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中国癌症防治杂志 ›› 2018, Vol. 10 ›› Issue (1): 24-28.doi: 10.3969/j.issn.1674-5671.2018.01.06

• 基础研究 • 上一篇    下一篇

高效液相色谱法同时测定水源水中三种微囊藻毒素

  

  1. 广西医科大学附属肿瘤医院实验研究部;广西医科大学附属肿瘤医院乳腺外科;广西壮族自治区肿瘤防治研究所
  • 出版日期:2018-02-25 发布日期:2018-03-23
  • 通讯作者: 邓伟 dengwei@gxmu.edu.cn;黎远冬 lyd641209@163.com
  • 基金资助:

    国家自然科学基金资助项目(81660561)

Simultaneous determination of three microcystins in source water using high performance liquid chromatography

  • Online:2018-02-25 Published:2018-03-23

摘要:

目的 建立一种同时测定水源水中三种微囊藻毒素(MC-LR、MC-RR、MC-YR)的高效液相色谱(high performance liquid chromatography,HPLC)方法。 方法 取500 mL水样,0.45 μm滤膜过滤,滤液过C18柱,依次用10 mL超纯水、20 mL 20%甲醇溶液淋洗,15 mL 80% 甲醇溶液(加入0.05%三氟乙酸)洗脱,蒸发浓缩吹干,溶于1 mL超纯水,待测。采用固相萃取柱,流动相为0.1%磷酸水溶液-乙腈(67∶33),流速1.0  mL/min,柱温45℃,在238 nm波长紫外线检测器检测。结果 MC-LR、MC-RR和MC-YR 在 0.05~1.00 μg/mL范围内线性良好(r=0.9987、0.9992和0.9997),且峰形较好;回收率均在80%~110%,相对标准偏差(relative standard deviation,RSD)为5.0%~9.6%;MC-LR、MC-RR和MC-YR的方法检出限(limit of detection,LOD)分别为0.028 μg/L、0.037 μg/L和0.056 μg/L。结论 本方法准确度、灵敏度、回收率高,重现性好,可用于水源水中MC-LR、MC-RR、MC-YR同时检测。

关键词: 水源水, 微囊藻毒素, 高效液相色谱, 水体富营养化

Abstract:

Objective A method was established for simultaneous determination of microcystins (microcystin-LR,-RR,-YR) in source water using high-performance liquid chromatography (HPLC). Methods Water samples (500 mL) were filtered through a 0.45 μm membrane on a C18 column,then eluted with sequential use of 10 ml of ultra-pure water,20 mL of 20% methanol and 15 mL of 80% methanol containing 0.05% tallow fatty acid(TFA). The eluate was dried and the residues were dissolved in 1 mL of ultra-pure water for testing. The eluate was fractionated on a C18  column with a mobile phase of 0.1% aqueous phosphoric acid-acetonitrile (67:33) at a flow rate of 1 ml/min at a column temperature of 45 ℃. Compounds were detected with a UV detector at a wavelength of 238 nm. Results Microcystin-LR,-RR,and -YR showed good peak shape and good linearity in the range of 0.05-1.0 μg/mL(r=0.9987, 0.9992,and 0.9997). Recoveries ranged from 80% to 110%,relative standard deviation(RSD) was 5.0%-9.6%,and limits of detection were 0.028,0.037,and 0.056 μg/L. Conclusions The method described here can be used for accurate,highly sensitive,and reproducible simultaneous detection of microcystin-LR,-RR and -YR in source water.

Key words: Source water, Microcystins, High performance liquid chromatography, Water eutrophication