Integrated identification-quantification (ID-Quant) workflow utilizing UPLC-QTOF-MS for the therapeutic drug monitoring of multi-component antibiotics without pure standards: Validation using teicoplanin

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-04-28 DOI:10.1016/j.jchromb.2024.124132
Xiaoli Ma , Yutong Zou , Jian Zhong , Songlin Yu , Ling Qiu
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Abstract

The lack of individual pure standard has hampered the application of therapeutic drug monitoring (TDM) for multi-component antibiotics in clinical laboratories. Here, we aimed to develop an integrated identification-quantification (ID-Quant) workflow based on ultra-high-performance liquid chromatography coupled with quadrupole/time-of-flight mass spectrometry (UHPLC-QTOF-MS) to enable the comprehensive determination of all teicoplanin components without needing pure standards. The workflow comprises three steps. First, non-targeted MSE full scanning was used to detect and identify all potential ingredients. Then, characteristic product ions were selected to generate a quantitative time-of-flight multiple reaction monitoring (Tof-MRM) method. Finally, the constituent composition of teicoplanin injection was determined and utilized as an alternative reference standard to monitor the teicoplanin ingredients in human serum samples. As a result, nine teicoplanin analogs were identified from teicoplanin injection (Sanofi-Aventis, France). The overall performance of the Tof-MRM method was satisfactory in terms of linearity, precision, accuracy, and limits of detection. Utilizing the drug as standard, the individual concentrations for each component in patient serum were determined to be 0.120 µg/mL (A3-1), 0.020 µg/mL (N-1), 0.550 µg/mL (N-2), 0.730 µg/mL (A2-1), 4.26 µg/mL (A2-2,3), 4.79 µg/mL (A2-4,5), and 0.290 µg/mL (N-3), respectively. The distribution pattern of teicoplanin components was also discovered to differ from that in the drug injection. Overall, this integrated ID-Quant workflow based on UHPLC-QTOF-MS enables the robust quantitation of all teicoplanin analogs without the need for individual pure standard. This approach could help address the standard unavailability problem in the TDM of multi-component antibiotics.

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利用 UPLC-QTOF-MS 对无纯标准的多组分抗生素进行治疗药物监测的综合鉴定-定量(ID-Quant)工作流程:使用替考拉宁进行验证
由于缺乏单独的纯净标准,临床实验室在应用多组分抗生素治疗药物监测(TDM)时受到了阻碍。在此,我们旨在开发一种基于超高效液相色谱-四极杆/飞行时间质谱(UHPLC-QTOF-MS)的鉴定-定量(ID-Quant)一体化工作流程,无需纯标准品即可全面测定替考拉宁的所有成分。工作流程包括三个步骤。首先,使用非靶向 MSE 全扫描来检测和识别所有潜在成分。然后,选择特征产物离子,生成定量飞行时间多反应监测(Tof-MRM)方法。最后,确定了替考拉宁注射液的成分组成,并将其用作替代参考标准,以监测人血清样本中的替考拉宁成分。结果,从替考拉宁注射液(法国赛诺菲-安万特公司)中鉴定出了九种替考拉宁类似物。Tof-MRM 方法在线性、精密度、准确度和检出限方面的总体性能令人满意。以药物为标准,病人血清中各成分的浓度分别为 0.120 微克/毫升(A3-1)、0.020 微克/毫升(N-1)、0.550 微克/毫升(N-2)、0.730 微克/毫升(A2-1)、4.26 微克/毫升(A2-2,3)、4.79 微克/毫升(A2-4,5)和 0.290 微克/毫升(N-3)。此外,还发现替考拉宁成分的分布模式与药物注射液中的分布模式不同。总之,这种基于超高效液相色谱-QTOF-质谱的集成 ID-Quant 工作流程能够对所有替考拉宁类似物进行可靠的定量,而无需使用单独的纯标准品。这种方法有助于解决多组分抗生素 TDM 中标准品不可用的问题。
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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