Wang Jing, Pang Xiaolu, Liu Zhengzheng, Hou Jingde
Zhejiang Province Environmental Monitoring Centre, Hangzhou 310012, China.
Se Pu. 2006 Jul;24(4):335-8.
An analytical method for the analysis of trace microcystins (MCYST) in water was developed using solid phase extraction (SPE) for enrichment and ultra performance liquid chromatography/tandem mass spectrometry (UPLC/MS/MS) for detection. One litre of water was passed through SPE columns, the extracted sample was rinsed off by 10 mL methanol, then evaporated to 1.0 mL before being analyzed with UPLC/MS/MS. The effect of formic acid concentration in the mobile phase on the sensitivity was studied and the results showed that 0.1% was the optimum concentration. Four microcystins, MCYST-LR, RR, LW, LF, can be separated and detected in 5 min, which is much shorter than that by the conventional liquid chromatography. The detection limits were 1.3 - 6.0 ng/L, and the recoveries were 91.1% - 111%. The calibration curves showed good linearity in the range of 1.0 microg/L - 1.0 mg/L with correlation coefficients larger than 0.99. The method was also applied to determine MCYST in real water samples from three reservoirs in Zhejiang Province, and the results showed that the concentrations of LR and RR were 0.044 7 - 2.73 microg/L and 0.020 8 - 1.36 microg/L respectively, and LW and LF were not detected.
建立了一种水中痕量微囊藻毒素(MCYST)的分析方法,该方法采用固相萃取(SPE)进行富集,超高效液相色谱/串联质谱(UPLC/MS/MS)进行检测。将1升水通过SPE柱,用10毫升甲醇冲洗萃取后的样品,然后蒸发至1.0毫升,再用UPLC/MS/MS进行分析。研究了流动相中甲酸浓度对灵敏度的影响,结果表明0.1%为最佳浓度。四种微囊藻毒素,MCYST-LR、RR、LW、LF,可在5分钟内分离并检测出来,这比传统液相色谱法所需时间短得多。检测限为1.3 - 6.0纳克/升,回收率为91.1% - 111%。校准曲线在1.0微克/升 - 1.0毫克/升范围内呈良好线性,相关系数大于0.99。该方法还应用于测定浙江省三个水库实际水样中的MCYST,结果表明LR和RR的浓度分别为0.044 7 - 2.73微克/升和0.020 8 - 1.36微克/升,未检测到LW和LF。