.0%, and the intraday repeatability and interday reproducibility were 2.0%-4.4% and 3.3%-7.0%, respectively. The developed method has good accuracy and precision. This quantitative method for morpholine is simple, sensitive, rapid, and low cost and can successfully be applied to analyze the residual morpholine in apple juices and drug samples.

摘要

已开发出一种可靠的衍生化方法,用于通过气相色谱-质谱法检测和定量苹果汁和布洛芬中的吗啉。吗啉在酸性条件下可与亚硝酸钠反应生成稳定且易挥发的N-亚硝基吗啉衍生物。在本实验中,对影响衍生化和萃取过程的各种因素进行了优化,包括盐酸的体积和浓度、亚硝酸钠的用量、衍生化温度、衍生化时间、萃取试剂和萃取时间。用二氯甲烷萃取衍生物,并通过气相色谱-质谱法进行测定。吗啉的线性范围为10-500 μg·L,具有良好的相关性,检测限(LOD)和定量限(LOQ)分别为7.3 μg·L和24.4 μg·L。向苹果汁和布洛芬样品中添加低、中、高浓度的吗啉,以评估标准回收率和相对标准偏差。加标回收率在94.3%至109.0%之间,日内重复性和日间重现性分别为2.0%-4.4%和3.3%-7.0%。所开发的方法具有良好的准确度和精密度。这种吗啉定量方法简单、灵敏、快速且成本低,可成功应用于分析苹果汁和药物样品中的吗啉残留量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/282f/5944257/77f08492733b/JAMC2018-9670481.001.jpg

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