Liu Honghe, Mao Lisha, Zhu Zhou, Liu Guihua, Chen Yuhua
Shenzhen Center for Disease Control & Prevention, Shenzhen 518055, China.
Wei Sheng Yan Jiu. 2012 Sep;41(5):793-8.
A high performance liquid chromatography-tandem mass spectrometric method was established for determination of five microcystins( MC-LR,MC-LW,MC-RR, MC-LF, MC-YR)in drinking water and source water.
The five microcystins in water was cleaned by 0.22 microm millipore filter, then detected by high performance liquid chromatography-tandem mass spectrometry. Identification was achieved by electrospray ionization (ESI) in positive mode using multiple reaction monitoring.
The calibration curves of five microcystins showed good linearity in the range of 0.5-50 microg/L with correlation coefficient in the range of 0.9994 -1.0000. The detection limit of the method was from 0.06 microg/L to 0.08 microg/L, the recoveries of two spiking levels ranged from 91.2% to 102%, and RSDs of range from 2.11% to 3.26% were obtained.
The method for determination of five microcystins in drinking water and source water by HPLC-MS/MS was of operation convenience, less interference from impurities and good accuracy, which could meet the requirements of national health standard method for the determination of microcystins in drinking water.
建立高效液相色谱 - 串联质谱法测定饮用水和水源水中5种微囊藻毒素(MC-LR、MC-LW、MC-RR、MC-LF、MC-YR)。
水样中的5种微囊藻毒素经0.22μm微孔滤膜过滤净化后,采用高效液相色谱 - 串联质谱法进行检测。采用电喷雾电离(ESI)正离子模式,多反应监测进行定性。
5种微囊藻毒素的校准曲线在0.5 - 50μg/L范围内呈良好线性,相关系数在0.9994 - 1.0000之间。方法的检出限为0.06μg/L至0.08μg/L,两个加标水平的回收率在91.2%至102%之间,相对标准偏差在2.11%至3.26%之间。
采用HPLC-MS/MS测定饮用水和水源水中5种微囊藻毒素的方法操作简便,杂质干扰少,准确度好,能够满足国家卫生标准方法对饮用水中微囊藻毒素测定的要求。