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本文引用的文献

1
Multidetection of paralytic, diarrheic, and amnesic shellfish toxins by an inhibition immunoassay using a microsphere-flow cytometry system.采用微球流式细胞仪系统的抑制免疫测定法对麻痹性、腹泻性和健忘性贝类毒素的多重检测。
Anal Chem. 2013 Aug 20;85(16):7794-802. doi: 10.1021/ac401146m. Epub 2013 Jul 31.
2
Multiplex screening of persistent organic pollutants in fish using spectrally encoded microspheres.利用光谱编码微球对鱼类中的持久性有机污染物进行多重筛选。
Anal Chem. 2011 Nov 15;83(22):8696-702. doi: 10.1021/ac201969z. Epub 2011 Oct 26.
3
Development of a multiplex flow cytometric microsphere immunoassay for mycotoxins and evaluation of its application in feed.建立一种用于真菌毒素的多重流式荧光微球免疫检测方法,并评估其在饲料中的应用。
Mycotoxin Res. 2011 Feb;27(1):63-72. doi: 10.1007/s12550-010-0077-0. Epub 2010 Nov 26.
4
Effect of uncontrolled factors in a validated liquid chromatography-tandem mass spectrometry method question its use as a reference method for marine toxins: major causes for concern.验证后的液相色谱-串联质谱法中不可控因素的影响质疑其作为海洋毒素参考方法的适用性:主要关注原因。
Anal Chem. 2011 Aug 1;83(15):5903-11. doi: 10.1021/ac200732m. Epub 2011 Jun 29.
5
First identification of azaspiracid and spirolides in Mesodesma donacium and Mulinia edulis from Northern Chile.首次在智利北部的多棘海盘车和紫贻贝中鉴定出azaspiracid 和 spirolides。
Toxicon. 2010 Feb-Mar;55(2-3):638-41. doi: 10.1016/j.toxicon.2009.07.014. Epub 2009 Jul 23.
6
Monoclonal antibodies with orthogonal azaspiracid epitopes.具有正交azaspiracid表位的单克隆抗体。
Chembiochem. 2009 Jul 6;10(10):1625-9. doi: 10.1002/cbic.200900201.
7
Mussel-associated azaspiracid intoxication in the United States.美国与贻贝相关的azaspiracid中毒事件
Ann Intern Med. 2009 Mar 3;150(5):361. doi: 10.7326/0003-4819-150-5-200903030-00023.
8
Isolation of azaspiracid-2 from a marine sponge Echinoclathria sp. as a potent cytotoxin.从海洋海绵Echinoclathria sp.中分离出氮杂螺旋酸-2作为一种强效细胞毒素。
Toxicon. 2009 May;53(6):680-4. doi: 10.1016/j.toxicon.2009.02.008.
9
Azaspiracid shellfish poisoning: a review on the chemistry, ecology, and toxicology with an emphasis on human health impacts.azaspiracid贝类中毒:关于化学、生态和毒理学的综述,重点关注对人类健康的影响。
Mar Drugs. 2008 May 7;6(2):39-72. doi: 10.3390/md20080004.
10
Discovery of new analogs of the marine biotoxin azaspiracid in blue mussels (Mytilus edulis) by ultra-performance liquid chromatography/tandem mass spectrometry.通过超高效液相色谱/串联质谱法在蓝贻贝(紫贻贝)中发现海洋生物毒素氮杂螺旋酸的新类似物。
Rapid Commun Mass Spectrom. 2008;22(4):549-58. doi: 10.1002/rcm.3385.

基于微球的免疫分析法检测azaspiracids。

Microsphere-based immunoassay for the detection of azaspiracids.

机构信息

Departamento de Farmacología, Facultad de Veterinaria, Universidad de Santiago de Compostela, 27002 Lugo, Spain.

Departamento de Farmacología, Facultad de Veterinaria, Universidad de Santiago de Compostela, 27002 Lugo, Spain.

出版信息

Anal Biochem. 2014 Feb 15;447:58-63. doi: 10.1016/j.ab.2013.10.035. Epub 2013 Nov 8.

DOI:10.1016/j.ab.2013.10.035
PMID:24215909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3947218/
Abstract

Azaspiracids (AZAs) are a group of lipophilic toxins discovered in mussels from Ireland in 1995 following a human poisoning incident. Nowadays the regulatory limit for AZAs in many countries is set at 160 μg of azaspiracid equivalents per kilogram of shellfish meat. In this work a microsphere-based immunoassay has been developed for the detection of AZAs using a Luminex system. This method is based on the competition between AZA-2 immobilized onto the surface of microspheres and free AZAs for the interaction with a monoclonal anti-azaspiracid antibody (mAb 8F4). In this inhibition immunoassay the amount of mAb 8F4 bound to AZA-2 microspheres was quantified using a phycoerythrin-labeled anti-mouse antibody, and the fluorescence was measured with a Luminex analyzer. Simple acetate/methanol or methanol extractions yielded final extracts with no matrix interferences and adequate recovery rates of 86.5 and 75.8%, respectively. In summary, this work presents a sensitive and easily performed screening method capable of detecting AZAs at concentrations below the range of the European regulatory limit using a microsphere/flow cytometry system.

摘要

azaspiracids(AZAs)是一组脂溶性毒素,于 1995 年在爱尔兰的贻贝类动物中发现,当时发生了一起人类中毒事件。如今,许多国家/地区对贝类中的 AZAs 设定的监管限量为 160μg azaspiracid 当量/千克贝类肉。在这项工作中,使用 Luminex 系统开发了一种基于微球的免疫测定法来检测 AZAs。该方法基于固定在微球表面上的 AZA-2 与游离 AZAs 之间的竞争,以与单克隆抗azaspiracid 抗体(mAb 8F4)相互作用。在这种抑制免疫测定法中,使用藻红蛋白标记的抗小鼠抗体定量测定与 AZA-2 微球结合的 mAb 8F4 的量,并使用 Luminex 分析仪测量荧光。简单的乙酸盐/甲醇或甲醇提取分别得到最终提取物,没有基质干扰,回收率分别为 86.5%和 75.8%。总之,这项工作提出了一种敏感且易于实施的筛选方法,使用微球/流式细胞术系统能够检测到低于欧洲监管限量范围的 AZAs 浓度。