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利用多转换光传感器间接测定啤酒中的黄曲霉毒素 B₁。

Indirect determination of aflatoxin B₁ in beer via a multi-commuted optical sensor.

机构信息

Department of Physical and Analytical Chemistry, University of Jaén, Jaén, Spain.

出版信息

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2012;29(3):392-402. doi: 10.1080/19440049.2011.643244. Epub 2012 Jan 23.

Abstract

This paper reports the determination of aflatoxin B₁ (AFB₁), one of the most carcinogenic substances known. A multi-commuted flow injection-solid phase spectroscopy (FI-SPS) system combined with photochemically induced fluorescence (PIF) was developed, for the first time, for its quantitative determination. A strongly fluorescent degradation product was obtained on-line by irradiation with ultraviolet light. The determination was carried out by measuring the fluorescence intensity of the photo-product at 353/424 (λ (ex)/λ (em)), once retained on C₁₈ silica-gel filling the flow-cell. A linear dynamic range of 0.09-12 µg l⁻¹, detection limit as sensitive as 29 ng l⁻¹ and a relative standard deviation (RSD) of 1.4% were obtained. The method proposed was satisfactorily applied to the determination of AFB₁ in different types of beer (normal and non-alcoholic). Hydrophobic compounds were eliminated from beer samples and AFB₁ was extracted with acetonitrile by solid-phase extraction on C₁₈ sorbent. Recoveries of the target compound from spiked beers were between 94 and 106%. The results obtained in the analysis of real samples are in good agreement with those provided by a reference chromatographic method.

摘要

本文报道了一种强致癌物质黄曲霉毒素 B₁(AFB₁)的测定方法。首次建立了多阶流动注射-固相光谱(FI-SPS)系统结合光化学诱导荧光(PIF)检测方法,用于定量测定。通过在线紫外线照射,获得了强荧光降解产物。通过测量保留在填充有流动池的 C₁₈硅胶中的光产物在 353/424(λ(ex)/λ(em))处的荧光强度,对产物进行定量分析。该方法的线性动态范围为 0.09-12μg/L,检测限低至 29ng/L,相对标准偏差(RSD)为 1.4%。该方法可用于不同类型啤酒(正常和无酒精)中 AFB₁的测定。采用 C₁₈固相萃取法,从啤酒样品中去除疏水性化合物,并用乙腈提取 AFB₁。目标化合物在加标啤酒中的回收率在 94%至 106%之间。实际样品分析结果与参考色谱法提供的结果一致。

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