Joint Mass Spectrometry Centre (JMSC), Chair of Analytical Chemistry, University of Rostock, Rostock, Germany.
Joint Mass Spectrometry Centre (JMSC), Cooperation Group "Comprehensive Molecular Analytics" (CMA), Helmholtz Zentrum München GmbH, German Research Center for Environmental Health, Neuherberg, Germany.
Anal Bioanal Chem. 2024 Feb;416(4):1033-1045. doi: 10.1007/s00216-023-05093-9. Epub 2023 Dec 21.
The reliability of analytical results is critical and indispensable when applied in regulated environments such as the pharmaceutical industry. Therefore, analytical workflows must be validated. However, validation guidelines are often designed for quantitative targeted analysis and rarely apply to qualitative untargeted approaches. In this study, we employ a risk assessment approach to identify critical parameters which might influence the qualitative results derived by online derivatisation - comprehensive two-dimensional gas chromatography coupled to a high-resolution time-of-flight mass spectrometer (GC × GC-HR-ToF-MS) for the analysis of the active pharmaceutical ingredient (API) sodium bituminosulfonate (SBS). To show the complexity and feasibility of such an approach, we focus on investigating three potential risk factors: sample preparation, vapourability, and the thermal stability of sulfonates. Through the individual evaluation of these potential risk factors due to the application of sample preparation approaches and thermal gravimetric analysis (TGA), we demonstrate the high derivatisation efficiency and repeatability of the online derivatisation method and confirm the absence of derivatisation-induced side reactions. In addition, we also show the potential thermal instability of an incompletely derivatised API. To address the limitation of these individual assessments, we applied a holistic evaluation step with negative electrospray ionisation Fourier transform ion cyclotron resonance mass spectrometry (ESI( -) FT-ICR MS) as an orthogonal technique. This confirms that most of the API is detected via the presented GC-based method. Thereby, we demonstrated the practical feasibility of the risk assessment-based approach to ensure the validity of the qualitative data for a complex untargeted method.
当应用于受监管的环境中,如制药行业时,分析结果的可靠性是至关重要且不可或缺的。因此,必须对分析工作流程进行验证。然而,验证指南通常是为定量靶向分析而设计的,很少适用于定性非靶向方法。在本研究中,我们采用风险评估方法来识别可能影响通过在线衍生化-全面二维气相色谱与高分辨率飞行时间质谱联用(GC×GC-HR-ToF-MS)分析活性药物成分(API)磺酸钠(SBS)所得定性结果的关键参数。为了展示这种方法的复杂性和可行性,我们专注于研究三个潜在的风险因素:样品制备、挥发性和磺酸盐的热稳定性。通过应用样品制备方法和热重分析(TGA)对这些潜在风险因素进行单独评估,我们证明了在线衍生化方法具有高衍生化效率和重复性,并确认不存在衍生化诱导的副反应。此外,我们还展示了未完全衍生化的 API 潜在的热不稳定性。为了解决这些单独评估的局限性,我们应用了整体评估步骤,采用负电喷雾电离傅里叶变换离子回旋共振质谱(ESI(-) FT-ICR MS)作为正交技术。这证实了大多数 API 通过所提出的基于 GC 的方法进行检测。由此,我们证明了基于风险评估的方法对于确保复杂非靶向方法的定性数据有效性的实际可行性。