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首页> 外文期刊>Chemistry central journal >New spectrofluorimetric methods for determination of melatonin in the presence of N-{2-[1-({3-[2-(acetylamino)ethyl]-5-methoxy-1H-indol-2-yl}methyl)-5-methoxy-1H-indol-3-yl]- ethyl}acetamide: a contaminant in commercial melatoni
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New spectrofluorimetric methods for determination of melatonin in the presence of N-{2-[1-({3-[2-(acetylamino)ethyl]-5-methoxy-1H-indol-2-yl}methyl)-5-methoxy-1H-indol-3-yl]- ethyl}acetamide: a contaminant in commercial melatoni

机译:N- {2- [1-({3- [2-(乙酰氨基)乙基] -5-甲氧基-1H-吲哚-2-基}甲基)-5-甲氧基存在下褪黑素测定的新的荧光光谱法-1H-吲哚-3-基]-乙基}乙酰胺:一种商品褪黑素中的污染物

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Background Melatonin (MLT) has many health implications, therefore it is of valuable importance to develop specific analytical methods for determination of MLT in the presence of its main contaminant, N-{2-[1-({3-[2-(acetylamino)ethyl]-5-methoxy-1H-indol-2-yl}methyl)-5-methoxy-1H-indol-3-yl]ethyl}acetamide (10). For development of these analytical methods, compound 10 had to be prepared in an adequate amount. Results Compound 10 was synthesized in six steps starting from 5-methoxyindole-2-carboxylic acid (1). Analytical performance of the proposed spectrofluorimetric methods was statistically validated with respect to linearity, accuracy, precision and specificity. The proposed methods were successfully applied for the assay of MLT in laboratory prepared mixtures containing up to 60 % of compound 10 and in commercial MLT tablets with recoveries not less than 99.00 %. No interference was observed from common pharmaceutical additives and the results were favorably compared with those obtained by a reference method. Conclusions This work describes simple, sensitive, and reliable second derivative spectrofluorimetric method in addition to two multivariate calibration methods, principal component regression (PCR) and partial least square (PLS), for the determination of MLT in the presence of compound 10.
机译:背景褪黑激素(MLT)对健康有许多影响,因此,开发一种在主要污染物N- {2- [1-({3- [2-(乙酰氨基) )乙基] -5-甲氧基-1H-吲哚-2-基}甲基)-5-甲氧基-1H-吲哚-3-基]乙基}乙酰胺(10)。为了开发这些分析方法,必须以足够的量制备化合物10。结果化合物10是从5-甲氧基吲哚-2-羧酸(1)开始的六步合成的。相对于线性,准确性,精密度和特异性,所提出的光谱荧光方法的分析性能得到了统计验证。所提出的方法已成功地用于实验室制备的混合物中,其含量最高为60%的化合物10,并且用于商业MLT片剂中的MLT分析,其回收率不少于99.00%。没有观察到普通药物添加剂的干扰,其结果与参考方法得到的结果相比具有优势。结论这项工作描述了简单,灵敏和可靠的二阶导数荧光光谱法,以及两种多元校准方法,主成分回归(PCR)和偏最小二乘(PLS),用于在化合物10存在下测定MLT。

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