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Review of Chromatographic Methods Coupled with Modern Detection Techniques Applied in the Therapeutic Drugs Monitoring (TDM)

机译:附加与现代检测技术的色谱方法综述施用于治疗药物监测(TDM)

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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.
机译:治疗药物监测(TDM)是用于整合药代动力学和药效学知识的工具,以优化和个性化各种药物治疗。药物给药的优化可以改善治疗结果,减少毒性,降低发育耐药性的风险。为了充分实现TDM,需要准确,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,越来越多地使用较少的侵入性样品,例如干血斑或无侵袭性唾液样品。样品制备方法的选择,柱填料,流动相组合物和检测方法的类型是重要的,以确保准确的药物测量并避免来自基质效应和药物代谢物的干扰。由于其高选择性和灵敏度,大多数报道的方法使用液相色谱耦合,液相色谱法与串联质谱(LC-MS / MS)技术相偶联。当临床监测期望更简单和更具成本效益的方法时,也使用具有紫外检测(HPLC-UV)方法的高性能色谱。用荧光检测(HPLC-FLD)在具有和不具有衍生化方法和具有电化学检测(HPLC-ED)的高性能色谱的高性能色谱(HPLC-ED)技术用于分析TDM的生物样品中的各种药物的高性能色谱(HPLC-ED)技术的应用已经较少描述。在色谱分析之前,通过蛋白质沉淀,液 - 液萃取和固相萃取,通过填充吸附剂,分散液 - 液微萃取来预处理样品。本文的目的是审查最近的文献(2010-2020),了解使用各种检测技术的液相色谱法为TDM。

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