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首页> 外文期刊>TrAC: Trends in Analytical Chemistry >Representative sampling of large kernel lots II. Application to soybean sampling for GMO control
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Representative sampling of large kernel lots II. Application to soybean sampling for GMO control

机译:大仁批次的代表性抽样II。在大豆样品中进行转基因生物控制

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摘要

Official testing and sampling of large kernel lots for impurities [e.g., genetically modified organisms (GMOs)] is regulated by normative documents and international standards of economic, trade and societal importance.In Part I, we reviewed current official guides and standards for sampling large contaminated kernel lots and the basic concepts of the Theory of Sampling (TOS) for chemical analysis. Here, we re-interpret the data collected in a recent field study (KeLDA) from a stringent TOS perspective, focusing on representative process sampling and variographic analysis in order to characterize the heterogeneities of large kernel lots and to estimate both Total Sampling Error (TSE) and Total Analytical Error (TAE). This is used as a basis for developing a general approach for optimization of kernel sampling protocols that are " fit for purpose" i.e. robust to heterogeneity and sufficiently accurate also to detect critically low levels of concentration.We demonstrate that both TSE and TAE are significantly large for GMO quantitation, but that TSE still can be up two orders of magnitude larger than TAE, depending on heterogeneity, sampling mode and GMO concentration, signifying that efforts to reduce uncertainties should focus on sampling plans and not on further refinements of analytical precision.For GMO testing based on the current labeling threshold (0.9%) in European Union regulations, we show that 42 is the absolute minimum number of increments needed for reliable characterization of all lots with a heterogeneity comparable to the most severely heterogeneous KeLDA lots (Lot #1).We demonstrate that the TOS is a comprehensive tool for reliable estimation of the effects of alternative sampling procedures and schemes, especially when using 1-D process variography, with which to optimize both sampling accuracy and precision. We show how it is always possible to estimate TSE from one simple variographic experiment based solely on the simple process-sampling requirements of TOS. This approach is universal and can be carried to very many other (static or dynamic) sampling scenarios and materials (e.g., impurities, contaminants and trace concentrations). The present variographic approach is crucial for meaningful definition of " appropriate sampling plans" (i.e. sampling plans minimizing TSE as function of the specific heterogeneity of any given lot).
机译:官方对大批仁中的杂质[例如,转基因生物(GMOs)]进行测试和采样受到规范性文件和具有经济,贸易和社会重要性的国际标准的监管。在第一部分中,我们回顾了当前对大批样品进行采样的官方指南和标准。被污染的内核批次以及用于化学分析的采样理论(TOS)的基本概念。在这里,我们从严格的TOS角度重新解释了最近的一项实地研究(KeLDA)中收集的数据,着重于代表性的过程采样和变异分析,以表征大粒仁的异质性并估算总采样误差(TSE) )和总分析误差(TAE)。这被用作开发通用方法的基础,该方法用于优化“适合目的”的内核采样协议,即对异质性很强,并且也足够准确,可以检测出极低的浓度水平。我们证明TSE和TAE都非常大对于GMO定量分析,但根据异质性,采样模式和GMO浓度,TSE仍可以比TAE高两个数量级,这表明减少不确定性的工作应侧重于采样计划而不是进一步提高分析精度。根据欧盟法规中的当前标记阈值(0.9%)进行GMO测试,我们显示,对于所有异质性能够与最严重异质的KeLDA批次媲美的批次,可靠鉴定所需的增量的绝对最小数量为42(批次1) )。我们证明,TOS是可靠评估替代抽样p的影响的综合工具解决方案和方案,尤其是在使用一维过程变异术时,可同时优化采样精度和精度。我们展示了总是有可能仅基于TOS的简单过程采样要求,通过一个简单的变异试验来估计TSE。这种方法是通用的,可用于许多其他(静态或动态)采样场景和材料(例如,杂质,污染物和痕量浓度)。当前的统计方法对于有意义地定义“适当的采样计划”(即,根据任何给定批次的特定异质性使TSE最小化的采样计划)至关重要。

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