Department of Analytical Chemistry, Chemistry Institute, Universidade Federal Fluminense (UFF), 24020-150 Niterói, RJ, Brazil.
Talanta. 2010 Nov 15;83(1):256-61. doi: 10.1016/j.talanta.2010.09.017. Epub 2010 Sep 21.
Laser-excited fluorescence was used for the selective determination of camptothecin in samples containing anti-cancer camptothecin-analogs (irinotecan and topotecan). The selectivity of the method was based on the UV photochemical derivatization in basic solution which increased the analyte fluorescence (337/450 nm) and eliminated fluorescence from the two campthotecin-analogs. The influence of UV exposure time and sodium hydroxide concentration was studied using an experimental design. Limit of detection was 4 × 10(-10) mol L(-1) with linear fluorescence response up to 1 × 10(-6)mol L(-1). Average recoveries of camptothecin (added to the samples to simulate a contamination) were 92 ± 4 and 94 ± 6% (n=3) respectively in irinotecan and topotecan based pharmaceuticals.
激光激发荧光用于选择性测定含有抗癌喜树碱类似物(伊立替康和拓扑替康)的样品中的喜树碱。该方法的选择性基于在碱性溶液中的 UV 光化学反应衍生化,该反应增加了分析物的荧光(337/450nm)并消除了两种喜树碱类似物的荧光。使用实验设计研究了 UV 照射时间和氢氧化钠浓度的影响。检测限为 4×10(-10)mol L(-1),线性荧光响应高达 1×10(-6)mol L(-1)。在以伊立替康和拓扑替康为基础的药物中,模拟污染时加入喜树碱的平均回收率分别为 92±4%和 94±6%(n=3)。