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首页> 外文期刊>Optics and Spectroscopy >New Spectrofluorimetric Method for the Determination of Nizatidine in Bulk Form and in Pharmaceutical Preparations
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New Spectrofluorimetric Method for the Determination of Nizatidine in Bulk Form and in Pharmaceutical Preparations

机译:新的荧光光谱法测定散装形式和药物制剂中的尼扎替丁。

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摘要

A simple, accurate and highly sensitive spectrofluorimetric method has been developed for determination of nizatidine in pure form and in pharmaceutical dosage forms. The method is based on the reaction between nizatidine and 1-dimethylaminonaphthalene-5-sulphonyl chloride in carbonate buffer, pH 10.5, to yield a highly fluorescent derivative peaking at 513 nm after excitation at 367 nm. Various factors affecting the fluorescence intensity of nizatidin-dansyl derivative were studied and conditions were optimized. The method was validated as per ICH guidelines. The fluorescence concentration plot was rectilinear over the range of 25-300 ng/mL. Limit of detection and limit of quantification were calculated as 11.71 and 35.73 ng/mL, respectively. The proposed method was successfully applied to pharmaceutical preparations.
机译:已经开发了一种简单,准确和高度灵敏的分光荧光法,用于测定纯净形式和药物剂型中的尼扎替丁。该方法基于尼扎替丁与1-碳酸二甲酯在pH 10.5的碳酸盐缓冲液中的反应,在367 nm激发后在513 nm处产生峰值的高荧光衍生物。研究了影响硝唑丁-丹磺酰基衍生物荧光强度的各种因素,并优化了条件。该方法已按照ICH指南进行了验证。荧光浓度图在25-300 ng / mL范围内呈直线。检测限和定量限分别计算为11.71和35.73 ng / mL。所提出的方法已成功地应用于药物制剂。

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