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Sensitive assay of pharmaceutical amines in environmental samples and formulations by oxygenated graphene quantum dots

机译:通过含氧石墨烯量子点的环境样品和制剂中药物胺的敏感试验

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Oxygenated graphene quantum dots (GQDs) were prepared and used as a new colorimetric reagent for analysis of pharmaceutical amines. Citric acid was thermalized to prepare GQDs with functional groups along their edges. The prepared GQDs were used as a coupling reagent in an azo dye formation for dapsone (DAP) and metoclopramide (MET) determination. The characterization was done by scanning electron microscopy, transmission electron microscopy, atomic force microscopy, X-ray diffraction spectroscopy, Energy dispersive X-ray spectroscopy, EDX-mapping, dynamic light scattering, photoluminescence spectroscopy, Raman and FT-IR spectroscopy. DAP and MET were diazotized by nitrite to their related diazonium cations in acidic condition through a flow injection manifold. Then they were coupled to GQDs to produce the yellow colored products. Detection of the products was performed by spectrophotometry at 423 nm. Various chemical and instrumental parameters were optimized by a univariate procedure and a central composite design (CCD) chemometrics approach. The analytical method showed the linear calibrations for DAP and MET in the ranges of 0.03-20 and 0.1-40 mu g mL(-1), respectively. The limit of detection for both DAP and MET was of 0.01 mu g mL(-1), respectively. The inter-day experiments showed a satisfactory robustness of the method for determination of DAP and MET. The sample throughput found in this method was about 60 h(-1). Lake, river and well water samples as well as soil samples along with some pharmaceutical formulations were analyzed. (C) 2018 Elsevier Ltd. All rights reserved.
机译:制备含氧石墨烯量子点(GQDS)并用作新的比色试剂,用于分析药物胺。热化柠檬酸以沿其边缘用官能团制备GQD。制备的GQDS用作偶氮染料形成的偶联试剂,用于双酮(DAP)和甲基丙普通(MET)测定。表征是通过扫描电子显微镜,透射电子显微镜,原子力显微镜,X射线衍射光谱,能量分散X射线光谱,EDX映射,动态光散射,光致发光光谱,拉曼和FT-IR光谱来完成的。通过流入歧管通过亚硝酸盐通过亚硝酸盐并通过流动注入歧管进行DAP并通过亚酸性条件进行重氮化。然后它们耦合到GQD以产生黄色产品。通过分光光度法在423nm下进行检测。通过单变量的程序和中央复合设计(CCD)化学计量方法进行了各种化学和乐器参数。分析方法显示了DAP的线性校准,分别在0.03-20和0.1-40μg(-1)的范围内。达到的检测极限分别为0.01μgml(-1)。日内的实验表明,用于测定DAP和满足的方法的令人满意的稳健性。该方法中发现的样品产量约为60小时(-1)。分析了湖泊,河流和水样以及土壤样品以及一些药物制剂的水样。 (c)2018年elestvier有限公司保留所有权利。

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