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Determination of lansoprazole in pharmaceutical capsules by flow injection analysis using UV-detection.

机译:使用紫外检测器通过流动注射分析法测定药物胶囊中的兰索拉唑。

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摘要

The direct determination of lansoprazole by using a flow injection analysis (FIA) with UV-detection and its application to the pharmaceutical capsules is described, in this study. The best carrier solvent was found to be 0.01M NaOH and it was determined at optimum conditions such as flow rate of 1mlmin(-1) and wavelength of 292nm. Examining the repeatability of the method that was found to be 1.72% for intra-day and 2.13% for inter-day precision using the [Formula: see text] M lansoprazole concentration has validated the method. The linear range of the method was [Formula: see text] to [Formula: see text] M. The limit of detection and quantification was found to be [Formula: see text] and [Formula: see text] M, respectively. The proposed method was applied to the pharmaceutical capsules and very good results obtained. Thus, the FIA method for the quantification of lansoprazole can be proposed as a cheap, rapid, easy, accurate, and precise method for the routine determination in pharmaceutical preparations.
机译:在这项研究中描述了通过使用带有紫外检测的流动注射分析(FIA)直接测定兰索拉唑的方法及其在药物胶囊中的应用。发现最佳的载体溶剂是0.01M NaOH,并在最佳条件下确定,例如流速1mlmin(-1)和波长292nm。使用[公式:参见文本]检查兰索拉唑浓度,该方法的日内重复精度和日间精密度分别为1.72%和2.13%,从而验证了该方法的有效性。该方法的线性范围为[公式:参见文本]至[公式:参见文本]M。发现和定量的极限分别为[公式:参见文本]和[公式:参见文本]M。所提出的方法被应用于药物胶囊并获得了很好的结果。因此,FIA方法用于兰索拉唑的定量分析可被提议为一种廉价,快速,简便,准确和精确的方法,用于药物制剂中的常规测定。

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