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Sensitive bromatometric methods for the assay of metaprolol tartrate in dosage forms

机译:灵敏的滴度法测定酒石酸美托洛尔剂型

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摘要

One titrimctric and two spectrophotomelric methods are described for the determination of metaprolol tartrate (MPT) using bromate-bromide mixture and two dyes,methyl orange and indigo carmine,as reagents.In titrimetry,an acidified solution of MPT is reacted with a known excess of bromatc-bromidc mixture and after a pre-determincd time,the unreacted bromine is determined by iodometric titration.The spectrophotometric methods involve the addition of a known excess of bromate-bromide mixture to MPT in acidic medium followed by determination of the residual bromine by reacting with fixed amount of either methyl orange and measuring the absorbance at 520 nm (Method A) or indigo carmine and measuring the absorbance at 610 nm (Method B).In all the methods,amount of bromine reacted corresponds to the amount of MPT.The working conditions of the methods have been optimised.Titrimetry allows the determination of MPT in 2.5 - 7.5 mg range and the calculations are based on a 1:1(MPT : KBrO_3) reaction stoichiometry.In the spectropholometric methods.Beer's law is valid over the concentration ranges 0.5 -5.0 and 1.5 - 15.0 mu g mL~(-1) MPT for method A and method B,respectively.Method A with a molar absorptivity of 8.17 x 10~4 L mol~(-1) cm~(-1) is more sensitive than method B (euro = 2.70 x 10~4 L mol~(-1) cm~(-1)).The limits of detection and quantification are reported for both the methods.The methods could usefully be applied to routine quality control of tablets containing MPT.No interference was observed from common pharmaceutical adjuvants.Statistical comparison of the results with those obtained by an established UV-spcctrophotometric method showed excellent agreement and indicated no significant difference in accuracy and precision.The reliability of the methods was further ascertained by recovery studies.
机译:描述了一种滴定法和两种分光光度法,使用溴酸盐-溴化物混合物和两种染料甲基橙和靛蓝胭脂红作为试剂测定酒石酸异丙酚(MPT)。滴定法中,MPT的酸化溶液与已知过量的在预定时间后,通过碘量滴定法测定未反应的溴。分光光度法包括向酸性介质中的MPT中添加已知过量的溴酸盐-溴化物混合物,然后通过反应确定残留的溴。使用固定量的甲基橙并测量520 nm(方法A)的吸光度或靛蓝胭脂红并测量610 nm(方法B)的吸光度。在所有方法中,反应的溴量与MPT的量相对应。优化了方法的工作条件。滴定法可测定2.5-7.5 mg范围内的MPT,计算基于1:1(MPT:KBrO_3)反应光谱法中的啤酒定律在方法A和方法B的浓度范围分别为0.5 -5.0和1.5-15.0μg mL〜(-1)MPT时有效。方法A的摩尔吸收率为8.17 x 10〜4 L mol〜(-1)cm〜(-1)比方法B更敏感(欧元= 2.70 x 10〜4 L mol〜(-1)cm〜(-1))。两种方法均进行了定量分析,该方法可有效地用于含MPT的片剂的常规质量控制,未见普通药物佐剂的干扰,结果与通过既定的紫外分光光度法获得的结果进行统计学比较显示出极好的一致性回收率研究进一步确定了方法的可靠性。

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