首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Identification of related substances in tofacitinib citrate by LC-MS techniques for synthetic process optimization
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Identification of related substances in tofacitinib citrate by LC-MS techniques for synthetic process optimization

机译:通过LC-MS技术鉴定TOFACITINIB柠檬酸盐的合成过程优化技术相关物质

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摘要

A specific LC-MS method was developed for separation, identification and characterization of the process related substances and degradation products in tofacitinib citrate. The separation was achieved on a LiChrospher C18 column (250 mm x 4.6 mm, 5 mu m) by linear gradient elution of 0.1% ammonium acetate solution (pH adjusted to 4.0 by formic acid) and acetonitrile at a flow rate of 1.0 mL/min. Forced degradation studies were conducted under hydrolytic (acidic, basic), oxidative, photolytic and thermal stress conditions as described in ICH. It was found that tofacitinib was stable under photolytic condition, but degraded obviously in acidic, basic, thermal and oxidative conditions. The high resolution TOF-MS and MS/MS were used for determination and structural identification of the related substances. Eleven major related substances were detected and identified as five process-related substances and six degradation products, and three of them were further synthesized and characterized by NMR spectroscopy. The most plausible mechanisms involved in the formation of the related substances were also proposed. Since related substances have a significant impact on drug safety, quality and efficacy, the data obtained are valuable for process monitoring and quality assurance of tofacitinib citrate. (C) 2017 Elsevier B.V. All rights reserved.
机译:开发了特异性LC-MS方法,用于分离,鉴定和表征所述加工相关物质和TOFACITINIB柠檬酸盐中的降解产物。通过线性梯度洗脱0.1%乙酸铵溶液(通过甲酸调节至4.0)和乙腈以1.0ml / min的流速,通过线性梯度洗脱来实现分离。 。如ICH中所述,在水解(酸性,碱性),氧化,光溶解和热应激条件下进行强制降解研究。发现Tofacitinib在光解条件下稳定,但在酸性,碱性,热和氧化条件下显而易见。高分辨率TOF-MS和MS / MS用于测定和结构鉴定相关物质。检测11个主要相关物质并将其鉴定为五种过程相关的物质和六种降解产物,并进一步合成其中三种的降解产物,并通过NMR光谱表征。还提出了形成相关物质的最合理的机制。由于相关物质对药物安全性,质量和功效产生重大影响,因此所获得的数据对于酸噻唑酯的过程监测和质量保证是有价值的。 (c)2017年Elsevier B.V.保留所有权利。

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