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DECAGLIP - Colorimetric Detection of Glyphosate Herbicide

机译:DECAGLIP-草甘膦除草剂的比色检测

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The project addresses the issue of the verification of the presence of pesticide N-(phosphonomethyl) glycine, commonly known as glyphosate, in small amounts through an innovative method of colorimetric detection. The purpose of this project is to find a facilitator of glyphosate residues’ identification in apple samples, which may be used in the inspection of the same. The importance of the research is precisely to detect glyphosate in human consumption, since this pesticide is considered probable carcinogen in humans by IARC (International Agency for Research on Cancer), and its use is growing in an exceptional way in the whole world. The current methods for detection of glyphosate are based in High Performance Liquid Chromatography (HPLC), which is more expensive and complex than the colorimetric analysis. The proposed method involves the formation of glyphosate complexes with copper (II) ions in aqueous media; followed by the colorimetric detection which is based on the enzymatic activity of copper (II) in peroxidase reactions. Copper catalyzes the peroxidase reaction that occurs between the chromogen 3,3,5,5-tetramethylbenzidine (TMB) and H2O2, producing a blue color change in the solution. When copper is complexed with glyphosate, it occurs the inhibition of catalysis and hence lesser intensity of the color produced. Thus, the concentration of glyphosate in solution can be determined by the formation of copper-glyphosate complexes, which prevent the color development. According to the results obtained so far, including the successfully glyphosate extraction from apple samples using the QuEChERS extraction method, it is possible to observe color changes in the solutions distinguished by naked eye and absorbance changes at very low concentrations, up to 1.185 ppm of glyphosate, by the method of UV–visible Molecular Absorption Spectroscopy using 655 nm of wavelength. Therefore, the proposed method shows high sensitivity, besides its simplicity of procedure and immediate response.
机译:该项目通过一种创新的比色检测方法,解决了少量验证农药N-(膦酰基甲基)甘氨酸(俗称草甘膦)的问题。该项目的目的是在苹果样品中寻找草甘膦残留物的鉴定辅助剂,可用于对其进行检查。这项研究的重要性恰恰在于检测人类食用中的草甘膦,因为该农药被IARC(国际癌症研究机构)认为是人类可能的致癌物质,并且其使用在全世界范围内都以特殊的方式增长。目前检测草甘膦的方法是基于高效液相色谱法(HPLC),该方法比比色分析更昂贵,更复杂。拟议的方法包括在水性介质中与铜离子形成草甘膦配合物。然后进行比色检测,该检测基于过氧化酶反应中铜(II)的酶活性。铜催化发色团3,3,5,5-四甲基联苯胺(TMB)和H2O2之间发生的过氧化物酶反应,在溶液中产生蓝色变化。当铜与草甘膦络合时,它会抑制催化作用,从而降低产生的颜色强度。因此,溶液中草甘膦的浓度可以通过形成铜-草甘膦络合物来确定,该络合物可防止显色。根据迄今获得的结果,包括使用QuEChERS提取方法成功从苹果样品中提取草甘膦,可以观察到肉眼可见的溶液颜色变化以及在浓度极低(高达1.185 ppm的草甘膦)下的吸光度变化。 ,通过使用655 nm波长的紫外可见分子吸收光谱法进行。因此,所提出的方法除了操作简单和即时响应外,还具有很高的灵敏度。

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