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Reinjection flow field-flow fractionation method for nanoparticle quantitative analysis in unknown and complex samples

机译:未知和复杂样品中纳米粒子定量分析的再注射流场流动分馏方法

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An analytical challenge that arises in environmental and food analysis is to quantify heterogeneous nanoparticles especially in polydisperse and complex samples. The method stated herein based on the reinjection asymmetrical flow field-flow fractionation (AF4 x AF4) coupled with inductively coupled plasma-mass spectrometer (ICP-MS) and statistical deconvolution allowed for identifying the molecular weight (Mw) and selenium abundance of the low Mw protein fractions (ca. < 132 kDa) in an unknown and complex sample (e.g., selenium-rich soybean protein isolates (Se-SPI)). A non-linear decay crossflow program was also developed to get better resolution and shorter elution time for both low and high Mw components. The concept of the reinjection method was based on the excellent ability for reducing sample complexity regarding the size fractionation, and peak reproducibility under the identical conditions of AF4 system. The standard protein mixture was used as a proof-of-principle sample. The results showed the underlying peaks predicted by the reinjection method were agreed with the separation result using the standard mixture (the relative standard deviation of peak locations < 1%), which indicated the reinjection method could provide an accurate assessment of the underlying peak number and location, and was promising to minimize the overfitting problem for statistic deconvolution. Interestingly, significant differences of Se abundance in protein fractions were observed in the low Mw range for Se-SPI, ranging from 0.28 to 1.66 cps/V with the Mw ranging from 13.75 kDa to 104.17 kDa, which indicated significant differences in the ability of binding Se for these selenium-rich proteins in Se-SPI. (C) 2021 Elsevier B.V. All rights reserved.
机译:环境和食品分析中出现的一个分析挑战是对异质纳米颗粒进行量化,尤其是在多分散和复杂的样品中。本文所述方法基于回注非对称流场流动分馏(AF4 x AF4),结合电感耦合等离子体质谱仪(ICP-MS)和统计反褶积,用于识别未知复杂样品中低分子量蛋白质组分(约<132 kDa)的分子量(Mw)和硒丰度(例如,富硒大豆分离蛋白(Se-SPI))。还开发了一个非线性衰变横流程序,以获得更好的分辨率,缩短低分子量和高分子量组分的洗脱时间。回注法的概念基于在AF4系统相同条件下降低样品粒度分级复杂性和峰重现性的卓越能力。标准蛋白质混合物被用作原则性样品的证明。结果表明,回注法预测的潜在峰与使用标准混合物的分离结果一致(峰位的相对标准偏差<1%),这表明回注法可以准确评估潜在峰的数量和位置,并承诺尽量减少统计反褶积的过度拟合问题。有趣的是,在Se-SPI的低分子量范围内,观察到蛋白质组分中硒丰度的显著差异,范围为0.28至1.66 cps/V,分子量范围为13.75 kDa至104.17 kDa,这表明Se-SPI中这些富硒蛋白质结合硒的能力存在显著差异。(c)2021爱思唯尔B.V.保留所有权利。

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