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采用顶空固相微萃取气相色谱-质谱法分析不同产地咖啡中的呋喃:冲泡程序的影响。

Analysis of furan in coffee of different provenance by head-space solid phase microextraction gas chromatography-mass spectrometry: effect of brewing procedures.

机构信息

Dipartimento Di Scienze degli Alimenti e dell'Ambiente, Universita di Messina, Messina, Italy.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2009 Jun;26(6):786-92. doi: 10.1080/02652030902751712.

Abstract

A simple, sensitive and accurate method for the analysis of furan in roasted coffee has been used based on headspace-solid-phase micro-extraction (HS-SPME) coupled to gas chromatography-mass spectrometry (GC-MS). The extraction was performed using 75-microm carboxen/polydimethylsiloxane fiber. Ionic strength, extraction time and temperature, and desorption time were assessed as the most important parameters affecting the HS-SPME procedure and d(4)-furan was used as the internal standard. The linearity range was in the range 0.0075-0.486 ng g(-1); the LOD and LOQ calculated using the signal-to-noise ratio approach were 0.002 and 0.006 ng g(-1), respectively. The inter- and intra-day precision was 8 and 10%, respectively. The concentration of furan found in batches of roasted coffee powder different producing countries ranged from 57.3 to 587.3 ng g(-1). The mean reduction in furan levels observed when brewing coffee by either infusion, using a moka pot or an expresso machine was 57, 67.5 and 63.3%, respectively.

摘要

一种基于顶空固相微萃取(HS-SPME)与气相色谱-质谱联用(GC-MS)的分析烤咖啡中呋喃的简单、灵敏、准确的方法已经被使用。萃取采用 75μm 羧基/聚二甲基硅氧烷纤维进行。离子强度、萃取时间和温度、以及解吸时间被评估为影响 HS-SPME 过程的最重要参数,并且 d(4)-呋喃被用作内标。线性范围在 0.0075-0.486ng g(-1)之间;采用信噪比法计算的检出限和定量限分别为 0.002 和 0.006ng g(-1)。日内和日间精密度分别为 8%和 10%。来自不同生产国的烤咖啡粉批次中呋喃的浓度范围为 57.3 至 587.3ng g(-1)。通过浸泡、摩卡壶或浓缩咖啡机冲泡咖啡时,呋喃水平的平均降低分别为 57%、67.5%和 63.3%。

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