首页> 美国卫生研究院文献>Toxins >Determination of Cyanotoxins and Phycotoxins in Seawater and Algae-Based Food Supplements Using Ionic Liquids and Liquid Chromatography with Time-Of-Flight Mass Spectrometry
【2h】

Determination of Cyanotoxins and Phycotoxins in Seawater and Algae-Based Food Supplements Using Ionic Liquids and Liquid Chromatography with Time-Of-Flight Mass Spectrometry

机译:离子液体和液相色谱-飞行时间质谱法测定海水和藻类食品补充剂中的氰毒素和藻毒素

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

An analytical procedure is proposed for determining three cyanotoxins (microcystin RR, microcystin LR, and nodularin) and two phycotoxins (domoic and okadaic acids) in seawater and algae-based food supplements. The toxins were first isolated by a salting out liquid extraction procedure. Since the concentration expected in the samples was very low, a dispersive liquid–liquid microextraction procedure was included for preconcentration. The ionic liquid 1-hexyl-3-methylimidazolium hexafluorophosphate (80 mg) was used as green extractant solvent and acetonitrile as disperser solvent (0.5 mL) for a 10 mL sample volume at pH 1.5, following the principles of green analytical chemistry. Liquid chromatography with electrospray ionization and quadrupole time of flight-mass spectrometry (LC-Q-TOF-MS) was used. The selectivity of the detection system, based on accurate mass measurements, allowed the toxins to be unequivocally identified. Mass spectra for quadrupole time of flight-mass spectrometry (Q-TOF-MS) and Q-TOF-MS/MS were recorded in the positive ion mode and quantification was based on the protonated molecule. Retention times ranged between 6.2 and 18.3 min using a mobile phase composed by a mixture of methanol and formic acid (0.1%). None of the target toxins were detected in any of the seawater samples analyzed, above their corresponding detection limits. However, microcystin LR was detected in the blue green alga sample.
机译:提出了一种分析程序,用于测定海水和藻类食品补充剂中的三种氰毒素(微囊藻毒素RR,微囊藻毒素LR和结节菌素)和两种藻毒素(十二烷酸和冈田酸)。首先通过盐析液体提取程序分离毒素。由于样品中的预期浓度非常低,因此采用了分散液-液微萃取程序进行预浓缩。遵循绿色分析化学原理,在pH 1.5时,将离子液体1-己基-3-甲基咪唑鎓六氟磷酸盐(80 mg)用作绿色萃取剂溶剂,将乙腈作为分散剂(0.5 mL)用于10 mL样品体积。使用具有电喷雾电离和四极杆飞行时间质谱的液相色谱(LC-Q-TOF-MS)。基于精确质量测量的检测系统的选择性可以明确鉴定毒素。以正离子模式记录四极飞行时间质谱(Q-TOF-MS)和Q-TOF-MS / MS的质谱,并基于质子化分子进行定量。使用由甲醇和甲酸(0.1%)的混合物组成的流动相,保留时间在6.2至18.3分钟之间。在所分析的任何海水样品中,均未超过其相应的检出限,未检出目标毒素。但是,在蓝绿色藻类样品中检测到了微囊藻毒素LR。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号