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首页> 外文期刊>European Chemical Bulletin >Spectrophotometric Determination of Cinnarizine through Charge-Transfer Complex Formation with Polynitro Compounds
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Spectrophotometric Determination of Cinnarizine through Charge-Transfer Complex Formation with Polynitro Compounds

机译:多硝基化合物的电荷转移配合物形成分光光度法测定肉桂酸

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Spectrophotometric studies were carried out to investigate the charge-transfer reaction between cinnarizine and dipicrylamine (DPA) or 2,6-dinitrophenol (DNP). Simple and rapid spectrophotometric methods were suggested for the determination of cinnarizine (CN) in pure and in its pharmaceutical dosage forms. The colored products are quantified spectrophotometrically at 430 and 440 nm for cinnarizine complexes with DPA in a mixture of 15% dioxane in dichloroethane (I) and 15% ethyl acetate in chloroform (II), respectively. On the other hand, cinnarizine complexes formed with DNP in acetonitrile (III) and in a mixture of 30% dichloroethane in ethyl alcohol (IV) were quantified at 460 and 430 nm, respectively. The proposed procedures were successfully utilized for the determination of the drug in its pharmaceutical formulation using standard addition and calibration curve methods. Beer's law was obeyed in the concentration ranges 1.00-22.00, 1.50-36.80, 1.50-36.80 and 3.60-36.80 μg mL-1 cinnarizine with molar absorpitivities of 1.64×104, 1.43×104, 5.16×104 and 3.60×104 (L mol-1 cm-1), for CN-DPA in mixture (I), CN-DPA in mixture (II), CN-DNP in acetonitrile (III) and CN-DNP in mixture (IV), respectively. The relative standard deviations are less than 1.02%. The results of analysis of commercial tablets (Cinnarizine-25) showed that there is no interference from any excipient. Statistical comparison of the results was performed with regard to accuracy and precision using student's t-test and F-ratio at 95% confidence level.
机译:进行了分光光度法研究,以研究肉桂利嗪与二吡啶胺(DPA)或2,6-二硝基苯酚(DNP)之间的电荷转移反应。建议使用简单,快速的分光光度法测定纯及其药物剂型中的肉桂利嗪(CN)。分别在15%二恶烷的二氯乙烷溶液(I)和15%乙酸乙酯的氯仿溶液(II)的混合物中分光光度法在430和440 nm处测定肉桂醛与DPA的配合物的有色配合物。另一方面,分别在460和430 nm处定量与DNP在乙腈(III)和30%二氯乙烷在乙醇(IV)的混合物中形成的肉桂嗪络合物。使用标准添加和校准曲线方法,所建议的程序已成功用于确定其药物制剂中的药物。在1.00-22.00、1.50-36.80、1.50-36.80和3.60-36.80μgmL-1桂利嗪的浓度范围内遵守比尔定律,摩尔吸光度为1.64×104、1.43×104、5.16×104和3.60×104(L mol -1 cm-1),分别用于混合物(I)中的CN-DPA,混合物(II)中的CN-DPA,乙腈(III)中的CN-DNP和混合物(IV)中的CN-DNP。相对标准偏差小于1.02%。商业片剂(Cinnarizine-25)的分析结果表明,没有任何赋形剂的干扰。使用学生的t检验和F比率以95%置信水平对结果的准确性和精密度进行统计比较。

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