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首页> 外文期刊>Spectroscopy >Development of a new analytical spectroscopic methodology based on the competitive aggregation in a dye–surfactant–drug system: Application to the determination of gemfibrozil
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Development of a new analytical spectroscopic methodology based on the competitive aggregation in a dye–surfactant–drug system: Application to the determination of gemfibrozil

机译:基于染料-表面活性剂-药物系统中竞争性聚集的新分析光谱方法的开发:在测定吉非贝齐中的应用

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A new analytical methodology based on the competitive aggregation in a dye–surfactant–drug system is developed for the determination of gemfibrozil. Eriochrome Blue Black R (EBBR) and Didodecyldimethylammonium bromide (DDABr) were the dye and surfactant used, respectively. In the proposed method, the anions of the dye bind to the cationic surfactant molecules to form dye–surfactant aggregates, which are monitored from changes in UV-Vis absorption features of the dye. In the ternary EBBR–DDABr–drug mixtures, the drug competes with the dye to interact with the surfactant, which results in a decrease in dye–surfactant aggregates formation. This, again, causes a change in absorption properties of the dye. The measurement parameter is the difference between the absorption of the dye in the presence and absence of the drug. In the appropriate experimental conditions the absorbance differences are directly proportional to the drug concentration. The influence of several experimental variables such as pH, concentrations of buffer, EBBR and DDABr on the measurement parameter were studied. Under the optimum conditions, the calibration graph was linear up to 6.0 μg ml−1with the correlation coefficient of 0.998. The limit of detection and quantification were found to be 0.044 and 0.15 μg ml−1, respectively. The method was validated and applied to the determination of gemfibrozil in pharmaceutical preparations.
机译:一种基于染料-表面活性剂-药物系统中竞争性聚集的新分析方法被开发出来,用于测定吉非贝齐。铬蓝黑R(EBBR)和十二烷基二甲基溴化铵(DDABr)分别用作染料和表面活性剂。在所提出的方法中,染料的阴离子与阳离子表面活性剂分子结合形成染料表面活性剂聚集体,可通过染料对UV-Vis吸收特征的变化进行监测。在三元EBBR-DDABr-药物混合物中,药物与染料竞争与表面活性剂相互作用,这导致染料-表面活性剂聚集体的形成减少。再次,这导致染料的吸收性质改变。测量参数是在存在和不存在药物的情况下染料吸收的差异。在适当的实验条件下,吸光度差异与药物浓度成正比。研究了pH,缓冲液浓度,EBBR和DDABr等几个实验变量对测量参数的影响。在最佳条件下,校准曲线线性至6.0μgml-1,相关系数为0.998。检出限和定量限分别为0.044和0.15μgml-1。该方法经过验证,可用于药物制剂中吉非贝齐的测定。

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