纯透明动力学分光光度法评价药物制剂中盐酸溴己辛

IF 0.4 Q4 CHEMISTRY, MULTIDISCIPLINARY Acta Chemica Iasi Pub Date : 2021-01-01 DOI:10.47743/achi-2021-2-0009
M. Al-Rufaie
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引用次数: 0

摘要

为评价盐酸溴己辛(BRO)在纯药物及其制剂中的含量,建立了一种灵敏的分光光度法。该方法的重点是通过二甲氨基苯甲醛(PDMB)产生希夫碱,使药物与试剂反应时呈现明亮的黄色。在其最大吸收λmax为420 nm时测定了各物种的黄色吸光度。在10 ~ 60 μg/ml浓度范围内符合比尔定律。光学值分别为8.693 x10 (L/mol/cm)、0.0005 (μg/cm2)、摩尔吸收系数和桑德尔灵敏度。该方法的定量限和定量限分别为3.280μg/ml和4.114 μg/ml。为了优化反应条件,对所有变量进行了研究。在传统辅料存在的情况下,确定了该方法的干扰。通过对其制剂中的BRO进行检测,检验了该方法的有效性,并通过统计检验客观地检验了其准确性。该方法回收率高;在其药物剂型中获得的结果进行了严格评估,并有效地用于确定BRO。
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PURELY CLEAR KINETIC SPECTROPHOTOMETRIC PROCESS FOR BROMHEXINE HYDROCHLORIDE EVALUATION IN PHARMACEUTICAL PREPARATIONS
For the evaluation of Bromhexine hydrochloride (BRO) in pure drugs as well as their pharmaceutical preparations, a successful, sensitivity spectrophotometric method has been proved as well as checked. The methodology is focused on the creation of the Schiff base by pdimethylaminobenzaldehyde (PDMB), giving a bright yellow color to the reaction of the drug with the reagent . The yellow colored absorbance of species was assessed at its maximum absorption λmax of 420 nm. The Beer’s law was obeyed in the 10-60 μg/ml as the concentration range. The optical values were measured to be 8.693 x10 (L/mol/cm), 0.0005 (μg/cm2), Molar absorption coefficient as well as Sandell sensitivity respectively. The LOD and the LOQ for the suggested methodology were measured 3.280μg/ml, 4.114 μg/ml, respectively. To maximize the reaction conditions, all the variables were studied. The interference for the suggested method was identified in the existence of traditional excipients of pharmaceutics. By testing BRO in its pharmaceutical formulations, the validity of the approach was checked and objectively tested by statistical tests for its accuracy. Strong recoveries were obtained by the method developed; the results obtained in its pharmaceutical dosage forms were critically evaluated and used effectively for determining BRO.
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来源期刊
Acta Chemica Iasi
Acta Chemica Iasi CHEMISTRY, MULTIDISCIPLINARY-
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