Faculdade de Ciências da Universidade do Porto, Departamento de Química e Bioquímica, Centro de Investigação em Química, Linha 4, Rua do Campo Alegre 687, 4169-007 Porto, Portugal.
Anal Chem. 2013 Feb 5;85(3):1582-90. doi: 10.1021/ac3028245. Epub 2013 Jan 24.
In this work, the ion transfer mechanism of the anticancer drug daunorubicin (DNR) at a liquid/liquid interface has been studied for the first time. This study was carried out using electrochemical techniques, namely cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The lipophilicity of DNR was investigated at the water/1,6-dichlorohexane (DCH) interface, and the results obtained were presented in the form of an ionic partition diagram. The partition coefficients of both neutral and ionic forms of the drug were determined. The analytical parameter for the detection of DNR was also investigated in this work. An electrochemical DNR sensor is proposed by means of simple ion transfer at the water/DCH interface, using DPV as the quantification technique. Experimental conditions for the analytical determination of DNR were established, and a detection limit of 0.80 μM was obtained.
本工作首次研究了抗癌药物柔红霉素(DNR)在液/液界面的离子传递机制。这项研究是用电化学技术,即循环伏安法(CV)和差分脉冲伏安法(DPV)进行的。DNR 的亲脂性在水/1,6-二氯己烷(DCH)界面进行了研究,并以离子分配图的形式呈现了结果。测定了药物中性和离子形式的分配系数。本工作还研究了检测 DNR 的分析参数。通过在水/DCH 界面简单的离子转移,使用 DPV 作为定量技术,提出了电化学 DNR 传感器。建立了分析测定 DNR 的实验条件,得到了 0.80 μM 的检测限。