Department of Physical Chemistry, Medical University of Lublin, Chodźki 4a, 20-093 Lublin, Poland.
Department of Inorganic Chemistry, Medical University of Lublin, Chodźki 4a, 20-093 Lublin, Poland.
Molecules. 2020 Sep 3;25(17):4026. doi: 10.3390/molecules25174026.
Therapeutic drug monitoring (TDM) is a tool used to integrate pharmacokinetic and pharmacodynamics knowledge to optimize and personalize various drug therapies. The optimization of drug dosing may improve treatment outcomes, reduce toxicity, and reduce the risk of developing drug resistance. To adequately implement TDM, accurate and precise analytical procedures are required. In clinical practice, blood is the most commonly used matrix for TDM; however, less invasive samples, such as dried blood spots or non-invasive saliva samples, are increasingly being used. The choice of sample preparation method, type of column packing, mobile phase composition, and detection method is important to ensure accurate drug measurement and to avoid interference from matrix effects and drug metabolites. Most of the reported procedures used liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) techniques due to its high selectivity and sensitivity. High-performance chromatography with ultraviolet detection (HPLC-UV) methods are also used when a simpler and more cost-effective methodology is desired for clinical monitoring. The application of high-performance chromatography with fluorescence detection (HPLC-FLD) with and without derivatization processes and high-performance chromatography with electrochemical detection (HPLC-ED) techniques for the analysis of various drugs in biological samples for TDM have been described less often. Before chromatographic analysis, samples were pretreated by various procedures-most often by protein precipitation, liquid-liquid extraction, and solid-phase extraction, rarely by microextraction by packed sorbent, dispersive liquid-liquid microextraction. The aim of this article is to review the recent literature (2010-2020) regarding the use of liquid chromatography with various detection techniques for TDM.
治疗药物监测(TDM)是一种用于整合药代动力学和药效动力学知识以优化和个性化各种药物治疗的工具。药物剂量的优化可以改善治疗效果,降低毒性,降低产生耐药性的风险。为了充分实施 TDM,需要准确和精确的分析程序。在临床实践中,血液是 TDM 最常用的基质;然而,越来越多地使用非侵入性样本,如干血斑或非侵入性唾液样本。选择样品制备方法、色谱柱填充类型、流动相组成和检测方法对于确保药物的准确测量和避免基质效应和药物代谢物的干扰很重要。由于其高选择性和灵敏度,大多数报道的程序都使用液相色谱与串联质谱(LC-MS/MS)技术。当需要更简单、更具成本效益的方法进行临床监测时,也使用带有紫外检测的高效液相色谱(HPLC-UV)方法。已经描述了带有和不带有衍生化过程的高效液相色谱与荧光检测(HPLC-FLD)和高效液相色谱与电化学检测(HPLC-ED)技术在生物样品中分析各种药物用于 TDM 的应用较少。在色谱分析之前,样品通过各种程序进行预处理-最常见的是通过蛋白质沉淀、液液萃取和固相萃取,很少通过填充吸附剂的微萃取、分散液液微萃取。本文的目的是回顾 2010 年至 2020 年期间关于使用各种检测技术的液相色谱进行 TDM 的最新文献。