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首页> 外文期刊>Central European Journal of Chemistry >Indirect spectrophotometric determination of diltiazem hydrochloride in pure form and pharmaceutical formulations
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Indirect spectrophotometric determination of diltiazem hydrochloride in pure form and pharmaceutical formulations

机译:间接分光光度法测定纯制盐酸地尔硫卓和药物制剂

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摘要

Three simple,accurate,and sensitive spectrophotometric methods(A,B and C) have been described for the indirect assay of diltiazem hydrochloride(DIL.HCl),either in pure form or in pharmaceutical formulations.The first method(A)is based on the oxidation of DIL.HCl by N-bromosuccinimide(NBS)and determination of unconsumed NBS by measuring the decrease in absorbance of amaranth dye(AM)at a suitable lambda_(max)=521 nm.Other methods (B)and(C)involve the addition of excess cerric ammonium sulfate(CAS)and subsequent determination of the unconsumed oxidant by a decrease in the red color of chromotrope 2R (C2R)at a suitable lambda _(max)=528 nm or a decrease in the orange-pink color of rhodamine 6G (Rh6G)at lambda_(max)=525 nm,respectively.Regression analysis of Beer-Lambert plots showed good correlation in the concentration ranges 3.0-9.0,3.5-7.0 and 3.5-6.3 mu g ml~(-1) for methods A,B and C,respectively.The apparent molar absorptivity,Sandell's sensitivity, detection and quantification limits were calculated.The proposed methods have been applied successfully for the analysis of the drug in its pure form and its dosage form.No interference was observed from a common pharmaceutical adjuvant.Statistical comparison of the results with the reference method shows excellent agreement and indicates no significant di?erence in accuracy and precision.
机译:已经描述了三种简单,准确和灵敏的分光光度法(A,B和C)用于盐酸地尔硫卓(DIL.HCl)的间接测定,以纯形式或药物制剂形式进行。第一种方法(A)基于N-溴琥珀酰亚胺(NBS)氧化DIL.HCl并通过在合适的λ(max)= 521 nm下测量of菜染料(AM)吸光度的降低来测定未消耗的NBS。其他方法(B)和(C)包括添加过量的硫酸铈铵(CAS),然后通过在合适的λ_(max)= 528 nm处降低发色团2R(C2R)的红色或减少橙色粉红色来确定未消耗的氧化剂罗丹明6G(Rh6G)在lambda_(max)= 525 nm处的颜色分别.Beer-Lambert图的回归分析显示在3.0-9.0、3.5-7.0和3.5-6.3μg ml〜(-1)浓度范围内具有良好的相关性)分别用于方法A,B和C.表观摩尔吸光度,Sandell灵敏度,检测和定量极限s的计算结果。所提出的方法已成功应用于纯净药物及其剂型的分析。普通药物佐剂未见干扰。与参考方法的统计比较显示出极好的一致性并表明在准确性和精确度上没有显着差异。

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