†Department of Chemistry and Green-Nano Materials Research Center, Kyungpook National University, 80 Daehakro, Buk-gu, Daegu-city, 702-701, Republic of Korea.
‡Centro de Investigação em Química-UP, L4, Departamento de Química e Bioquímica da Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre, 687, 4169-007 Porto, Portugal.
Anal Chem. 2015 May 19;87(10):5356-62. doi: 10.1021/acs.analchem.5b00653. Epub 2015 May 1.
An amperometric ion sensor featuring a microhole supported water/organic gel interface was developed for the quantitative analysis of a water-soluble anticancer drug species, namely, topotecan, which has been used for ovarian and lung cancer treatments. Voltammetric responses associated with topotecan transfer across a polarized water/1,2-dichloroethane (1,2-DCE) interface were first investigated at different aqueous pH values to provide information on a topotecan partition diagram for understanding the lipophilicity of the topotecan drug species. The well-defined voltammetric characteristics for topotecan transfer in pH 4.0 buffer was then employed in conjunction with a microhole supported water/polyvinyl chloride-2-nitrophenyloctyl ether (PVC-NPOE) gel interface to develop a topotecan sensor. Current responses due to the direct transfer of topotecan molecules across the microhole interface increased linearly with respect to topotecan concentration when using cyclic voltammetry and differential pulse stripping voltammetry (DPSV). Improvements in sensitivity were obtained using DPSV and preconcentrating topotecan in the gel layer by holding the transferring potential at 1 V (vs Ag/AgCl) for 30 s followed by stripping of the drug. The topotecan drug sensor shows a low detectable concentration of 0.1 μM with a good selectivity over other anticancer drug molecules and interfering reagents. As a practical demonstration, the sensing platform was applied for the analysis of topotecan in a diluted serum sample. The results were also compared to those using high performance liquid chromatography (HPLC).
一种基于微孑 L 支撑的水/有机凝胶界面的安培型离子传感器,用于水溶性抗癌药物拓扑替康的定量分析。拓扑替康已用于卵巢癌和肺癌的治疗。在不同的水相 pH 值下,首先研究了与拓扑替康在极化水/1,2-二氯乙烷(1,2-DCE)界面之间传递相关的伏安响应,以提供拓扑替康分配图的信息,从而了解拓扑替康药物的亲脂性。然后,在 pH 4.0 缓冲液中,采用具有良好定义的拓扑替康转移伏安特性,结合微孑 L 支撑的水/聚氯乙烯-2-硝基苯辛醚(PVC-NPOE)凝胶界面,开发了一种拓扑替康传感器。使用循环伏安法和差分脉冲溶出伏安法(DPSV),由于拓扑替康分子直接通过微孑 L 界面传递,电流响应与拓扑替康浓度呈线性关系。使用 DPSV 并通过将转移电位保持在 1 V(相对于 Ag/AgCl)30 s 来浓缩凝胶层中的拓扑替康,然后对药物进行洗脱,从而提高了灵敏度。该拓扑替康药物传感器的检测下限低至 0.1 μM,对其他抗癌药物分子和干扰试剂具有良好的选择性。作为实际演示,该传感平台用于分析稀释血清样品中的拓扑替康。并将结果与高效液相色谱法(HPLC)的结果进行了比较。