Asensio-Ramos María, Hernández-Borges Javier, Ravelo-Pérez Lidia M, Rodríguez-Delgado Miguel Angel
Departamento de Química Analítica, Nutrición y Bromatología, Universidad de La Laguna, La Laguna, Tenerife, Islas Canarias, Spain.
Electrophoresis. 2008 Nov;29(21):4412-21. doi: 10.1002/elps.200800254.
In this work, NACE with UV detection is combined with SPE using multi-walled carbon nanotubes (MWCNT) as stationary phase to determine a group of seven pesticides (pirimicarb, pyrifenox, penconazol, carbendazim, cyromazine, pyrimethanil and cyprodinil) in mineral water samples using ametryn as internal standard. The optimized BGE, consisting of a mixture of MeOH and ACN (1:2 v/v) with 90 mM SDS and 20.5 mM HClO(4), was satisfactory to get a good resolution of the seven compounds in less than 13 min. On-line preconcentration was carried out by electrokinetic injection of the sample dissolved in 78:22 v/v MeOH/ACN, 1.11 mM HClO(4). Repeatability was studied for the same day (n=4), for nine different days (n=36) and for four different capillaries. RSD values were appropriate in all cases, i.e. in the range 4.3-9.4% between different capillaries. MWCNT of 10-15 nm od, 2-6 nm id and 0.1-10 mum length were used as SPE materials for the preconcentration of these pesticides from water samples. SPE parameters influencing the enrichment were optimized and the most favorable conditions were as follows: the amount of stationary phase, eluent, sample pH and sample volume were 40 mg MWCNT, 10 mL ACN and 10 mL dichloromethane containing 5% v/v formic acid, pH 8.0, and 750 mL, respectively. Mean recovery values ranged between 53 and 94% for Milli-Q water and between 47 and 93% for mineral waters (RSD values were in the range 2-16%). The method allowed the determination of these pesticides at concentrations below the maximum residue limits established by the European Union legislation (LOD in the range 27-58 ng/L). When the cost, amount and type of the carbon nanotubes used in this work are compared with those carbon nanotubes previously used in the literature it is clear that the proposed materials can be used as economical stationary phases, even cheaper than conventional SPE cartridges.
在本工作中,将带有紫外检测的非水毛细管电泳(NACE)与以多壁碳纳米管(MWCNT)为固定相的固相萃取(SPE)相结合,以莠灭净为内标物,测定矿泉水中的一组七种农药(抗蚜威、氯苯嘧啶醇、戊菌唑、多菌灵、环丙氨嗪、嘧霉胺和嘧菌环胺)。优化后的背景电解质(BGE)由甲醇和乙腈(1:2 v/v)的混合物与90 mM十二烷基硫酸钠(SDS)和20.5 mM高氯酸(HClO₄)组成,能在不到13分钟的时间内使这七种化合物获得良好的分离度。通过电动进样对溶解于78:22 v/v甲醇/乙腈、1.11 mM高氯酸中的样品进行在线预富集。研究了同一天(n = 4)、九个不同日期(n = 36)以及四根不同毛细管的重复性。在所有情况下,相对标准偏差(RSD)值均合适,即在不同毛细管之间为4.3 - 9.4%。外径为10 - 15 nm、内径为2 - 6 nm、长度为0.1 - 10 µm的多壁碳纳米管用作固相萃取材料,用于从水样中预富集这些农药。对影响富集的固相萃取参数进行了优化,最适宜的条件如下:固定相用量、洗脱剂、样品pH值和样品体积分别为40 mg多壁碳纳米管、10 mL乙腈、10 mL含5% v/v甲酸的二氯甲烷、pH 8.0和750 mL。超纯水的平均回收率在53%至94%之间,矿泉水的平均回收率在47%至93%之间(RSD值在2%至16%范围内)。该方法能够测定低于欧盟法规规定的最大残留限量浓度的这些农药(检测限在27 - 58 ng/L范围内)。当将本工作中使用的碳纳米管的成本、用量和类型与文献中先前使用的碳纳米管进行比较时,很明显所提出的材料可用作经济的固定相,甚至比传统的固相萃取柱更便宜。