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首页> 外文期刊>Analytica chimica acta >Determination of trace amount of microcystins in water samples using liquid chromatography coupled with triple quadrupole mass spectrometry
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Determination of trace amount of microcystins in water samples using liquid chromatography coupled with triple quadrupole mass spectrometry

机译:液相色谱-三重四极杆质谱联用法测定水样中的微量微囊藻毒素

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摘要

Microcystins,a group of cyclic heptapeptide heaptoxins and tumor promoters,are bio-generated by cyanobacteria occurring in eutrophic lakes,rivers and reservoirs.In the present work,a novel liquid chromatography electrospray ionization (ESI-MS) tandem triple quadrupole mass spectrometry method was developed to determine the trace amounts of major microcystin variants in waters.Solid phase extraction (SPE) consuming 10 mL of water samples was used for sample cleaning-up and analyte enrichment.A reverse phase LC separation system consisting a symmetry~(300) C-18 column (4.6 mm x 75 mm i.d.,3.5 mum,pore size 300 A) and binary gradient methanol-water mobile phase was applied for the separation of microcystin variants (MC-RR,-LR,-LW and -LF).Formic acid was spiked into the mobile phase to enhance the ionization efficiency.Tandem MS/MS analysis was performed in multi-reaction monitoring mode (MRM).Product-ion traces at m/z 519.9 -> 135.0 for MC-RR,498.4 -> 135.0 for MC-LR,1025.8 -> 891.7 for MC-LW and 986.8 -> 852.5 for MC-LF was used for quantification of the corresponding microcystin variants,and trace at m/z 556.1 -> 278.0 used for internal standard enkephalin.Limits of quantification (LOQs) were 0.16,0.04,2.0,1.0 and 0.10 mug/L for MC-RR,MC-LR,MC-LW,MC-LF and enkephalin,respectively.Intra- and inter-day precisions for the determination of the four variants were better than 5 and 6% in relative standard deviations (R.S.D.s),and recoveries for the four variants were in the range of 95-105%.The developed approach has been applied for the determination of the trace amounts of miccocystins in water samples of Taihu Lake of eastern China.The results showed that MC-RR and MC-LR were major variants detected in the water samples,and their concentrations significantly increased with the season changing from Spring to Summer.
机译:微囊藻毒素是一类环状七肽堆毒素和肿瘤启动子,是由富营养化湖泊,河流和水库中的蓝细菌生物生成的。用于确定水中痕量主要微囊藻毒素变异体的方法开发。使用固相萃取(SPE)消耗10 mL的水样品进行样品净化和分析物富集。反相LC分离系统由〜(300)C对称性组成-18柱(4.6毫米x 75毫米内径,3.5毫米,孔径300 A)和二元梯度甲醇-水流动相用于分离微囊藻毒素变体(MC-RR,-LR,-LW和-LF)。将甲酸加标到流动相中以提高电离效率。在多反应监测模式(MRM)中进行串联MS / MS分析。MC-RR,498.4-的产物离子痕量为m / z 519.9-> 135.0。 > MC-LR,135.8为135.0-> 891.7为MC-LW和MC-LF的986.8-> 852.5用于定量相应的微囊藻毒素变体,内标脑啡肽的m / z 556.1-> 278.0示踪。定量限(LOQs)为0.16,0.04,2.0 MC-RR,MC-LR,MC-LW,MC-LF和脑啡肽分别为1.0和0.10 mug / L。测定这四个变量的日内和日间精度分别优于5和6%。四个变体的相对标准偏差(RSD)和回收率在95%至105%之间。该方法已用于测定东部太湖水样中的微量微囊藻毒素。结果结果表明,MC-RR和MC-LR是在水样中检测到的主要变种,并且其浓度随春季到夏季的变化而显着增加。

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