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全球视角下的真菌毒素标准物质(第一部分):多供应商比较研究的新见解,涵盖黄曲霉毒素 B1、脱氧雪腐镰刀菌烯醇和玉米赤霉烯酮。

Global Perspectives on Mycotoxin Reference Materials (Part I): Insights from Multi-Supplier Comparison Study Including Aflatoxin B1, Deoxynivalenol and Zearalenone.

机构信息

LVA GmbH, Magdeburggasse 10, 3400 Klosterneuburg, Austria.

Fumizol Ltd., Kisfaludy u. 6/B, H-6725 Szeged, Hungary.

出版信息

Toxins (Basel). 2024 Sep 17;16(9):397. doi: 10.3390/toxins16090397.

Abstract

We conducted a comprehensive examination of liquid mycotoxin reference standards. A total of 30 different standards were tested, each containing 10 samples of three distinct substances: Aflatoxin B1, Deoxynivalenol, and Zearalenone. The standards were sourced from 10 different global market leading manufacturers. To facilitate comparison, all the standard sets were adjusted to the same concentration level. The standards were analyzed using the techniques LC-MS/MS, HPLC-DAD, and LC-HRMS to assess their quality attributes. Regarding the validation of the reference values, it was observed that 30% of the suppliers provided reference standards that were either below the lower acceptance limit or above the higher acceptance limit, confirmed by both the LC-MS/MS and HPLC-DAD methods. Furthermore, a total of 12 impurities were found in the DON standards, 10 in the AFB standards, and 8 in the ZON standards, distributed across all the suppliers. Therefore, this study suggests relevant adjustments to the ISO 17034 standard, proposing that the purity of a raw material should be uniformly based on q-NMR analysis, as most manufacturers state the purity of their certificates is determined using HPLC-UV or LC-MS/MS. Liquid standards with a shelf life of ≤1 year should not exceed an uncertainty of 3%. Standards that have a longer shelf life should not have more than 5% uncertainty. This study also emphasizes the importance of stability. The standards should undergo continuous long-term monitoring; otherwise, products may exhibit a target value of only 80%, as seen in one instance. It is also recommended to include proof of HPLC and LC-MS/MS analyses on the certificate of each released batch of a final product.

摘要

我们对液体霉菌毒素参考标准进行了全面检查。共测试了 30 种不同的标准品,每种标准品包含三种不同物质的 10 个样品:黄曲霉毒素 B1、脱氧雪腐镰刀菌烯醇和玉米赤霉烯酮。这些标准品来自 10 家不同的全球领先市场制造商。为了便于比较,所有标准品集都调整到相同的浓度水平。使用 LC-MS/MS、HPLC-DAD 和 LC-HRMS 技术分析了标准品,以评估它们的质量属性。关于参考值的验证,观察到 30%的供应商提供的参考标准品要么低于较低的可接受限,要么高于较高的可接受限,这两种方法都由 LC-MS/MS 和 HPLC-DAD 方法证实。此外,在 DON 标准品中发现了总共 12 种杂质,在 AFB 标准品中发现了 10 种,在 ZON 标准品中发现了 8 种,分布在所有供应商中。因此,本研究建议对 ISO 17034 标准进行相关调整,提议原材料的纯度应统一基于 q-NMR 分析,因为大多数制造商表示其证书的纯度是使用 HPLC-UV 或 LC-MS/MS 确定的。有效期≤1 年的液体标准品的不确定度不应超过 3%。保质期较长的标准品的不确定度不应超过 5%。本研究还强调了稳定性的重要性。标准品应进行持续的长期监测;否则,产品可能表现出只有 80%的目标值,正如一个实例中所见。还建议在每个最终产品放行批次的证书上包含 HPLC 和 LC-MS/MS 分析的证明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c20/11435901/5515391b8a94/toxins-16-00397-g001.jpg

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