Optimization of the Method for Spectrofluorimetric Determination of Aluminum Impurities in Substances

E. V. Vishnyakov, A. A. Tolstikova, J. E. Generalova, A. K. Kaldybaeva, I. I. Terninko
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Abstract

Introduction. Evaluation of the content of impurities is the most important step in confirming the safety and efficacy in the quality control of the medicinal product. Aluminum, being an acceptable impurity in a number of pharmaceutical substances, can adversely affect the human body, as a result of which its content is normalized. The admixture of aluminum in the State Pharmacopoeia of the Russian Federation XV is determined by the spectrofluorimetric method using the ligand – 8-hydroxyquinoline in chloroform. In the present work, it is proposed to replace 8-hydroxyquinoline with the more accessible rutin, which also forms fluorescent complexes with metals. This approach involves the exclusion of the stage of extraction of the aluminum complex into chloroform from sample preparation, which improves the accuracy of the technique, and the replacement of chloroform has a positive effect on safety.Aim. To create an alternative approach for the spectrofluorimetric determination of aluminum impurities using rutin and "potassium chloride" as an active pharmaceutical ingredient.Materials and methods. The following substances and reagents were used as research materials: CRS of aluminum ion 1 mg/ml (LLC "EKROSHIM", Russia), CRS of iron ion (II) 1 mg/ml (LLC "EKROSHIM", Russia), CRS of zinc ion 1 mg/ml (LLC "EKROSHIM", Russia), CRS of lead-ion 1 mg/ml (LLC "EKROSHIM", Russia), CRS nickel-ion 1 mg/ml (LLC "EKROSHIM", Russia), CRS copper-ion 1 mg/ml (LLC "EKROSHIM", Russia), chromium (III) cation standard 1 mg/ml (imp., Sigma-Aldrich, USA) rutin (imp., Sichuan Guangsong Pharmaceutical Co., Ltd., China), ammonium acetic acid (imp., Molekula GmbH, Germany), glacial acetic acid (chemically pure, JSC "Base No. 1 Himreaktivov", Russia), potassium chloride (pharmaceutical substance, LLC "MZHR", Russia). The spectrofluorimetric study was carried out on an FL 6500 instrument (PerkinElmer Inc., USA). The aluminum impurity content was also evaluated using an Optima 8000 inductively coupled plasma atomic emission spectrometer (ICP AES) (PerkinElmer Inc., USA) and a Multi-Element Solution standard sample (PerkinElmer Inc., USA).Results and discussion. The approach given in the article eliminates the use of 8-hydroxyquinoline in chloroform and replaces it with rutin in 70 % ethyl alcohol. The aluminum-rutin complex has an excitation wavelength at 445 nm and an emission wavelength at 565 nm. The proposed method was tested on the substance "Potassium chloride" to assess the indicator "Aluminum", the content of which should not exceed 0.0001 %. Method validation was carried out according to three parameters "Specificity", "Linearity" and "Limit of detection". Comparison of the data obtained was carried out using atomic emission spectroscopy, during which the relevance of the technique was proved.Conclusion. An ergonomic approach has been developed for the spectrofluorimetric determination of aluminum impurities using rutin with approbation on the substance "Potassium chloride". The results obtained during the experiment were confirmed by the ICP AES method.
优化光谱荧光法测定物质中铝杂质的方法
导言。杂质含量评估是在药品质量控制中确认安全性和有效性的最重要步骤。铝是许多药物中可接受的杂质,但会对人体产生不良影响,因此铝的含量必须符合标准。俄罗斯联邦国家药典》XV 中的铝含量是通过氯仿中的配体--8-羟基喹啉的分光荧光法测定的。在本研究中,建议用更容易获得的芦丁来替代 8-羟基喹啉,因为芦丁也能与金属形成荧光络合物。这种方法在样品制备过程中省去了将铝络合物提取到氯仿中的步骤,从而提高了技术的准确性,而且氯仿的替代对安全性也有积极影响。材料和方法。使用以下物质和试剂作为研究材料:铝离子 CRS 1 mg/ml(LLC "EKROSHIM",俄罗斯),铁离子(II)CRS 1 mg/ml(LLC "EKROSHIM",俄罗斯),锌离子 CRS 1 mg/ml(LLC "EKROSHIM",俄罗斯)、1 毫克/毫升的铅离子 CRS(LLC "EKROSHIM",俄罗斯)、1 毫克/毫升的镍离子 CRS(LLC "EKROSHIM",俄罗斯)、1 毫克/毫升的铜离子 CRS(LLC "EKROSHIM",俄罗斯)、1 毫克/毫升的铬(III)阳离子标准(imp.,芦丁(进口,四川广松药业股份有限公司,中国)、醋酸铵(进口,Molekula GmbH,德国)、冰醋酸(化学纯,JSC "Base No.使用 FL 6500 仪器(PerkinElmer Inc.)此外,还使用 Optima 8000 电感耦合等离子体原子发射光谱仪(ICP AES)(PerkinElmer 公司,美国)和多元素溶液标准样品(PerkinElmer 公司,美国)对铝杂质含量进行了评估。文章中给出的方法取消了氯仿中 8-羟基喹啉的使用,代之以 70% 乙醇中的芦丁。铝-芦丁复合物的激发波长为 445 纳米,发射波长为 565 纳米。建议的方法在 "氯化钾 "物质上进行了测试,以评估指标 "铝",其含量不得超过 0.0001%。根据 "特异性"、"线性 "和 "检测限 "三个参数对方法进行了验证。使用原子发射光谱对获得的数据进行了比较,证明了该技术的相关性。利用芦丁对 "氯化钾 "物质进行光谱荧光测定铝杂质的方法符合人体工程学。实验结果得到了 ICP AES 方法的证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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