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在线固相萃取-超高效液相色谱-串联质谱法作为测定土壤中磺胺类残留的强大技术。

On-line solid phase extraction-ultra high performance liquid chromatography-tandem mass spectrometry as a powerful technique for the determination of sulfonamide residues in soils.

作者信息

Tetzner Natália Fernanda, Maniero Milena Guedes, Rodrigues-Silva Caio, Rath Susanne

机构信息

Institute of Chemistry, Department of Analytical Chemistry, University of Campinas, P.O. Box 6154, 13083-970 Campinas, SP, Brazil.

School of Civil Engineering, Architecture and Urban Design, University of Campinas, P.O. Box 6143, 13083-889 Campinas, SP, Brazil.

出版信息

J Chromatogr A. 2016 Jun 24;1452:89-97. doi: 10.1016/j.chroma.2016.05.034. Epub 2016 May 11.

Abstract

Sulfonamides are antimicrobials used widely as veterinary drugs, and their residues have been detected in environmental matrices. An analytical method for determining sulfadiazine, sulfathiazole, sulfamethazine, sulfamethoxazole, sulfadimethoxine and sulfaquinoxaline residues in soils employing a solid phase extraction on-line technique coupled with ultra-high performance liquid chromatography and tandem mass spectrometry (SPE-UHPLC-MS/MS) was developed and validated in this study. SPE and chromatographic separation were performed using an Oasis HLB column and an Acquity UPLC BEH C18 analytical column, respectively, at 40°C. Samples were prepared by extracting sulfonamides from soil using a solid-liquid extraction method with water:acetonitrile, 1:1v/v (recovery of 70.2-99.9%). The following parameters were evaluated to optimize the on-line SPE process: sorbent type (Oasis and C8), sample volume (100-400μL), loading solvent (water and different proportions of water:methanol) and washing volume (0.19-0.66mL). The method produced linear results for all sulfonamides from 0.5 to 12.5ngg(-1) with a linearity greater than 0.99. The precision of the method was less than 15%, and the matrix effect was -27% to -87%. The accuracy was in the range of 77-112% for all sulfonamides. The limit of quantitation in the two soils (clay and sand) was 0.5ngg(-1). The SPE column allowed for the analysis of many (more than 2000) samples without decreasing the efficiency.

摘要

磺胺类药物作为兽药被广泛使用,其残留物已在环境基质中被检测到。本研究开发并验证了一种采用固相萃取在线技术结合超高效液相色谱和串联质谱(SPE-UHPLC-MS/MS)测定土壤中磺胺嘧啶、磺胺噻唑、磺胺二甲嘧啶、磺胺甲恶唑、磺胺二甲氧嘧啶和磺胺喹恶啉残留量的分析方法。固相萃取和色谱分离分别使用Oasis HLB柱和Acquity UPLC BEH C18分析柱在40℃下进行。采用水:乙腈(1:1 v/v)的固液萃取方法从土壤中提取磺胺类药物制备样品(回收率为70.2-99.9%)。评估了以下参数以优化在线固相萃取过程:吸附剂类型(Oasis和C8)、进样体积(100-400μL)、上样溶剂(水和不同比例的水:甲醇)和清洗体积(0.19-0.66mL)。该方法对所有磺胺类药物在0.5至12.5ng g⁻¹范围内产生线性结果,线性度大于0.99。该方法的精密度小于15%,基质效应为-27%至-87%。所有磺胺类药物的准确度在77-112%范围内。两种土壤(粘土和砂土)中的定量限为0.5ng g⁻¹。固相萃取柱可用于分析许多(超过2000个)样品而不降低效率。

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