研究牙科凝胶中丙种球蛋白真实性和定量检测方法的验证特性

Golovanenko A.L., Berezina E.S., Alekseeva I.V., Oleshko O.A.
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引用次数: 0

摘要

在医药产品的质量保证体系中,分析方法在开发、测试、技术和批量生产阶段的验证程序发挥着重要作用。之所以需要在药物开发阶段进行验证,是因为这样可以及时发现方法的不足之处,并对其进行重大改进。本研究的目的是验证牙科凝胶中乙酰唑 "真实性 "和 "定量测定 "的检测方法。材料和方法。为实现这一目标,使用了一种符合药典质量标准的活性药物。在制定 "真伪 "检测方法时,使用了草酸与酰唑成分中确定的锌阳离子发生反应的方法。在定量测定酰唑时,使用了络合法。研究对象是三个系列的凝胶样品。结果与讨论研究结果表明,所提出的方法在不含被分析成分和安慰剂的模型混合物上的分析信号为负,而在含有被分析成分的各种成分的模型混合物上的分析信号为正。研究了凝胶中丙烯唑定量测定方法的验证特性。建议的方法可用于将其纳入所开发凝胶的监管文件中。结论在评估拟议方法的验证特性时,确定了检测凝胶中 "真实性 "和 "定量测定 "酰唑的方法是特异性的,定量测定方法的特点是准确性和可重复性,在酰唑申报量的±20%的分析范围内具有线性依赖性,可用于对开发的牙科凝胶进行可靠的质量评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
STUDYING THE VALIDATION CHARACTERISTICS OF TESTING METHODS FOR AUTHENTICITY AND QUANTITATING DETERMINATION OF ACYSOLE IN DENTAL GEL
In the quality assurance system for medicinal products, an important role is played by the procedure for validation of analytical methods at the stages of development, testing, technology and serial production. The need for validation at the stage of drug development is due to the fact that it is possible to promptly identify the shortcomings of the method and significantly improve it. The purpose of this study is to validate methods for testing «The authenticity» and «Quantitative determination» of acyzole in dental gel. Materials and methods. To achieve this goal, an active pharmaceutical substance of pharmacopoeial quality was used. When developing methods for testing for “Authenticity,” a reaction with oxalic acid to the zinc cation determined in the composition of acyzole was used. For the quantitative determination of acyzole, the complexometric method was used. The objects of the study were three series of gel samples. Results and discussion. As a result of the research, a method for testing «Authenticity» was developed; it was found that the proposed method is characterized by a negative analytical signal on model mixtures free of the analyte component and placebo, and a positive analytical signal on model mixtures of various compositions containing the analyte component. The validation characteristics of methods for the quantitative determination of acyzole in the gel were studied. positive results were obtained. The proposed methods can be used for inclusion in the regulatory documentation for the developed gel. Conclusion. When assessing the validation characteristics of the proposed methods, it was established that the methods for testing the «Authenticity» and «Quantitative determination» of acyzole in the gel are specific, the methods of quantitative determination are characterized by accuracy and repeatability, a linear dependence in the analytical range of ±20% of the declared amount of acyzole, which allows them to be used for a reliable assessment quality of the developed dental gel.
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