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通过实时无限稀释的流动注射分析实现定量质谱对基质效应和检测器饱和的独立性。

Quantitative mass spectrometry independence from matrix effects and detector saturation achieved by flow injection analysis with real-time infinite dilution.

机构信息

DuPont Crop Protection, Stine-Haskell Research Center, 1090 Elkton Road, Newark, Delaware 19714, United States.

出版信息

Anal Chem. 2013 Dec 17;85(24):11866-75. doi: 10.1021/ac402567w. Epub 2013 Dec 2.

Abstract

A high-throughput quantitative analysis method is presented to determine analyte concentrations at the infinite dilution limit, where the presence and effects of matrix become null, achieving mathematical independence from the detrimental phenomenon of matrix effects. Dilution is achieved online, reproducibly and in seconds by diffusion/mixing that occurs in flow injection analysis, while analyte concentration measurements are made by electrospray ionization tandem mass spectrometry. Because of matrix effects, the measured analyte concentration (Am) was inaccurate at high matrix concentrations, but accuracy consistently improved as matrix concentration was reduced by dilution. The method provides a practical solution around the decades-long matrix effects problem in quantitative analytical chemistry without separation of analytes from the matrix (e.g., chromatography) or use of corrective procedures, such as matrix-matched standards or isotopically labeled internal standards. Broad applications were demonstrated for part-per-billion quantitation of bioactive molecules (pesticides) in extracts of food, plant tissues, and body fluids by coupling the method to a high-throughput sample extraction/cleanup based on salting out with ammonium formate. The technique provides an assessment of matrix effects with remarkable comprehensiveness, simplicity, and speed. A limit of quantitation of 10 ng/g, a level appropriate for pesticide residue analysis and bioanalytical applications, was demonstrated. The method is also independent of detector saturation; this feature increased the applicable concentration range 20-100-fold above that of conventional techniques. In the abstract graphic, the measured analyte concentration (Am) approaches the accurate value (A0) when matrix effects disappear as measurements are conducted while lowering the normalized sample concentration (Snorm) by real-time dilution.

摘要

一种高通量定量分析方法被提出,以确定在无限稀释极限下的分析物浓度,在该极限下,基质的存在和影响变得为零,从而从基质效应的有害现象中实现数学独立性。通过扩散/混合在线、可重现地在几秒钟内实现稀释,该混合发生在流动注射分析中,而分析物浓度测量则通过电喷雾串联质谱法进行。由于基质效应,在高基质浓度下,测量的分析物浓度(Am)是不准确的,但随着基质浓度通过稀释降低,准确性一致提高。该方法提供了一种实用的解决方案,解决了定量分析化学中数十年来的基质效应问题,而无需将分析物与基质(例如色谱)分离,也无需使用校正程序,例如基质匹配标准品或同位素标记内标。通过将该方法与基于甲酸铵盐析的高通量样品提取/净化相结合,广泛应用于食品、植物组织和体液提取物中生物活性分子(农药)的十亿分之几定量。该技术提供了对基质效应的全面、简单和快速评估。证明了 10ng/g 的定量下限,这是适合农药残留分析和生物分析应用的水平。该方法还独立于检测器饱和;该特征将传统技术的适用浓度范围提高了 20-100 倍。在抽象图形中,当基质效应消失时,测量的分析物浓度(Am)接近准确值(A0),当通过实时稀释降低归一化样品浓度(Snorm)时。

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