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阐明基质效应并优化固相萃取条件,用于 LC-MS/MS 分析蓝藻中的β-N-甲基氨基-L-丙氨酸(BMAA)和 2,4-二氨基丁酸(DAB)神经毒素。

Elucidation of matrix effects and performance of solid-phase extraction for LC-MS/MS analysis of β-N-methylamino-L-alanine (BMAA) and 2,4-diaminobutyric acid (DAB) neurotoxins in cyanobacteria.

机构信息

Key Laboratory of Marine Environment and Ecology, Ocean University of China, Ministry of Education, Qingdao, 266100, China.

出版信息

Analyst. 2012 Mar 7;137(5):1210-9. doi: 10.1039/c2an15887f. Epub 2012 Jan 16.

Abstract

A liquid chromatography-mass spectrometry (LC-MS/MS) method using hydrophilic interaction liquid chromatography (HILIC) was developed for the analysis of neurotoxins β-N-methylamino-L-alanine (BMAA) and 2,4-diaminobutyric acid (DAB), using multiple reaction monitoring (MRM) scan mode. Oasis-MCX and Strata-X-C polymeric cation-exchange cartridges were used to clean extracts of cyanobacterial cultures, including two strains of Microcystis aeruginosa and one strain of Nostoc sp. The performance of the solid-phase extraction (SPE) cartridges for BMAA and DAB were evaluated using mixed standards and spiked cyanobacterial extracts, which demonstrated recoveries of BMAA and DAB ranging from 66% to 91%. Matrix effects in LC-MS/MS were evaluated, and while there was no effect on BMAA quantitation, suppression of DAB was found. Full scan (Q1) and enhanced product ion (EPI) monitoring showed that the DAB suppression may be due to closely eluting compounds, including lysine, histidine, arginine and three other compounds with M + H m/z of 88, 164 and 191. The procedures developed allow the sensitive and effective analysis of trace BMAA and DAB levels in cyanobacteria. While DAB was confirmed to be present, no BMAA was found in the cyanobacterial samples tested in the present study.

摘要

建立了一种采用亲水作用色谱(HILIC)的液质联用(LC-MS/MS)方法,用于分析神经毒素β-N-甲基氨基-L-丙氨酸(BMAA)和 2,4-二氨基丁酸(DAB),采用多重反应监测(MRM)扫描模式。Oasis-MCX 和 Strata-X-C 聚合型阳离子交换小柱用于清洁蓝藻培养物的提取物,包括两株铜绿微囊藻和一株念珠藻。采用混合标准品和加标蓝藻提取物评估固相萃取(SPE)小柱对 BMAA 和 DAB 的性能,结果表明 BMAA 和 DAB 的回收率在 66%至 91%之间。评估了 LC-MS/MS 中的基质效应,虽然对 BMAA 的定量没有影响,但发现 DAB 受到抑制。全扫描(Q1)和增强子离子(EPI)监测表明,DAB 抑制可能是由于存在紧密洗脱的化合物,包括赖氨酸、组氨酸、精氨酸和另外三种化合物,它们的 M + H m/z 分别为 88、164 和 191。所建立的方法可用于灵敏有效地分析蓝藻中痕量 BMAA 和 DAB 水平。虽然在本研究中检测到 DAB 的存在,但在测试的蓝藻样本中未发现 BMAA。

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