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摩洛哥市场上销售的氟康唑仿制药的固态表征及杂质测定

Solid-state characterization and impurities determination of fluconazol generic products marketed in Morocco.

作者信息

Bourichi Houda, Brik Youness, Hubert Philipe, Cherrah Yahia, Bouklouze Abdelaziz

机构信息

Research Team of Pharmaceutical and Toxicological Analysis-Laboratory of Pharmacology and Toxicology, Faculty of Medicine and Pharmacy, Mohammed V University, Soussi, Rabat, Morocco.

Physicochemical Service, Drugs Quality Control Laboratory, Division of Drugs and Pharmacy, Ministry of Health, Rabat, Morocco.

出版信息

J Pharm Anal. 2012 Dec;2(6):412-421. doi: 10.1016/j.jpha.2012.05.007. Epub 2012 Aug 17.

Abstract

In this paper, we report the results of quality control based in physicochemical characterization and impurities determination of three samples of fluconazole drug substances marketed in Morocco. These samples were supplied by different pharmaceuticals companies. The sample A, as the discovered product, was supplied by Pfizer, while samples B and C (generics), were manufactured by two different Indian industries. Solid-state characterization of the three samples was realized with different physicochemical methods as: X-ray powder diffraction, Fourier-transformation infrared spectroscopy, differential scanning calorimetry. High performance liquid chromatography was used to quantify the impurities in the different samples. The results from the physicochemical methods cited above, showed difference in polymorph structure of the three drug substances. Sample A consisted in pure polymorph III, sample B consisted in pure polymorph II, sample C consisted in a mixture of fluconazole Form III, form II and the monohydrate. This result was confirmed by differential scanning calorimetry. Also it was demonstrated that solvents used during the re-crystallization step were among the origins of these differences in the structure form. On the other hand, the result of the stability study under humidity and temperature showed that fluconazole polymorphic transformation could be owed to the no compliance with the conditions of storage. The HPLC analysis of these compounds showed the presence of specific impurities for each polymorphic form, and a possible relationship could be exist between impurities and crystalline form of fluconazole.

摘要

在本文中,我们报告了对摩洛哥市场上销售的三种氟康唑原料药样品进行基于物理化学表征和杂质测定的质量控制结果。这些样品由不同的制药公司提供。样品A作为已发现的产品,由辉瑞公司提供,而样品B和C(仿制药)则由两家不同的印度企业生产。采用不同的物理化学方法对这三个样品进行固态表征,如:X射线粉末衍射、傅里叶变换红外光谱、差示扫描量热法。使用高效液相色谱法定量测定不同样品中的杂质。上述物理化学方法的结果表明,这三种原料药的多晶型结构存在差异。样品A由纯多晶型III组成,样品B由纯多晶型II组成,样品C由氟康唑III型、II型和一水合物的混合物组成。差示扫描量热法证实了这一结果。此外,还证明了重结晶步骤中使用的溶剂是这些结构形式差异的来源之一。另一方面,湿度和温度条件下的稳定性研究结果表明,氟康唑的多晶型转变可能归因于储存条件不符合要求。对这些化合物的高效液相色谱分析表明,每种多晶型形式都存在特定杂质,并且氟康唑的杂质与晶型之间可能存在某种关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d1/5760925/bc7f51d3f3ef/gr1.jpg

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