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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Spectrophotometric determination of magnesium in pharmaceutical preparations by cost-effective sequential injection analysis
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Spectrophotometric determination of magnesium in pharmaceutical preparations by cost-effective sequential injection analysis

机译:成本有效的顺序注射分析光度法测定药物制剂中的镁

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A simple and rapid,inexpensive Spectrophotometric method was proposed for magnesium assay in pharmaceutical preparations by sequential injection analysis(SIA).The method is based on the reaction between o-cresolphthalein complexone(CPC)and Mg(II)in alkaline media,yielding a pink colored complexwith absorption maximum at 570 nm.Since the formation constant between Ca-CPC and Mg-CPC is similar,initially a sample/standard solution was aspirated into the holding coil followed by a mixture of masking-buffer solutions.This was done because masking of calcium should be accomplished before Mg-CPC complexation.Then the reagent was introduced into the reaction coil to produce a colored complex,which is measured spectrophotometrically at 570 nm.In this way the interference of calcium was reduced.Furthermore,all the parameters that affect the reaction were evaluated.The calibration curve is linear over a range of 0-20 mg I~(-1)of Mg(II)with a detection limit of 0.24 mg I~(-1).A sample throughput of 80 samples per hour and relative standard deviation <2.0%were achieved.The proposed method was successfully applied for the assay of magnesium in three different compositions of pharmaceutical preparations(tablets).The results were found to be in good agreement with the manual flame atomic absorption spectrophotometry(FAAS)and UV-Vis spectrophotometry methods and with the claimed values by the manufactures.The f-test shows no significant difference at 95%confidence level.
机译:提出了一种简便,快速,便宜的分光光度法,通过顺序注射分析(SIA)进行药物制剂中镁的测定。该方法基于邻甲酚酞络合物(CPC)与Mg(II)在碱性介质中的反应,从而得到一种粉色复合物,最大吸收在570 nm。由于Ca-CPC和Mg-CPC之间的形成常数相似,因此首先将样品/标准溶液吸入保持线圈中,然后再加入掩蔽缓冲液的混合物。在将Mg-CPC络合之前,应先对钙进行掩蔽处理,然后将试剂引入反应线圈中以生成有色的络合物,然后在570 nm处用分光光度法进行测量。这样可以减少钙的干扰。此外,所有参数校正曲线在0-20 mg I〜(-1)的Mg(II)范围内呈线性,检出限为0.24 mg I〜(-1)。每小时f样品80次,相对标准偏差<2.0%。该方法成功地用于三种药物制剂(片剂)中镁的测定,结果与手动火焰法相吻合原子吸收分光光度法(FAAS)和紫外可见分光光度法,并具有制造商要求的值。f检验表明,置信度为95%时,无明显差异。

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