首页> 外文期刊>Журнал аналитической химии >RAPID TITRIMETRIC AND SPECTROPHOTOMETRIC ASSAY METHODS FOR THE DETERMINATION OF LAMIVUDINE IN PHARMACEUTICALS USING IODATE AND TWO DYES
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RAPID TITRIMETRIC AND SPECTROPHOTOMETRIC ASSAY METHODS FOR THE DETERMINATION OF LAMIVUDINE IN PHARMACEUTICALS USING IODATE AND TWO DYES

机译:碘酸盐和两种染料的快速滴定和分光光度法测定药品中的拉米夫定。

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One titrimetric and two spectrophotometric methods which are simple, sensitive and rapid, are described for the assay of lamivudine in bulk drag and in tablet dosage forms using potassium iodate and two dyes, methyl orange and indigocarmine. as reagents. In titrimetry, aqueous solution of lamivudine is titrated directly with iodate in acidic medium, and in the presence of excess of bromide using methyl orange as indicator. After the decolouration of red colour of methyl orange, the residual bromine is titrated iodometrically to a starch end point. Spectrophotometric methods involve the addition of a known excess of iodate in acidic medium and in the presence of excess of bromide followed by the determination of residual bromine by the reaction witha fixed amount of either methyl orange and measuring the absorbance at 520 nrn (method A), or indigo carmine and measuring the absorbance at 610 nm (method B). In all the methods, the amount of iodate reacted corresponds to the amount of lamivudine content. Titrimetric method is applicable over 1.5-8.0 mg range. The systems obey Beer's law for 0.5-5.0 mug/mL (method A) and 1.25-12.5 mug/mL (method B). The calculated apparent molar absorptivity values are found to be 3.3 x 10~4 and 9.3 x 10 L mol~(-1) cm~(-1), for method A and method B. respectively, and the corresponding Sandell sensitivity values are 6.94 and 24.62 ng/cm~2. The limits of detection and quantification are also reported for both spectrophotometric methods. Intra-day and inter-day precision and accuracy for the developed methods have been evaluated. The methods were successfully applied to the assay of lamivudine in tablet formulation and the results were compared with those of a reference method by applying Student's t-test and F-test.No interference were observed from common tablet adjuvants. The accuracy and reliability of the methods were further ascertained by recovery experiments using standard addition technique.
机译:描述了一种简单,灵敏和快速的滴定法和两种分光光度法,用于使用碘酸钾和两种染料甲基橙和靛蓝胭脂红测定拉米夫定的散装和片剂剂型。作为试剂。在滴定法中,拉米夫定的水溶液直接在酸性介质中用碘酸盐滴定,并在存在过量溴化物的情况下使用甲基橙作为指示剂。甲基橙红色脱色后,碘量法将残留的溴滴定至淀粉终点。分光光度法包括在酸性介质中和过量溴化物的存在下添加已知过量的碘酸盐,然后通过与固定量的甲基橙反应并在520 nrn下测量吸光度来测定残留的溴(方法A)或靛蓝胭脂红,并测量610 nm处的吸光度(方法B)。在所有方法中,反应的碘酸盐的量对应于拉米夫定含量的量。滴定法适用于1.5-8.0 mg范围。该系统遵循比尔定律,适用于0.5-5.0杯/毫升(方法A)和1.25-12.5杯/毫升(方法B)。方法A和方法B的表观摩尔吸光系数分别为3.3 x 10〜4和9.3 x 10 L mol〜(-1)cm〜(-1),相应的Sandell灵敏度值为6.94和24.62 ng / cm〜2。还报道了两种分光光度法的检测和定量限。已评估了开发方法的日间和日间精度和准确性。该方法已成功应用于片剂中拉米夫定的测定,并通过Student's t检验和F检验将结果与参考方法进行了比较。普通片剂佐剂均未观察到干扰。通过使用标准添加技术进行回收率实验进一步确定了方法的准确性和可靠性。

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