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一种结合固相萃取和差分脉冲伏安法快速检测血浆样品中伊立替康的方法。

A fast method for the detection of irinotecan in plasma samples by combining solid phase extraction and differential pulse voltammetry.

机构信息

Department of Molecular Science and Nanosystems, Ca' Foscari University of Venice, Via Torino 155, Mestre-Venezia, 30172, Venice, Italy.

Clinical and Experimental Pharmacology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Via Franco Gallini 2, 33081, Aviano, Pordenone, Italy.

出版信息

Anal Bioanal Chem. 2020 Mar;412(7):1585-1595. doi: 10.1007/s00216-020-02386-1. Epub 2020 Jan 25.

DOI:10.1007/s00216-020-02386-1
PMID:31982924
Abstract

In this paper, a fast method for the detection of irinotecan (CPT-11) in plasma samples was investigated. CPT-11 is widely used in a number of chemotherapeutic treatments of several solid tumors. The method is based on the combination of a solid phase extraction and an electrochemical detection step. The extraction of CPT-11 from plasma was performed using solid phase extraction (SPE) columns and acetonitrile as eluent. The procedure included also a cleaning step to eliminate interference due to plasma endogenous compounds and the co-therapeutics 5-fluoroacil (5-FU) and folinic acid (FA). The latter are administered together with CPT-11 in the FOLFIRI regimen. The detection of CPT-11 was performed by differential pulse voltammetry at a glassy carbon electrode (GCE) in basified acetonitrile media. Under these conditions, a well-defined peak due to the oxidation of the tertiary ammine end of CPT-11, also free from interference due to main metabolites, was obtained. Calibration plots showed a good linear response with limit of detection and quantification of 1.10 × 10 and 3.74 × 10 M, respectively. The suitability of the method proposed here for clinical applications was verified by determining the concentration of CPT-11 in plasma samples of an oncological patient, collected after 30 and 180 min from the infusion of the drug. Graphical abstract.

摘要

本文研究了一种快速检测伊立替康(CPT-11)在血浆样品中的方法。CPT-11 广泛应用于多种实体肿瘤的多种化疗治疗中。该方法基于固相萃取和电化学检测步骤的结合。CPT-11 从血浆中的提取采用固相萃取(SPE)柱和乙腈作为洗脱液。该过程还包括一个清洗步骤,以消除由于血浆内源性化合物和共同治疗药物 5-氟尿嘧啶(5-FU)和甲酰四氢叶酸(FA)引起的干扰。后两者与 CPT-11 一起用于 FOLFIRI 方案中。CPT-11 的检测通过在碱性乙腈介质中的玻碳电极(GCE)进行差分脉冲伏安法进行。在这些条件下,获得了由于 CPT-11 的叔胺末端的氧化而产生的定义良好的峰,并且也没有主要代谢物引起的干扰。校准曲线显示出良好的线性响应,检测限和定量限分别为 1.10×10 和 3.74×10 M。通过测定在药物输注后 30 和 180 分钟从患者采集的血浆样品中 CPT-11 的浓度,验证了该方法在临床应用中的适用性。

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