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Application of Chloranil and Fluoranil π-Acceptors for the Spectrophotometric Determination of Mesalamine in Pharmaceutical Bulk and Dosage Forms

机译:氯腈和氟腈π受体在分光光度法测定药物散装和剂量形式中的美沙拉敏中的应用

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摘要

Two simple, sensitive and accurate spectrophotometric methods for the determination of mesalamine are described. The methods are based on charge-transfer complex formation reactions of the drug with two π -electron acceptors, p -chloranil and p -fluoranil, in aqueous medium. The coloured complexes having maximum absorbance at 346 nm and 347 nm by using p -chloranil and p -fluoranil reagents respectively. Under the optimized experimental conditions, the calibration curves showed a linear relationship over the concentration ranges of 1–35 and 1-30 μgml ? 1 with molar absorptivity values 4.60×10 3 and 5.67×10 3 L. mol -1 .cm -1 . using above reagents respectively. The limits of detection and quantitation were found 0.376 and 1.25 μgml ? 1 using p- chloranil, respectively, and 0.333 and 1.111 μgml ? 1 using p- fluoranil, respectively. The complexes were found to be formed in ratio of 1:1 species in both methods, with stability constants of 6.9′10 4 and 5.1′10 5 L.mol -1 for mesalamine complexes with p -chloranil and p -fluoranil respectively. The methods were applied successfully to the assay of mesalamine in pharmaceutical formulations and was agreed well with its certified value.
机译:介绍了两种简单,灵敏和准确的分光光度法测定美沙拉敏的方法。该方法基于药物与两种π电子受体,对氯苯醌和对氟芴在水性介质中的电荷转移复合物形成反应。通过分别使用对氯苯胺和对氟苯胺试剂,有色配合物在346 nm和347 nm处具有最大吸收。在优化的实验条件下,校准曲线在1–35和1-30μgml?的浓度范围内显示线性关系。 1具有摩尔吸收率值4.60×10 3和5.67×10 3 L. mol -1 .cm -1。分别使用上述试剂。检出限和定量限为0.376和1.25μg/ ml。 1分别使用对氯甲腈和0.333和1.111μgml? 1分别使用对-芴基。在两种方法中均发现复合物的形成比例为1:1,对于美沙明胺与对氯苯胺和对氟苯胺的配合物,稳定常数分别为6.9'10 4和5.1'10 5 L.mol -1。该方法已成功地应用于药物制剂中美沙拉敏的测定,并与其认证价值相吻合。

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