以神经-2a细胞为基础的毒性等效因子测定-智利受污染贝类样品的建议和评价

Ambbar Aballay-González, J. Gallardo-Rodríguez, Macarena Silva-Higuera, Alejandra Rivera, V. Ulloa, Lorena Delgado-Rivera, Andrea Rivera-Belmar, Allisson Astuya
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引用次数: 4

摘要

有两种官方的PSP检测方法(小鼠生物测定法和HLPC-FLD)和许多替代方法。出于伦理方面的考虑,一些国家通过了限制或禁止小鼠生物测定应用的法规。分析方法(如HPLC-FLD或LC-MSMS)的缺点是不能检测新的毒素或类似物,也不能反映样品的整体毒性。此外,它们需要训练有素的人员和昂贵的设备,而这些并不总是可以得到的。在这项工作中,我们评估了一种基于神经-2a细胞的检测方法,以检测抑制电压依赖性钠通道的物质(Manger方法)。我们检测了PSP标准品和被PSP污染的天然样品。在这里,我们证明了适应的Manger方法适用于计算stx类似物的毒性等效因子(TEF)。结果表明,该方法可用于筛选这些毒素浓度超过规定限值(80 μg STX当量/100 g贝类)的受污染天然样品。尽管存在其他海洋毒素,但我们能够在智利南部的19个天然软体动物样本中检测到PSP。这些初步结果表明,该方法可以作为筛选方案的第一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuro-2a cell-based assay for toxicity equivalency factor - proposal and evaluation in Chilean contaminated shellfish samples
ABSTRACT There are two official PSP detection methods (mouse bioassay and HLPC-FLD) and a number of alternative methods. Ethical considerations have led to regulations being adopted in some countries that limit or prohibit the application of mouse bioassay. Analytical methodologies (e.g. HPLC-FLD or LC-MSMS) have the disadvantages of not being able to detect new toxins or analogues or reflecting the overall toxicity of the sample. In addition, they require highly trained personnel and expensive equipment, which are not always available. In this work, we have evaluated a method based on the Neuro-2a cell-based assay to detect substances that inhibit voltage-dependent sodium channels (Manger’s method). We tested PSP standards and natural samples contaminated with PSP. Here we demonstrate that the adapted Manger’s method is suitable for calculating Toxicity Equivalency Factors (TEF) for STX-analogues. The method was shown to be useful for screening contaminated natural samples in concentrations above the regulatory limit for these toxins (80 μg STX equivalents/100 g shellfish). We were able to detect PSP in 19 natural mollusc samples from South Chile despite the presence of other marine toxins. These preliminary results suggest that the method could be used as a first step in screening programmes.
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