Solvents in the industrial synthesis of naphazoline nitrate: implementation of the principles of "Green chemistry" and analysis

Q3 Pharmacology, Toxicology and Pharmaceutics
Tetiana Solominchuk, V. Rudiuk, Lyudmila Sidorenko, N. Kobzar, Maryna Rakhimova, Olha Vislous, V. Georgiyants
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Abstract

The aim: implementation of the principles of green chemistry by regenerating the synthesis solvent 1,2,4-trichlorobenzene and reusing it during the synthesis of the Naphazoline nitrate substance. Study of the influence of the regenerated solvent on the quality of the final product by controlling analytical quality parameters. Development of a method for the quantitative determination and validation of synthesis solvents in a substance. Materials and methods: samples of the substance were synthesized according to the optimized proprietary technology of Farmak JSC. The obtained batches of fresh and regenerated 1,2,4-trichlorobenzene were analyzed according to the monograph of the European Pharmacopoeia on Naphazoline nitrate 0147. Results: the possibility of using regenerated 1,2,4-trichlorobenzene for the synthesis of the substance Naphazoline nitrate has been proven. It is shown that the regenerated solvent does not have a negative effect on the profile of impurities and the polymorphic form of the substance. Analytical quality parameters met the requirements of the internal specification and the requirements of the European Pharmacopoeia monograph. The developed and validated method of quantitative determination of synthesis solvents makes it possible to determine them at the required level. Conclusions: the introduction of regenerated 1,2,4-trichlorobenzene into the synthesis scheme made it possible to significantly reduce the amount of waste per 1 kg of product, which in turn significantly reduced the negative impact on the environment. Analytical quality parameters for regenerated 1,2,4-trichlorobenzene meet the requirements of the internal specification. Industrial series obtained on the regenerated solvent meet the requirements of the monograph of the European Pharmacopoeia. The polymorphic form of the substance batches manufactured on regenerated 1,2,4-trichlorobenzene corresponds to the polymorphic form of the substance batches manufactured on the fresh solvent. The obtained results on the influence of the regenerated solvent on the profile of impurities in the finished substance show the similarity of the profile of the series manufactured on both solvents. According to the requirements of ICH Q3C Impurities: Guideline for residual solvents, a method for quantitative determination of the residual content of 1,2,4-trichlorobenzene in the final product by gas chromatography was developed and validated. The absence of synthesis solvents at the limit of detection is shown
硝酸萘甲唑啉工业合成中的溶剂:"绿色化学 "原则的实施与分析
目的:通过再生合成溶剂 1,2,4-三氯苯并在硝酸萘甲唑啉物质的合成过程中重复使用该溶剂,落实绿色化学原则。通过控制分析质量参数,研究再生溶剂对最终产品质量的影响。材料和方法:根据 Farmak 股份公司优化的专利技术合成物质样品。根据《欧洲药典》关于硝酸萘甲唑啉的专著 0147,对获得的新鲜和再生 1,2,4-三氯苯批次进行了分析。结果:使用再生 1,2,4-三氯苯合成硝酸萘甲唑啉的可能性已经得到证实。结果表明,再生溶剂不会对杂质和物质的多晶型产生负面影响。分析质量参数符合内部规范和欧洲药典专著的要求。结论:在合成方案中引入再生的 1,2,4-三氯苯可显著减少每公斤产品的废物量,从而大大减少对环境的负面影响。再生 1,2,4-三氯苯的分析质量参数符合内部规范要求。再生溶剂的工业系列符合《欧洲药典》专论的要求。用再生的 1,2,4-三氯苯生产的物质批次的多形态形式与用新鲜溶剂生产的物质批次的多形态形式一致。再生溶剂对成品物质中杂质分布的影响结果表明,用这两种溶剂生产的系列物质的杂质分布具有相似性。根据 ICH Q3C 杂质:根据 ICH Q3C《杂质:残留溶剂指南》的要求,开发并验证了利用气相色谱法定量测定成品中 1,2,4-三氯苯残留量的方法。结果表明,在检测限内不存在合成溶剂。
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来源期刊
ScienceRise: Pharmaceutical Science
ScienceRise: Pharmaceutical Science Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.70
自引率
0.00%
发文量
39
审稿时长
6 weeks
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