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基于高效液相色谱法,采用样品预柱净化技术测定血液透析盐溶液中的三嗪类和硫代氨基甲酸盐类物质。

HPLC based method using sample precolumn cleanup for the determination of triazines and thiolcarbamates in hemodialysis saline solutions.

作者信息

do Nascimento Paulo C, Rohlfes Ana L B, Bohrer Denise, de Carvalho Leandro M, Pilau Eduardo J

机构信息

Departamento de Quimica, Universidade Federal de Santa Maria, 97111-970 Santa Maria, RS, Brazil.

出版信息

Talanta. 2005 Jan 15;65(1):211-6. doi: 10.1016/j.talanta.2004.06.009.

Abstract

Solid-phase extraction (SPE) procedures for cleanup and preconcentration followed by HPLC-UV method were investigated for the simultaneous determination of seven low-dosed pesticides in saline concentrates for hemodialysis. The target compounds were ametryn, desmetryn, prometryn, terbutryn, molinate, triallate and butylate. Polyethylene (three different types), teflon, polyurethane and polystyrene, in powder form, were investigated as adsorbents for solid-phase extraction of the analytes from the saline samples. Quantification was performed at 222nm and the analytes were separated on a LiChrosorb RP-18 (5mum, 125mm x 4mm i.d.) column using gradient elution with water/acetonitrile as mobile phase. The duration each chromatographic run was 18min including column reconditioning. The efficiency of the different SPE substrates for retaining the analytes from the highly concentrated saline (HCS) samples was discussed. The best performance was achieved with polystyrene as SPE material considering preconcentration factor, precolumn clogging, reusing capability and similarity between the mobile phases for SPE and HPLC procedures. Analyte concentrations as low as 1mugL(-1) could be determined in spiked HCS samples after preconcentration on polystyrene SPE precolumns. Recoveries between 98.7 and 102.2% were obtained from commercial spiked samples. Detection limits ranging from 4.8 (for prometryn) to 46mugL(-1) (for butylate) were calculated (without preconcentration). The within-day relative standard deviations (n = 9) ranged from 2.3 to 4.8%.

摘要

研究了采用固相萃取(SPE)进行净化和预浓缩,随后结合高效液相色谱 - 紫外检测法,用于同时测定血液透析浓缩液中七种低剂量农药的方法。目标化合物为莠灭净、去草净、扑草净、特丁净、禾草敌、野麦畏和丁草胺。对粉末状的三种不同类型聚乙烯、聚四氟乙烯、聚氨酯和聚苯乙烯作为吸附剂,从盐水样品中固相萃取分析物进行了研究。在222nm处进行定量分析,分析物在LiChrosorb RP - 18(5μm,125mm×4mm内径)柱上分离,以水/乙腈作为流动相进行梯度洗脱。每次色谱运行时间为18分钟,包括柱重新平衡。讨论了不同SPE基质从高浓度盐水(HCS)样品中保留分析物的效率。考虑到预浓缩因子、柱前堵塞、重复使用能力以及SPE和HPLC程序流动相之间的相似性,以聚苯乙烯作为SPE材料时性能最佳。在聚苯乙烯SPE预柱上进行预浓缩后,加标HCS样品中低至1μg L⁻¹的分析物浓度均可测定。从市售加标样品中获得的回收率在98.7%至102.2%之间。计算得到的检测限范围为4.8(对于扑草净)至46μg L⁻¹(对于丁草胺)(未进行预浓缩)。日内相对标准偏差(n = 9)范围为2.3%至4.8%。

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