Fang Lanyun, Yao Xunping, Wang Li, Li Jige
Ningbo Key Laboratory of Poison Research and Control, Ningbo Municipal Center for Disease Control and Prevention, Ningbo 315010, China
Ningbo Key Laboratory of Poison Research and Control, Ningbo Municipal Center for Disease Control and Prevention, Ningbo 315010, China.
J Chromatogr Sci. 2015 Feb;53(2):373-9. doi: 10.1093/chromsci/bmu054. Epub 2014 Jun 16.
A solid-phase extraction (SPE) method for ultra-sensitive determination of four lipophilic marine biotoxins in bivalve samples by coupling high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS-MS) was developed. Azaspiracid-2 (AZA2), pectenotoxins-2, spirolide (SPX) and gymnodimine were simultaneously determined by HPLC-MS-MS in a positive multiple reaction monitoring mode. Separation was achieved on a reversed-phase C18 column with an acetonitrile-water gradient containing formic acid. During the analysis, solvent effects on the analytes were eliminated by using 1 : 1 water-methanol as dissolving solvent instead of pure methanol. Matrix effects in post-SPE extract and crude extract were seriously evaluated. Increased matrix effects in post-SPE extract countervailed the concentration purpose to some extent. The limits of detection of the SPE-HPLC-MS-MS method were determined to be in the range of 0.013-0.085 µg kg(-1), and the linear range of the method was in the range of 0.128-55.2 ng mL(-1) for the detected toxins. The proposed method was validated in terms of linearity (matrix-matched standard curves), precision, recovery, repeatability and limits of quantification. The recoveries of fortified samples at three different concentration levels were satisfactory, and the intra- and interday precisions were <7 and 10%, respectively.Several bivalve samples were analyzed to demonstrate the applicability of the proposed method. Different target toxins were detected in different kind of bivalves. Among them, AZA2 and SPX1 were first detected in Chinese shellfish. The levels of detected toxins were below the current European Union regulatory limits.
建立了一种通过高效液相色谱 - 串联质谱联用(HPLC-MS-MS)超灵敏测定双壳贝类样品中四种亲脂性海洋生物毒素的固相萃取(SPE)方法。采用正离子多反应监测模式,通过HPLC-MS-MS同时测定氮杂螺旋酸 - 2(AZA2)、扇贝毒素 - 2、螺旋环肽(SPX)和裸甲藻毒素。在含甲酸的乙腈 - 水梯度的反相C18柱上实现分离。分析过程中,使用1:1水 - 甲醇作为溶解溶剂代替纯甲醇,消除了溶剂对分析物的影响。对固相萃取后提取物和粗提取物中的基质效应进行了严格评估。固相萃取后提取物中增加的基质效应在一定程度上抵消了浓缩目的。该固相萃取 - HPLC-MS-MS方法的检测限为0.013 - 0.085 μg kg⁻¹,所测毒素的方法线性范围为0.128 - 55.2 ng mL⁻¹。该方法在线性(基质匹配标准曲线)、精密度、回收率、重复性和定量限方面得到了验证。三个不同浓度水平加标样品的回收率令人满意,日内和日间精密度分别<7%和10%。分析了几个双壳贝类样品以证明该方法的适用性。在不同种类的双壳贝类中检测到了不同的目标毒素。其中,AZA2和SPX1首次在中国贝类中被检测到。所测毒素水平低于当前欧盟监管限值。