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Isotope-labelling derivatisation: a broadly applicable approach to quantitation of algal toxins by isotope dilution LC-MS/MS

机译:同位素标记衍生化:通过同位素稀释LC-MS / MS定量藻类毒素的广泛适用方法

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Two methods were developed for the analysis of algal biotoxins in complex biological and environmental samples to demonstrate the concept of isotope-labelling derivatisation for quantitation. These methods are based on dansyl chloride derivatisation of samples and dansyl-d6 chloride derivatisation of toxin standards. Derivatised sample and standard are then mixed to achieve isotope dilution calibration in liquid chromatographya€“tandem mass spectrometry analyses. Quantitation of the marine toxin domoic acid (DA) in mussel tissues and the freshwater toxins anatoxin-a (ATX) and homoanatoxin-a (hATX) in cyanobacteria is demonstrated. For DA, isotope-labelling was incorporated into existing dansylation methodology using inexpensive and commercially available reagents. For ATXs, a novel sample preparation procedure is presented that involves solid phase extraction on a mixed reverse phase/weak anion exchange column that facilitates simultaneous clean-up of the derivatised toxins and removal of excess dansylation reagent through covalent bonding. The challenge of achieving co-elution in LC between deuterated and non-deuterated dansylated toxins was addressed by modifying separation conditions from the usual reverse phase (RP) separation to hydrophilic interaction liquid chromatography in the case of DA and a shortened RP separation with high organic modifier content in the case of the ATXs. The new methods gave limits of detection between 10 and 60 ??g kga?’1 and allowed for precise, accurate and fast determination of toxins in spiked control samples and matrix reference materials. This work demonstrates that isotope-labelling derivatisation is broadly applicable to the field of algal toxin analysis where derivatisation is well established but isotopically-labelled standards are not available.
机译:开发了两种方法来分析复杂的生物和环境样品中的藻类生物毒素,以证明用于定量的同位素标记衍生化的概念。这些方法基于样品的丹磺酰氯衍生化和毒素标准品的丹磺酰-d6氯化物衍生化。然后将衍生化的样品和标准液混合,以在液相色谱和串联质谱分析中实现同位素稀释校准。定量了贻贝组织中的海洋毒素海藻酸(DA)以及蓝细菌中的淡水毒素Anatoxin-a(ATX)和homoanatoxin-a(hATX)。对于DA,使用便宜的和可商购的试剂将同位素标记法引入现有的丹磺酰化方法中。对于ATX,提出了一种新颖的样品制备程序,该程序涉及在混合的反相/弱阴离子交换柱上进行固相萃取,这有利于同时净化衍生毒素并通过共价键去除多余的丹磺酰化试剂。通过修改分离条件,从常规的反相(RP)分离到亲水相互作用的液相色谱,在DA的情况下,缩短了高有机物的RP分离,解决了氘代和非氘代丹磺酰毒素在LC中共洗脱的挑战。对于ATX而言,修饰符内容。新方法的检出限在10至60 gga?1之间,并且可以精确,准确和快速地测定加标对照样品和基质参考物质中的毒素。这项工作表明,同位素标记衍生化广泛适用于藻毒素分析领域,在该领域中,衍生化已得到很好的确立,但同位素标记的标准尚不可用。

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