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Optimizing LC-MS-MS determination of microcystin toxins in natural water and drinking water supplies

机译:优化LC-MS-MS测定天然水和饮用水中微囊藻毒素的含量

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The performance of a solid phase extraction (SPE) LC-MS-MS procedure for determining microcystins (MC) in water was investigated. Six MC, MCRR, MCYR, MCLR, MCLA, MCLF and MCLW, were determined using positive ion electrospray (+ESI) with separation on a C8 column eluted with a methanol-water gradient containing 15 mM ammonium formate and 0.006% acetic acid. Each MC, as well as the internal standard and surrogate, were detected by two transitions. Isocratic and gradient separations were examined to increase the resolution of MCRR and MCLF as all known naturally occurring MC elute between these two variants. Analysis of fortified laboratory reagent water as well as bloom samples from northern California provided performance information. Cell lysis, accomplished by f reeze-thawing samples, was required to determine total sample toxins as 93 to 99% of the toxins were intracellular. Up to 98% of dissolved MC were lost by sorption in filter cartridges, but satisfactory recoveries were obtained with polypropylene filters after the filtrate was combined with a methanol rinse. C18 SPE required elution with trifluoroacetic acid (TFA) for acceptable recoveries of the arginine-containing MC Freezing was required to preserve MC which degraded rapidly by microbial metabolism at 4 °C after an approximate 10 day lag period. With the optimized method the experimental Method Detection Limits (MDL) for both quantitation and confirmation transitions for the arginine-containing MC ranged from 0.03 to 0.04 ng L~(-1) Laboratory reporting limits (or LOQ) of 0.1 and 0.2 ng L~(-1) were confirmed by analyzing surface water samples where accuracy averaged 65 to 70%. Measurement of total MC in bloom samples was reproducible with relative standard deviations of 8.3 to 12%. The study demonstrates the importance of sample preservation, sample workup and quality control procedures in reliable MC determination using modern LC-MS-MS instruments.
机译:研究了固相萃取(SPE)LC-MS-MS方法测定水中微囊藻毒素(MC)的性能。使用正离子电喷雾(+ ESI)在C8色谱柱上分离,用含15 mM甲酸铵和0.006%乙酸的甲醇-水梯度洗脱,测定了六种MC,MCRR,MCR,MCLR,MCLA,MCLF和MCLW。每个MC以及内标和替代品均通过两次转换检测到。检查了等度分离和梯度分离,以提高MCRR和MCLF的分离度,因为这两个变体之间均存在所有已知的自然存在的MC洗脱液。分析强化的实验室试剂水以及北加州的水华样品提供了性能信息。需要通过冻融样品完成的细胞裂解来确定样品中的总毒素,因为93至99%的毒素在细胞内。高达98%的溶解MC通过吸附在滤芯中而损失,但是在将滤液与甲醇冲洗液合并后,使用聚丙烯滤器可获得令人满意的回收率。 C18 SPE需要用三氟乙酸(TFA)洗脱才能得到可接受的精氨酸含MC回收率。冷冻约10天后,为了保存在4°C下因微生物代谢迅速降解的MC,需要冷冻保存。采用优化的方法,用于精氨酸的MC定量和确认过渡的实验方法检测限(MDL)介于0.03至0.04 ng L〜(-1)实验室报告极限(或LOQ)为0.1和0.2 ng L〜 (-1)是通过分析地表水样品确定的,平均精度为65%至70%。大花样样品中总MC的测定是可重复的,相对标准偏差为8.3%至12%。该研究证明了使用现代LC-MS-MS仪器进行可靠的MC测定时,样品保存,样品处理和质量控制程序的重要性。

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