A General Strategy to Rapid and Sensitive Determination of Five High Boiling Point Solvents in Pharmaceuticals by RP-HPLC Combined with Precipitation Method.

IF 1.5 4区 化学 Q4 BIOCHEMICAL RESEARCH METHODS
Chenxia Zhang, Zeyi Wu, Meiyan Qiu, Yanhua Li, Zhongqing Wang, Xiaomei Fan, Shaoyu Cai, Wanbing Rao
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引用次数: 0

Abstract

The difficulty on determination of high boiling point solvents, always exist due to their low vapor pressure in headspace (HS) vial. What's worse, the commonly used GC diluents, such as N, N-dimethylacetamide, 1,3-dimethyl-2-imidazolidinone, dimethyl sulfoxide, N, N-dimethylformamide and N-methylpyrrolidone are often remained in HS instrument after frequent injection into HS, thus would result in terrible positive interference problem. In this work, a fast and sensitive HPLC method in combination with a sample precipitation method, was proposed for the determination of above five high boiling point solvents in drug substances within 14.5 min. The final method was validated with regard to limit of detection and limit of quantitation, precision, linearity and accuracy in accordance with ICH Q2 (R1). Finally, the proposed strategy was successfully applied for the analysis of high boiling point solvents used in three active pharmaceutical ingredients. The established generic strategy would provide another choice for the determination of high boiling point solvents in pharmaceuticals.

结合沉淀法的 RP-HPLC 快速灵敏测定药物中五种高沸点溶剂的一般策略
由于高沸点溶剂在顶空(HS)瓶中的蒸汽压较低,因此在测定高沸点溶剂时总是存在困难。更糟糕的是,常用的气相色谱稀释剂,如 N, N-二甲基乙酰胺、1,3-二甲基-2-咪唑烷酮、二甲亚砜、N, N-二甲基甲酰胺和 N-甲基吡咯烷酮等,在频繁注入顶空样品瓶后,往往会残留在顶空样品瓶中,从而导致严重的正干扰问题。本研究提出了一种快速、灵敏的高效液相色谱法,结合样品沉淀法,可在 14.5 分钟内测定药物中的上述五种高沸点溶剂。根据 ICH Q2 (R1),对最终方法的检出限、定量限、精密度、线性度和准确度进行了验证。最后,该方法成功地用于分析三种活性药物成分中使用的高沸点溶剂。所建立的通用策略为测定药物中的高沸点溶剂提供了另一种选择。
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来源期刊
CiteScore
2.90
自引率
7.70%
发文量
94
审稿时长
5.6 months
期刊介绍: The Journal of Chromatographic Science is devoted to the dissemination of information concerning all methods of chromatographic analysis. The standard manuscript is a description of recent original research that covers any or all phases of a specific separation problem, principle, or method. Manuscripts which have a high degree of novelty and fundamental significance to the field of separation science are particularly encouraged. It is expected the authors will clearly state in the Introduction how their method compares in some markedly new and improved way to previous published related methods. Analytical performance characteristics of new methods including sensitivity, tested limits of detection or quantification, accuracy, precision, and specificity should be provided. Manuscripts which describe a straightforward extension of a known analytical method or an application to a previously analyzed and/or uncomplicated sample matrix will not normally be reviewed favorably. Manuscripts in which mass spectrometry is the dominant analytical method and chromatography is of marked secondary importance may be declined.
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