建立了固相萃取-超高效液相色谱-电喷雾串联三重四极杆质谱(SPE-UPLC-ESI-MS/MS)联用技术分析水中9种微囊藻毒素的方法.样品经SPE提取和净化后,以Waters ACQUITY UPLCTM BEH C18色谱柱为分离柱,以含0.1%甲酸乙腈和含0.1%甲酸水作为流动相进行梯度洗脱,电喷雾离子源电离、正离子多反应监测模式质谱进行定性和定量分析.9种微囊藻毒素在0.1~50 μg/L或0.5~100 μg/L质量浓度范围内线性良好,相关系数为0.999 0~0.999 8,方法的检出限(以3倍信噪比计)为0.1~0.5 ng/L;高、中、低3个添加水平的回收率为75.8% ~109%,相对标准偏差为0.49%~10.0%.结果表明,该方法灵敏、准确,检测范围广,分析速度快.应用该方法检测了杭州市两处水库水样中的微囊藻毒素,分别检出了3种和8种微囊藻毒素.
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