舌下免疫治疗药用形式屋尘螨混合过敏原水盐提取物标准化的实际问题

V. Berzhets, S. Petrova, L. Nesterenko, P. V. Samoilikov, S. Khlgatian, N. S. Petrova, A. V. Vasilyeva
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引用次数: 0

摘要

背景:过敏原医学形态标准化是建立和应用统一的质量指标体系和控制方法的过程。过敏原治疗形式的质量控制是保证过敏原特异性免疫治疗(ASIT)临床疗效和安全性的必要条件。在过敏原Mechnikov疫苗和血清研究所的过敏原实验室中,开发了从室内尘螨中获得用于口服的混合状翼状螨和粉状螨的颗粒状技术。目的:确定螨虫Der p和Der f混合过敏原的非酚水盐提取物的真实性,用于药物的治疗形式。材料与方法:所得过敏原提取液采用奈斯勒法蛋白氮单元进行标准化。用Bradford法测定蛋白浓度。采用十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)研究了混合过敏原中蛋白质组成的存在。pH值用电位法测定。采用反向免疫分析法(REAST)比较标准过敏原和实验混合过敏原的比活性。结果:SDS-PAGE显示混合变应原Der p和Der f的水盐提取物的蛋白谱保存,与屋尘螨变应原的蛋白谱相对应。在所研究的过敏原(四个药物系列)与参考血清中含有对Der p或Der f特异性IgE的标准过敏原在REAST中与3类参考血清反应时,光密度无统计学差异(0.05)。结论:以上内容符合俄罗斯联邦国家药典第十四版,是对该药品真实性的确认。不酚提取不影响混合过敏原Der p和Der f的主要致敏成分,使其保持高度特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Actual questions of standardization of water-salt extracts of house dust mites mixed allergens intended for medicinal forms of sublingual immunotherapy
Background: Standardization of medical forms of allergens is the process of establishing and applying a unified system of quality indicators and control methods. Quality control of therapeutic forms of allergens is an essential condition for guaranteeing the clinical efficacy and safety of allergen-specific immunotherapy (ASIT). The technology for obtaining the granular form of the mixed allergen from house dust mites Dermatophagoides pteronyssinus (Der p) and Dermatophagoides farinae (Der f) for oral use was developed in the laboratory of allergens Mechnikov Research Institute of Vaccines and Sera. Aims: to determine the authenticity of the anphenolic water-salt extract of the mixed allergen from mites Der p and Der f, intended for the therapeutic form of the drug. Materials and methods: Standardization of the obtained allergen extract was carried out by protein nitrogen unit by the Nessler method. The protein concentration was determined by the Bradford method. Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was used to study the presence of protein composition in mixed allergen. The pH value was determined potentiometrically. The comparison of the specific activity of the standard allergen and the experimental mixed allergen was carried out by the method of reverse immunoassay (REAST). Results: SDS-PAGE showed the preservation of the protein profile of the water-salt extract of the mixed allergen Der p and Der f, corresponding to the protein profile of allergens of house dust mites. There were no statistically significant differences in the optical density of the studied allergen (four drug series) and the standard allergen with reference serums containing specific IgE to Der p or Der f when reacting with a Class 3 reference serum in REAST(р0,05). Conclusions: The above in accordance with the State Pharmacopoeia of the Russian Federation XIV edition is a confirmation of the authenticity of the drug. Not phenolic extraction did not affect the main allergenic components of the mixed allergen Der p and Der f and allowed it to maintain a high degree of specificity.
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