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用于低成本测定草甘膦的纸质等速电泳预浓缩技术

Paper-based isotachophoretic preconcentration technique for low-cost determination of glyphosate.

作者信息

Franck Nicolás, Stopper Pascal, Ude Lukas, Urteaga Raul, Kler Pablo A, Huhn Carolin

机构信息

Centro de Investigación en Métodos Computacionales, UNL-CONICET, Predio CCT CONICET RN 168, S3000GLN, Santa Fe, Argentina.

Instituto de Física del Litoral, UNL-CONICET, Güemes 3450, S3000GLN, Santa Fe, Argentina.

出版信息

Anal Bioanal Chem. 2024 Dec;416(29):6745-6757. doi: 10.1007/s00216-024-05544-x. Epub 2024 Oct 1.

Abstract

Electrophoretic microfluidic paper-based analytical devices (e-µPADs) are promising for low-cost and portable technologies, but quantitative detection remains challenging. In this study, we develop a paper-based isotachophoretic preconcentration and separation method for the herbicide glyphosate as a model analyte. The device, consisting of two electrode chambers filled with leading and terminating electrolytes and a nitrocellulose strip as the separation carrier, was illuminated by a flat light source and operated with a voltage supply of 400 V. Detection was accomplished using a simple camera. Colorimetric detection was optimized through competitive complexation between glyphosate, copper ions, and pyrocatechol violet as a dye. The buffer system was optimized using simulations, (i) ensuring the pH was optimal for the demetallation of the blue pyrocatechol violet-copper complex [PV] to the yellow free dye and (ii) ensuring the electrophoretic migration of glyphosate into the slower [PV] for the colorimetric reaction. A new data evaluation method is presented, analyzing the RGB channel intensities. The linear range was between 0.8 and 25 µM, with a LOD of approximately 0.8 µM. The ITP separation preconcentrated glyphosate by a factor of 820 in numerical simulations. The method may be applied to control glyphosate formulations, especially in developing countries where herbicide sales and applications are poorly regulated.

摘要

基于电泳的微流控纸基分析装置(e-µPADs)在低成本和便携式技术方面前景广阔,但定量检测仍然具有挑战性。在本研究中,我们开发了一种基于纸的等速电泳预浓缩和分离方法,以除草剂草甘膦作为模型分析物。该装置由两个分别装有先导电解质和终端电解质的电极室以及一条作为分离载体的硝酸纤维素条带组成,由一个平面光源照射,并在400 V的电压供应下运行。使用一个简单的相机完成检测。通过草甘膦、铜离子和作为染料的邻苯二酚紫之间的竞争性络合优化了比色检测。使用模拟对缓冲系统进行了优化,(i)确保pH值对于蓝色邻苯二酚紫 - 铜络合物[PV]脱金属形成黄色游离染料是最佳的,(ii)确保草甘膦电泳迁移到较慢的[PV]中进行比色反应。提出了一种新的数据评估方法,分析RGB通道强度。线性范围在0.8至25 µM之间,检测限约为0.8 µM。在数值模拟中,等速电泳分离将草甘膦预浓缩了820倍。该方法可应用于草甘膦制剂的控制,特别是在除草剂销售和使用监管不力的发展中国家。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08ff/11579070/3ee93ddf0024/216_2024_5544_Fig1_HTML.jpg

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