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Determination of Aristolochic Acid in Botanicals and Dietary Supplements by Liquid Chromatography with Ultraviolet Detection and by Liquid Chromatography/Mass Spectrometry: Single Laboratory Validation Confirmation

机译:液相色谱-紫外检测和液相色谱/质谱法测定植物药和膳食补充剂中的马兜铃酸:单实验室验证确认

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摘要

The presence of aristolochic acid in some dietary supplements is a concern to regulators and consumers. A method has been developed, by initially using a reference method as a guide, during single laboratory validation (SLV) for the determination of aristolochic acid I, also known as aristolochic acid A, in botanical species and dietary supplements at concentrations of approximately 2 to 32 μg/g. Higher levels were determined by dilution to fit the standard curve. Through the SLV, the method was optimized for quantification by liquid Chromatography with ultraviolet detection (LC-UV) and LC/mass Spectrometry (MS) confirmation. The test samples were extracted with organic solvent and water, then injected on a reverse phase LC column. Quantification was achieved with linear regression using a laboratory automation system. The SLV study included systematically optimizing the LC-UV method with regard to test sample size, fine grinding of solids, and solvent extraction efficiency. These parameters were varied in increments (and in separate optimization studies), in order to ensure that each parameter was individually studied; the test results include corresponding tables of parameter variations. In addition, the chromatographic conditions were optimized with respect to injection volume and detection wavelength. Precision studies produced overall relative standard deviation values from 2.44 up to 8.26% for aristolochic acid I. Mean recoveries were between 100 and 103% at the 2 μg/g level, between 102 and 103% at the 10 μg/g level, and 104% at the 30 μg/g level.
机译:一些饮食补品中存在马兜铃酸是监管者和消费者关注的问题。已经开发出一种方法,该方法最初是通过参考方法作为指导,在单实验室验证(SLV)期间用于测定植物物种和膳食补充剂中浓度约为2至5的马兜铃酸I(也称为马兜铃酸A)的。 32微克/克。通过稀释确定更高的水平以符合标准曲线。通过SLV,该方法针对液相色谱法进行了优化,并带有紫外检测(LC-UV)和LC /质谱(MS)确认。用有机溶剂和水萃取测试样品,然后注入反相LC柱中。使用实验室自动化系统通过线性回归实现定量。 SLV研究包括系统地优化LC-UV方法的测试样品大小,固体的精细研磨和溶剂萃取效率。这些参数以递增方式变化(并在单独的优化研究中),以确保分别研究每个参数;测试结果包括相应的参数变化表。此外,针对进样量和检测波长优化了色谱条件。精密度研究得出,马兜铃酸I的总体相对标准偏差值从2.44到8.26%。在2μg/ g的水平下,平均回收率在100至103%之间;在10μg/ g的水平下,平均回收率在102至103%之间;在104时%在30μg/ g的水平。

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