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Micro Spectrophotometric Determination and Cloud Point Extraction of Sulphadimidine Sodium in Pure form and Pharmaceutical Drug

机译:纯度和药物中磺酰咪啶钠的微量分光光度法测定和浊点萃取

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摘要

Two simple, rapid, and useful spectrophotometric methods were suggest or the determination of sulphadimidine sodium (SDMS) with and without using cloud point extraction technique in pure form and pharmaceutical preparation. The first  method was based on  diazotization of the Sulphdimidine Sodium drug by sodium nitrite at 5 ºC, followed by coupling with α –Naphthol in basic medium to form an orange colored product . The product was stabilized and its absorption was measured at 473 nm. Beer’s law was obeyed in the concentration range of (1-12) μg∙ml-1. Sandell’s sensitivity was 0.03012 μg∙cm-1, the detection limit was 0.0277 μg∙ml-1, and the limit of Quantitation was 0.03605μg∙ml-1.The second method was the cloud point extraction (CPE) using Trtion X-114 as surfactant. Beer’s law was obeyed in the concentration range of (1-12) μg∙ml-1. Sandell’s sensitivity was 0.02958 μg∙cm-1, the detection limit was 0.01745 μg∙ml-1, and the limit of quantitation was 0.028303 μg∙ml-1. All variables including the reagent concentration, reaction time, color stability period, and mole ratio were studied in order to optimize the reaction conditions. The mole ratio for the composition of product is (1:1). Both methods were effectively useful to the determination of sulphdimidine sodium in pharmaceutical dose form.  The attained results were in a good agreement with the official and other methods in the literature .No interference were observed from the commonly encountered additives and excipients.
机译:两个简单的,快速的和有用的分光光度方法是建议或磺胺钠(SDMS)具有和不具有以纯的形式和药物制剂使用浊点萃取技术的确定。第一种方法是基于在5ºC的Sulphdimidine钠药物由亚硝酸钠重氮化,接着在碱性介质中与α萘酚偶联以形成橙色产物。将产物稳定,其吸收在473nm的测量。 Beer定律在的(1-12)微克∙ml-1的浓度范围内符合。桑德尔的灵敏度为0.03012微克∙-1,检测限为0.0277微克∙毫升-1,和定量限为0.03605μg∙毫升-1,第二个方法是浊点萃取(CPE)使用Trtion X-114作为表面活性剂。 Beer定律在的(1-12)微克∙ml-1的浓度范围内符合。桑德尔的灵敏度为0.02958微克∙-1,检测限为0.01745微克∙毫升-1,和定量限为0.028303微克∙ml-1的。所有变量,包括反应物浓度,反应时间,颜色稳定性周期,和摩尔比,以优化反应条件进行了研究。为产品的组合物中的摩尔比为(1:1)。这两种方法都对sulphdimidine钠的药物剂量形式的有效判定有用。达到的结果与文献。没有干扰官方等方法从经常遇到的添加剂和辅料,观察有很好的一致性。

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    Dhahir Et al.;

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  • 年度 2019
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  • 原文格式 PDF
  • 正文语种 ara;eng
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