硝基呋喃衍生物的研制:固体分散泡腾片的组成与工艺

A. Elagina, A. Belyatskaya, I. I. Krasnyuk (jr.), I. Krasnyuk, O. I. Stepanova, T. V. Fateeva, E. Smolyarchuk, S. V. Kozin, O. Plakhotnaya, O. V. Rаstopchina, J. Rau
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引用次数: 2

摘要

考虑到目前的产品规范文件,该工作的目的是开发基于呋喃唑酮固体分散体的水剂型外用泡腾片的组合物和技术。材料和方法。所用物质为:呋喃唑酮、无水碳酸钠(化学纯)、聚乙烯吡啶酮-24000±2000(化学纯)、苹果酸(分析纯)、酒石酸(化学纯)、柠檬酸(化学纯)、苯甲酸钠(化学纯)、乙醇96%(化学纯)、纯净水。颗粒的制备是在流化床中分离的湿制粒(Mycrolab, BOSCH,德国)。获得片剂是在手动液压压力机(“PRG”,VNIR,俄罗斯)上按压的过程。研究了复合材料的崩解性、耐磨性和抗破碎性与压实压力的关系。根据《俄罗斯联邦国家药典》第14版对颗粒剂、所得泡腾片的工艺参数、保质期和贮存条件进行了考察。制备了两种以呋喃唑酮固体分散体为活性物质的泡腾片组合物,在室温(20℃)下将其溶解于100ml水中,在不到5分钟的时间内形成浓度为0.004%的呋喃唑酮溶液。建立了泡腾片中呋喃唑酮含量的定量测定方法。采用综合理化方法对片剂进行了分析。制定了质量标准。实验证实了速溶片剂的成分在加速和长期贮存过程中的稳定性。初步确定了保鲜期和贮存条件。对呋喃唑酮泡腾片新型速溶剂型进行了工艺和化学药学研究,并对其质量进行了评价。
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DEVELOPMENT OF NITROFURAN DERIVATIVE: COMPOSITION AND TECHNOLOGY OF EFFERVESCENT TABLETS WITH SOLID DISPERSIONS
Taking into account the current Product specification file, the aim of the work was to develop the composition and technology for obtaining effervescent tablets based on solid dispersions of furazolidone in the form of an aqueous solution for external use.Materials and methods. The used substances were: furazolidone, anhydrous sodium carbonate (chemically pure), polyvinylpyrrolidone-24000±2000 (chemically pure), malic acid (analytically pure), tartaric acid (chemically pure), citric acid (chemically pure), sodium benzoate (chemically pure), ethyl alcohol 96% (chemically pure), purified water. Preparation of granulates is separate wet granulation in a fluidized bed (Mycrolab, BOSCH, Germany). Obtaining tablets is the process of pressing on a manual hydraulic test press (“PRG”, VNIR, Russia). The dependence of disintegration, abrasion capacity and crushing resistance on compacting pressure was investigated. Technological parameters of granulates, еру obtained effervescent tablets, shelf life and storage conditions were investigated according to the State Pharmacopoeia of the Russian Federation XIVth ed.Results. Two compositions of effervescent tablets containing solid dispersions of furazolidone as an active substance were obtained, which, when dissolved in 100 ml of water at room temperature (20°C), form a solution of furazolidone with a concentration of 0.004% in less than 5 minutes. The method of quantitative determination of the furazolidone content in the effervescent tablets was validated. A complex of physicochemical methods for the analysis of tablets was carried out. Quality standards have been developed. The developed compositions stability of instant tablets during storage during accelerated and long-term tests has been experimentally confirmed. The preliminary shelf life and storage conditions have been determined.Conclusion. The result of technological and chemical-pharmaceutical research is the creation and evaluation of the quality of a new instant furazolidone dosage form as effervescent tablet formulations.
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